Results for:
chemical Classification: Sulfur compounds

Sulfane

Compound Details

Synonymous names
hydrogen sulfide
sulfane
Hydrosulfuric acid
Dihydrogen monosulfide
Stink DAMP
Hydrogen sulphide
Dihydrogen sulfide
Sulfureted hydrogen
7783-06-4
Sewer gas
Hydrogene sulfure
Acide sulfhydrique
Schwefelwasserstoff
Netzschwefel
Zwavelwaterstof
Kolospray
Liquamat
Micowetsulf
Microflotox
Siarkowodor
Colsul
Crystex
Elosal
Hexasul
Kolofog
Kumulus
Sastid
Cosan
Hydrogen sulfide (H2S)
Polsulkol Extra
Hydrogen-sulfide
Idrogeno solforato
Corosul D and S
RC-Schwefel Extra
Hydrogen monosulfide
Kolloidschwefel 95
Sulfuretted hydrogen
Cosan 80
Hepatic acid
Hydrogene sulphure
Kolo 100
Acide sulphhydrique
RCRA waste number U135
Hydrogen sulfuric acid
dihydridosulfur
FEMA No. 3779
UN 1053
YY9FVM7NSN
CHEBI:16136
Hepatic gas
Hydrogen sulfure
H2S
dihydrogen(sulfide)
sulfure d'hydrogene
Sulfur-32S
HSDB 576
CHEBI:26833
UNII-YY9FVM7NSN
EINECS 231-977-3
NSC-403664
SULPHUR HYDROGENISATUM
DIHYDROGEN MONOSULPHIDE
DTXSID4024149
Collokit
Kristex
Microthiol
Shreesul
Kumulus FL
Sulfur-(32-S)
EC 231-977-3
Magnetic 6
Caswell No. 812
azufre
HYDROGEN SULFIDE (MART.)
HYDROGEN SULFIDE [MART.]
mercaptans
thiols
(SH2)
[SH2]
Proactiv
Transact
Schwefel, feinverteilter
Thiol
Sulfide, Hydrogen
Siarkowodor [Polish]
Hydrogen sulfide H2S
Magnetic 70, 90, and 95
HSDB 5166
Sulfur - S @ 0 microg/g in Heavy Mineral Oil
Sulfur - S @ 1.00 wt% in Heavy Mineral Oil
Sulfur Standard: S @ 10000 microg/mL in H2O
Sulfur Standard: S BLK (0 wt%) in Crude Oil
Zwavelwaterstof [Dutch]
Sulfur - S @ 500 microg/g in Heavy Mineral Oil
EINECS 231-722-6
NA1350
NA2448
UN1350
UN2448
Hydrogen sulfure [French]
RCRA waste no. U135
EPA Pesticide Chemical Code 077501
Hydrogene sulfure [French]
NSC 403664
Acide sulfhydrique [French]
monosulfane
Schwefelwasserstoff [German]
theion
Hydrosulfurate
Idrogeno solforato [Italian]
Acnaveen
Cuticura
Eskamel
Hepatate
Merkaptan
Schwefel
Acnil
Meted
Sulfur,sublimed
a thiol
Sulfur Standard: S @ 1000 microg/g (0.100 wt%) in Crude Oil
Sulfur Standard: S @ 10000 microg/g (1.00 wt%) in Crude Oil
Sulfur Standard: S @ 20000 microg/g (2.00 wt%) in Crude Oil
Sulfur Standard: S @ 2500 microg/g (0.250 wt%) in Crude Oil
Sulfur Standard: S @ 30000 microg/g (3.00 wt%) in Crude Oil
Sulfur Standard: S @ 40000 microg/g (4.00 wt%) in Crude Oil
Sulfur Standard: S @ 5000 microg/g (0.500 wt%) in Crude Oil
Sulfur Standard: S @ 50000 microg/g (5.00 wt%) in Crude Oil
Sulfur,colloidal
Sour gas
Sulfur, molten
37331-50-3
Colloidal sulphur
Dome-Acne
intracellular S0
Sulfur Standard: S @ 7500 microg/g (0.750 wt%) in 20 cSt Mineral Oil
Sulfur (Powder)
Sulfur, colloidal
Bensulfoid (TN)
Dihydrogen sulphide
Sulfur,precipitated
RSH
Sastid (TN)
UN1053
component of Bensulfoid
SULFUR DIHYDRIDE
Sour gas (Salt/Mix)
Sulfur (>80%)
Sulfur (>98%)
Magnetic 70, and 95
EC 231-722-6
SULPHURETTED HYDROGEN
HYDROGEN SULFIDE [MI]
SULFUR HYDRIDE (SH2)
DTXCID404149
Hydrogen sulfide, >=99.5%
HYDROGEN SULFIDE [FHFI]
HYDROGEN SULFIDE [HSDB]
CHEMBL1200739
CHEMBL2105487
NIOSH/MX1229000
CHEBI:29256
Sulfur Blank (0%) in Isooctane
PXQLVRUNWNTZOS-UHFFFAOYSA-N
DTXSID201029845
HYDROGEN SULFIDE, LIQUEFIED
HYDROGEN SULPHIDE, LIQUEFIED
Sulfur Blank (0 wt%) in Kerosene
Sulfur [NA1350] [Class 9]
BDBM50147625
BDBM50498447
NSC403664
Sulfur Blank (0 wt%) in Isooctane
SULPHUR HYDROGENISATUM [HPUS]
Hydrogen sulfide, purum, >=99.0%
AKOS015833648
AKOS015950634
Sulfur - S @15microg/g, 500 mL
Sulphur in Diesel, Low (7.2 mg/kg)
Sulfur [UN1350] [Flammable solid]
Sulfur Blank (0%) in Synthetic Diesel
Sulfur @ 7000microg/g in Residual Oil
BP-21056
Q682
Sulfur Blank (0%) in Heavy Mineral Oil
Sulfur Blank (0%) in Light Mineral Oil
Sulfur Blank (0%) in Odourless Kerosene
Sulfur, molten [NA2448] [Class 9]
Hydrogen sulfide [UN1053] [Poison gas]
Sulfur @ 0.0005% (5ppm) in Isooctane
Sulfur @ 0.001% (10ppm) in Isooctane
Sulfur @ 0.005% (50ppm) in Isooctane
Sulfur @ 0.01% (100ppm) in Isooctane
Sulfur @ 0.03% (300ppm) in Isooctane
Sulfur @ 0.05% (500ppm) in Isooctane
Sulfur @ 0.07% (700ppm) in Isooctane
Sulfur @ 0.1% (1000ppm) in Isooctane
Sulfur @ 0.3% (3000ppm) in Isooctane
Sulfur Blank (0 wt%) in #2 Diesel Fuel
MX12290000
NS00075432
PTP Sample for Sulfur in Isooctane Analysis
Sulfur - S @ 2.00 wt% in Heavy Mineral
Sulfur @ 0.0025% (25ppm) in Isooctane
Sulfur @ 0.025% (250ppm) in Isooctane
Sulfur @ 0.075% (750ppm) in Isooctane
Sulfur @ 0.25% (2500ppm) in Isooctane
Sulfur @ 10 microg/g, from Polysulfide Oil
U0149
Sulfur - S @ 2% in Residual Oil, 500mL
Sulfur, powder, 99.998% trace metals basis
C00087
C00283
D00024
F21255
Sulfur - S @ 0ug/g in Light Mineral, 1 gal
Sulfur - S @ 1% in Residual Oil, 1 Gallon
Sulfur - S @ 200microg/g in #2 Diesel fuel
Sulfur - S @ 4% in Residual Oil, 1 Gallon
Sulfur - S @ 400microg/g in #2 Diesel fuel
Sulfur - S @ 5% in Residual Oil, 1 Gallon
Sulfur @ 1% (10000ppm) in Synthetic Diesel
Sulfur @ 2% (20000ppm) in Synthetic Diesel
Sulfur @ 3% (30000ppm) in Synthetic Diesel
Sulfur @ 4% (40000ppm) in Synthetic Diesel
Sulfur @ 5% (50000ppm) in Synthetic Diesel
Sulfur Blank (0 wt%) in 20 cSt Mineral Oil
Sulfur Blank (0 wt%) in 75 cSt Mineral Oil
Sulfur, molten [UN2448] [Flammable solid]
di-n-butyl sulfide, S @ 22% nominally, 100g
Sulfur - S @ 2% in Resdidual Oil , 1 Gallon
Sulfur - S @ 3% in Residual Oil , 1 Gallon
Sulfur - S @ 3.00 wt% in Heavy Mineral Oil
Sulfur - S @ 4.00 wt% in Heavy Mineral Oil
Sulfur - S @ 400ug/g in #2 Diesel Fuel, L
Sulfur - S @ 5 microg/g in Heavy Mineral Oil
Sulfur - S @ 5.00 wt% in Heavy Mineral Oil
Sulfur @ 0.0005% (5ppm) in Synthetic Diesel
Sulfur @ 0.001% (10ppm) in Synthetic Diesel
Sulfur @ 0.005% (50ppm) in Synthetic Diesel
Sulfur @ 0.01% (100ppm) in Synthetic Diesel
Sulfur @ 0.03% (300ppm) in Synthetic Diesel
Sulfur @ 0.05% (500ppm) in Synthetic Diesel
Sulfur @ 0.07% (700ppm) in Synthetic Diesel
Sulfur @ 0.1% (1000ppm) in Synthetic Diesel
Sulfur @ 0.3% (3000ppm) in Synthetic Diesel
Sulfur @ 0.5% (5000ppm) in Synthetic Diesel
Sulfur @ 1% (10000ppm) in Odourless Kerosene
Sulfur @ 2% (20000ppm) in Odourless Kerosene
Sulfur @ 3% (30000ppm) in Odourless Kerosene
Sulfur @ 4% (40000ppm) in Odourless Kerosene
Sulfur @ 5% (50000ppm) in Odourless Kerosene
Sulfur in Residual Oil @ 10,000microg/g, 1L
Sulfur in Residual Oil @ 20,000microg/g, 1L
Sulfur in Residual Oil @ 30,000microg/g, 1L
Sulfur in Residual Oil @ 40,000microg/g, 1L
Sulfur in Residual Oil @ 50,000microg/g, 1L
Sulfur Standard: S @ 250microg/g in Isooctane
A857440
PTP Sample for Sulfur in #2 Diesel Fuel Analysis
PTP Sample for Sulfur in B100 Biodiesel Analysis
Q170591
Sulfur - S @ 0.300 wt% in Heavy Mineral Oil
Sulfur - S @ 0.500 wt% in Heavy Mineral Oil
Sulfur - S @ 0.750 wt% in Heavy Mineral Oil
Sulfur - S @ 0ug/g in #2 Diesel Fuel, 500mL
Sulfur - S @ 10 microg/g in Heavy Mineral Oil
Sulfur - S @ 100microg/g in Heavy Mineral Oil
Sulfur - S @ 1500microg/g in Heavy Mineral Oil
Sulfur - S @ 20 microg/g in Heavy Mineral Oil
Sulfur - S @ 200 microg/g in Heavy Mineral Oil
Sulfur - S @ 25 microg/g in Heavy Mineral Oil
Sulfur - S @ 2wt% in #2 Diesel Fuel, 1 Liter
Sulfur - S @ 3.00wt% in #2 Diesel, 500mL
Sulfur - S @ 3.00wt% in Residual Oil, 500mL
Sulfur - S @ 300 microg/g in Heavy Mineral Oil
Sulfur - S @ 4.00wt% in Residual Oil, 500mL
Sulfur - S @ 5.00wt% in Residual Oil, 500mL
Sulfur - S @ 50 microg/g in Heavy Mineral Oil
Sulfur - S @ 5ug/g in #2 Diesel Fuel, 1 Gal
Sulfur - S @ 5ug/g in #2 Diesel Fuel, 500mL
Sulfur - S @ 750 microg/g in Heavy Mineral Oil
Sulfur @ 0.0005% (5ppm) in Heavy Mineral Oil
Sulfur @ 0.0005% (5ppm) in Light Mineral Oil
Sulfur @ 0.0005% (5ppm) in Odourless Kerosene
Sulfur @ 0.001% (10ppm) in Heavy Mineral Oil
Sulfur @ 0.001% (10ppm) in Light Mineral Oil
Sulfur @ 0.001% (10ppm) in Odourless Kerosene
Sulfur @ 0.0025% (25ppm) in Synthetic Diesel
Sulfur @ 0.005% (50ppm) in Heavy Mineral Oil
Sulfur @ 0.005% (50ppm) in Light Mineral Oil
Sulfur @ 0.005% (50ppm) in Odourless Kerosene
Sulfur @ 0.01% (100ppm) in Heavy Mineral Oil
Sulfur @ 0.01% (100ppm) in Light Mineral Oil
Sulfur @ 0.01% (100ppm) in Odourless Kerosene
Sulfur @ 0.025% (250ppm) in Synthetic Diesel
Sulfur @ 0.03% (300ppm) in Heavy Mineral Oil
Sulfur @ 0.03% (300ppm) in Light Mineral Oil
Sulfur @ 0.03% (300ppm) in Odourless Kerosene
Sulfur @ 0.05% (500ppm) in Heavy Mineral Oil
Sulfur @ 0.05% (500ppm) in Light Mineral Oil
Sulfur @ 0.05% (500ppm) in Odourless Kerosene
Sulfur @ 0.07% (700ppm) in Heavy Mineral Oil
Sulfur @ 0.07% (700ppm) in Light Mineral Oil
Sulfur @ 0.07% (700ppm) in Odourless Kerosene
Sulfur @ 0.075% (750ppm) in Synthetic Diesel
Sulfur @ 0.1% (1000ppm) in Heavy Mineral Oil
Sulfur @ 0.1% (1000ppm) in Light Mineral Oil
Sulfur @ 0.1% (1000ppm) in Odourless Kerosene
Sulfur @ 0.25% (2500ppm) in Synthetic Diesel
Sulfur @ 0.3% (3000ppm) in Heavy Mineral Oil
Sulfur @ 0.3% (3000ppm) in Light Mineral Oil
Sulfur @ 0.3% (3000ppm) in Odourless Kerosene
Sulfur @ 0.5% (5000ppm) in Heavy Mineral Oil
Sulfur @ 0.5% (5000ppm) in Light Mineral Oil
Sulfur @ 0.5% (5000ppm) in Odourless Kerosene
Sulfur @ 1% (10000ppm) in Heavy Mineral Oil
Sulfur @ 1% (10000ppm) in Light Mineral Oil
Sulfur @ 1.5% (15000ppm) in Synthetic Diesel
Sulfur @ 2% (20000ppm) in Heavy Mineral Oil
Sulfur @ 2% (20000ppm) in Light Mineral Oil
Sulfur @ 3% (30000ppm) in Heavy Mineral Oil
Sulfur @ 3% (30000ppm) in Light Mineral Oil
Sulfur @ 3500microg/g in Residual Oil, 100mL
Sulfur @ 4% (40000ppm) in Heavy Mineral Oil
Sulfur @ 4% (40000ppm) in Light Mineral Oil
Sulfur @ 5% (50000ppm) in Heavy Mineral Oil
Sulfur @ 5% (50000ppm) in Light Mineral Oil
Sulfur @ 7000microg/g in Residual Oil, 500mL
Sulfur Standard: S @ 250 microg/g in Isooctane
Q7636182
Sulfur - S @ 0ug/g in #2 Diesel Fuel, 1 gallon
Sulfur - S @ 0ug/g in Light Mineral Oil, 500mL
Sulfur - S @ 1.00wt% in Residual Oil, 500mL
Sulfur - S @ 1000 microg/g in Heavy Mineral Oil
Sulfur - S @ 10ug/g in #2 Diesel Fuel, 1 Gal
Sulfur - S @ 10ug/g in #2 Diesel Fuel, 500mL
Sulfur - S @ 15ug/g in #2 Diesel Fuel, 1 Gal
Sulfur - S @ 15ug/g in #2 Diesel Fuel, 500mL
Sulfur - S @ 20ug/g in #2 Diesel Fuel, 500mL
Sulfur - S @ 25ug/g in #2 Diesel Fuel, 1 Gal
Sulfur - S @ 25ug/g in #2 Diesel Fuel, 500mL
Sulfur - S @ 300ug/g in #2 Diesel Fuel, 50mL
Sulfur - S @ 5000microg/g in Residual Oil, 1L
Sulfur - S @ 500ug/g in #2 Diesel Fuel, 50mL
Sulfur - S @ 50ug/g in #2 Diesel Fuel, 500mL
Sulfur - S @ 5ug/g in Light Mineral Oil, 500mL
Sulfur - S @ 75ug/g in #2 Diesel Fuel, 500mL
Sulfur @ 0.0025% (25ppm) in Heavy Mineral Oil
Sulfur @ 0.0025% (25ppm) in Light Mineral Oil
Sulfur @ 0.0025% (25ppm) in Odourless Kerosene
Sulfur @ 0.025% (250ppm) in Heavy Mineral Oil
Sulfur @ 0.025% (250ppm) in Light Mineral Oil
Sulfur @ 0.025% (250ppm) in Odourless Kerosene
Sulfur @ 0.075% (750ppm) in Heavy Mineral Oil
Sulfur @ 0.075% (750ppm) in Light Mineral Oil
Sulfur @ 0.075% (750ppm) in Odourless Kerosene
Sulfur @ 0.25% (2500ppm) in Heavy Mineral Oil
Sulfur @ 0.25% (2500ppm) in Light Mineral Oil
Sulfur @ 0.25% (2500ppm) in Odourless Kerosene
Sulfur @ 1.5% (15000ppm) in Heavy Mineral Oil
Sulfur @ 1.5% (15000ppm) in Light Mineral Oil
Sulfur @ 1.5% (15000ppm) in Odourless Kerosene
ASTM D5453 Curve 1, S @ 0.5-10ppm in p-xylene
ASTM D5453 Curve 2, S @ 5-100 ppm in isooctane
ASTM D5453 Curve 2, S @ 5-100 ppm in p-xylene
PTP Sample for Sulfur in 20 cSt Mineral Oil Analysis
Q60998679
Sulfur - S @ 400ug/g in #2 Diesel Fuel, 250mL
Sulfur - S @ 1.00wt% in #2 Diesel Fuel, 1 Gal
Sulfur - S @ 1.00wt% in #2 Diesel Fuel, 1 Liter
Sulfur - S @ 1.00wt% in #2 Diesel Fuel, 500mL
Sulfur - S @ 1.0wt% in Light Mineral Oil, 500mL
Sulfur - S @ 100ug/g in #2 Diesel Fuel, 500mL
Sulfur - S @ 100ug/g in Light Mineral Oil, 500mL
Sulfur - S @ 10ug/g in #2 Diesel Fuel, 1 Liter
Sulfur - S @ 10ug/g in Light Mineral Oil, 500mL
Sulfur - S @ 15ug/g in #2 Diesel Fuel, 1 Liter
Sulfur - S @ 15ug/g in Light Mineral Oil, 500mL
Sulfur - S @ 2.00wt% in #2 Diesel Fuel, 500mL
Sulfur - S @ 200ug/g in #2 Diesel Fuel, 500mL
Sulfur - S @ 200ug/g in Light Mineral Oil, 500mL
Sulfur - S @ 20microg/g in #2 Diesel Fuel, 1 Gal
Sulfur - S @ 20ug/g in Light Mineral Oil, 500mL
Sulfur - S @ 25ug/g in #2 Diesel Fuel, 1 Liter
Sulfur - S @ 25ug/g in Light Mineral Oil, 500mL
Sulfur - S @ 3,500ug/g in Residual Oil, 500mL
Sulfur - S @ 300ug/g in #2 Diesel Fuel, 500mL
Sulfur - S @ 4.00wt% in #2 Diesel Fuel, 500mL
Sulfur - S @ 400ug/g in #2 Diesel Fuel, 1 Gal
Sulfur - S @ 400ug/g in #2 Diesel Fuel, 500mL
Sulfur - S @ 5,000ug/g in Residual Oil, 1 Gallon
Sulfur - S @ 5.00wt% in #2 Diesel Fuel, 500mL
Sulfur - S @ 5000microg/g in #2 Diesel, 500mL
Sulfur - S @ 5000microg/g in Residual Oil, 500mL
Sulfur - S @ 500ug/g in #2 Diesel Fuel, 1 Gal
Sulfur - S @ 500ug/g in #2 Diesel Fuel, 500mL
Sulfur - S @ 500ug/g in Light Mineral Oil, 500mL
Sulfur - S @ 50ug/g in Light Mineral Oil, 500mL
Sulfur - S @ 750ug/g in #2 Diesel Fuel, 1 Gal
Sulfur - S @ 750ug/g in #2 Diesel Fuel, 1 Liter
Sulfur - S @ 750ug/g in #2 Diesel Fuel, 500mL
Sulfur - S @ 75microg/g in #2 Diesel Fuel, 1 Gal
Sulfur - S @ 75ug/g in Light Mineral Oil, 500mL
Sulfur - S @0.050wt% in #2 Diesel Fuel, 1 Liter
Sulfur - S @0.300wt% in #2 Diesel Fuel, 1 Liter
Sulfur - S @0.500wt% in #2 Diesel Fuel, 1 Liter
Sulfur @ 500microg/g in #2 Diesel Fuel, 1/2Gallon
Sulfur Calibration Set: S @ 0-100 mg/kg in Toluene
Sulfur Calibration Set: S @ 0-50 mg/kg in Toluene
Sulfur Standard: S @ 10 microg/g in B100 Biodiesel
Sulfur Standard: S @ 15 microg/g in B100 Biodiesel
Sulfur Standard: S @ 20 microg/g in B100 Biodiesel
Sulfur Standard: S @ 25 microg/g in B100 Biodiesel
Sulfur Standard: S @ 5 microg/g in B100 Biodiesel
Sulfur Standard: S @ 50 microg/g in B100 Biodiesel
Sulfur, S @ 3000 ug/g in #2 Diesel Fuel, 1 Gal
ASTM D5453 Curve 1, S @ 0.5 -10ppm in isooctane
ASTM D5453 Curve 1, S @ 0.5 -10ppm in Toluene
ASTM D5453 Curve 2, S @ 5 -100 ppm in Toluene
Sulfur - S @ 2.00wt% in Light Mineral Oil, 500mL
Sulfur - S @ 3.00wt% in Light Mineral Oil, 500mL
Sulfur - S @ 4.00wt% in Light Mineral Oil, 500mL
Sulfur - S @ 0.100wt% in #2 Diesel Fuel, 1 Liter
Sulfur - S @ 0.100wt% in #2 Diesel Fuel, 500mL
Sulfur - S @ 0.300wt% in #2 Diesel Fuel, 500mL
Sulfur - S @ 0.750wt% in #2 Diesel Fuel, 500mL
Sulfur - S @ 1,000ug/g in #2 Diesel Fuel, 1 Gal
Sulfur - S @ 1000ug/g in Light Mineral Oil, 500mL
Sulfur - S @ 200microg/g in #2 Diesel Fuel, 1 Gal
Sulfur - S @ 4000microg/g in 75 cSt Oil Heavy Oil
Sulfur - S @ 5,000ug/g in #2 Diesel Fuel, 1 Gal
Sulfur - S @ 5.00wt% in Light Mineral Oil, 500mL
Sulfur - S @ 5000ug/g in Light Mineral Oil, 500mL
Sulfur - S @ 5microg/g in 90% Isooctane/10% Ethanol
Sulfur - S @0.0100wt% in #2 Diesel Fuel, 1 Liter
Sulfur Calibration Set: S @ 0-100 mg/kg in Isooctane
Sulfur Standard: S @ 100 microg/g in B100 Biodiesel
Sulfur Standard: S @ 500 microg/g in B100 Biodiesel
ASTM D5453 Curve 3, S @ 100 -1000 ppm in Toluene
ASTM D5453 Curve 3, S @ 100-1000 ppm in isooctane
ASTM D5453 Curve 3, S @ 100-1000 ppm in p-xylene
Sulfur - S @ 0.150wt% S in #2 Diesel Fuel, 500mL
Sulfur - S @ 100microg/g in 90% Isooctane/10% Ethanol
Sulfur - S @ 10microg/g in 90% Isooctane/10% Ethanol
Sulfur - S @ 15microg/g in 90% Isooctane/10% Ethanol
Sulfur - S @ 20 microg/g in 90% Isooctane/10% Ethanol
Sulfur - S @ 200 microg/g in 90% Isooctane/10% Ethanol
Sulfur - S @ 250 microg/g in 90% Isooctane/10% Ethanol
Sulfur - S @ 25microg/g in 90% Isooctane/10% Ethanol
Sulfur - S @ 300 microg/g in 90% Isooctane/10% Ethanol
Sulfur - S @ 50microg/g in 90% Isooctane/10% Ethanol
Sulfur - S @ 75microg/g in 90% Isooctane/10% Ethanol
Sulfur - S @0.00050wt% in #2 Diesel Fuel, 1 Liter
F5FD384D-E823-4920-B313-6476A1F3F0C5
Polysulfide Oil Standard: 30,000 microg/g S in Mineral Oil
Polysulfide Oil Standard: 40,000 microg/g S in Mineral Oil
Sulfur - S @ 1500microg/g in Light Mineral Oil, 500mLs
Sulfur - S @ 3000microg/g in Light Mineral Oil, 500mLs
Sulfur - S @ 300microg/g in Light Mineral Oil, 500mLs
Sulfur - S @ 400microg/g in Light Mineral Oil, 500mLs
Sulfur - S @ 750microg/g in Light Mineral Oil, 500mLs
Sulfur - S @ 0 microg/g (blank) in #2 Diesel Fuel, 1 Liter
Sulfur Calibration Set: S @ 0-10 mg/Kg in Synthetic Diesel
Sulfur Calibration Set: S @ 0-25 mg/kg in Synthetic Diesel
Sulfur Standard: S @ 10 microg/g (0.0010 wt%) in Isooctane
Sulfur Standard: S @ 10 microg/g (0.0010 wt%) in Kerosene
Sulfur Standard: S @ 10 ug/g in 70% Isooctane/30% Toluene
Sulfur Standard: S @ 10 ug/g in 75% Isooctane/25% Toluene
Sulfur Standard: S @ 10 ug/g in 80% Isooctane/20% Toluene
Sulfur Standard: S @ 100 ug/g in 70% Isooctane/30% Toluene
Sulfur Standard: S @ 100 ug/g in 75% Isooctane/25% Toluene
Sulfur Standard: S @ 100 ug/g in 80% Isooctane/20% Toluene
Sulfur Standard: S @ 15 microg/g (0.0015 wt%) in Isooctane
Sulfur Standard: S @ 15 ug/g in 70% Isooctane/30% Toluene
Sulfur Standard: S @ 15 ug/g in 75% Isooctane/25% Toluene
Sulfur Standard: S @ 15 ug/g in 80% Isooctane/20% Toluene
Sulfur Standard: S @ 20 microg/g (0.0020 wt%) in Isooctane
Sulfur Standard: S @ 20 ug/g in 70% Isooctane/30% Toluene
Sulfur Standard: S @ 20 ug/g in 75% Isooctane/25% Toluene
Sulfur Standard: S @ 20 ug/g in 80% Isooctane/20% Toluene
Sulfur Standard: S @ 25 microg/g (0.0025 wt%) in Isooctane
Sulfur Standard: S @ 25 ug/g in 70% Isooctane/30% Toluene
Sulfur Standard: S @ 25 ug/g in 75% Isooctane/25% Toluene
Sulfur Standard: S @ 25 ug/g in 80% Isooctane/20% Toluene
Sulfur Standard: S @ 250 microg/g (0.0250 wt%) in Diesel
Sulfur Standard: S @ 250 ug/g in 80% Isooctane/20% Toluene
Sulfur Standard: S @ 2500 microg/g (0.2500 wt%) in Diesel
Sulfur Standard: S @ 5 microg/g (0.0005 wt%) in Isooctane
Sulfur Standard: S @ 5 microg/g (0.0005 wt%) in Kerosene
Sulfur Standard: S @ 5 ug/g in 70% Isooctane/30% Toluene
Sulfur Standard: S @ 5 ug/g in 75% Isooctane/25% Toluene
Sulfur Standard: S @ 5 ug/g in 80% Isooctane/20% Toluene
Sulfur Standard: S @ 50 microg/g (0.0050 wt%) in Isooctane
Sulfur Standard: S @ 50 microg/g (0.0050 wt%) in Kerosene
Sulfur Standard: S @ 50 ug/g in 70% Isooctane/30% Toluene
Sulfur Standard: S @ 50 ug/g in 75% Isooctane/25% Toluene
Sulfur Standard: S @ 50 ug/g in 80% Isooctane/20% Toluene
