Results for:
chemical Classification: sulfoxides

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Topsym (rescinded)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


[2-(benzenesulfinylmethyl)-3-phenylcyclopropyl]benzene

Compound Details

Synonymous names
(2,3-diphenylcyclopropyl)methyl phenyl sulfoxide
131758-71-9
[2-(benzenesulfinylmethyl)-3-phenylcyclopropyl]benzene
(2,3-Diphenylcyclopropyl)methyl phenyl sulfoxide, trans-
1,1'-{3-[(phenylsulfinyl)methyl]cyclopropane-1,2-diyl}dibenzene
CHEBI:84273
DTXSID70880917
MVULGCSHGFLUBH-UHFFFAOYSA-N
(2,3-Diphenylcyclopropyl)methyl phenyl sulphoxide
Q27157635
(2-Phenyl-3-[(phenylsulfinyl)methyl]cyclopropyl)benzene #
(PHENYL-[(PHENYLSULFINYL)METHYL]CYCLOPROPYL)BENZENE
1,1'-{3-[(phenylsulphinyl)methyl