Sulfur Standard: S @ 500 ug/g in 70% Isooctane/30% Toluene
Sulfur Standard: S @ 500 ug/g in 80% Isooctane/20% Toluene
Sulfur Standard: S @ 75 microg/g (0.0075 wt%) in Isooctane
Sulfur Standard: S @ 75 ug/g in 70% Isooctane/30% Toluene
Sulfur Standard: S @ 75 ug/g in 80% Isooctane/20% Toluene
IP 336, Sulfur Set D in Heavy Mineral Oil: S @ 2, 3, 4, 5 %
IP 336, Sulfur Set D in Light Mineral Oil: S @ 2, 3, 4, 5 %
IP 336, Sulfur Set D in Odourless Kerosene: S @ 2, 3, 4, 5 %
IP 336, Sulfur Set D in Synthetic Diesel: S @ 2, 3, 4, 5 %
Polysulfide Oil Standard: 100 microg/g S in 13 cSt Mineral Oil
Polysulfide Oil Standard: 15 microg/g S in 13 cSt Mineral Oil
Polysulfide Oil Standard: 20,000 microg/g S in 13 cSt Mineral Oil
Polysulfide Oil Standard: 250 microg/g S in 13 cSt Mineral Oil
Polysulfide Oil Standard: 300 microg/g S in 13 cSt Mineral Oil
Polysulfide Oil Standard: 50 microg/g S in 13 cSt Mineral Oil
Polysulfide Oil Standard: 5000 microg/g S in 13 cSt Mineral Oil
Polysulfide Oil Standard: 750 microg/g S in 13 cSt Mineral Oil
Polysulfide Oil Standard: S @ 1500 microg/g in 13 cSt Mineral Oil
Polysulfide Oil Standard: S @ 20 microg/g in 13 cSt Mineral Oil
Polysulfide Oil Standard: S @ 200 microg/g in 13 cSt Mineral Oil
Polysulfide Oil Standard: S @ 25 microg/g in 13 cSt Mineral Oil
Polysulfide Oil Standard: S @ 3000 microg/g in 13 cSt Mineral Oil
Polysulfide Oil Standard: S @ 400 microg/g in 13 cSt Mineral Oil
Polysulfide Oil Standard: S @ 75 microg/g in 13 cSt Mineral Oil
Sulfur Calibration Set: S @ 25-1000 mg/Kg in Synthetic Diesel
Sulfur Standard: S @ 100 microg/g (0.0100 wt%) in Isooctane
Sulfur Standard: S @ 100 microg/g (0.0100 wt%) in Kerosene
Sulfur Standard: S @ 1000 microg/g (0.100 wt%) in Isooctane
Sulfur Standard: S @ 1000 microg/g (0.100 wt%) in Kerosene
Sulfur Standard: S @ 1000 ug/g in 70% Isooctane/30% Toluene
Sulfur Standard: S @ 10000 microg/g (1.00 wt%) in Residual Oil
Sulfur Standard: S @ 200 microg/g (0.0200 wt%) in Isooctane
Sulfur Standard: S @ 20000 microg/g (2.00 wt%) in Residual Oil
Sulfur Standard: S @ 250 microg/g (0.0250 wt%) in Kerosene
Sulfur Standard: S @ 300 microg/g (0.0300 wt%) in Isooctane
Sulfur Standard: S @ 300 microg/g (0.0300 wt%) in Kerosene
Sulfur Standard: S @ 3000 microg/g (0.300 wt%) in Isooctane
Sulfur Standard: S @ 3000 microg/g (0.300 wt%) in Kerosene
Sulfur Standard: S @ 30000 microg/g (3.00 wt%) in Residual Oil
Sulfur Standard: S @ 400 microg/g (0.0400 wt%) in Isooctane
Sulfur Standard: S @ 40000 microg/g (4.00 wt%) in Residual Oil
Sulfur Standard: S @ 5 microg/g (0.0005 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 500 microg/g (0.0500 wt%) in Isooctane
Sulfur Standard: S @ 500 microg/g (0.0500 wt%) in Kerosene
Sulfur Standard: S @ 5000 microg/g (0.500 wt%) in Residual Oil
Sulfur Standard: S @ 50000 microg/g (5.00 wt%) in Residual Oil
Sulfur Standard: S @ 750 microg/g (0.0750 wt%) in Isooctane
Sulfur Standard: S @ 750 microg/g (0.0750 wt%) in Kerosene
Total Sulfur by UV Fluorescence Set for ASTM D5453 - in toluene
Total Sulfur by UV Fluorescence Set for ASTM D5453 -in toluene
ASTM D2622, Sulfur Set C in Heavy Mineral Oil: S @ 1, 2, 3, 4, 5 %
ASTM D2622, Sulfur Set C in Light Mineral Oil: S @ 1, 2, 3, 4, 5 %
ASTM D2622, Sulfur Set C in Odourless Kerosene: S @ 1, 2, 3, 4, 5 %
ASTM D2622, Sulfur Set C in Synthetic Diesel: S @ 1, 2, 3, 4, 5 %
ASTM D4294, Sulfur Set C in Heavy Mineral Oil: S @ 1, 2, 3, 4, 5 %
ASTM D4294, Sulfur Set C in Light Mineral Oil: S @ 1, 2, 3, 4, 5 %
ASTM D4294, Sulfur Set C in Odourless Kerosene: S @ 1, 2, 3, 4, 5 %
ASTM D4294, Sulfur Set C in Synthetic Diesel: S @ 1, 2, 3, 4, 5 %
ASTM D5453 Curve 1, S @ 0.5 -10ppm in 75% Isooctane/25% Toluene
ASTM D5453 Curve 2, S @ 5 -100 ppm in 75% Isooctane/25% Toluene
ASTM D5453 Curve 3, S @ 100 -1000 ppm in 75% Isooctane/25% Toluene
IP 336, Sulfur Set C in Heavy Mineral Oil: S @ 0.5, 1, 1.5, 2 %
IP 336, Sulfur Set C in Light Mineral Oil: S @ 0.5, 1, 1.5, 2 %
IP 336, Sulfur Set C in Odourless Kerosene: S @ 0.5, 1, 1.5, 2 %
IP 336, Sulfur Set C in Synthetic Diesel: S @ 0.5, 1, 1.5, 2 %
Mercaptan Sulphur in Hydrocarbons, Jet Aviation Fuel (Nominal: 15.2 mg/kg)
Sulfur Standard: S @ 10 microg/g (0.0010 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 10 microg/g (0.0010 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 10 microg/g (0.0010 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 100 microg/g (0.0100 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 100 microg/g (0.0100 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 100 microg/g (0.0100 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 1000 microg/g (0.100 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 1000 microg/g (0.100 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 1000 microg/g (0.100 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 1000 ug/g (0.1 wt%) in 80% Isooctane/20% Toluene
Sulfur Standard: S @ 10000 microg/g (1.00 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 10000 microg/g (1.00 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 10000 microg/g (1.00 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 15 microg/g (0.0015 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 15 microg/g (0.0015 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 15 microg/g (0.0015 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 1500 microg/g (0.150 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 1500 microg/g (0.150 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 1500 microg/g (0.150 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 20 microg/g (0.0020 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 20 microg/g (0.0020 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 20 microg/g (0.0020 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 200 microg/g (0.0200 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 200 microg/g (0.0200 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 200 microg/g (0.0200 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 20000 microg/g (2.00 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 20000 microg/g (2.00 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 20000 microg/g (2.00 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 25 microg/g (0.0025 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 25 microg/g (0.0025 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 25 microg/g (0.0025 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 250 microg/g (0.0250 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 250 microg/g (0.0250 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 250 microg/g in Isooctane (75%) & Toluene (25%)
Sulfur Standard: S @ 2500 microg/g (0.2500 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 2500 microg/g (0.2500 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 250microg/g in Isooctane (70%) and Toluene (30%)
Sulfur Standard: S @ 300 microg/g (0.0300 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 300 microg/g (0.0300 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 300 microg/g (0.0300 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 3000 microg/g (0.300 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 3000 microg/g (0.300 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 3000 microg/g (0.300 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 30000 microg/g (3.00 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 30000 microg/g (3.00 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 30000 microg/g (3.00 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 400 microg/g (0.0400 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 400 microg/g (0.0400 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 400 microg/g (0.0400 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 40000 microg/g (4.00 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 40000 microg/g (4.00 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 40000 microg/g (4.00 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 5 microg/g (0.0005 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 5 microg/g (0.0005 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 50 microg/g (0.0050 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 50 microg/g (0.0050 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 50 microg/g (0.0050 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 500 microg/g (0.0500 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 500 microg/g (0.0500 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 500 microg/g (0.0500 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 5000 microg/g (0.500 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 5000 microg/g (0.500 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 5000 microg/g (0.500 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 50000 microg/g (5.00 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 50000 microg/g (5.00 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 50000 microg/g (5.00 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 7 microg/g (0.0007 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 700 microg/g (0.0700 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 700 microg/g (0.0700 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 75 microg/g (0.0075 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 75 microg/g (0.0075 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 75 microg/g (0.0075 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 750 microg/g (0.0750 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 750 microg/g (0.0750 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 750 microg/g (0.0750 wt%) in 75 cSt Mineral Oil
Sulfur Standard: S @ 7500 microg/g (0.750 wt%) in #2 Diesel Fuel
Sulfur Standard: S @ 7500 microg/g (0.750 wt%) in 75 cSt Mineral Oil
"ASTM D4294, Sulfur Set B in Diesel: S @ 1000, 2500, 5000, 10000 microg/g"
"ASTM D7220, Sulfur Set A in Diesel: S @ 0, 5, 10, 25, 50 microg/g"
"ASTM D7220, Sulfur Set A in Light Oil (20 cSt): S @ 0, 5, 10, 25, 50 microg/g"
"IP 336, Sulfur Set B in Light Oil (20 cSt): S @ 0, 1000, 3000, 5000 microg/g"
ASTM D2622, Sulfur Set B in Heavy Mineral Oil: S @ 0.1, 0.25, 0.5, 1 %
ASTM D2622, Sulfur Set B in Light Mineral Oil: S @ 0.1, 0.25, 0.5, 1 %
ASTM D2622, Sulfur Set B in Odourless Kerosene: S @ 0.1, 0.25, 0.5, 1 %
ASTM D2622, Sulfur Set B in Synthetic Diesel: S @ 0.1, 0.25, 0.5, 1 %
ASTM D4294, Sulfur Set B in Heavy Mineral Oil: S @ 0.1, 0.25, 0.5, 1 %
ASTM D4294, Sulfur Set B in Light Mineral Oil: S @ 0.1, 0.25, 0.5, 1 %
ASTM D4294, Sulfur Set B in Odourless Kerosene: S @ 0.1, 0.25, 0.5, 1 %
ASTM D4294, Sulfur Set B in Synthetic Diesel: S @ 0.1, 0.25, 0.5, 1 %
IP 336, Sulfur Set A in Heavy Mineral Oil: S @ Blank, 0.03, 0.05, 0.07, 0.1 %
IP 336, Sulfur Set A in Light Mineral Oil: S @ Blank, 0.03, 0.05, 0.07, 0.1 %
IP 336, Sulfur Set A in Odourless Kerosene: S @ Blank, 0.03, 0.05, 0.07, 0.1 %
IP 336, Sulfur Set A in Synthetic Diesel: S @ Blank, 0.03, 0.05, 0.07, 0.1 %
IP 336, Sulfur Set B in Heavy Mineral Oil: S @ Blank, 0.1, 0.3, 0.5 %
IP 336, Sulfur Set B in Light Mineral Oil: S @ Blank, 0.1, 0.3, 0.5 %
IP 336, Sulfur Set B in Odourless Kerosene: S @ Blank, 0.1, 0.3, 0.5 %
IP 336, Sulfur Set B in Synthetic Diesel: S @ Blank, 0.1, 0.3, 0.5 %
IP 336, Sulfur Set F in Heavy Mineral Oil: S @ 0.5, 1, 1.5, 2, 3, 4, 5 %
IP 336, Sulfur Set F in Light Mineral Oil: S @ 0.5, 1, 1.5, 2, 3, 4, 5 %
IP 336, Sulfur Set F in Odourless Kerosene: S @ 0.5, 1, 1.5, 2, 3, 4, 5 %
IP 336, Sulfur Set F in Synthetic Diesel: S @ 0.5, 1, 1.5, 2, 3, 4, 5 %
Sulfur Set for ASTM D5453 - S @ 0, 1, 2.5, 5, 7.5, 10 ng/microL in toluene.
Sulfur Set for ASTM D5453 - S @ 0, 100, 250, 500, 750, 1000 ng/microL in Toluene
Sulfur Set for ASTM D5453: S @ 0, 1.0, 2.5, 5, 7.5, 10 ng/microL in Isooctane
Sulfur Set for ASTM D5453: S @ 0, 100, 250, 500, 750, 1000 ng/microL in Isooctane
Sulfur Set for ASTM D5453: S @ 0, 2.5, 5, 7.5, 15, 20 ng/microL in p-xylene
Sulfur Set for ASTM D5453: S @ 0, 5, 25, 50, 100, 200 ng/microL in Isooctane
Sulfur Standard: S @ 15000 microg/g (1.5000 wt%) in 20 cSt Mineral Oil
Sulfur Standard: S @ 15000 microg/g (1.5000 wt%) in 75 cSt Mineral Oil
"ASTM D2622, Sulfur Set A in Diesel: S @ 0, 5, 10, 100, 250, 500, 750, 1000 microg/g"
"ASTM D2622, Sulfur Set A in Heavy Oil (75 cSt): S @ 0, 5, 10, 100, 250, 500, 750, 1000 microg/g"
"ASTM D2622, Sulfur Set A in Light Oil (20 cSt): S @ 0, 5, 10, 100, 250, 500, 750, 1000 microg/g"
"ASTM D2622, Sulfur Set B in Heavy Oil (75 cSt): S @ 1000, 2500, 5000, 10000 microg/g"
"ASTM D2622, Sulfur Set B in Light Oil (20 cSt): S @ 1000, 2500, 5000, 10000 microg/g"
"ASTM D2622, Sulfur Set C in Diesel: S @ 10000, 20000, 30000, 40000, 50000 microg/g"
"ASTM D2622, Sulfur Set C in Heavy Oil (75 cSt): S @ 10000, 20000, 30000, 40000, 50000 microg/g"
"ASTM D2622, Sulfur Set C in Light Oil (20 cSt): S @ 10000, 20000, 30000, 40000, 50000 microg/g"
"ASTM D4294, Sulfur Set A in Diesel: S @ 0, 5, 10, 100, 250, 500, 750, 1000 microg/g"
"ASTM D4294, Sulfur Set A in Heavy Oil (75 cSt): S @ 0, 5, 10, 100, 250, 500, 750, 1000 microg/g"
"ASTM D4294, Sulfur Set A in Kerosene: S @ 0, 5, 10, 100, 250, 500, 750, 1000 microg/g"
"ASTM D4294, Sulfur Set A in Light Oil (20 cSt): S @ 0, 5, 10, 100, 250, 500, 750, 1000 microg/g"
"ASTM D4294, Sulfur Set B in Heavy Oil (75 cSt): S @ 1000, 2500, 5000, 10000 microg/g"
"ASTM D4294, Sulfur Set B in Light Oil (20 cSt): S @ 1000, 2500, 5000, 10000 microg/g"
"ASTM D4294, Sulfur Set C in Diesel: S @ 10000, 20000, 30000, 40000, 50000 microg/g"
"ASTM D4294, Sulfur Set C in Heavy Oil (75 cSt): S @ 10000, 20000, 30000, 40000, 50000 microg/g"
"ASTM D4294, Sulfur Set C in Light Oil (20 cSt): S @ 10000, 20000, 30000, 40000, 50000 microg/g"
"IP 336, Sulfur Set A in Light Oil (20 cSt): S @ 0, 300, 500, 700, 1000 microg/g"
"IP 336, Sulfur Set C in Light Oil (20 cSt): S @ 5000, 10000, 15000, 20000 microg/g"
"IP 336, Sulfur Set D in Light Oil (20 cSt): S @ 20000, 30000, 40000, 50000 microg/g"
"IP 336, Sulfur Set E in Heavy Oil (75 cSt): S @ 0, 300, 500, 700, 1000, 3000, 5000 microg/g"
"IP 336, Sulfur Set E in Light Oil (20 cSt): S @ 0, 300, 500, 700, 1000, 3000, 5000 microg/g"
"IP 336, Sulfur Set F in Heavy Oil (75 cSt): S @ 5000, 10000, 15000, 20000, 30000, 40000, 50000 microg/g"
"IP 336, Sulfur Set F in Light Oil (20 cSt): S @ 5000, 10000, 15000, 20000, 30000, 40000, 50000 microg/g"
ASTM D2622, Sulfur Set A in Heavy Mineral Oil: S @ Blank, 0.0005, 0.001, 0.01, 0.025, 0.05, 0.075, 0.1 %
ASTM D2622, Sulfur Set A in Light Mineral Oil: S @ Blank, 0.0005, 0.001, 0.01, 0.025, 0.05, 0.075, 0.1 %
ASTM D2622, Sulfur Set A in Odourless Kerosene: S @ Blank, 0.0005, 0.001, 0.01, 0.025, 0.05, 0.075, 0.1 %
ASTM D2622, Sulfur Set A in Synthetic Diesel: S @ Blank, 0.0005, 0.001, 0.01, 0.025, 0.05, 0.075, 0.1 %
ASTM D4294, Sulfur Set A in Heavy Mineral Oil: S @ Blank, 0.0005, 0.001, 0.01, 0.025, 0.05, 0.075, 0.1 %
ASTM D4294, Sulfur Set A in Light Mineral Oil: S @ Blank, 0.0005, 0.001, 0.01, 0.025, 0.05, 0.075, 0.1 %
ASTM D4294, Sulfur Set A in Odourless Kerosene: S @ Blank, 0.0005, 0.001, 0.01, 0.025, 0.05, 0.075, 0.1 %
ASTM D4294, Sulfur Set A in Synthetic Diesel: S @ Blank, 0.0005, 0.001, 0.01, 0.025, 0.05, 0.075, 0.1 %
ASTM D7039, Sulfur Set A in Heavy Mineral Oil: S @ Blank, 0.0005, 0.005, 0.025, 0.05 %
ASTM D7039, Sulfur Set A in Light Mineral Oil: S @ Blank, 0.0005, 0.005, 0.025, 0.05 %
ASTM D7039, Sulfur Set A in Odourless Kerosene: S @ Blank, 0.0005, 0.005, 0.025, 0.05 %
ASTM D7039, Sulfur Set A in Synthetic Diesel: S @ Blank, 0.0005, 0.005, 0.025, 0.05 %
ASTM D7039, Sulfur Set B in Heavy Mineral Oil: S @ Blank, 0.0025, 0.01, 0.05, 0.1, 0.3 %
ASTM D7039, Sulfur Set B in Light Mineral Oil: S @ Blank, 0.0025, 0.01, 0.05, 0.1, 0.3 %
ASTM D7039, Sulfur Set B in Odourless Kerosene: S @ Blank, 0.0025, 0.01, 0.05, 0.1, 0.3 %
ASTM D7039, Sulfur Set B in Synthetic Diesel: S @ Blank, 0.0025, 0.01, 0.05, 0.1, 0.3 %
ASTM D7220, Sulfur Set A in Heavy Mineral Oil: S @ Blank, 0.0005, 0.001, 0.0025, 0.005 %
ASTM D7220, Sulfur Set A in Light Mineral Oil: S @ Blank, 0.0005, 0.001, 0.0025, 0.005 %
ASTM D7220, Sulfur Set A in Odourless Kerosene: S @ Blank, 0.0005, 0.001, 0.0025, 0.005 %
ASTM D7220, Sulfur Set A in Synthetic Diesel: S @ Blank, 0.0005, 0.001, 0.0025, 0.005 %
ASTM D7220, Sulfur Set B in Heavy Mineral Oil: S @ 0.005, 0.01, 0.025, 0.05, 0.075, 0.1 %
ASTM D7220, Sulfur Set B in Light Mineral Oil: S @ 0.005, 0.01, 0.025, 0.05, 0.075, 0.1 %
ASTM D7220, Sulfur Set B in Odourless Kerosene: S @ 0.005, 0.01, 0.025, 0.05, 0.075, 0.1 %
ASTM D7220, Sulfur Set B in Synthetic Diesel: S @ 0.005, 0.01, 0.025, 0.05, 0.075, 0.1 %
IP 336, Sulfur Set E in Heavy Mineral Oil: S @ Blank, 0.03, 0.05, 0.07, 0.1, 0.3, 0.5 %
IP 336, Sulfur Set E in Light Mineral Oil: S @ Blank, 0.03, 0.05, 0.07, 0.1, 0.3, 0.5 %
IP 336, Sulfur Set E in Odourless Kerosene: S @ Blank, 0.03, 0.05, 0.07, 0.1, 0.3, 0.5 %
IP 336, Sulfur Set E in Synthetic Diesel: S @ Blank, 0.03, 0.05, 0.07, 0.1, 0.3, 0.5 %
IP 496, Sulfur Set A in Heavy Mineral Oil: S @ Blank, 0.01, 0.03, 0.05, 0.07, 0.1 %
IP 496, Sulfur Set A in Light Mineral Oil: S @ Blank, 0.01, 0.03, 0.05, 0.07, 0.1 %
IP 496, Sulfur Set A in Odourless Kerosene: S @ Blank, 0.01, 0.03, 0.05, 0.07, 0.1 %
IP 496, Sulfur Set A in Synthetic Diesel: S @ Blank, 0.01, 0.03, 0.05, 0.07, 0.1 %
IP 497, Sulfur Set A in Heavy Mineral Oil: S @ Blank, 0.005, 0.01, 0.025, 0.03, 0.05 %
IP 497, Sulfur Set A in Light Mineral Oil: S @ Blank, 0.005, 0.01, 0.025, 0.03, 0.05 %
IP 497, Sulfur Set A in Odourless Kerosene: S @ Blank, 0.005, 0.01, 0.025, 0.03, 0.05 %
IP 497, Sulfur Set A in Synthetic Diesel: S @ Blank, 0.005, 0.01, 0.025, 0.03, 0.05 %
Mercaptan Sulfur Set for UOP 163 and ASTM D3227: S @ 10 microg/g in 80% Isooctane/20% Toluene
Sulfur Set for ASTM D4045: S @ 0, 0.1, 0.5, 1.0, 2.5, 5.0, 10 microg/g in Isooctane
Total Sulfur by UV Fluorescence Set for ASTM D5453 - S @ 0, 1, 2.5, 5, 7.5, 10 ng/microL. Set of 6x2mL ampoules in toluene.
Microorganism:

Yes

IUPAC namesulfane
SMILESS
InchiInChI=1S/H2S/h1H2
FormulaH2S
PubChem ID402
Molweight34.08
LogP0.5
Atoms1
Bonds0
H-bond Acceptor1
H-bond Donor1
Chemical Classificationsulfur compounds thioethers sulfides
CHEBI-ID16136
Supernatural-IDSN0337276

mVOC Specific Details

Boiling Point
DegreeReference
-60.33 °C peer reviewed
Volatilization
The Henry's Law constant for hydrogen sulfide has been measured as 0.0098 atm-cu m/mole at 25 °C(1). This Henry's Law constant indicates that hydrogen sulfide is expected to volatilize rapidly from water surfaces(2). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(2) is estimated as 1.8 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as 2.3 days(SRC). Hydrogen sulfide is a weak base and has two pKa values of pKa1 = 7.04 and pKa2 = 11.96(3) which indicate some dissociation at environmental pHs(4). At pH 5-6, the water-air transfer rate was found to behave like an unreactive gas, but as the pH increases to pH10, the transfer rate was enhanced and nearly 200 times faster at pH10 than pH 5(4). Hydrogen sulfide's Henry's Law constant indicates that volatilization from moist soil surfaces will occur(SRC). Hydrogen sulfide is a gas at ambient temperatures(3) and expected to volatilize from dry soil surfaces(SRC); however, hydrogen sulfide gas can adsorb to both moist and dry soil surfaces(5) which may attenuate the rate of volatilization(SRC).
Soil Adsorption
Hydrogen sulfide gas was found to absorb rapidly to six different soil types(1). For example, when hydrogen sulfide gas was passed over six air-dried and moist (50% field capacity) soils, 15.4-65.2 mg/g and 11.0-65.2 mg/g of hydrogen sulfide rapidly adsorbed to the dry and moist soils, respectively(1). Neither the capacity or rate of sorption was correlated to soil pH, organic matter content, or clay content; sterile controls ruled out the involvement of microorganisms(1); it was suggested that adsorption to soil surfaces might be an environmental sink for gaseous hydrogen sulfide(1).

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaBurkholderia CepaciaNANAThorn et al. 2011
ProkaryotaBurkholderia CepaciaNANADryahina et al. 2016
ProkaryotaEnterococcus FaecalisNANAThorn et al. 2011
ProkaryotaEscherichia ColiNANAAllardyce et al. 2006
ProkaryotaEscherichia ColiNANAAllardyce et al. 2006
ProkaryotaEscherichia ColiNANAScotter et al. 2006
ProkaryotaEscherichia ColiNANAThorn et al. 2011
ProkaryotaNeisseria MeningitidisNANAScotter et al. 2006
ProkaryotaProteus MirabilisNANAThorn et al. 2011
ProkaryotaPseudomonas AeruginosaNANAAllardyce et al. 2006
ProkaryotaPseudomonas AeruginosaNANAAllardyce et al. 2006
ProkaryotaPseudomonas AeruginosaNANAThorn et al. 2011
ProkaryotaPseudomonas AeruginosaNANADryahina et al. 2016
ProkaryotaStaphylococcus AureusNANAAllardyce et al. 2006
ProkaryotaStaphylococcus AureusNANAAllardyce et al. 2006
ProkaryotaStaphylococcus AureusNANAThorn et al. 2011
ProkaryotaStaphylococcus AureusNANADryahina et al. 2016
ProkaryotaStenotrophomonas MaltophiliaNANADryahina et al. 2016
ProkaryotaStreptococcus PneumoniaeNANAAllardyce et al. 2006
ProkaryotaStreptococcus PneumoniaeNANAScotter et al. 2006
ProkaryotaMycobacterium BovisNANAMcNerney et al. 2012
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaBurkholderia CepaciaTYESIFT-MSno
ProkaryotaBurkholderia CepaciaMHBSIFT-MSno
ProkaryotaBurkholderia CepaciaBHISIFT-MSno
ProkaryotaBurkholderia CepaciaNBSIFT-MSno
ProkaryotaEnterococcus FaecalisTYESIFT-MSno
ProkaryotaEscherichia Colihuman bloodSIFT-MSno
ProkaryotaEscherichia ColiBacT/ALERT FASIFT-MSno
ProkaryotaEscherichia ColiTYESIFT-MSno
ProkaryotaNeisseria Meningitidishuman bloodSIFT-MSno
ProkaryotaProteus MirabilisTYESIFT-MSno
ProkaryotaPseudomonas Aeruginosahuman bloodSIFT-MSno
ProkaryotaPseudomonas AeruginosaBacT/ALERT FASIFT-MSno
ProkaryotaPseudomonas AeruginosaTYESIFT-MSno
ProkaryotaPseudomonas AeruginosaBHISIFT-MSno
ProkaryotaPseudomonas AeruginosaMHBSIFT-MSno
ProkaryotaPseudomonas AeruginosaNBSIFT-MSno
ProkaryotaStaphylococcus Aureushuman bloodSIFT-MSno
ProkaryotaStaphylococcus AureusBacT/ALERT FASIFT-MSno
ProkaryotaStaphylococcus AureusTYESIFT-MSno
ProkaryotaStaphylococcus AureusMHBSIFT-MSno
ProkaryotaStaphylococcus AureusNBSIFT-MSno
ProkaryotaStaphylococcus AureusBHISIFT-MSno
ProkaryotaStenotrophomonas MaltophiliaBHISIFT-MSno
ProkaryotaStenotrophomonas MaltophiliaMHBSIFT-MSno
ProkaryotaStenotrophomonas MaltophiliaNBSIFT-MSno
ProkaryotaStreptococcus Pneumoniaehuman bloodSIFT-MSno
ProkaryotaMycobacterium BovisLG + glycerolTD/GC-MS and SIFT-MSno


3-methylsulfanylpropanoic Acid

Mass-Spectra

Compound Details

Synonymous names
3-(Methylthio)propionic acid
646-01-5
3-methylthiopropionate
3-methylthiopropionic acid
3-(Methylthio)propanoic acid
4-Thiapentanoic acid
Propanoic acid, 3-(methylthio)-
3-methylsulfanylpropanoic acid
3-(Methylsulfanyl)propanoic acid
Propanoic acid 3-(methylthio)-
Propionic acid, 3-(methylthio)-
3-Methythiopropionic acid
3-methylthiopropanoic acid
3-methyl-thiopropionic acid
3-(Methythio)propionic acid
C4H8O2S
CHEBI:1438
F523ALI47D
3-Methylsulfanyl-Propionic Acid
3-(Methylmercapto)propionic Acid
3-(methyl-sulfanyl)-propanoic acid
3-(methylsulfanyl)propanoate
MFCD00059635
3-(methylthio)propanoate
UNII-F523ALI47D
3-methylsulfanylpropionic acid
4-Thiapentanoate
EINECS 211-460-9
3-METHYLTHIOPROPIONA
3(methylthio)propanoic acid
3-(Methylthio)propionicacid
SCHEMBL342851
CHEMBL116212
DTXSID70862354
3-(Methylsulfanyl)propanoic acid #
LMFA01130006
s6341
AKOS000202219
CS-6296
3-(METHYLMERCAPTO)PROPANOIC ACID
AS-10364
DA-69853
PD063944
HY-101401
M0811
NS00007379
EN300-16207
C08276
D87669
Q27105456
Z54719251
A8C
Microorganism:

Yes

IUPAC name3-methylsulfanylpropanoic acid
SMILESCSCCC(=O)O
InchiInChI=1S/C4H8O2S/c1-7-3-2-4(5)6/h2-3H2,1H3,(H,5,6)
FormulaC4H8O2S
PubChem ID563
Molweight120.17
LogP0.4
Atoms7
Bonds3
H-bond Acceptor3
H-bond Donor1
Chemical Classificationacids carboxylic acids sulfides thioethers sulfur compounds
CHEBI-ID1438
Supernatural-IDSN0040531

Species emitting the compound
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaStaphylococcus Xylosusn/an/ano
ProkaryotaOenococcus Oenin/an/ano
ProkaryotaLactobacillus Brevisn/an/ano
ProkaryotaLactobacillus Hilgardiin/an/ano
ProkaryotaLactobacillus Plantarumn/an/ano


Methylsulfinylmethane

Mass-Spectra

Compound Details

Synonymous names
dimethyl sulfoxide
DMSO
67-68-5
Methyl sulfoxide
Methylsulfinylmethane
Dimethylsulfoxide
Dimethyl sulphoxide
Methane, sulfinylbis-
Demasorb
Demsodrox
Demavet
Domoso
Infiltrina
Somipront
Dimexide
Dolicur
Dromisol
Durasorb
Syntexan
Deltan
Demeso
Hyadur
sulfinylbismethane
Dimethyl sulfur oxide
Doligur
Dipirartril-tropico
Gamasol 90
Sulfinylbis(methane)
Dermasorb
Kemsol
Dimethylsulphoxide
Rimso-50
Topsym
Dimethylsulfoxid
Dimethylsulfoxyde
SQ 9453
NSC-763
Rimso 50
Dimetil sulfoxido
Sulfinylbis-methane
Dimethyli sulfoxidum
Dimexidum
Caswell No. 381
(methylsulfinyl)methane
Dimetilsolfossido
(CH3)2SO
DMS-90
Sulfoxide, dimethyl
methanesulfinylmethane
A 10846
CCRIS 943
M 176
DMS 70
DMS 90
DMS-70
DTXSID2021735
NSC 763
Methyl sulphoxide
dimethyl-sulfoxide
S(O)Me2
EPA Pesticide Chemical Code 000177
SQ-9453
NSC763
YOW8V9698H
CHEBI:28262
AI3-26477
(methanesulfinyl)methane
MFCD00002089
(DMSO)
C2H6OS
CHEMBL504
Methane, 1,1'-sulfinylbis-
DTXCID401735
Dimethyl sulfoxide, HPLC Grade
METHYL-13C SULFOXIDE
Dimethylsulphinyl
Dimethyl sulfoxide, 99%
103759-08-6
Topsym (rescinded)
Rimso-5
Domoso (Veterinary)
DIMETHYL SULFOXIDE (II)
DIMETHYL SULFOXIDE [II]
methylsulfoxide
DIMETHYL SULFOXIDE (MART.)
DIMETHYL SULFOXIDE [MART.]
DIMETHYL SULFOXIDE (USP-RS)
DIMETHYL SULFOXIDE [USP-RS]
sulfinyldimethane
Dimetilsolfossido [DCIT]
Dimethyl sulpoxide
DIMETHYL SULFOXIDE (EP MONOGRAPH)
DIMETHYL SULFOXIDE [EP MONOGRAPH]
DIMETHYL SULFOXIDE (USP MONOGRAPH)
DIMETHYL SULFOXIDE [USP MONOGRAPH]
HSDB 80
Sulphoxide, Dimethyl
Dimethylsulfoxyde [INN-French]
Dimetil sulfoxido [INN-Spanish]
Dimethyli sulfoxidum [INN-Latin]
DMSO, sterile filtered
EINECS 200-664-3
UNII-YOW8V9698H
dimethysulfoxide
dimethlysulfoxide
dimethvlsulfoxide
dimethyisulfoxide
dimethylsulphoxid
Domoso Solution
dimethy sulfoxide
dimetyl sulfoxide
Domoso Gel
dimethyisulphoxide
dimethyl sulfoxyde
dimethyl-sulfoxyde
dimethyl suiphoxide
dimethyl-sulphoxide
dirnethyl sulfoxide
Dimethyl sulfoxixde
methylsulfmylmethane
DMSO (anydrous)
dimethyl sulf oxide
Dimethylis sulfoxidum
DIMEHTYLSULFOXYDE
Dimethyl sulfoxide [USAN:USP:INN:BAN]
Methyl sulfoxide (8CI)
Rimso-50 (TN)
dimethyl sulfoxide (dmso)
DMSO (Sterile-filtered)
DMSO [INCI]
DMSO (Dimethyl sulfoxide)
EC 200-664-3
H3C-SO-CH3
BIDD:PXR0182
Dimethyl sulfoxide, >=99%
Dimethyl sulfoxide, anhydrous
Dimethyl sulfoxide, for HPLC
Methane, sulfinylbis- (9CI)
WLN: OS1&1
DIMETHYL SULFOXIDE [MI]
DIMETHYL SULFOXIDE [INN]
DIMETHYL SULFOXIDE [JAN]
Dimethyl sulfoxide, >=99.5%
Dimethyl sulfoxide, PCR Reagent
DIMETHYL SULFOXIDE [HSDB]
DIMETHYL SULFOXIDE [USAN]
Dimethyl sulfoxide, ACS reagent
G04BX13
M02AX03
Methyl sulfoxide, >=99%, FG
Dimethyl sulfoxide, p.a., 99%
DIMETHYL SULFOXIDE [VANDF]
Dimethyl sulfoxide, LR, >=99%
Pharmakon1600-01506122
AMY14894
CS-B1637
Dimethyl sulfoxide (JAN/USP/INN)
DIMETHYL SULFOXIDE [WHO-DD]
HY-Y0320
METHYLSULFINYLMETHANE [FHFI]
Tox21_300957
BDBM50026472
HB3262
HB8591
NSC760436
STL264194
Dimethyl sulfoxide, AR, >=99.5%
AKOS000121107
CCG-213615
DB01093
DIMETHYL SULFOXIDE [GREEN BOOK]
Dimethyl sulfoxide, analytical standard
MCULE-2005841258
NSC-760436
CAS-67-68-5
DIMETHYL SULFOXIDE [ORANGE BOOK]
MRF-0000764
USEPA/OPP Pesticide Code: 000177
(methanesulfinyl)methanedimethyl sulfoxide
Dimethyl sulfoxide, for molecular biology
Dimethyl sulfoxide; AIF; CE0; MS2Dec
NCGC00163958-01
NCGC00163958-02
NCGC00163958-03
NCGC00254859-01
8070-53-9
Dimethyl sulfoxide, anhydrous, >=99.9%
Dimethyl sulfoxide, HPLC grade, 99.9%
Dimethyl Sulfoxide [for Spectrophotometry]
Dimethyl sulfoxide, for HPLC, >=99.5%
Dimethyl sulfoxide, for HPLC, >=99.7%
DS-015031
D0798
D1159
D5293
Dimethyl sulfoxide solution 50 wt.% in H2O
Dimethyl sulfoxide, ACS reagent, >=99.9%
Dimethyl sulfoxide, AldraSORB(TM), 99.8%
InChI=1/C2H6OS/c1-4(2)3/h1-2H
NS00001957
EN300-24544
D01043
Dimethyl sulfoxide, >=99.6%, ReagentPlus(R)
Dimethyl sulfoxide, ReagentPlus(R), >=99.5%
AB01563146_01
Dimethyl Sulfoxide (DMSO), cell culture reagent
Dimethyl sulfoxide, p.a., ACS reagent, 99.9%
Dimethyl sulfoxide, SAJ first grade, >=99.0%
Dimethyl sulfoxide, JIS special grade, >=99.0%
Dimethyl sulfoxide, Vetec(TM) reagent grade, 99%
Q407927
Dimethyl sulfoxide, UV HPLC spectroscopic, 99.9%
Dimethyl sulfoxide solution 50 wt.% in distilled H2O
Dimethyl sulfoxide, anhydrous, ZerO2(TM), >=99.9%
Dimethyl sulfoxide, meets EP, USP testing specifications
Z199055774
Dimethyl sulfoxide, ACS spectrophotometric grade, >=99.9%
Dimethyl sulfoxide, puriss. p.a., dried, <=0.02% water
4H-1,3-oxazine,2-cyclopentyl-5,6-dihydro-4,4,7-trimethyl-
Dimethyl sulfoxide, >=99.5% (GC), plant cell culture tested
Dimethyl sulfoxide, BioUltra, for molecular biology, >=99.5% (GC)
Dimethyl sulfoxide, European Pharmacopoeia (EP) Reference Standard
Dimethyl sulfoxide, puriss. p.a., ACS reagent, >=99.9% (GC)
Dimethyl sulfoxide, Vetec(TM) reagent grade, anhydrous, >=99.7%
Dimethyl sulfoxide, >=99.0%, suitable for absorption spectrum analysis
Dimethyl sulfoxide, United States Pharmacopeia (USP) Reference Standard
Dimethyl sulfoxide, for inorganic trace analysis, >=99.99995% (metals basis)
Dimethyl sulfoxide, meets EP testing specifications, meets USP testing specifications
Dimethyl sulfoxide, Hybri-Max(TM), sterile-filtered, BioReagent, suitable for hybridoma, >=99.7%
Dimethyl sulfoxide, puriss., absolute, over molecular sieve (H2O <=0.005%), >=99.5% (GC)
Dimethyl sulfoxide, sterile-filtered, BioPerformance Certified, meets EP, USP testing specifications, suitable for hybridoma
Microorganism:

Yes

IUPAC namemethylsulfinylmethane
SMILESCS(=O)C
InchiInChI=1S/C2H6OS/c1-4(2)3/h1-2H3
FormulaC2H6OS
PubChem ID679
Molweight78.14
LogP-0.6
Atoms4
Bonds0
H-bond Acceptor2
H-bond Donor0
Chemical Classificationsulfoxides sulfur compounds
CHEBI-ID28262
Supernatural-IDSN0140812

mVOC Specific Details

Boiling Point
DegreeReference
189 °C peer reviewed
Volatilization
The Henry's Law constant for dimethyl sulfoxide is 1.03X10-8 atm-cu m/mole at 25 deg C(SRC) based upon a measured air/water partition coefficient equation of 136,600-1570T where T is in deg C and the partition coefficient is in mol/kg-atm(1). This Henry's Law constant indicates that dimethyl sulfoxide is expected to be essentially nonvolatile from moist soil and water surfaces(2). The observation that the concentration of dimethyl sulfoxide in marine air is about 1/100 that of dimethyl sulfide suggests that little or no dimethyl sulfoxide is volatilizing from the sea surface(3). Dimethyl sulfoxide's Henry's Law constant indicates that volatilization from moist soil surfaces is not expected to be an important(SRC). Dimethyl sulfoxide is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure 0.60 mm Hg at 25 deg C(4).
Literature: (1) Watts SF, Brimblecombe P; Environ Technol Lett 8: 483-86 (1987) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Harvey GR, Lang RG; Geophys Res Let 13: 49-51 (1986) (4) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, DC: Taylor and Francis (2002)
Literature: #The volatilization rate of a pool of dimethyl sulfoxide was measured at 0 and -17.5 deg C(1). The flux was found to be proportional to the cube root of the wind speed. At a wind speed of 1 m/s, the volatilization rate was approximately 1.2 and 9 ug/min at -17.5 and 0 deg C, respectively. The calculated volatilization rate at zero wind velocity is 0.8 and 0.07 ug/min at 0 and -20 deg C, respectively(1). For volatilization of droplets, as opposed to a pool, surface affects (droplet spreading), would be important(SRC).
Literature: (1) Podoll RT, Parish HJ; Experimental Measurements of the Properties of Chemical Surety Materials Under Conditions of Extreme Cold. CREDC-CR-88051 AD B122 961 Aberdeen Proving Ground, MD: US Army CREDC (1988)
Soil Adsorption
Using a structure estimation method based on molecular connectivity indices(1), the Koc of dimethyl sulfoxide can be estimated to be 2(SRC). According to a classification scheme(2), this estimated Koc value suggests that dimethyl sulfoxide is expected to have very high mobility in soil.
Literature: (1) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.11. Nov, 2012. Available from, as of June 16, 2014: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (2) Swann RL et al; Res Rev 85: 17-28 (1983)
Vapor Pressure
PressureReference
0.60 mm Hg at 25 deg CDaubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, DC: Taylor and Francis (2002)
MS-Links
1D-NMR-Links
Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaTsukamurella Sp.nanaTyc et al. 2015
EukaryotaTuber Aestivumn/aAgricultural Centre of Castilla and León Community (Monasterio de la Santa Espina, Valladolid, Spain) and Navaleno (Soria, Spain).Diaz et al. 2003
EukaryotaTuber Melanosporumn/aAgricultural Centre of Castilla and León Community (Monasterio de la Santa Espina, Valladolid, Spain) and Navaleno (Soria, Spain).Diaz et al. 2003
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaTsukamurella Sp.Tryptic soy broth agarGC/MS-Q-TOFno
EukaryotaTuber Aestivumn/an/ano
EukaryotaTuber Melanosporumn/an/ano


Methanethiol

Mass-Spectra

Compound Details

Synonymous names
methanethiol
METHYL MERCAPTAN
Methylmercaptan
Mercaptomethane
74-93-1
Methyl sulfhydrate
Thiomethanol
Methanthiol
Thiomethyl alcohol
Metilmercaptano
Methvtiolo
Methylmercaptaan
Mercaptan methylique
Methaanthiol
Thiomethane
RCRA waste number U153
FEMA No. 2716
Methanethiole
CH3SH
methyl-mercaptan
Methyl thioalcohol
MeSH
UN 1064
2X8406WW9I
Methaanthiol [Dutch]
Methanthiol [German]
Methvtiolo [Italian]
Methylmercaptaan [Dutch]
Metilmercaptano [Italian]
Metilmercaptano [Spanish]
SCH 54292
Methyl mercaptan (natural)
Mercaptan methylique [French]
HSDB 813
EINECS 200-822-1
UN1064
RCRA waste no. U153
BRN 1696840
methylsulfanyl
methane thiol
methyl sulfides
methyl thiol
methyl-thiol
UNII-2X8406WW9I
(methyl)sulfane
Methylthioalcohol
a methyl thioether
sulfonium methylide
Methanethiol, purum
Methanethiol, 98.0%
METHANETHIOL [MI]
EC 200-822-1
Methanethiol, >=98.0%
4-01-00-01273 (Beilstein Handbook Reference)
METHYL MERCAPTAN [FHFI]
METHYL MERCAPTAN [HSDB]
DTXSID5026382
CHEBI:16007
CHEBI:86315
DTXSID10168842
DTXSID60992376
InChI=1/CH4S/c1-2/h2H,1H
NSC229573
AKOS009157032
NSC-229573
Methyl mercaptan [UN1064] [Poison gas]
NS00020025
C00409
Q409309
17719-48-1
Z22
Microorganism:

Yes

IUPAC namemethanethiol
SMILESCS
InchiInChI=1S/CH4S/c1-2/h2H,1H3
FormulaCH4S
PubChem ID878
Molweight48.11
LogP0.5
Atoms2
Bonds0
H-bond Acceptor1
H-bond Donor1
Chemical Classificationsulfur compounds thiols
CHEBI-ID16007
Supernatural-IDSN0213930

mVOC Specific Details

Boiling Point
DegreeReference
5.95 °C peer reviewed
Volatilization
The Henry's Law constant for methyl mercaptan is estimated as 0.0031 atm-cu m/mole(SRC) derived from its vapor pressure, 1,510 mm Hg(1), and water solubility, 15,400 mg/L(2). This Henry's Law constant indicates that methyl mercaptan is expected to volatilize rapidly from water surfaces(3). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(3) is estimated as 0.8 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(3) is estimated as 2.8 days(SRC). Methyl mercaptan's Henry's Law constant indicates that volatilization from moist soil surfaces is expected to occur(SRC). Methyl mercaptan is expected to volatilize rapidly from dry soil surfaces based upon its vapor pressure and because it is a gas a temperatures above 6 deg C(SRC). However, gaseous methyl mercaptan gas has been found to strongly adsorb to moist and dry soil surfaces suggesting that adsorption might be an environmental sink for methyl mercaptan(4). Therefore, the importance of volatilization from soil surfaces may be attenuated by adsorption(SRC).
Literature: (1) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, DC: Taylor and Francis (1989) (2) Hine J, Mookerjee PK; J Org Chem 40: 292-8 (1975) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (4) Smith KA et al; Soil Sci 116: 313-9 (1973)
Soil Adsorption
Using a structure estimation method based on molecular connectivity indices(1), the Koc of methyl mercaptan can be estimated to be 13(SRC). According to a classification scheme(2), this estimated Koc value suggests that methyl mercaptan is expected to have very high mobility in soil. Gaseous methyl mercaptan has been observed to partition to soils(3). For example, when gaseous methyl mercaptan was passed over six air-dried and moist (50% field capacity) soils, 2.4-32.1 mg/g and 2.2-21.4 mg/g of methyl mercaptan rapidly adsorbed to the dry and moist soils, respectively(3). Neither the capacity or rate of sorption was correlated to soil pH, organic matter content, or clay content; sterile controls ruled out the involvement of microorganisms(3); it was suggested that adsorption to soil surfaces might be an environmental sink for gaseous methyl mercaptan(3).
Literature: (1) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.1. Jan, 2011. Available from, as of July 19, 2012: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (2) Swann RL et al; Res Rev 85: 17-28 (1983) (3) Smith KA et al; Soil Sci 116: 313-9 (1973)
Vapor Pressure
PressureReference
1,510 mm Hg at 25 deg CDaubert, T.E., R.P. Danner. Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, D.C.: Taylor and Francis, 1989.
MS-Links
MS-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAspergillus FumigatusNANAChippendale et al. 2014
ProkaryotaEscherichia ColiNANADolch et al. 2012
ProkaryotaPseudomonas AeruginosaNANADolch et al. 2012
ProkaryotaBurkholderia CepaciaNANAThorn et al. 2011
ProkaryotaBurkholderia CepaciaNANADryahina et al. 2016
ProkaryotaEnterococcus FaecalisNANAThorn et al. 2011
ProkaryotaEscherichia ColiNANAAllardyce et al. 2006
ProkaryotaEscherichia ColiNANAAllardyce et al. 2006
ProkaryotaEscherichia ColiNANAScotter et al. 2006
ProkaryotaEscherichia ColiNANAThorn et al. 2011
ProkaryotaNeisseria MeningitidisNANAScotter et al. 2006
ProkaryotaProteus MirabilisNANAThorn et al. 2011
ProkaryotaPseudomonas AeruginosaNANACarroll et al. 2005
ProkaryotaPseudomonas AeruginosaNANAAllardyce et al. 2006
ProkaryotaPseudomonas AeruginosaNANAThorn et al. 2011
ProkaryotaPseudomonas AeruginosaNANADryahina et al. 2016
ProkaryotaStaphylococcus AureusNANAAllardyce et al. 2006
ProkaryotaStaphylococcus AureusNANAAllardyce et al. 2006
ProkaryotaStaphylococcus AureusNANAThorn et al. 2011
ProkaryotaStaphylococcus AureusNANADryahina et al. 2016
ProkaryotaStenotrophomonas MaltophiliaNANADryahina et al. 2016
ProkaryotaStreptococcus PneumoniaeNANAAllardyce et al. 2006
ProkaryotaStreptococcus PneumoniaeNANAScotter et al. 2006
ProkaryotaStreptococcus PyogenesNANAThorn et al. 2011
ProkaryotaHaemophilus InfluenzaeNANAFilipiak et al. 2012
ProkaryotaPseudomonas AeruginosaNANANA
ProkaryotaPseudomonas AeruginosaNANAFilipiak et al. 2012
ProkaryotaStaphylococcus AureusNANAFilipiak et al. 2012
ProkaryotaStreptococcus PneumoniaeNANAFilipiak et al. 2012
ProkaryotaKlebsiella PneumoniaeNARees et al. 2017
EukaryotaFusarium OxysporumonionWang et al. 2018
EukaryotaFusarium ProliferatumonionWang et al. 2018
ProkaryotaPseudomonas Fluorescens0Medicago spp. plant rhizospheresHernández-León et al. 2015
ProkaryotaPseudomonas Sp.antifungal activity against Thielaviopsis ethacetica mycelial growthBrazilian Biorenewables National Laboratory – LNBR/CNPEM Microorganism Collection, Campinas, SP; isolatedfrom soil and roots of highly productive sugarcane-producing regions; BrazilFreitas et al. 2022
ProkaryotaPaenibacillus PolymyxaNAMülner et al. 2021
EukaryotaCandida AlbicansATCC MYA-2876, American Type Culture CollectionCosta et al. 2020
EukaryotaCandida GlabrataATCC 90030, American Type Culture CollectionCosta et al. 2020
EukaryotaCandida TropicalisATCC 750, American Type Culture CollectionCosta et al. 2020
ProkaryotaBacillus AtrophaeusLeibnitz Institute DSMZ-German Collection of Microorganisms and Cell Cultures GmbHMülner et al. 2020
ProkaryotaBacillus AmyloliquefaciensLeibnitz Institute DSMZ-German Collection of Microorganisms and Cell Cultures GmbHMülner et al. 2020
ProkaryotaBacillus LicheniformisLeibnitz Institute DSMZ-German Collection of Microorganisms and Cell Cultures GmbHMülner et al. 2020
ProkaryotaBacillus PumilusLeibnitz Institute DSMZ-German Collection of Microorganisms and Cell Cultures GmbHMülner et al. 2020
EukaryotaTuber Magnatumcollected from natural truffle orchards in Istria (Croatia) during one truffle season (October 2018–January 2019)Niimi et al. 2021
EukaryotaTuber Magnatumcollected from natural truffle orchards in Baranya (Hungary) during one truffle season (October 2018–January 2019)Niimi et al. 2021
EukaryotaTuber Magnatumcollected from natural truffle orchards in Somogy (Hungary) during one truffle season (October 2018–January 2019)Niimi et al. 2021
EukaryotaTuber Magnatumcollected from natural truffle orchards in Abruzzo (Italy) during one truffle season (October 2018–January 2019)Niimi et al. 2021
EukaryotaTuber Magnatumcollected from natural truffle orchards in Kalubara (Serbia) during one truffle season (October 2018–January 2019)Niimi et al. 2021
EukaryotaTuber Magnatumcollected from natural truffle orchards in Srem (Serbia) during one truffle season (October 2018–January 2019)Niimi et al. 2021
ProkaryotaBacillus Amyloliquefaciensn/aNALee et al. 2012
ProkaryotaBacillus Subtilisn/aNALee et al. 2012
ProkaryotaPaenibacillus Polymyxan/aNALee et al. 2012
ProkaryotaAlpha Proteobacterian/aNASchulz and Dickschat 2007
ProkaryotaGamma Proteobacterian/aNASchulz and Dickschat 2007
ProkaryotaAlcaligenes Faecalisn/aNASchulz and Dickschat 2007
ProkaryotaDesulfovibrio Acrylicusn/aNASchulz and Dickschat 2007
ProkaryotaParasporobacterium Paucivoransn/aNASchulz and Dickschat 2007
ProkaryotaLactococcus Sp.n/aNASchulz and Dickschat 2007
ProkaryotaLactobacillus Sp.n/aNASchulz and Dickschat 2007
ProkaryotaLactobacillus Lactisn/aNASchulz and Dickschat 2007
ProkaryotaBrevibacterium Linensn/aNASchulz and Dickschat 2007
ProkaryotaOenococcus Oenin/aNASchulz and Dickschat 2007
ProkaryotaLactobacillus Brevisn/aNASchulz and Dickschat 2007
ProkaryotaLactobacillus Hilgardiin/aNASchulz and Dickschat 2007
ProkaryotaLactobacillus Plantarumn/aNASchulz and Dickschat 2007
ProkaryotaPorphyromonas Gingivalisn/aNASchulz and Dickschat 2007
ProkaryotaFusobacterium Nucleatumn/aNASchulz and Dickschat 2007
ProkaryotaTreponema Denticolan/aNASchulz and Dickschat 2007
ProkaryotaCitrobacter Freundiin/aNASchulz and Dickschat 2007
ProkaryotaEscherichia Colin/aNABunge et al. 2008
ProkaryotaShigella Flexnerin/aNABunge et al. 2008
ProkaryotaSalmonella Enterican/aNABunge et al. 2008
EukaryotaCandida Tropicalisn/aNABunge et al. 2008
EukaryotaTuber Magnatumn/aItalian geographical areas (Piedmont, Marche, Emilia Romagna, Border region area between Emilia Romagna and Marche)Gioacchini et al. 2008
ProkaryotaPseudomonas PutidananaSchöller et al. 1997
ProkaryotaPseudomonas TolaasiinanaLo Cantore et al. 2015
ProkaryotaPseudomonas Putidanarhizosphere of bean plants, southern ItalyGiorgio et al. 2015
ProkaryotaRalstonia SolanacearumnanaSpraker et al. 2014
ProkaryotaKlebsiella PneumoniaeNARees et al. 2016a
EukaryotaSchizophyllum Communen/aNAStotzky and Schenck 1976
ProkaryotaStreptococcus PneumoniaeclinicPreti et al. 2009
ProkaryotaPseudomonas Perolensnasterile fish muscle (Sebastes melanops)Miller et al. 1973
ProkaryotaAchromobacter Sp.NANAAlmeida et al. 2022
ProkaryotaSerratia Sp.NANAAlmeida et al. 2022
ProkaryotaEnterobacter Sp.NANAAlmeida et al. 2022
ProkaryotaEscherichia ColiNANAAlmeida et al. 2022
ProkaryotaPeribacillus Sp.NANAToral et al. 2021
ProkaryotaPsychrobacillus VulpisNANAToral et al. 2021
MicrobacteriumBallot et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAspergillus FumigatusBHIGC-MSno
ProkaryotaEscherichia ColiLBIMR-MSno
ProkaryotaPseudomonas AeruginosaLBIMR-MSno
ProkaryotaBurkholderia CepaciaTYESIFT-MSno
ProkaryotaBurkholderia CepaciaMHBSIFT-MSno
ProkaryotaBurkholderia CepaciaNBSIFT-MSno
ProkaryotaBurkholderia CepaciaBHISIFT-MSno
ProkaryotaEnterococcus FaecalisTYESIFT-MSno
ProkaryotaEscherichia Colihuman bloodSIFT-MSno
ProkaryotaEscherichia ColiBacT/ALERT FASIFT-MSno
ProkaryotaEscherichia ColiTYESIFT-MSno
ProkaryotaNeisseria Meningitidishuman bloodSIFT-MSno
ProkaryotaProteus MirabilisTYESIFT-MSno
ProkaryotaPseudomonas AeruginosaPseudomonas selectiveSIFT-MSno
ProkaryotaPseudomonas AeruginosaBlood agarSIFT-MSno
ProkaryotaPseudomonas AeruginosaBacT/ALERT FASIFT-MSno
ProkaryotaPseudomonas AeruginosaTYESIFT-MSno
ProkaryotaPseudomonas AeruginosaBHISIFT-MSno
ProkaryotaPseudomonas AeruginosaMHBSIFT-MSno
ProkaryotaPseudomonas AeruginosaNBSIFT-MSno
ProkaryotaStaphylococcus Aureushuman bloodSIFT-MSno
ProkaryotaStaphylococcus AureusBacT/ALERT FASIFT-MSno
ProkaryotaStaphylococcus AureusTYESIFT-MSno
ProkaryotaStaphylococcus AureusNBSIFT-MSno
ProkaryotaStaphylococcus AureusMHBSIFT-MSno
ProkaryotaStaphylococcus AureusBHISIFT-MSno
ProkaryotaStenotrophomonas MaltophiliaMHBSIFT-MSno
ProkaryotaStenotrophomonas MaltophiliaBHISIFT-MSno
ProkaryotaStenotrophomonas MaltophiliaNBSIFT-MSno
ProkaryotaStreptococcus Pneumoniaehuman bloodSIFT-MSno
ProkaryotaStreptococcus PyogenesTYESIFT-MSno
ProkaryotaHaemophilus InfluenzaeTryptic soya supp. factors X&VTD/GC-MSno
ProkaryotaPseudomonas Aeruginosatrypticase soy agarTD/GC-MSno
ProkaryotaPseudomonas Aeruginosatryptic soy brothTD/GC-MSno
ProkaryotaStaphylococcus Aureustryptic soy brothTD/GC-MSno
ProkaryotaStreptococcus PneumoniaeTryptic soyaTD/GC-MSno
ProkaryotaKlebsiella PneumoniaeLBSPME / GCxGC-TOFMSno
EukaryotaFusarium OxysporumLiquid onion extract medium (LOM)SPME, GC-MSyes
EukaryotaFusarium ProliferatumLiquid onion extract medium (LOM)SPME, GC-MSyes
ProkaryotaPseudomonas FluorescensNutrient AgarSPME-GC-MSno
ProkaryotaPseudomonas Sp.LB media, DYGS mediaHS-SPME/GC-MSno
ProkaryotaPseudomonas Sp.LB mediaHS-SPME/GC-MSno
ProkaryotaPaenibacillus PolymyxaNA media, TSA mediaHS-SPME/GC-MSno
ProkaryotaPaenibacillus PolymyxaTSA mediaHS-SPME/GC-MSno
EukaryotaCandida AlbicansYGC mediaHS-SPME/GC-GC-ToFMSno
EukaryotaCandida GlabrataYGC mediaHS-SPME/GC-GC-ToFMSno
EukaryotaCandida TropicalisYGC mediaHS-SPME/GC-GC-ToFMSno
ProkaryotaBacillus Atrophaeusnutrient agarHS-SPME/GC-MSno
ProkaryotaBacillus Amyloliquefaciensnutrient agarHS-SPME/GC-MSno
ProkaryotaBacillus Licheniformisnutrient agarHS-SPME/GC-MSno
ProkaryotaBacillus Pumilusnutrient agarHS-SPME/GC-MSno
EukaryotaTuber MagnatumGC-MS-Ono
ProkaryotaBacillus AmyloliquefaciensTryptic soy agarSPME coupled with GC-MSno
ProkaryotaBacillus SubtilisTryptic soy agarSPME coupled with GC-MSno
ProkaryotaPaenibacillus PolymyxaTryptic soy agarSPME coupled with GC-MSno
ProkaryotaAlpha Proteobacterian/an/ano
ProkaryotaGamma Proteobacterian/an/ano
ProkaryotaAlcaligenes Faecalisn/an/ano
ProkaryotaDesulfovibrio Acrylicusn/an/ano
ProkaryotaParasporobacterium Paucivoransn/an/ano
ProkaryotaLactococcus Sp.n/an/ano
ProkaryotaLactobacillus Sp.n/an/ano
ProkaryotaLactobacillus Lactisn/an/ano
ProkaryotaBrevibacterium Linensn/an/ano
ProkaryotaOenococcus Oenin/an/ano
ProkaryotaLactobacillus Brevisn/an/ano
ProkaryotaLactobacillus Hilgardiin/an/ano
ProkaryotaLactobacillus Plantarumn/an/ano
ProkaryotaPorphyromonas Gingivalisn/an/ano
ProkaryotaFusobacterium Nucleatumn/an/ano
ProkaryotaTreponema Denticolan/an/ano
ProkaryotaCitrobacter Freundiin/an/ano
ProkaryotaEscherichia Colin/an/ano
ProkaryotaShigella Flexnerin/an/ano
ProkaryotaSalmonella Enterican/an/ano
EukaryotaCandida Tropicalisn/an/ano
EukaryotaTuber Magnatumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)no
ProkaryotaPseudomonas PutidaAB medium + 1% citrate or 0,02% citrate or 1% glucose +1% casaminoacid GC-FID,GC/MSno
ProkaryotaPseudomonas TolaasiiKBSPME-GCno
ProkaryotaPseudomonas PutidaKing's B AgarSPME-GC/MSno
ProkaryotaRalstonia SolanacearumCasamino Acid Peptone Glucose agarSPME-GC/MSno
ProkaryotaKlebsiella PneumoniaeLB GCxGC-TOF-MSno
EukaryotaSchizophyllum Communen/an/ano
ProkaryotaStreptococcus PneumoniaeBlood agar/chocolate blood agaHS-SPME/GC-MS no
ProkaryotaPseudomonas PerolensTrypticase soil agar (BBL)GC/MSno
ProkaryotaAchromobacter Sp.LB broth supplemented with cryoprotectant solution (25 g L−1 gelatin, 50 g L−1 lactose, 10 g L−1 peptone, and 250 g L−1 glycerol)SPME with gas chromatograph (Agilent 7890A, Agilent Technologies) connected to a mass spectrometer (Pegasus® HT TOFMS, LECO Corporation)no
ProkaryotaSerratia Sp.LB broth supplemented with cryoprotectant solution (25 g L−1 gelatin, 50 g L−1 lactose, 10 g L−1 peptone, and 250 g L−1 glycerol)SPME with gas chromatograph (Agilent 7890A, Agilent Technologies) connected to a mass spectrometer (Pegasus® HT TOFMS, LECO Corporation)no
ProkaryotaEnterobacter Sp.LB broth supplemented with cryoprotectant solution (25 g L−1 gelatin, 50 g L−1 lactose, 10 g L−1 peptone, and 250 g L−1 glycerol)SPME with gas chromatograph (Agilent 7890A, Agilent Technologies) connected to a mass spectrometer (Pegasus® HT TOFMS, LECO Corporation)no
ProkaryotaEscherichia ColiLB broth supplemented with cryoprotectant solution (25 g L−1 gelatin, 50 g L−1 lactose, 10 g L−1 peptone, and 250 g L−1 glycerol)SPME with gas chromatograph (Agilent 7890A, Agilent Technologies) connected to a mass spectrometer (Pegasus® HT TOFMS, LECO Corporation)no
ProkaryotaPeribacillus Sp.tryptic soy agar (TSA, Panreac Applichem) mediumHS-SPME-GC/MSno
ProkaryotaPsychrobacillus VulpisMOLPHS-SPME-GC/MSno
ProkaryotaPsychrobacillus VulpisSchaeffer’s growth (SG) mediumHS-SPME-GC/MSno
ProkaryotaPsychrobacillus Vulpistryptic soy agar (TSA, Panreac Applichem) mediumHS-SPME-GC/MSno
Microbacteriumtryptone soy (TS medium; Carl Roth, Karlsruhe, Germany)GC-QQQ-MSno


Methylsulfanylmethane

Mass-Spectra

Compound Details

Synonymous names
dimethyl sulfide
Methyl sulfide
75-18-3
Methane, thiobis-
dimethyl sulphide
dimethylsulfide
Methyl thioether
Dimethylsulphide
2-Thiapropane
Dimethyl thioether
Methyl sulphide
METHYLSULFANYLMETHANE
Methylthiomethane
Dimethylsulfid
(Methylsulfanyl)methane
Methyl monosulfide
Dimethyl monosulfide
Thiobismethane
2-Thiopropane
Methanethiomethane
Thiobis(methane)
Exact-S
Sulfure de methyle
Dimethyl sulfide (natural)
dimethylsulfane
FEMA No. 2746
Methylthiomethyl radical
MFCD00008562
Methane, 1,1'-thiobis-
[SMe2]
QS3J7O7L3U
CHEBI:17437
(CH3)2S
31533-72-9
methylsulfide
Dimethylsulfid [Czech]
Sulfure de methyle [French]
HSDB 356
EINECS 200-846-2
UN1164
UNII-QS3J7O7L3U
BRN 1696847
Methylsulphide
Thiopropane
Thiobis-methane
di-methylsulfide
AI3-25274
Dimethyl sulfane
Sulfide, methyl-
(methylthio)methane
Me2S
REDUCED-DMSO
SMe2
Dimethyl sulfide, 98%
reduced dimethyl sulfoxide
(Methylsulfanyl)methane #
Dimethyl sulfide [UN1164] [Flammable liquid]
Dimethyl sulfoxide(Reduced)
EC 200-846-2
(Me)2S
Dimethyl sulfide, >=99%
4-01-00-01275 (Beilstein Handbook Reference)
CHEMBL15580
DIMETHYL SULFIDE [MI]
METHYL SULFIDE [FHFI]
DIMETHYL SULFIDE [FCC]
DIMETHYL SULFIDE [HSDB]
DTXSID9026398
S(CH3)2
Dimethyl sulfide, >=99%, FCC
Dimethyl sulfide, analytical standard
STL481894
Dimethyl sulfide, >=95.0% (GC)
AKOS009031411
MCULE-4525381422
UN 1164
Dimethyl sulfide, anhydrous, >=99.0%
InChI=1/C2H6S/c1-3-2/h1-2H
M0431
NS00005000
NS00124710
Dimethyl sulfide, puriss., >=99.0% (GC)
C00580
Dimethyl sulfide, natural, >=99%, FCC, FG
Dimethyl sulfide [UN1164] [Flammable liquid]
A838342
Dimethyl sulfide, redistilled, >=99%, FCC, FG
Q423133
Q-100810
Microorganism:

Yes

IUPAC namemethylsulfanylmethane
SMILESCSC
InchiInChI=1S/C2H6S/c1-3-2/h1-2H3
FormulaC2H6S
PubChem ID1068
Molweight62.14
LogP0.9
Atoms3
Bonds0
H-bond Acceptor1
H-bond Donor0
Chemical Classificationsulfides thioethers sulfur compounds
CHEBI-ID17437
Supernatural-IDSN0309416

mVOC Specific Details

Boiling Point
DegreeReference
37.3 °C peer reviewed
Volatilization
The Henry's Law constant for dimethyl sulfide has been measured as 1.61X10-3 atm-cu m/mole(1). This Henry's Law constant indicates that dimethyl sulfide is expected to volatilize rapidly from water surfaces(2). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(2) is estimated as 3 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as 3 days(SRC). Dimethyl sulfides's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of dimethyl sulfide from dry soil surfaces may exist(SRC) based upon a vapor pressure of 502 mm Hg(3).
Literature: (1) Gaffney, JS et al; Env Sci Tech 21: 519-23 (1987) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals: Data Compilation. Vol 4. Design Inst Phys Prop Data, Amer Inst Chem Eng, NY, NY: Hemisphere Pub Corp (1989)
Soil Adsorption
The Koc of dimethyl sulfide is estimated as 6.3(SRC), using a water solubility of 22,000 mg/L(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that dimethyl sulfide is expected to have very high mobility in soil.
Literature: (1) Suzuki T; J Comp-Aided Molec Des 5: 149-66 (1991) (2) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.0. Jan, 2009. Available from http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm as of Oct 1, 2009. (3) Swann RL et al; Res Rev 85: 17-28 (1983)
Literature: #Air-dried, unsterilized moist, and sterilized moist soils exposed to air initially containing 500 ppm dimethyl sulfide adsorbed an avg of 32, 308, and 10 ug dimethyl sulfide/g soil, respectively, in 15 days(1). Time required for complete sorption of dimethyl sulfide by moist soil from air initially containing 100 ppm dimethyl sulfide: soil 1 (Weller) - 1st exposure 150 min, 2nd exposure 100 min, 3rd exposure 95 min; soil 2 (Harps) - 1st exposure 45 min, 2nd exposure 24 min, 3rd exposure 19 min(1). These data suggest that moist soils have a greater tendency to adsorb dimethyl sulfide than dry soils, and that microbial activity in moist soils may be responsible for greater adsorption(1). When natural gas containing 0.5 pounds of dimethyl sulfide per million cubic feet of gas was passed through a bed of pulverized, dry, montmorillonite clay, dimethyl sulfide exhibited a fast breakthrough (2 hours) and a fast build-up rate in effluent gas (85% of influent concn 4 hours after breakthrough), suggesting that dimethyl sulfide does not adsorb to dry soils(2).
Literature: (1) Bremner JM, Banwart WL; Soil Biol Biochem 8: 79-83 (1976) (2) Williams RP; Oper Sect Proc - Am Gas Assoc pp. T29-T37 (1976)
Vapor Pressure
PressureReference
502 mm Hg at 25 deg CDaubert, T.E., R.P. Danner. Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, D.C.: Taylor and Francis, 1989.
MS-Links
1D-NMR-Links
Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAspergillus FumigatusNANAChippendale et al. 2014
ProkaryotaBurkholderia CepaciaNANADryahina et al. 2016
ProkaryotaEscherichia ColiNANAAllardyce et al. 2006
ProkaryotaEscherichia ColiNANAAllardyce et al. 2006
ProkaryotaNeisseria MeningitidisNANAAllardyce et al. 2006
ProkaryotaPseudomonas AeruginosaNANAAllardyce et al. 2006
ProkaryotaPseudomonas AeruginosaNANAAllardyce et al. 2006
ProkaryotaPseudomonas AeruginosaNANADryahina et al. 2016
ProkaryotaStaphylococcus AureusNANAAllardyce et al. 2006
ProkaryotaStaphylococcus AureusNANADryahina et al. 2016
ProkaryotaStenotrophomonas MaltophiliaNANADryahina et al. 2016
ProkaryotaStreptococcus PneumoniaeNANAAllardyce et al. 2006
ProkaryotaStreptococcus PneumoniaeNANAAllardyce et al. 2006
ProkaryotaEscherichia ColiNANAHewett et al. 2020
ProkaryotaPseudomonas AeruginosaNANABean et al. 2016
ProkaryotaKlebsiella PneumoniaeNANARees et al. 2016a
ProkaryotaPseudomonas AeruginosaNANABean et al. 2012
ProkaryotaPseudomonas AeruginosaNANADavis et al. 2020
ProkaryotaEscherichia ColiNANADixon et al. 2022
ProkaryotaHaemophilus InfluenzaeNANAFilipiak et al. 2012
ProkaryotaPseudomonas AeruginosaNANAFilipiak et al. 2012
ProkaryotaPseudomonas AeruginosaNANAAhmed et al. 2023
ProkaryotaStreptococcus PneumoniaeNANAFilipiak et al. 2012
ProkaryotaMycobacterium BovisNANAMcNerney et al. 2012
ProkaryotaEnterobacter CloacaeNALawal et al. 2018
EukaryotaAspergillus Versicolorwild strainsSchleibinger et al. 2005
EukaryotaChaetomium Globosumwild strainsSchleibinger et al. 2005
EukaryotaEurotium Amstelodamiwild strainsSchleibinger et al. 2005
ProkaryotaShigella SonneiChina Center of Industrial Culture collectionWang et al. 2018
ProkaryotaVibrio ParahaemolyticusChina Center of Industrial Culture collectionWang et al. 2018
EukaryotaFusarium OxysporumonionWang et al. 2018
EukaryotaFusarium ProliferatumonionWang et al. 2018
ProkaryotaPseudomonas Fluorescens0Medicago spp. plant rhizospheresHernández-León et al. 2015
ProkaryotaPseudomonas Sp.antifungal activity against Thielaviopsis ethacetica mycelial growthBrazilian Biorenewables National Laboratory – LNBR/CNPEM Microorganism Collection, Campinas, SP; isolatedfrom soil and roots of highly productive sugarcane-producing regions; BrazilFreitas et al. 2022
ProkaryotaPseudomonas AeruginosaNational Collections of Industrial Food and Marine Bacteria, American Type Culture CollectionSlade et al. 2022
EukaryotaTuber Magnatumcollected from natural truffle orchards in Istria (Croatia) during one truffle season (October 2018–January 2019)Niimi et al. 2021
EukaryotaTuber Magnatumcollected from natural truffle orchards in Baranya (Hungary) during one truffle season (October 2018–January 2019)Niimi et al. 2021
EukaryotaTuber Magnatumcollected from natural truffle orchards in Somogy (Hungary) during one truffle season (October 2018–January 2019)Niimi et al. 2021
EukaryotaTuber Magnatumcollected from natural truffle orchards in Abruzzo (Italy) during one truffle season (October 2018–January 2019)Niimi et al. 2021
EukaryotaTuber Magnatumcollected from natural truffle orchards in Kalubara (Serbia) during one truffle season (October 2018–January 2019)Niimi et al. 2021
EukaryotaTuber Magnatumcollected from natural truffle orchards in Srem (Serbia) during one truffle season (October 2018–January 2019)Niimi et al. 2021
EukaryotaSerendipita IndicaInstitute of Phytopathology, Justus-Liebig-Universität, Gießen, Germany; origin: isolates from sudangrass roots growing in soil-based trap systemsVenneman et al. 2020
EukaryotaSerendipita WilliamsiiInstitute of Phytopathology, Justus-Liebig-Universität, Gießen, Germany; origin: isolates from sudangrass roots growing in soil-based trap systemsVenneman et al. 2020
ProkaryotaAlpha Proteobacterian/aNASchulz and Dickschat 2007
ProkaryotaGamma Proteobacterian/aNASchulz and Dickschat 2007
ProkaryotaAlcaligenes Faecalisn/aNASchulz and Dickschat 2007
ProkaryotaDesulfovibrio Acrylicusn/aNASchulz and Dickschat 2007
ProkaryotaParasporobacterium Paucivoransn/aNASchulz and Dickschat 2007
ProkaryotaLactococcus Sp.n/aNASchulz and Dickschat 2007
ProkaryotaLactobacillus Sp.n/aNASchulz and Dickschat 2007
ProkaryotaClostridium Sp.n/aNAStotzky and Schenck 1976
ProkaryotaCollimonas Fungivoransn/aNAGarbeva et al. 2014
EukaryotaTuber Magnatumn/aItalian geographical areas ( Umbria, Piedmont, Marche, Emilia Romagna, Border region area between Emilia Romagna and Marche, Tuscany, Molise)Gioacchini et al. 2008
EukaryotaTuber Simonean/aAyme Truffe of Grignan, 26230 FranceMarch et al. 2006
EukaryotaTuber Rufumn/aAyme Truffe of Grignan, 26230 FranceMarch et al. 2006
EukaryotaTuber Mesentericumn/aAyme Truffe of Grignan, 26230 FranceMarch et al. 2006
EukaryotaTuber Melanosporumn/aAyme Truffe of Grignan, 26230 FranceMarch et al. 2006
EukaryotaTuber Aestivumn/aAyme Truffe of Grignan, 26230 FranceMarch et al. 2006
EukaryotaTuber Uncinatumn/aFrance, Italy, Switzerland, the UK, Austria, Romania, and HungarySplivallo et al. 2012
ProkaryotaCollimonas Pratensisn/aNAGarbeva et al. 2014
ProkaryotaPseudomonas FluorescensNACheng et al. 2016
EukaryotaFusarium Sp.NABrock et al. 2011
EukaryotaPenicillium Sp.NALarsen 1998
ProkaryotaPseudonocardia ThermophilanasoilWilkins 1996
ProkaryotaSaccharomonospora RectivirgulanasoilWilkins 1996
ProkaryotaStreptomyces Sp.nabreathing zone of a waste collection workerWilkins 1996
ProkaryotaPseudomonas Aeruginosastimulates growth of Aspergillus fumigatusnaBriard et al. 2016
ProkaryotaSerratia Plymuthicanamaize rhizosphere, NetherlandsGarbeva et al. 2014
ProkaryotaPaenibacillus Sp.narhizosphere of Marram grass in sandy dune soils, NetherlandsGarbeva et al. 2014
ProkaryotaPedobacter Sp.narhizosphere of Marram grass in sandy dune soils, NetherlandsGarbeva et al. 2014
ProkaryotaRalstonia SolanacearumnanaSpraker et al. 2014
EukaryotaPenicillium Communenain dry-cured meat products, cheeseSunesson et al. 1995
ProkaryotaSerratia Sp.the results led us to propose a possible new direct long-distance mechanism of action for WT antagonistic F. oxysporum that is mediated by vocsNAMinerdi et al. 2009
EukaryotaTuber Aestivumn/aT. melanosporum was from the cultivated truffle zones in the province and T. aestivum from the natural truffle zones in the same regionCullere et al. 2010
EukaryotaTuber Melanosporumn/aT. melanosporum was from the cultivated truffle zones in the province and T. aestivum from the natural truffle zones in the same regionCullere et al. 2010
ProkaryotaPseudomonas PutidananaSchöller et al. 1997
EukaryotaTuber Mesentericumn/aProf. Mattia Bentivenga (Università di Perugia, Perugia, Italy) and in the fortywoodland of the Basilicata regionMauriello et al. 2004
EukaryotaTuber Excavatumn/aProf. Mattia Bentivenga (Università di Perugia, Perugia, Italy) and in the fortywoodland of the Basilicata regionMauriello et al. 2004
EukaryotaTuber Magnatumn/aProf. Mattia Bentivenga (Università di Perugia, Perugia, Italy) and in the fortywoodland of the Basilicata regionMauriello et al. 2004
EukaryotaTuber Aestivumn/aProf. Mattia Bentivenga (Università di Perugia, Perugia, Italy) and in the fortywoodland of the Basilicata regionMauriello et al. 2004
EukaryotaTuber Brumalen/aProf. Mattia Bentivenga (Università di Perugia, Perugia, Italy) and in the fortywoodland of the Basilicata regionMauriello et al. 2004
EukaryotaTuber Melanosporumn/aProf. Mattia Bentivenga (Università di Perugia, Perugia, Italy) and in the fortywoodland of the Basilicata regionMauriello et al. 2004
ProkaryotaPseudomonas AeruginosaclinicPreti et al. 2009
ProkaryotaEnterobacter AgglomeransNARobacker and Lauzon 2002
ProkaryotaClostridium Difficilenastool specimens, from patients infected with clostridium difficileKuppusami et al. 2015
ProkaryotaClostridium DifficilenanaKuppusami et al. 2015
EukaryotaTuber MesentericumNoneNoneMarch et al. 2006
ProkaryotaSerratia Sp.NANAAlmeida et al. 2022
ProkaryotaEnterobacter Sp.NANAAlmeida et al. 2022
ProkaryotaEscherichia ColiNANAAlmeida et al. 2022
ProkaryotaPseudomonas SegetisNANAToral et al. 2021
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAspergillus FumigatusBHIGC-MSno
ProkaryotaBurkholderia CepaciaMHBSIFT-MSno
ProkaryotaBurkholderia CepaciaNBSIFT-MSno
ProkaryotaBurkholderia CepaciaBHISIFT-MSno
ProkaryotaEscherichia Colihuman bloodSIFT-MSno
ProkaryotaEscherichia ColiBacT/ALERT FASIFT-MSno
ProkaryotaNeisseria Meningitidishuman bloodSIFT-MSno
ProkaryotaPseudomonas Aeruginosahuman bloodSIFT-MSno
ProkaryotaPseudomonas AeruginosaBacT/ALERT FASIFT-MSno
ProkaryotaPseudomonas AeruginosaNBSIFT-MSno
ProkaryotaPseudomonas AeruginosaBHISIFT-MSno
ProkaryotaPseudomonas AeruginosaMHBSIFT-MSno
ProkaryotaStaphylococcus Aureushuman bloodSIFT-MSno
ProkaryotaStaphylococcus AureusMHBSIFT-MSno
ProkaryotaStaphylococcus AureusNBSIFT-MSno
ProkaryotaStaphylococcus AureusBHISIFT-MSno
ProkaryotaStenotrophomonas MaltophiliaNBSIFT-MSno
ProkaryotaStenotrophomonas MaltophiliaMHBSIFT-MSno
ProkaryotaStenotrophomonas MaltophiliaBHISIFT-MSno
ProkaryotaStreptococcus Pneumoniaehuman bloodSIFT-MSno
ProkaryotaStreptococcus PneumoniaeBacT/ALERT FASIFT-MSno
ProkaryotaEscherichia ColiLBSPME/GC-MSno
ProkaryotaPseudomonas AeruginosaLB-LennoxSPME/GC-MSno
ProkaryotaKlebsiella Pneumoniaehuman bloodSPME/GCxGC-MSno
ProkaryotaPseudomonas Aeruginosalysogeny brothSPME/GCxGC-MSno
ProkaryotaPseudomonas AeruginosaLB brothSPME/GCxGC-MSno
ProkaryotaEscherichia ColiLBTD/GC-MSno
ProkaryotaHaemophilus InfluenzaeTryptic soya supp. factors X&VTD/GC-MSno
ProkaryotaPseudomonas Aeruginosatryptic soy brothTD/GC-MSno
ProkaryotaPseudomonas AeruginosaNBTD/GC-MSno
ProkaryotaStreptococcus PneumoniaeTryptic soyaTD/GC-MSno
ProkaryotaMycobacterium BovisLG + glycerolTD/GC-MS and SIFT-MSno
ProkaryotaEnterobacter CloacaeLevine EMB agar (LEA) (Fluka Analytical, UK)GC-MSno
EukaryotaAspergillus Versicoloringrain (woodchip)SIM/GCMS / Tenaxno
EukaryotaChaetomium Globosumingrain (woodchip)SIM/GCMS / Tenaxno
EukaryotaEurotium Amstelodamiingrain (woodchip)SIM/GCMS / Tenaxno
ProkaryotaShigella SonneiSodium chloride brothSPME, GC-MSno
ProkaryotaVibrio ParahaemolyticusSodium chloride brothSPME, GC-MSno
EukaryotaFusarium OxysporumLiquid onion extract medium (LOM)SPME, GC-MSyes
EukaryotaFusarium ProliferatumLiquid onion extract medium (LOM)SPME, GC-MSyes
ProkaryotaPseudomonas FluorescensNutrient AgarSPME-GC-MSno
ProkaryotaPseudomonas Sp.LB media, DYGS media, ANGLE mediaHS-SPME/GC-MSno
ProkaryotaPseudomonas AeruginosaTS agar/blood agarHS-SPME/GC-MSno
EukaryotaTuber MagnatumGC-MS-Ono
EukaryotaSerendipita IndicaPD agarPTR-TOF-MSno
EukaryotaSerendipita WilliamsiiPD agarPTR-TOF-MSno
ProkaryotaAlpha Proteobacterian/an/ano
ProkaryotaGamma Proteobacterian/an/ano
ProkaryotaAlcaligenes Faecalisn/an/ano
ProkaryotaDesulfovibrio Acrylicusn/an/ano
ProkaryotaParasporobacterium Paucivoransn/an/ano
ProkaryotaLactococcus Sp.n/an/ano
ProkaryotaLactobacillus Sp.n/an/ano
ProkaryotaClostridium Sp.n/an/ano
ProkaryotaCollimonas Fungivoranssand supplemented with artificial root exudatesHeadspace trapping/GC-MSno
EukaryotaTuber Magnatumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)no
EukaryotaTuber Simonean/aPressure balanced head-space sampling and GC/TOF-MSno
EukaryotaTuber Rufumn/aPressure balanced head-space sampling and GC/TOF-MSno
EukaryotaTuber Mesentericumn/aPressure balanced head-space sampling and GC/TOF-MSno
EukaryotaTuber Melanosporumn/aPressure balanced head-space sampling and GC/TOF-MSno
EukaryotaTuber Aestivumn/aPressure balanced head-space sampling and GC/TOF-MSno
EukaryotaTuber Uncinatumn/aSPME-GC-MSno
ProkaryotaCollimonas Pratensissand supplemented with artificial root exudatesHeadspace trapping/GC-MSno
ProkaryotaPseudomonas FluorescensKings B + rif,+kann; PDA GC-Q-TOF-MSno
EukaryotaFusarium Sp.no
EukaryotaPenicillium Sp.no
ProkaryotaPseudonocardia ThermophilaNutrient agar CM3GC/MSno
ProkaryotaSaccharomonospora RectivirgulaNutrient agar CM3GC/MSno
ProkaryotaStreptomyces Sp.Nutrient agar CM3 + 50mg/l actidioneGC/MSno
ProkaryotaPseudomonas Aeruginosaminimal medium/ Brian mediumSPME-GC/MSno
ProkaryotaSerratia Plymuthicasand containing artificial root exudatesGC/MSno
ProkaryotaPaenibacillus Sp.sand containing artificial root exudatesGC/MSno
ProkaryotaPedobacter Sp.sand containing artificial root exudatesGC/MSno
ProkaryotaRalstonia SolanacearumCasamino Acid Peptone Glucose agarSPME-GC/MSno
EukaryotaPenicillium CommuneMEAGC/MSno
ProkaryotaSerratia Sp.LB mediumSPME/GC-MS no
EukaryotaTuber Aestivumn/aGas chromatography-olfactometry (GC-O)no
EukaryotaTuber Melanosporumn/aGas chromatography-olfactometry (GC-O)no
ProkaryotaPseudomonas PutidaAB medium + 1% citrate or 0,02% citrate or 1% glucose +1% casaminoacid GC-FID,GC/MSno
EukaryotaTuber Mesentericumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)no
EukaryotaTuber Excavatumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)no
EukaryotaTuber Aestivumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)no
EukaryotaTuber Brumalen/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)no
EukaryotaTuber Melanosporumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)no
ProkaryotaPseudomonas AeruginosaBlood agar/chocolate blood agaHS-SPME/GC-MS no
ProkaryotaEnterobacter Agglomeransno
ProkaryotaClostridium Difficilebrain heart infusion agar with 7% horse bloodPTR-ToF-MSno
EukaryotaTuber MesentericumNonePressure balanced head-space sampling and GC/TOF-MSno
ProkaryotaSerratia Sp.LB broth supplemented with cryoprotectant solution (25 g L−1 gelatin, 50 g L−1 lactose, 10 g L−1 peptone, and 250 g L−1 glycerol)SPME with gas chromatograph (Agilent 7890A, Agilent Technologies) connected to a mass spectrometer (Pegasus® HT TOFMS, LECO Corporation)no
ProkaryotaEnterobacter Sp.LB broth supplemented with cryoprotectant solution (25 g L−1 gelatin, 50 g L−1 lactose, 10 g L−1 peptone, and 250 g L−1 glycerol)SPME with gas chromatograph (Agilent 7890A, Agilent Technologies) connected to a mass spectrometer (Pegasus® HT TOFMS, LECO Corporation)no
ProkaryotaEscherichia ColiLB broth supplemented with cryoprotectant solution (25 g L−1 gelatin, 50 g L−1 lactose, 10 g L−1 peptone, and 250 g L−1 glycerol)SPME with gas chromatograph (Agilent 7890A, Agilent Technologies) connected to a mass spectrometer (Pegasus® HT TOFMS, LECO Corporation)no
ProkaryotaPseudomonas SegetisMOLPHS-SPME-GC/MSno
ProkaryotaPseudomonas SegetisSchaeffer’s growth (SG) mediumHS-SPME-GC/MSno
ProkaryotaPseudomonas Segetistryptic soy agar (TSA, Panreac Applichem) mediumHS-SPME-GC/MSno


Dioxido-oxo-sulfanylidene-lambda6-sulfane

Compound Details

Synonymous names
thiosulfate
THIOSULFATE ION
Thiosulphate
Thiosulfate ion(2-)
thiosulfate(2-)
Thiosulfate (2-)
14383-50-7
Thiosulphate ion
UNII-LLT6XV39PY
LLT6XV39PY
Thiosulfate (S2O32-)
trioxidosulfidosulfate(2-)
THIOSULPHATE ION(2-)
CHEBI:16094
THIOSULPHATE (S2O32-)
S2O3(2-)
trioxido-1kappa(3)O-disulfate(S--S)(2-)
(SO3S)(2-)
[SO3S](2-)
sulfurothioate
Thiosulfates
DTXSID80932118
DHCDFWKWKRSZHF-UHFFFAOYSA-L
dioxido-oxo-sulfanylidene-lambda6-sulfane
Q410739
Microorganism:

Yes

IUPAC namedioxido-oxo-sulfanylidene-lambda6-sulfane
SMILES[O-]S(=O)(=S)[O-]
InchiInChI=1S/H2O3S2/c1-5(2,3)4/h(H2,1,2,3,4)/p-2
FormulaO3S2-2
PubChem ID1084
Molweight112.13
LogP0.2
Atoms5
Bonds0
H-bond Acceptor4
H-bond Donor0
Chemical Classificationsulfur compounds
CHEBI-ID16094

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaBurkholderia ArborisNANAZhu et al. 2022
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaBurkholderia Arborisnutrient agar (NA) mediumUPLC-QTOF/MSno


Sulfur Dioxide

Mass-Spectra

Compound Details

Synonymous names
sulfur dioxide
sulphur dioxide
Sulfurous anhydride
7446-09-5
Sulfurous oxide
Sulfur superoxide
Fermenicide liquid
Fermenicide powder
Sulfur oxide (SO2)
Sulfurous acid anhydride
Schwefeldioxid
Siarki dwutlenek
Sulfur dioxide (SO2)
dioxidosulfur
Schwefeldioxyd
Oxosulfane oxide
Caswell No. 813
FEMA No. 3039
Surfur dioxide (anhydrous)
Fermenticide liquid
Schwefel(IV)-oxid
UN 1079
SULFUROXIDE
CCRIS 9001
HSDB 228
SO2
Sulfur dioxide (NF)
SULFUR-DIOXIDE
CHEBI:18422
0UZA3422Q4
EINECS 231-195-2
EPA Pesticide Chemical Code 077601
UNII-0UZA3422Q4
INS NO.220
DTXSID6029672
Sulfon
INS-220
SULFUR DIOXIDE (E 220)
Sulfur dioxide (SO2) 10% by volume or more SO2
SULFUROUS ANHYDRIDE (E220)
Sulfur dioxide [NF]
E220
E-220
R-764
EC 231-195-2
SULFUR DIOXIDE (II)
SULFUR DIOXIDE [II]
SULFUR DIOXIDE (IARC)
SULFUR DIOXIDE [IARC]
Sulfur dioxide, >=99.9%
SULFUR DIOXIDE (MART.)
SULFUR DIOXIDE [MART.]
Sulfurdioxide
(SO2)
[SO2]
Schwefeldioxyd [German]
Siarki dwutlenek [Polish]
sulfonyl
sulfuryl
sulphonyl
sulfer dioxide
Dioxide, Sulfur
Oxosulfane oxide #
Anhydride, Sulfurous
UN1079
67015-63-8
Sulfur dioxide [UN1079] [Poison gas]
Sulphur dioxide, liquified
SULFUR DIOXIDE [MI]
SULFUR DIOXIDE [FCC]
SULFUR DIOXIDE [FHFI]
SULFUR DIOXIDE [HSDB]
DTXCID009672
Sulfur dioxide, >=99.98%
CHEMBL1235997
FEMA 3039
InChI=1/O2S/c1-3-2
RAHZWNYVWXNFOC-UHFFFAOYSA-
SULFUR DIOXIDE, LIQUEFIED
SULPHUR DIOXIDE, LIQUEFIED
SULFUR DIOXIDE (ANHYDROUS)
AKOS015904447
Sulfur dioxide, puriss., >=99.9%
USEPA/OPP Pesticide Code: 077601
Sulfur dioxide [UN1079] [Poison gas]
NS00076361
Q5282
U0147
U0148
C09306
D05961
Sulfur Dioxide (ca. 2.5% in Dichloromethane, ca. 0.5 mol/L)
Sulfur Dioxide (ca. 8% in Tetrahydrofuran, ca. 1.2 mol/L)
Microorganism:

Yes

IUPAC namesulfur dioxide
SMILESO=S=O
InchiInChI=1S/O2S/c1-3-2
FormulaO2S
PubChem ID1119
Molweight64.07
LogP0.1
Atoms3
Bonds0
H-bond Acceptor3
H-bond Donor0
Chemical Classificationsulfur compounds oxides
CHEBI-ID18422
Supernatural-IDSN0320022

mVOC Specific Details

Boiling Point
DegreeReference
-10.05 °C peer reviewed
Volatilization
The Henry's Law constant for sulfur dioxide is 8.10X10-4 atm-cu m/mole(1). This Henry's Law constant indicates that sulfur dioxide is expected to volatilize from water surfaces(2). Sulfur dioxide's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). However volatilization may be attenuated by reaction with water to form sulfuric acid(SRC). Sulfur dioxide is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 3.0X10+3 mm Hg(3).
Soil Adsorption
Sulfur dioxide uptake is dependent upon soil pH and moisture content.
Literature: Payrissat M, Beilke S; Atmos Environ 9: 211 (1975) as cited in Monitoring and Assessment Research Centre; Report #7 p.21 (1978)
Vapor Pressure
PressureReference
3X10+3 mm Hg at 25 deg C (est)Daubert, T.E., R.P. Danner. Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, D.C.: Taylor and Francis, 1989.
MS-Links
MS-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaChryseobacterium Sp.nanaTyc et al. 2015
ProkaryotaJanthinobacterium Sp.nanaTyc et al. 2015
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaChryseobacterium Sp.Tryptic soy broth agarGC/MS-Q-TOFno
ProkaryotaJanthinobacterium Sp.Tryptic soy broth agarGC/MS-Q-TOFno


2-sulfanylethanol

Mass-Spectra

Compound Details

Synonymous names
2-mercaptoethanol
Mercaptoethanol
60-24-2
Beta-Mercaptoethanol
Thioglycol
2-Sulfanylethanol
Ethanol, 2-mercapto-
2-Thioethanol
Thioethylene glycol
2-Hydroxyethanethiol
2-Hydroxyethyl mercaptan
Monothioglycol
Thiomonoglycol
2-Hydroxy-1-ethanethiol
1-Ethanol-2-thiol
Hydroxyethyl mercaptan
Monothioethylene glycol
2-Mercapto-1-ethanol
1-Hydroxy-2-mercaptoethane
2-Mercaptoethyl alcohol
2-ME
Ethylene glycol, monothio-
1-Mercapto-2-hydroxyethane
beta-Hydroxyethanethiol
2-sulfanylethan-1-ol
2-Hydroxyethylmercaptan
Emery 5791
USAF EK-4196
.beta.-Hydroxyethanethiol
.beta.-Mercaptoethanol
NSC 3723
.beta.-Hydroxyethylmercaptan
14R9K67URN
DTXSID4026343
CHEBI:41218
NSC-3723
155613-89-1
Mercaptoetanol
BME
Monothioethyleneglycol
2-Mercaptoethanol, >=99.0%
beta-Hydroxyethylmercaptan
|A-mercaptoethanol
2-mercapto ethanol
Cuprate(6-), .mu.-2,2-(1-methyl-1,2-ethanediyl)bisimino(6-fluoro-1,3,5-triazine-4,2-diyl)imino(2-hyd
CCRIS 2097
HSDB 5199
EINECS 200-464-6
UN2966
BRN 0773648
UNII-14R9K67URN
2mercaptoethanol
AI3-07710
b-mercaptoethanol
2-mercapto-ethanol
2-sulfanyl-ethanol
beta-sulfanylethanol
hydroxyethyl sulfide
mercaptoethyl alcohol
MFCD00004890
beta -mercaptoethanol
2-Sulfanylethanol #
2-hydroxy-ethanethiol
2-mercaptoethan-1-ol
HSCH2CH2OH
?-MERCAPTOETHANOL
WLN: SH2Q
EC 200-464-6
4-01-00-02428 (Beilstein Handbook Reference)
DivK1c_000784
BDBM7971
CHEMBL254951
2-MERCAPTOETHANOL [MI]
FEMA NO. 4582
HMS502H06
KBio1_000784
NSC3723
NINDS_000784
Thioglycol [UN2966] [Poison]
STL482546
2-Mercaptoethanol, for electrophoresis
AKOS000118900
CCG-231050
DB03345
MCULE-2252943288
UN 2966
IDI1_000784
BP-21398
2-Mercaptoethanol, for synthesis, 99.0%
DS-014379
M0058
M1948
NS00005734
EN300-19346
C00928
2-Mercaptoethanol, SAJ special grade, >=99.0%
A832651
Q411084
InChI=1/C2H6OS/c3-1-2-4/h3-4H,1-2H
Q-200296
3-Pyridinecarbonitrile, 4-methyl-2,6-di-5-morpholinyl-
F0001-1577
Z104473584
2-Mercaptoethanol, for HPLC derivatization, >=99.0% (GC)
2-Mercaptoethanol, BioUltra, for molecular biology, >=99.0% (GC)
2-Mercaptoethanol, for molecular biology, for electrophoresis, suitable for cell culture, BioReagent, 99% (GC/titration)
Cuprate(6-), [.mu.-[[2,2'-[(1-methyl-1,2-ethanediyl)bis[imino(6-fluoro-1,3,5-triazine-4,2-diyl)imino[2-(hydroxy-.kappa.O)-5-sulfo-3,1-phenylene](2,1-diazenediyl
Microorganism:

Yes

IUPAC name2-sulfanylethanol
SMILESC(CS)O
InchiInChI=1S/C2H6OS/c3-1-2-4/h3-4H,1-2H2
FormulaC2H6OS
PubChem ID1567
Molweight78.14
LogP-0.2
Atoms4
Bonds1
H-bond Acceptor2
H-bond Donor2
Chemical Classificationalcohols sulfur compounds thiols
CHEBI-ID41218
Supernatural-IDSN0065398

mVOC Specific Details

Boiling Point
DegreeReference
157 °C peer reviewed
Volatilization
The Henry's Law constant for 2-mercaptoehtanol is estimated as 1.8X10-7 atm-cu m/mole(SRC) derived from its vapor pressure, 1.76 mm Hg(1), and an assigned value for water solubility of 1.00X10+6 mg/L (miscible)(2). This Henry's Law constant indicates that 2-mercaptoethanol is expected to be essentially nonvolatile from water surfaces(3). 2-Mercaptoethanol's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may not occur(SRC). 2-Mercaptoethanol is expected to volatilize from dry soil surfaces(SRC) based upon its extrapolated vapor pressure(1).
Literature: (1) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, DC: Taylor and Francis (1989) (2) O'Neil MJ, ed; The Merck Index. 13th ed Whitehouse Station, NJ: Merck and Co., Inc., p. 1050 (2001) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)
Soil Adsorption
Using a structure estimation method based on molecular connectivity indices(1), the Koc of 2-mercaptoethanol can be estimated to be 1.3(SRC). According to a classification scheme(2), this estimated Koc value suggests that 2-mercaptoethanol is expected to have very high mobility in soil.
Literature: (1) Meylan WM et al; Environ Sci Technol 26: 1560-67 (1992) (2) Swann RL et al; Res Rev 85: 17-28 (1983) (3) Doucette WJ; pp. 141-188 in Handbook of Property Estimation Methods for Chemicals. Boethling RS, Mackay D, eds. Boca Raton, FL: Lewis Publ (2000)
Vapor Pressure
PressureReference
1.756 mm Hg at 25 deg C /Extrapolated/Daubert, T.E., R.P. Danner. Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, D.C.: Taylor and Francis, 1989.
Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaStreptomyces Philanthiantifungal activity against Aspergillus parasiticus TISTR 3276 and Aspergillus flavus PSRDC-4NABoukaew and Prasertsan 2020
EukaryotaTuber Magnatumn/aItalian geographical areas (Piedmont, Molise)Gioacchini et al. 2008
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaStreptomyces Philanthisterile wheat seedsGC-MSyes
EukaryotaTuber Magnatumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)no


4-(2-aminoethyl)benzenesulfonyl Fluoride

Compound Details

Synonymous names
4-(2-Aminoethyl)benzenesulfonyl fluoride
34284-75-8
AEBSF
4-(2-Aminoethyl)benzenesulfonylfluoride
4-(2-aminoethyl)benzene-1-sulfonyl fluoride
Benzenesulfonyl fluoride, 4-(2-aminoethyl)-
F5D36L5354
AES
4-beta-Aminoethylbenzolsulfofluoride
CHEMBL1256178
SR-01000075690
ABSF
Lopac-A-8456
Lopac0_000132
SCHEMBL77781
CHEMBL1096339
UNII-F5D36L5354
DTXSID40187844
BDBM50398077
CCG-204227
DB07347
SDCCGSBI-0050120.P002
NCGC00015097-01
NCGC00015097-02
NCGC00015097-03
NCGC00015097-12
NCGC00162071-01
PD005322
NS00015316
[4-(2-Aminoethyl)-benzenesulphonyl fluoride]
G22633
EN300-1581783
Q290992
BENZENESULFONYL FLUORIDE, P-(2-AMINOETHYL)-
SR-01000075690-6
Microorganism:

Yes

IUPAC name4-(2-aminoethyl)benzenesulfonyl fluoride
SMILESC1=CC(=CC=C1CCN)S(=O)(=O)F
InchiInChI=1S/C8H10FNO2S/c9-13(11,12)8-3-1-7(2-4-8)5-6-10/h1-4H,5-6,10H2
FormulaC8H10FNO2S
PubChem ID1701
Molweight203.24
LogP1.7
Atoms13
Bonds3
H-bond Acceptor4
H-bond Donor1
Chemical Classificationaromatic compounds nitrogen compounds sulfur compounds benzenoids amines halogenated compounds sulfonyls
Supernatural-IDSN0225208

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaStreptomyces ThermocarboxydusNANAPassari et al. 2019
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaStreptomyces Thermocarboxydusactinomycetes isolation agar (AIA)GC-MSno


Dibenzothiophene

Compound Details

Synonymous names
dibenzothiophene
132-65-0
Diphenylene sulfide
Dibenzo[b,d]thiophene
9-Thiafluorene
alpha-Thiafluorene
2,2'-Biphenylylene sulfide
Dibenzothiophene [USAN]
Dibenzo(b,d)thiophene
[1,1'-Biphenyl]-2,2'-diyl sulfide
.alpha.-Thiafluorene
NSC-2843
MFCD00004969
(1,1'-Biphenyl)-2,2'-diyl sulfide
Z3D4AJ1R48
DTXSID0047741
CHEBI:23681
NCGC00094646-01
Dibenzothiophene (USAN)
Dibenzothiophene 10 microg/mL in Acetonitrile
DTXCID0027725
C12H8S
Dibenzothiophene, analytical standard
CAS-132-65-0
CCRIS 5307
HSDB 7409
NSC 2843
EINECS 205-072-9
UNII-Z3D4AJ1R48
Dibenzthiophene
AI3-00043
Dibenzo[b]thiophene
Dibenzothiophene-Sulfur
Spectrum_000926
[1,2'-diyl sulfide
Dibenzothiophene, 98%
Spectrum2_001011
Spectrum3_000383
Spectrum4_000504
Spectrum5_000863
Dibenzothiophene, >=99%
SCHEMBL13294
BSPBio_002165
KBioGR_001047
KBioSS_001406
BIDD:GT0331
DivK1c_000393
SPECTRUM1500235
SPBio_001161
DIBENZOTHIOPHENE [HSDB]
DIBENZOTHIOPHENE [IARC]
DIBENZOTHIOPHENE [INCI]
CHEMBL219828
HMS501D15
KBio1_000393
KBio2_001406
KBio2_003974
KBio2_006542
KBio3_001385
NSC2843
NINDS_000393
HMS1920E12
HMS2091K22
HMS3652N11
Pharmakon1600-01500235
HY-B0973
Tox21_111308
Tox21_303415
CCG-40229
NSC756732
s4205
STK367232
AKOS000278427
Tox21_111308_1
AC-1025
CS-4462
FD14022
MCULE-2582244078
NSC-756732
SB66387
IDI1_000393
NCGC00094646-02
NCGC00094646-03
NCGC00094646-04
NCGC00257449-01
AS-12976
SBI-0051339.P003
DB-042124
AM20050251
D0148
NS00003432
SW219819-1
EN300-20188
C20125
D03777
AB00051965_02
AB00051965_03
A936927
Dibenzothiophene, purified by sublimation, >=99%
Q544767
SR-05000002089
Q-101161
SR-05000002089-1
Z104477204
8-thiatricyclo[7.4.0.0,2,7]trideca-1(9),2(7),3,5,10,12-hexaene
InChI=1/C12H8S/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8
83R
Microorganism:

No

IUPAC namedibenzothiophene
SMILESC1=CC=C2C(=C1)C3=CC=CC=C3S2
InchiInChI=1S/C12H8S/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8H
FormulaC12H8S
PubChem ID3023
Molweight184.26
LogP4.4
Atoms13
Bonds0
H-bond Acceptor1
H-bond Donor0
Chemical Classificationbenzenoids sulfur compounds heterocyclic compounds aromatic compounds
CHEBI-ID23681
Supernatural-IDSN0159082

mVOC Specific Details

Boiling Point
DegreeReference
332.5 °C peer reviewed
Volatilization
The Henry's Law constant for dibenzothiophene is estimated as 3.4X10-5 atm-cu m/mole(SRC) derived from its vapor pressure, 2.05X10-4 mm Hg(1), and water solubility, 1.47 mg/L(2). This Henry's Law constant indicates that dibenzothiophene is expected to volatilize from water surfaces(3). However, volatilization from water surfaces is expected to be severely attenuated by adsorption to suspended solids and sediment in the water column(SRC). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(3) is estimated as 24 hours when adsorption is neglected(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(3) is estimated as 16 days when neglecting adsorption(SRC). The volatilization half-life from a model pond is about 217 days when adsorption is considered(4). Dibenzothiophene's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur, but adsorption may attenuate this process(SRC). Dibenzothiophene is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(1).
Soil Adsorption
The Koc of dibenzothiophene was measured in 14 soil and sediment samples collected from the Ohio, Missouri, Mississippi, and Illinois Rivers and their watersheds(1). The adsorption isotherms were determined to be linear over the entire concentration range and adsorption was shown to be strongly correlated with the percentage of organic carbon in the soil and sediment. The Koc values ranged from 5,273 to 18,937 with an average value of 11,120(1). Koc values in the range of 11,584 to 20,535 were calculated for dibenzothiophene from adsorption isotherms using marine sediment obtained from the South China Sea(2). According to a classification scheme(3), these Koc values suggest that dibenzothiophene is expected to be immobile in soil(SRC).
Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaChromera VeliaCulture Collection of Algae and Protozoa (CCAP) at the SAMS Limited Scottish Marine Institute (Oban, Argyll, Scotland, UK)Koteska et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaChromera Veliaseawater media L1OSSA/GC-MSno


4-hydroxybenzenesulfonic Acid

Compound Details

Synonymous names
4-Hydroxybenzenesulfonic acid
98-67-9
p-Phenolsulfonic acid
phenolsulfonic acid
4-Phenolsulfonic acid
Sulfocarbolic acid
p-Sulfophenol
p-Hydroxybenzenesulfonic acid
Benzenesulfonic acid, 4-hydroxy-
4-HYDROXYPHENYLSULFONIC ACID
Phenol-4-sulfonic acid
Benzenesulfonic acid, p-hydroxy-
4-Sulfophenol
4-Hydroxybenzenesulphonic acid
Hydroxybenzene-4-sulfonic acid
p-Phenolsulfonate
NSC 227908
4-hydroxybenzene-1-sulfonic acid
para-phenolsulfonic acid
4-Hydroxybenzenesulfonic acid, 65% in Water
NSC-227908
L74LRO149A
DTXSID1046421
CHEBI:32354
Phenolsulfonic acid (JAN)
DTXCID9026421
PHENOLSULFONIC ACID [JAN]
CAS-98-67-9
HSDB 5319
NCGC00164534-01
NCGC00164534-02
EINECS 202-691-6
BRN 1869034
UNII-L74LRO149A
4-phenolsulfonic-acid
p-phenol sulfonic acid
4hydroxybenzenesulfonic acid
EC 202-691-6
p-Hydroxyphenylsulfonic acid
SCHEMBL18275
p-hydroxybenzenesulphonic acid
4-11-00-00582 (Beilstein Handbook Reference)
Phenol-4-sulfonic Acid Hydrate
CHEMBL1398657
P-PHENOLSULFONIC ACID [MI]
Tox21_112165
MFCD00007506
NSC227908
P-PHENOLSULFONIC ACID [HSDB]
STL280368
AKOS009159072
Tox21_112165_1
CS-W017509
DB14739
MCULE-9642506548
P-PHENOLSULFONIC ACID [WHO-DD]
PARA-PHENOLSULFONIC ACID [VANDF]
AM804627
AS-39421
BP-31158
4-Hydroxybenzenesulfonic Acid (85per cent)
NS00006802
P0104
EN300-36331
D01403
4-Hydroxybenzenesulfonic acid;p-Phenolsulfonic acid
Q1534677
W-100070
Microorganism:

No

IUPAC name4-hydroxybenzenesulfonic acid
SMILESC1=CC(=CC=C1O)S(=O)(=O)O
InchiInChI=1S/C6H6O4S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4,7H,(H,8,9,10)
FormulaC6H6O4S
PubChem ID4765
Molweight174.18
LogP0.2
Atoms11
Bonds1
H-bond Acceptor4
H-bond Donor2
Chemical Classificationaromatic compounds acids phenols sulfonyls benzenoids sulfur compounds
CHEBI-ID32354
Supernatural-IDSN0083605

mVOC Specific Details

Volatilization
The Henry's Law constant for 4-hydroxyphenylsulfonic acid is estimated as 2.62X10-13 atm-cu/mole(1,SRC). This indicates that 4-hydroxyphenylsulfonic acid will essentially not volatilize from water surfaces(2).
Literature: (1) Meylan W, Howard PH; Environ Toxicol Chem 10: 1283-93 (1991) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods Washington, DC: Amer Chem Soc p. 15-15 to 15-29 (1990)
Solubility
MISCIBLE WITH WATER, ALCOHOL
Literature: Budavari, S. (ed.). The Merck Index - Encyclopedia of Chemicals, Drugs and Biologicals. Rahway, NJ: Merck and Co., Inc., 1989., p. 1151
Soil Adsorption
Based on an estimated log Kow of -1.65(1), the Koc of 4-hydroxyphenylsulfonic acid is estimated as approximately 3.0 using a regression-derived equation(2,SRC). According to a suggested classification scheme, this estimated Koc value suggests that 4-hydroxyphenylsulfonic acid has very high mobility in soil(3).
Literature: (1) Meylan WM, Howard PH; J Pharm Sci 84: 83-92 (1995) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington DC: Amer Chem Soc pp. 4-9 (1990) (3) Swann RL et al; Res Rev 85: 23 (1983)
Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaTuber Magnatumn/aItalian geographical areas ( Piedmont)Gioacchini et al. 2008
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaTuber Magnatumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)no


2-(2-hydroxyethylsulfanyl)ethanol

Mass-Spectra

Compound Details

Synonymous names
thiodiglycol
2,2'-Thiodiethanol
111-48-8
Thiodiethanol
Thiodiethylene glycol
Tedegyl
Bis(2-hydroxyethyl) sulfide
Kromfax solvent
Ethanol, 2,2'-thiobis-
Bis(2-hydroxyethyl)sulfide
2,2'-THIOBISETHANOL
2,2'-Thiodiglycol
Glyecine A
Di(2-hydroxyethyl) sulfide
2,2-Thiodiethanol
2-(2-hydroxyethylsulfanyl)ethanol
Bis(2-hydroxyethyl) thioether
bis(hydroxyethyl)sulfide
beta-Hydroxyethyl sulfide
Sulfide, bis(2-hydroxyethyl)
Thiodiglycol [INN]
Thiodiglycolum
Tiodiglicol
Tiodiglicolo
Ethanol, 2,2'-thiodi-
Dihydroxyethyl sulfide
Diethanol sulfide
Bis(beta-hydroxyethyl) sulfide
beta,beta'-Dihydroxyethyl sulfide
beta,beta'-Dihydroxydiethyl sulfide
Bis(beta-hydroxyethyl)sulfide
2-[(2-hydroxyethyl)sulfanyl]ethan-1-ol
2,2'-Thiobis(ethanol)
3-Thiapentane-1,5-diol
beta-Thiodiglycol
Kromfax@ Solvent
NSC 6289
Bis(2-hydroxyethyl) sulphide
.beta.-Thiodiglycol
2-[(2-hydroxyethyl)thio]ethanol
NSC-6289
2,2'-Thiobis[ethanol]
2,2'-sulfanediyldiethanol
.beta.-Hydroxyethyl sulfide
Bis(b-hydroxyethyl) sulfide
beta-Bis(hydroxyethyl) sulfide
DTXSID6026878
CHEBI:75184
.beta.-Bis(hydroxyethyl) sulfide
Bis(.beta.-hydroxyethyl) sulfide
9BW5T43J04
MFCD00002910
.beta.,.beta.'-Dihydroxyethyl sulfide
.beta.,.beta.'-Dihydroxydiethyl sulfide
NCGC00095074-01
DTXCID506878
Tiodiglicolo [DCIT]
2,2'-sulfobisethanol
Tiodiglicol [INN-Spanish]
Thiodiglycolum [INN-Latin]
28516-38-3
CAS-111-48-8
HSDB 7482
EINECS 203-874-3
BRN 1236325
UNII-9BW5T43J04
AI3-05541
Ethanol,2'-thiodi-
Ethanol,2'-thiobis-
2-Hydroxyethyl Sulfide
Spectrum_001701
2-Methylsulfone ethanol
beta-hydroxyethyl sulfid
2,2'-Thiodi-Ethanol
2,2'-Thiobis-Ethanol
Spectrum2_000407
Spectrum4_000213
EC 203-874-3
THIODIGLYCOL [HSDB]
THIODIGLYCOL [INCI]
WLN: Q2S2Q
SCHEMBL40132
KBioGR_000845
KBioSS_002181
1,5-dihydroxy-3-thiapentane
2,2'-thiobis(ethan-1-ol)
SPECTRUM1503325
2-(2-hydroxyethylthio)ethanol
bis-(2-hydroxyethyl) sulphide
SPBio_000334
CHEMBL444480
SCHEMBL6679983
KBio2_002181
KBio2_004749
KBio2_007317
2,2'-Thiodiethanol, >=99%
NSC6289
HMS1922I18
Pharmakon1600-01503325
2,2'-THIODIETHANOL [MI]
HY-B0913
Tox21_111413
Tox21_200827
CCG-39716
NSC758456
STL302034
AKOS009031578
Tox21_111413_1
MCULE-5502656030
NSC-758456
1ST159274_C
NCGC00095074-02
NCGC00095074-03
NCGC00095074-05
NCGC00258381-01
2,2'-Thiodiethanol, >=99.0% (GC)
SBI-0051909.P002
DB-060096
NS00009553
T0202
2,2'-Thiodiethanol, purum, >=95.0% (GC)
2,2'-Thiodiethanol 1000 microg/mL in Methanol
AB00052435_02
2,2'-Thiodiethanol, puriss., >=98.5% (GC)
A802371
Q418117
SR-01000872773
J-002590
SR-01000872773-1
InChI=1/C4H10O2S/c5-1-3-7-4-2-6/h5-6H,1-4H
2,2'-Thiodiethanol, >=99.0%, suitable for amino acid analysis
2,2'-Thiodiethanol; 2,2'-Thiobis(ethanol), Bis(2-hydroxyethyl) sulfide, Thiodiethylene glycol, Thiodiglycol
Microorganism:

No

IUPAC name2-(2-hydroxyethylsulfanyl)ethanol
SMILESC(CSCCO)O
InchiInChI=1S/C4H10O2S/c5-1-3-7-4-2-6/h5-6H,1-4H2
FormulaC4H10O2S
PubChem ID5447
Molweight122.19
LogP-0.6
Atoms7
Bonds4
H-bond Acceptor3
H-bond Donor2
Chemical Classificationalcohols sulfides sulfur compounds thioethers
CHEBI-ID75184
Supernatural-IDSN0455751

mVOC Specific Details

Boiling Point
DegreeReference
282 deg CLide, D.R. CRC Handbook of Chemistry and Physics 86TH Edition 2005-2006. CRC Press, Taylor & Francis, Boca Raton, FL 2005, p. 3-52
Volatilization
The Henry's Law constant for thiodiglycol is estimated as 1.9X10-9 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that thiodiglycol is expected to be essentially nonvolatile from water surfaces(2) and moist soil surfaces(SRC). Thiodiglycol is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 0.00323 mm Hg(3).
Literature: (1) Meylan WM, Howard PH; Environ Toxicol Chem 10: 1283-93 (1991) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, DC: Taylor and Francis (1989)
Soil Adsorption
The Koc of thiodiglycol is estimated as 11(SRC), using a log Kow of -0.63(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that thiodigylcol is expected to have very high mobility in soil. The sorption of thiodiglycol was determined in 6 soils that were characteristic of US military installations(4). After 24 hours of equilibration, 99-100% of the original mass of thiodiglycol remained in the aqueous phase for 5 of the 6 soils(4).
Literature: (1) Hansch C et al; Exploring QSAR. Hydrophobic, Electronic, and Steric Constants. ACS Prof Ref Book. Heller SR, consult. ed., Washington, DC: Amer Chem Soc p. 10 (1995) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 4-9 (1990) (3) Swann RL et al; Res Rev 85: 17-28 (1983) (4) Lee KP, Allen HE; Environ Toxicol Chem 17: 1720-6 (1998)
Vapor Pressure
PressureReference
0.00323 at 25 deg CDaubert, T.E., R.P. Danner. Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, D.C.: Taylor and Francis, 1989.
MS-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaTuber Magnatumn/aItalian geographical areas ( Piedmont, Marche, Border region area between Emilia Romagna and Marche, Molise)Gioacchini et al. 2008
EukaryotaTuber Magnatumn/aItalian geographical areas ( Marche, Emilia Romagna, Border region area between Emilia Romagna and Marche)Gioacchini et al. 2008
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaTuber Magnatumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)no


Methylsulfonylmethane

Mass-Spectra

Compound Details

Synonymous names
Dimethyl sulfone
Methyl sulfone
67-71-0
Methylsulfonylmethane
DIMETHYLSULFONE
Dimethyl sulphone
Sulfonylbismethane
Methane, sulfonylbis-
sulfonyldimethane
(methylsulfonyl)methane
Sulphonylbismethane
Methylsulfonyl methane
METHANESULFONYLMETHANE
METHYL SULFONYL METHANE
DMSO2
NSC 63345
9H4PO4Z4FT
CHEMBL25028
Methane, 1,1'-sulfonylbis-
CHEBI:9349
DTXSID4043937
NSC-63345
methylsulfone
CCRIS 2938
EINECS 200-665-9
UNII-9H4PO4Z4FT
dimethylsulfon
dimethylsulphone
methy sulfone
methyl sulphone
AI3-25306
Lignisul MSM
Sulfonylbis-methane
Opti MSM
Sulfone, dimethyl-
MFCD00007566
(methylsulphonyl)methane
Dimethyl sulfone, 98%
METHOSULFONYLMETHANE
MolMap_000019
DIMETHYL SULFONE [MI]
SPECTRUM1505358
DIMETHYL SULFONE [INCI]
DTXCID2023937
DIMETHYL SULFONE [MART.]
AMY25756
HY-Y1314
NSC63345
METHYLSULFONYLMETHANE [VANDF]
Tox21_303712
BDBM50026473
METHYLSULFONYLMETHANE [USP-RS]
METHYLSULFONYLMETHANE [WHO-DD]
AKOS015897615
CCG-214558
DB14090
MCULE-3320409932
CAS-67-71-0
NCGC00095990-01
NCGC00357027-01
DB-050533
MYTHYLSULFONYLMETHANE (MSM) [VANDF]
CS-0017786
M0509
M1239
NS00006500
EN300-79559
D70240
InChI=1/C2H6O2S/c1-5(2,3)4/h1-2H
A835859
Q423842
DIMETHYL SULFOXIDE IMPURITY A [EP IMPURITY]
F0001-1776
Z417007936
Dimethyl sulfone, Standard for quantitative NMR, TraceCERT(R)
Methylsulfonylmethane, United States Pharmacopeia (USP) Reference Standard
Methylsulfonylmethane, Pharmaceutical Secondary Standard; Certified Reference Material
Microorganism:

Yes

IUPAC namemethylsulfonylmethane
SMILESCS(=O)(=O)C
InchiInChI=1S/C2H6O2S/c1-5(2,3)4/h1-2H3
FormulaC2H6O2S
PubChem ID6213
Molweight94.14
LogP-0.4
Atoms5
Bonds0
H-bond Acceptor2
H-bond Donor0
Chemical Classificationsulfones sulfur compounds sulfonyls
CHEBI-ID9349
Supernatural-IDSN0126036

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaPaenibacillus PolymyxaNAMülner et al. 2021
ProkaryotaBacillus Subtilisgrowth stimulation effects on Solanum tuberosum tubers (potato) and Zea mays seeds (maize)NAMülner et al. 2020
ProkaryotaBacillus SubtilisNAMülner et al. 2020
ProkaryotaBacillus Atrophaeusgrowth stimulation effects on Solanum tuberosum tubers (potato) and Zea mays seeds (maize)NAMülner et al. 2020
ProkaryotaBacillus AmyloliquefaciensNAMülner et al. 2020
ProkaryotaBacillus Velezensisgrowth stimulation effects on Solanum tuberosum tubers (potato) and Zea mays seeds (maize)Leibnitz Institute DSMZ-German Collection of Microorganisms and Cell Cultures GmbHMülner et al. 2020
ProkaryotaBacillus Velezensisgrowth stimulation effects on Solanum tuberosum tubers (potato) and Zea mays seeds (maize)NAMülner et al. 2020
ProkaryotaBacillus LicheniformisNAMülner et al. 2020
ProkaryotaCollimonas Fungivoransn/aNAGarbeva et al. 2014
ProkaryotaSerratia Plymuthicanamaize rhizosphere, NetherlandsGarbeva et al. 2014
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaPaenibacillus PolymyxaNA mediaHS-SPME/GC-MSno
ProkaryotaBacillus Subtilisnutrient agarHS-SPME/GC-MSno
ProkaryotaBacillus Atrophaeusnutrient agarHS-SPME/GC-MSno
ProkaryotaBacillus Amyloliquefaciensnutrient agarHS-SPME/GC-MSno
ProkaryotaBacillus Velezensisnutrient agarHS-SPME/GC-MSno
ProkaryotaBacillus Licheniformisnutrient agarHS-SPME/GC-MSno
ProkaryotaCollimonas FungivoransHeadspace trapping/GC-MSno
ProkaryotaSerratia Plymuthicasand containing artificial root exudatesGC/MSno


Ethanethiol

Mass-Spectra

Compound Details

Synonymous names
Ethanethiol
ETHYL MERCAPTAN
75-08-1
Mercaptoethane
Ethyl sulfhydrate
Thioethanol
Ethyl thioalcohol
Thioethyl alcohol
Ethyl hydrosulfide
Aethylmercaptan
Etilmercaptano
Aethanethiol
Etantiolo
1-Mercaptoethane
Ethaanthiol
Ethylmercaptaan
Ethylmerkaptan
ethyl-mercaptan
Mercaptan C2
LPG ethyl mercaptan 1010
NSC 93877
stench
HSDB 814
stench gas
1-ethanethiol
EINECS 200-837-3
UNII-M439R54A1D
AI3-26618
M439R54A1D
NSC-93877
DTXSID9026394
FEMA NO. 4258
CHEBI:46511
EC 200-837-3
ETHANETHIOL (MART.)
ETHANETHIOL [MART.]
Etantiolo [Italian]
Ethaanthiol [Dutch]
Aethanethiol [German]
ethanthiol
ethylmercaptan
Ethylmerkaptan [Czech]
Ethylmercaptaan [Dutch]
Aethylmercaptan [German]
Etilmercaptano [Italian]
UN2363
ethanethioi
ethanethiolate
ethanothiol
ethane thiol
1-Ethylthiol
EtSH
HSEt
Ethanethiol, 97%
Ethanethiol, >=97%
ETHANETHIOL [MI]
ETHANETHIOL [FHFI]
C2H5SH
WLN: SH2
ETHYL MERCAPTAN [HSDB]
DTXCID506394
Ethanethiol, analytical standard
NSC93877
MFCD00004887
AKOS000120313
MCULE-5717309901
UN 2363
DB-004032
E0036
NS00005388
EN300-20602
InChI=1/C2H6S/c1-2-3/h3H,2H2,1H
Ethyl mercaptan [UN2363] [Flammable liquid]
Ethanethiol (ethyl mercaptan), analytical standard
Q407918
J-520442
F0001-1889
QuadraPure(R) DET, 450-650 mum, extent of labeling: 1.0-2.0 mmol/g loading, macroporous
EUF
Microorganism:

Yes

IUPAC nameethanethiol
SMILESCCS
InchiInChI=1S/C2H6S/c1-2-3/h3H,2H2,1H3
FormulaC2H6S
PubChem ID6343
Molweight62.14
LogP0.9
Atoms3
Bonds0
H-bond Acceptor1
H-bond Donor1
Chemical Classificationsulfur compounds thiols
CHEBI-ID46511
Supernatural-IDSN0070346

mVOC Specific Details

Boiling Point
DegreeReference
35.1 °C peer reviewed
Volatilization
The Henry's Law constant for ethyl mercaptan is 4.53X10-3 atm-cu m/mole(1). This Henry's Law constant indicates that ethyl mercaptan is expected to volatilize from water surfaces(2). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(2) is estimated as 2.4 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as 3.2 days(SRC). Ethyl mercaptan's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Ethyl mercaptan is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 529 mm Hg(3).
Literature: (1) Vitenberg AG et al; J Chromat 112: 319-27 (1975) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals: Data Compilation. Design Inst Phys Prop Data, Amer Inst Chem Eng. NY, NY: Hemisphere Pub Corp. 4 vol (1989)
Soil Adsorption
The Koc of ethyl mercaptan is estimated as 22(SRC), using a water solubility of 1.56X10+4 mg/L(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that ethyl mercaptan is expected to have very high mobility in soil.
Literature: (1) Wakita K et al; Chem Pharm Bull 34: 4463-81 (1986) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 4-5 (1990) (3) Swann RL et al; Res Rev 85: 17-28 (1983)
Vapor Pressure
PressureReference
529 mm Hg at 25 deg C /Extrapolated/Daubert, T.E., R.P. Danner. Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, D.C.: Taylor and Francis, 1989.
Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaClostridium Difficileoutbreak 2006 UKRees et al. 2016
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaClostridium Difficilebrain heart infusionGCxGC-TOF-MSyes


Compound Details

Synonymous names
CARBON DISULFIDE
Carbon disulphide
Carbon bisulfide
75-15-0
Carbon bisulphide
Dithiocarbonic anhydride
Schwefelkohlenstoff
Weeviltox
Wegla dwusiarczek
Solfuro di carbonio
methanedithione
Sulphocarbonic anhydride
Sulphuret of carbon
disulfidocarbon
CARBONDISULFIDE
RCRA waste number P022
Caswell No. 162
NCI-C04591
Carbon bisulfuret
Alcohol of sulfur
Sulfure de carbone
Koolstofdisulfide (zwavelkoolstof)
Kohlendisulfid (schwefelkohlenstoff)
HSDB 52
Carbone (sulfure de)
Carbonio (solfuro di)
CCRIS 5570
Carbon sulfide (CS2)
Carbon sulphide
UN 1131
EINECS 200-843-6
EPA Pesticide Chemical Code 016401
UNII-S54S8B99E8
BRN 1098293
CS2
DTXSID6023947
CHEBI:23012
Sulfocarbonic anhydride
AI3-08935
Sulfure de carbone [ISO-French]
S54S8B99E8
CARBONEUM SULPHURATUM
Carbon disulfide, ACS reagent
DTXCID103947
CARBON DISULFIDE (13C)
EC 200-843-6
4-03-00-00395 (Beilstein Handbook Reference)
12539-80-9
NCGC00091108-01
Carbondisulphide
CARBON DISULFIDE (MART.)
CARBON DISULFIDE [MART.]
Sulfure de carbone (ISO-French)
Carbon disulfide cation
Wegla dwusiarczek [Polish]
Disulfide, Carbon
CAS-75-15-0
Schwefelkohlenstoff [German]
Carbon disulfide [BSI:ISO]
Carbon disulfide, ACS reagent, >=99.9%
Solfuro di carbonio [Italian]
Carbone (sulfure de) [French]
Carbonio (solfuro di) [Italian]
UN1131
RCRA waste no. P022
Carbon disulfide, puriss., low in benzene, >=99.5% (GC)
Dithioxomethane
Kohlendisulfid
Koolstofdisulfide (zwavelkoolstof) [Dutch]
Koolstofdisulfide
carbon-disulphide
Kohlendisulfid (schwefelkohlenstoff) [German]
Dithioxomethane #
Carbon-disulphide-
Carbone (sufure de)
Caswell No 162
Carbon disulfide, CP
Carbon disulphide, BSI
HEADACHE RHEUMATISM
CARBON DISULFIDE [MI]
CARBON DISULFIDE [ISO]
CARBON DISULFIDE [HSDB]
CHEMBL1365180
CARBON DISULFIDE [WHO-DD]
Carbon disulfide, p.a., 99.5%
CARBONEUM SULPHURATUM [HPUS]
Tox21_111082
Tox21_201168
CARBON DISULFIDE [GREEN BOOK]
Carbon disulfide, anhydrous, >=99%
AKOS009075983
USEPA/OPP Pesticide Code: 016401
NCGC00091108-02
NCGC00258720-01
Carbon disulfide, for HPLC, >=99.9%
CARBON DISULFIDE (CARBON BISULFIDE)
Carbondisulfide 100 microg/ml in Methanol
Carbon disulfide, purum, >=99.0% (GC)
Carbondisulfide 5000 microg/mL in Methanol
C1955
Carbon-12C disulfide, 99.9 atom % 12C
NS00040573
Carbon disulfide 5000 microg/mL in Methanol
Carbon disulfide, puriss., >=99.5% (GC)
C19033
Carbon disulfide, SAJ first grade, >=98.0%
Carbon disulfide [UN1131] [Flammable liquid]
Carbon disulfide, JIS special grade, >=99.0%
Carbon disulfide, spectrophotometric grade, >=99%
Q243354
Carbon disulfide, puriss. p.a., >=99.9% (GC)
Carbon disulfide, ReagentPlus(R), low benzene, >=99.9%
Carbon disulfide, ReagentPlus(R), purified by redistillation, >=99.9%
Carbon disulfide, for IR spectroscopy, puriss. p.a., ACS reagent, reag. Ph. Eur., >=99.9% (GC)
Microorganism:

Yes

IUPAC name
SMILESC(=S)=S
InchiInChI=1S/CS2/c2-1-3
FormulaCS2
PubChem ID6348
Molweight76.15
LogP2.1
Atoms3
Bonds0
H-bond Acceptor2
H-bond Donor0
Chemical Classificationsulfides sulfur compounds
CHEBI-ID23012
Supernatural-IDSN0304680

mVOC Specific Details

Boiling Point
DegreeReference
46.2 °C peer reviewed
Volatilization
The Henry's Law constant for carbon disulfide is 1.44X10-2 atm-cu m/mole at 24 deg C(1). This Henry's Law constant indicates that carbon disulfide is expected to volatilize rapidly from water surfaces(2). Based on this Henry's Law constant, the estimated volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec) (2) is approximately 2.6 hours(SRC). The estimated volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec) (2)is approximately 3.5 days(SRC). Carbon disulfide's Henry's Law constant(1) indicates that volatilization from moist soil surfaces is expected to occur(SRC). The potential for volatilization of carbon disulfide from dry soil surfaces may exist(SRC) based upon the vapor pressure of 359 mm Hg(3).
Literature: (1) Elliot S; Atmos Environ 23: 1977-80 (1989) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Yaws CL; Handbook of Vapor Pressure, Vol 1, Houston,TX: Gulf Pub Co (1994)
Soil Adsorption
The Koc of carbon disulfide is estimated as approximately 270(SRC), using a log Kow of 1.94(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that carbon disulfide is expected to have moderate mobility in soil(SRC). The avg adsorption of carbon disulfide after 10 minutes by 4 air-dried soils was 46% but only 12% by the same soils at 50% water-holding capacity(4). However, after 8 hr the rate of adsorption was greater by moist soil, but only when the soil was unsterilized(4). Further experiments suggest that this 'adsorption' in moist soils is the result of microbial action(4).
Literature: (1) Hansch C et al; Exploring QSAR. Hydrophobic, Electronic, and Steric Constants. ACS Prof Ref Book. Heller SR (consult ed) Washington,DC: Amer Chem Soc p 3 (1995) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington,DC: Amer Chem Soc pp. 4-9 (1990) (3) Swann RL et al; Res Rev 85: 23 (1983) (4) Bremner JM, Banwart WL; Soil Biol Biochem 8: 79-83 (1976)
Vapor Pressure
PressureReference
359 mm Hg at 25 deg CYaws CL; Handbook of Vapor Pressure, Vol 1, Houston,TX: Gulf Pub Co. (1994)
MS-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaBurkholderia CepaciaNANADryahina et al. 2016
ProkaryotaPseudomonas AeruginosaNANADryahina et al. 2016
ProkaryotaStaphylococcus AureusNANADryahina et al. 2016
ProkaryotaStenotrophomonas MaltophiliaNANADryahina et al. 2016
ProkaryotaKlebsiella PneumoniaeNANARees et al. 2016a
ProkaryotaHaemophilus InfluenzaeNANAFilipiak et al. 2012
ProkaryotaStreptococcus PneumoniaeNANAFilipiak et al. 2012
EukaryotaFusarium OxysporumonionWang et al. 2018
EukaryotaFusarium ProliferatumonionWang et al. 2018
ProkaryotaPseudomonas Putidan/aNASchulz and Dickschat 2007
ProkaryotaSerratia Proteamaculansn/aNAErcolini et al. 2009
ProkaryotaCarnobacterium Divergensn/aNAErcolini et al. 2009
ProkaryotaPseudomonas Fragin/aNAErcolini et al. 2009
EukaryotaOgataea Pininamycangia of Dendroctonus brevicomisDavis et al. 2011
ProkaryotaPseudomonas PutidananaSchöller et al. 1997
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaBurkholderia CepaciaNBSIFT-MSno
ProkaryotaBurkholderia CepaciaBHISIFT-MSno
ProkaryotaBurkholderia CepaciaMHBSIFT-MSno
ProkaryotaPseudomonas AeruginosaMHBSIFT-MSno
ProkaryotaPseudomonas AeruginosaNBSIFT-MSno
ProkaryotaPseudomonas AeruginosaBHISIFT-MSno
ProkaryotaStaphylococcus AureusNBSIFT-MSno
ProkaryotaStaphylococcus AureusBHISIFT-MSno
ProkaryotaStaphylococcus AureusMHBSIFT-MSno
ProkaryotaStenotrophomonas MaltophiliaNBSIFT-MSno
ProkaryotaStenotrophomonas MaltophiliaBHISIFT-MSno
ProkaryotaStenotrophomonas MaltophiliaMHBSIFT-MSno
ProkaryotaKlebsiella Pneumoniaehuman bloodSPME/GCxGC-MSno
ProkaryotaHaemophilus InfluenzaeTryptic soya supp. factors X&VTD/GC-MSno
ProkaryotaStreptococcus PneumoniaeTryptic soyaTD/GC-MSno
EukaryotaFusarium OxysporumLiquid onion extract medium (LOM)SPME, GC-MSyes
EukaryotaFusarium ProliferatumLiquid onion extract medium (LOM)SPME, GC-MSyes
ProkaryotaPseudomonas Putidan/an/ano
ProkaryotaSerratia Proteamaculansn/an/ano
ProkaryotaCarnobacterium Divergensn/an/ano
ProkaryotaPseudomonas Fragin/an/ano
EukaryotaOgataea PiniMEAGC/MSno
ProkaryotaPseudomonas PutidaAB medium + 1% citrate or 0,02% citrate or 1% glucose +1% casaminoacid GC-FID,GC/MSno


1-thiophen-2-ylethanone

Compound Details

Synonymous names
2-ACETYLTHIOPHENE
88-15-3
1-thiophen-2-yl-ethanone
1-(2-Thienyl)ethanone
2-Acetothienone
Methyl 2-thienyl ketone
1-(thiophen-2-yl)ethanone
2-Acetothiophene
Ethanone, 1-(2-thienyl)-
2-acetyl thiophene
2-Thienyl methyl ketone
Ketone, methyl 2-thienyl
1-thiophen-2-ylethanone
alpha-Acetylthiophene
2-Acethylthiophene
1-(2-thienyl)-ethanone
1-(thiophen-2-yl)ethan-1-one
Methyl-2-thienyl ketone
2-Acetylthiophen
NSC 2345
97511-16-5
THIOPHENE,2-ACETYL
CHEMBL401911
5ASO208T20
NSC-2345
MFCD00005442
2-Aceto thiophene
EINECS 201-804-6
BRN 0107910
2acetylthiophene
acetyl-thiophene
2-acetylthiole
AI3-08491
2-Acetyl-thiophene
ACETYLTHIOPHENE
2-Acetylthiophene, 98%
SCHEMBL3798
WLN: T5SJ BV1
2-(ACETYL)THIOFURAN
5-17-09-00387 (Beilstein Handbook Reference)
BIDD:GT0210
UNII-5ASO208T20
1-(2-Thienyl)ethanone, 9CI
DTXSID2058960
NSC2345
CHEBI:179841
2-Acetylthiophene, >=98%, FG
BCP24442
STR01324
BDBM50376211
STL183822
2-Acetylthiophene, analytical standard
AKOS000119817
AC-4918
AM82005
CS-W020047
MCULE-7771755380
PS-3261
HY-20585
DB-038374
A0724
NS00022862
EN300-17951
W18336
A842486
Q-100875
Q27261757
Z57127896
F0001-2186
InChI=1/C6H6OS/c1-5(7)6-3-2-4-8-6/h2-4H,1H
Microorganism:

Yes

IUPAC name1-thiophen-2-ylethanone
SMILESCC(=O)C1=CC=CS1
InchiInChI=1S/C6H6OS/c1-5(7)6-3-2-4-8-6/h2-4H,1H3
FormulaC6H6OS
PubChem ID6920
Molweight126.18
LogP1.2
Atoms8
Bonds1
H-bond Acceptor2
H-bond Donor0
Chemical Classificationaromatic compounds heterocyclic compounds aromatic ketones ketones sulfur compounds
CHEBI-ID179841
Supernatural-IDSN0423348

mVOC Specific Details

Boiling Point
DegreeReference
213 median
Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaStreptococcus PneumoniaeNANAKaeslin et al. 2021
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaStreptococcus PneumoniaeBHISESI-MSno


1-benzothiophene

Mass-Spectra

Compound Details

Synonymous names
Benzo[b]thiophene
Thianaphthene
1-Benzothiophene
95-15-8
BENZOTHIOPHENE
Benzothiofuran
Thionaphthene
1-Thiaindene
Thianaphtene
Thianaphthen
1-benzothiophen
BENZO(B)THIOPHENE
Benzothiophen
Benzothiophene-5-D
2,3-Benzothiophene
11095-43-5
Benzo[b]thiophene-D6
MFCD00005864
NSC 47196
CHEMBL87112
CHEBI:35858
NSC-47196
073790YQ2G
13730-27-3
C8H6S
Thianaftene
Thianapthene
UNII-073790YQ2G
hydrobenzothiophene
benzo[b]-thiophene
EINECS 202-395-7
Thianaphthene, 95%
Thianaphthene, 98%
AI3-15523
THIANAPHTHENE [MI]
SCHEMBL7023
BIDD:GT0845
DTXSID2052736
CS-D1193
NSC47196
BDBM50167948
GEO-00284
MFCD31699976
STK053859
AKOS005258172
MCULE-7277751906
PS-5775
SY246286
AM20041456
B0093
NS00020042
EN300-36787
A845195
A847764
Q419709
Q-100899
F0001-2267
Z370711590
InChI=1/C8H6S/c1-2-4-8-7(3-1)5-6-9-8/h1-6
Microorganism:

Yes

IUPAC name1-benzothiophene
SMILESC1=CC=C2C(=C1)C=CS2
InchiInChI=1S/C8H6S/c1-2-4-8-7(3-1)5-6-9-8/h1-6H
FormulaC8H6S
PubChem ID7221
Molweight134.2
LogP3.1
Atoms9
Bonds0
H-bond Acceptor1
H-bond Donor0
Chemical Classificationbenzenoids heterocyclic compounds sulfur compounds aromatic compounds
CHEBI-ID35857
Supernatural-IDSN0081749

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaChromera VeliaCulture Collection of Algae and Protozoa (CCAP) at the SAMS Limited Scottish Marine Institute (Oban, Argyll, Scotland, UK)Koteska et al. 2023
EukaryotaTuber BrumaleFortywoodland of the Basilicata regionMauriello et al. 2004
ProkaryotaClostridium Difficileoutbreak 2006 UKRees et al. 2016
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaChromera Veliaseawater media L1OSSA/GC-MSno
EukaryotaTuber Brumalemicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)no
ProkaryotaClostridium Difficilebrain heart infusionGCxGC-TOF-MSyes


1,3-benzothiazole

Mass-Spectra

Compound Details

Synonymous names
BENZOTHIAZOLE
95-16-9
BENZO[D]THIAZOLE
1,3-Benzothiazole
Benzosulfonazole
1-Thia-3-azaindene
Vangard BT
benzothiazol
USAF EK-4812
FEMA No. 3256
CHEBI:45993
O-2857
MFCD00005775
G5BW2593EP
DTXSID7024586
NSC-8040
BT
DTXCID204586
benzthiazole
FEMA Number 3256
CAS-95-16-9
CCRIS 7893
HSDB 2796
NSC 8040
EINECS 202-396-2
BRN 0109468
UNII-G5BW2593EP
s-benzothiazole
AI3-05742
Benzothiazole, 96%
1,3-Benzothiazole #
BENZOTHIAZOLE [MI]
Epitope ID:138946
EC 202-396-2
SCHEMBL8430
BENZOTHIAZOLE [FHFI]
BENZOTHIAZOLE [HSDB]
WLN: T56 BN DSJ
4-27-00-01069 (Beilstein Handbook Reference)
MLS001050134
Benzothiazole, >=96%, FG
CHEMBL510309
SCHEMBL9304593
NSC8040
Benzothiazole, analytical standard
AMY23315
Tox21_201853
Tox21_303232
BDBM50444460
LT0034
STL268890
AKOS000120178
AC-3297
CS-W013350
FS-4155
HY-W012634
MCULE-5257468117
NCGC00091399-01
NCGC00091399-02
NCGC00257070-01
NCGC00259402-01
BOT
SMR001216577
DB-057562
B0092
NS00000291
Benzothiazole, Vetec(TM) reagent grade, 96%
EN300-19148
D77749
AC-907/25014160
Q419096
Q-100900
F0001-2268
Z104472964
InChI=1/C7H5NS/c1-2-4-7-6(3-1)8-5-9-7/h1-5
Microorganism:

Yes

IUPAC name1,3-benzothiazole
SMILESC1=CC=C2C(=C1)N=CS2
InchiInChI=1S/C7H5NS/c1-2-4-7-6(3-1)8-5-9-7/h1-5H
FormulaC7H5NS
PubChem ID7222
Molweight135.19
LogP2
Atoms9
Bonds0
H-bond Acceptor2
H-bond Donor0
Chemical Classificationnitrogen compounds benzenoids heterocyclic compounds thiazoles aromatic compounds sulfur compounds
CHEBI-ID45993
Supernatural-IDSN0150933

mVOC Specific Details

Boiling Point
DegreeReference
227-228 DEG C AT 765 MM HGBudavari, S. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Whitehouse Station, NJ: Merck and Co., Inc., 1996., p. 186
Volatilization
The Henry's Law constant for benzothiazole is estimated as 3.7 X 10-7 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This value indicates that benzothiazole will volatilize slowly from water surfaces(2,SRC). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec) is estimated as approximately 114 days(2,SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec) is estimated as approximately 832 days(2,SRC). Benzothiazole's Henry's Law constant(1,SRC) indicates that volatilization from moist soil surfaces should be slow(SRC).
Literature: (1) Meylan WM, Howard PH; Environ Toxicol Chem 10: 1283-93 (1991) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)
Soil Adsorption
The Koc of benzothiazole is estimated as approximately 295(SRC), using an experimental log Kow of 2.01(1,SRC) and a regression-derived equation(2,SRC). According to a recommended classification scheme(3), this estimated Koc value suggests that benzothiazole has moderate mobility in soil(SRC).
Literature: (1) Hansch C et al; Exploring QSAR Hydrophobic, Electronic and Stearic Constants Washington DC: Amer Chem Soc (1995) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington DC: Amer Chem Soc pp. 4-9 (1990) (3) Swann RL et al; Res Rev 85: 23 (1983)
MS-Links
1D-NMR-Links
Massbank-Links
Massbank Spectrum MSBNK-Antwerp_Univ-AN124202
Massbank Spectrum MSBNK-Antwerp_Univ-AN124204
Massbank Spectrum MSBNK-Antwerp_Univ-AN124208
Massbank Spectrum MSBNK-Athens_Univ-AU405606
Massbank Spectrum MSBNK-Athens_Univ-AU405608
Massbank Spectrum MSBNK-BAFG-CSL2311108601
Massbank Spectrum MSBNK-BAFG-CSL2311108602
Massbank Spectrum MSBNK-BAFG-CSL2311108603
Massbank Spectrum MSBNK-BAFG-CSL2311108604
Massbank Spectrum MSBNK-BAFG-CSL2311108605
Massbank Spectrum MSBNK-CASMI_2016-SM882102
Massbank Spectrum MSBNK-Eawag-EA034302
Massbank Spectrum MSBNK-Eawag-EA034303
Massbank Spectrum MSBNK-Eawag-EA034304
Massbank Spectrum MSBNK-Eawag-EA034305
Massbank Spectrum MSBNK-Eawag-EA034306
Massbank Spectrum MSBNK-Eawag-EA034307
Massbank Spectrum MSBNK-Eawag-EA034308
Massbank Spectrum MSBNK-Eawag-EA034309
Massbank Spectrum MSBNK-Eawag-EA034310
Massbank Spectrum MSBNK-Eawag-EA034311
Massbank Spectrum MSBNK-Eawag-EA034312
Massbank Spectrum MSBNK-Eawag-EA034313
Massbank Spectrum MSBNK-Fac_Eng_Univ_Tokyo-JP000473
Massbank Spectrum MSBNK-Fac_Eng_Univ_Tokyo-JP008217
Massbank Spectrum MSBNK-Fac_Eng_Univ_Tokyo-JP012060
Massbank Spectrum MSBNK-UFZ-UF420801
Massbank Spectrum MSBNK-UFZ-UF420802
Massbank Spectrum MSBNK-UFZ-UF420803
Massbank Spectrum MSBNK-UFZ-WANA042101AD6CPH
Massbank Spectrum MSBNK-UFZ-WANA042103B085PH
Massbank Spectrum MSBNK-UFZ-WANA042105070APH
Massbank Spectrum MSBNK-UFZ-WANA042111C9CFPH
Massbank Spectrum MSBNK-UFZ-WANA042113D9F1PH
Massbank Spectrum MSBNK-UFZ-WANA0421155BE0PH
Massbank Spectrum MSBNK-UFZ-WANA0421213166PH
Massbank Spectrum MSBNK-UFZ-WANA0421237762PH
Massbank Spectrum MSBNK-UFZ-WANA042125AF82PH

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaStenotrophomonas MaltophiliaNANAKaeslin et al. 2021
ProkaryotaEscherichia ColiNANADixon et al. 2022
ProkaryotaBacillus SubtilisNAGao et al. 2018
ProkaryotaBacillus Velezensistoxic effects on fungal mycelial growthmaize seedMassawe et al. 2018
ProkaryotaBacillus Muralisantifungal activity against mycelial growth and spore germination of phytopathogenic Moniliophtora roreriphytopathology strain collection of El Colegio de la Frontera Sur (ECOSUR), Tapachula, Chiapas, MexicoDe la Cruz-López et al. 2022
ProkaryotaNovosphingobium Lindaniclasticumantifungal activity against mycelial growth and spore germination of phytopathogenic Moniliophtora roreriphytopathology strain collection of El Colegio de la Frontera Sur (ECOSUR), Tapachula, Chiapas, MexicoDe la Cruz-López et al. 2022
ProkaryotaBacillus Subtilisantifungal activity against mycelial growth and spore germination of phytopathogenic Moniliophtora roreriphytopathology strain collection of El Colegio de la Frontera Sur (ECOSUR), Tapachula, Chiapas, MexicoDe la Cruz-López et al. 2022
ProkaryotaBacillus Megateriumantifungal activity against mycelial growth and spore germination of phytopathogenic Moniliophtora roreriphytopathology strain collection of El Colegio de la Frontera Sur (ECOSUR), Tapachula, Chiapas, MexicoDe la Cruz-López et al. 2022
ProkaryotaBacillus Subtilisantifungal activity against Alternaria solaniisolate from rhizosphere of potato in Shandong and Hebei Province in ChinaZhang et al. 2020
ProkaryotaPaenibacillus Polymyxaantifungal effects against Rhizopus stoloniferisolated from an ancient tree Cryptomeria fortune and deposited in China General Microbiological Culture Collection Center (CGMCC No. 15733)Wu et al. 2020
ProkaryotaStenotrophomonas Maltophiliaantifungal activity against Colletotrichum nymphaeaeisolated from the healthy strawberry leaf in Kamyaran, Kurdistan provinceAlijani et al. 2020
ProkaryotaBacillus Subtilisinhibited the mycelial growth of Lasiodiplodia theobromae L26NASudha et al. 2021
EukaryotaTrichoderma Viriden/anot shownWheatley et al. 1997
EukaryotaTrichoderma Viriden/aNAWheatley et al. 1997
ProkaryotaChondromyces Crocatusn/aNASchulz et al. 2004
ProkaryotaPseudomonas ChlororaphisIt has been shown to inhibit development of sclerotia of fungi.NASchulz and Dickschat 2007
ProkaryotaStreptomyces Sp.It has been shown to inhibit development of sclerotia of fungi.NASchulz and Dickschat 2007
ProkaryotaCyanobacteria Sp.It has been shown to inhibit development of sclerotia of fungi.NASchulz and Dickschat 2007
ProkaryotaMyxobacterium Sp.It has been shown to inhibit development of sclerotia of fungi.NASchulz and Dickschat 2007
ProkaryotaPseudomonas FluorescensInhibition of mycelium growth and spore germinationNAFernando et al. 2005
ProkaryotaPseudomonas CorrugataInhibition of mycelium growth and spore germinationNAFernando et al. 2005
ProkaryotaPseudomonas AurantiacaInhibition of mycelium growth and spore germinationNAFernando et al. 2005
ProkaryotaBacillus Sp.Inhibition of Mycelium growth of Paecilomyces lilacinus and Pochonia chlamydosporia.NAZou et al. 2007
ProkaryotaStenotrophomonas MaltophiliaInhibition of Mycelium growth of Paecilomyces lilacinus and Pochonia chlamydosporia.NAZou et al. 2007
ProkaryotaAlcaligenes FaecalisInhibition of Mycelium growth of Paecilomyces lilacinus and Pochonia chlamydosporia.NAZou et al. 2007
ProkaryotaArthrobacter NitroguajacolicusInhibition of Mycelium growth of Paecilomyces lilacinus and Pochonia chlamydosporia.NAZou et al. 2007
ProkaryotaLysobacter GummosusInhibition of Mycelium growth of Paecilomyces lilacinus and Pochonia chlamydosporia.NAZou et al. 2007
ProkaryotaSporosarcina GinsengisoliInhibition of Mycelium growth of Paecilomyces lilacinus and Pochonia chlamydosporia.NAZou et al. 2007
ProkaryotaStreptomyces Sp.n/aNADickschat et al. 2005_2
ProkaryotaNannocystis Exedensn/aNADickschat et al. 2007
EukaryotaTuber Magnatumn/aItalian geographical areas (Umbria, Emilia Romagna, Border region area between Emilia Romagna and Marche)Gioacchini et al. 2008
EukaryotaTrichoderma Sp.NANemcovic et al. 2008
EukaryotaAspergillus Sp.NASeifert and King 1982
ProkaryotaSalinispora Tropicanamarine sedimentGroenhagen et al. 2016
ProkaryotaPseudomonas Simiaenarhizosphere of a soybean field in the province of Rajasthan, IndiaVaishnav et al. 2016
ProkaryotaStreptomyces ThermocarboxydusNANAPassari et al. 2019
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaStenotrophomonas MaltophiliaBHISESI-MSno
ProkaryotaEscherichia ColiLBTD/GC-MSno
ProkaryotaBacillus SubtilisLuria-Bertani (LB) agarHS / SPME / GC-MSno
ProkaryotaBacillus VelezensisMinimal salt mediumSPME, GC-MSno
ProkaryotaBacillus MuralisNA mediaSPME/GC-MSno
ProkaryotaNovosphingobium LindaniclasticumNA mediaSPME/GC-MSno
ProkaryotaBacillus SubtilisNA mediaSPME/GC-MSno
ProkaryotaBacillus MegateriumNA mediaSPME/GC-MSno
ProkaryotaBacillus SubtilisLB mediaHS-SPME/GC-MSyes
ProkaryotaPaenibacillus PolymyxaLB agar and M49 (minimal) mediaSPME/GC-MSyes
ProkaryotaStenotrophomonas MaltophiliaNA mediaGC-MSno
ProkaryotaBacillus Subtilisnutrient agar mediumSPME/GC-MSno
EukaryotaTrichoderma Virideminimal agarVOCS were analysed by Integrated Automated Thermal Desorbtion-GC-MS. The isolates were grown on a minimal agar medium with the carbon:nitrogen levels similar to that found in Scots pine wood. Covered cultures were incubated at 25°C for 48h.no
EukaryotaTrichoderma VirideMalt extract/Low mediumGC/MSno
ProkaryotaChondromyces Crocatusn/an/ano
ProkaryotaPseudomonas Chlororaphisn/an/ano
ProkaryotaStreptomyces Sp.n/an/ano
ProkaryotaCyanobacteria Sp.n/an/ano
ProkaryotaMyxobacterium Sp.n/an/ano
ProkaryotaPseudomonas Fluorescensn/an/ano
ProkaryotaPseudomonas Corrugatan/an/ano
ProkaryotaPseudomonas Aurantiacan/an/ano
ProkaryotaBacillus Sp.n/an/ano
ProkaryotaStenotrophomonas Maltophilian/an/ano
ProkaryotaAlcaligenes Faecalisn/an/ano
ProkaryotaArthrobacter Nitroguajacolicusn/an/ano
ProkaryotaLysobacter Gummosusn/an/ano
ProkaryotaSporosarcina Ginsengisolin/an/ano
ProkaryotaNannocystis Exedensn/an/ano
EukaryotaTuber Magnatumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)no
EukaryotaTrichoderma Sp.no
EukaryotaAspergillus Sp.no
ProkaryotaSalinispora Tropicaseawater-based A1GC/MSno
ProkaryotaPseudomonas SimiaeNutrient broth; King's B agarGC/MSno
ProkaryotaStreptomyces Thermocarboxydusactinomycetes isolation agar (AIA)GC-MSno


2-hydroxy-5-sulfobenzoic Acid

Compound Details

Synonymous names
2-Hydroxy-5-sulfobenzoic acid
5-Sulfosalicylic acid
SULFOSALICYLIC ACID
97-05-2
5-Sulphosalicylic acid
Salicylsulfonic acid
Benzoic acid, 2-hydroxy-5-sulfo-
Salicylic acid, sulfo-
2-Hydroxybenzoic-5-sulfonic acid
Benzoic acid, 2-hydroxysulfo-
Sulphosalicylic acid
Salicylic acid, 5-sulfo-
3-Carboxy-4-hydroxybenzenesulfonic acid
NSC 190565
5-Sulfosalicylate
5-sulfo-Salicylic acid
L8XED79U3U
CHEMBL229241
CHEBI:68555
NSC-190565
2-hydroxy-5-sulfo-benzoic acid
WLN: WSQR DQ CVQ
Kalcolor anodizing acid
Sulfosalicylic acid (VAN)
Salicylsulfonic acid (VAN)
Sulphosalicylic acid (VAN)
EINECS 202-555-6
UNII-L8XED79U3U
BRN 0650741
CP 18121
AI3-18246
AI3-32582
sulfo salicylic acid
SULFOSALICYLIC
5-sulfosalicyclic acid
2-hydroxysulfo-Benzoate
2-hydroxysulfo-Benzoic acid
SCHEMBL34766
2-Hydroxy-5-sulfobenzoicacid
4-11-00-00702 (Beilstein Handbook Reference)
DTXSID7059145
SULFOSALICYLIC ACID [MI]
NSC4741
HY-B1785
NSC-4741
BBL008587
BDBM50219498
NSC190565
STK301570
SULFOSALICYLIC ACID [WHO-DD]
AKOS000120294
MCULE-1452035534
AC-11271
CS-0013816
NS00014762
S0830
EN300-20563
G76479
A845677
Q238569
W-100120
Z104478882
InChI=1/C7H6O6S/c8-6-2-1-4(14(11,12)13)3-5(6)7(9)10/h1-3,8H,(H,9,10)(H,11,12,13
Microorganism:

No

IUPAC name2-hydroxy-5-sulfobenzoic acid
SMILESC1=CC(=C(C=C1S(=O)(=O)O)C(=O)O)O
InchiInChI=1S/C7H6O6S/c8-6-2-1-4(14(11,12)13)3-5(6)7(9)10/h1-3,8H,(H,9,10)(H,11,12,13)
FormulaC7H6O6S
PubChem ID7322
Molweight218.19
LogP1.3
Atoms14
Bonds2
H-bond Acceptor6
H-bond Donor3
Chemical Classificationacids carboxylic acids benzenoids organic acids aromatic compounds phenols sulfur compounds
CHEBI-ID68555
Supernatural-IDSN0446705

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaFlammulina VelutipesnaKoreaKim et al. 2008
EukaryotaSparassis CrispanaKoreaKim et al. 2008
EukaryotaGanoderma LucidumnaKoreaKim et al. 2008
EukaryotaPhellinus LinteusnaKoreaKim et al. 2008
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaFlammulina VelutipesnaHPLCyes
EukaryotaSparassis CrispanaHPLCyes
EukaryotaGanoderma LucidumnaHPLCyes
EukaryotaPhellinus LinteusnaHPLCyes


Furan-2-ylmethanethiol

Compound Details

Synonymous names
Furfuryl mercaptan
98-02-2
2-FURANMETHANETHIOL
2-Furylmethanethiol
furan-2-yl-methanethiol
Furfuryl thiol
furan-2-ylmethanethiol
2-Furylmethyl mercaptan
2-Furfurylmercaptan
Furfurylmercaptan
2-Furfurylthiol
2-(Mercaptomethyl)furan
175236-33-6
(2-Furanyl)methylmercaptan
USAF B-58
FEMA No. 2493
2-furanmethanthiol
2-mercaptomethylfuran
29W096TCPG
DTXSID7052654
NSC 41142-d2
MFCD00003254
NSC-41142
Furfuryl mercaptan (natural)
alpha-Furfuryl mercaptan
EINECS 202-628-2
NSC 41142
BRN 0383594
UNII-29W096TCPG
furylmethanethiol
AI3-36709
fufuryl mercaptan
furfuryl-mercaptan
2-furanylmethanethiol
2-Furfuryl mercaptan
2-furylmethylmercaptan
furanylmethyl mercaptan
uran-2-ylmethanethiol
starbld0016618
(furan-2-yl)methanethiol
.alpha.-Furfuryl mercaptan
WLN: T5OJ B1SH
2-Furanmethanethiol, 98%
5-17-03-00351 (Beilstein Handbook Reference)
SCHEMBL125084
CHEMBL3560314
DTXCID4031227
FURFURYL MERCAPTAN [FCC]
FEMA 2493
FURFURYL MERCAPTAN [FHFI]
CHEBI:166536
Furfuryl mercaptan, >=97%, FG
NSC41142
Tox21_303886
STK802294
AKOS000119240
2-Furanmethanethiol, analytical standard
CAS-98-02-2
Furfuryl mercaptan, natural, 98%, FG
NCGC00357144-01
LS-13041
DB-003671
F0077
NS00012489
EN300-19031
E78916
A845789
J-640072
Q-100003
Q5509474
F0001-2311
InChI=1/C5H6OS/c7-4-5-2-1-3-6-5/h1-3,7H,4H
19980-20-2
Microorganism:

Yes

IUPAC namefuran-2-ylmethanethiol
SMILESC1=COC(=C1)CS
InchiInChI=1S/C5H6OS/c7-4-5-2-1-3-6-5/h1-3,7H,4H2
FormulaC5H6OS
PubChem ID7363
Molweight114.17
LogP1.3
Atoms7
Bonds1
H-bond Acceptor2
H-bond Donor1
Chemical Classificationthiols sulfur compounds furan derivatives ethers aromatic compounds
CHEBI-ID166536
Supernatural-IDSN0468798

mVOC Specific Details

Boiling Point
DegreeReference
263 median
Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
Lactobacillus PlantarumZhang et al. 2023
Staphylococcus AureusWang et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
Lactobacillus PlantarumHabanero pepperGC–IMSno
Staphylococcus Aureusraw Shiyang chickenHS-GC-IMS/HS-SPME-GC-MSno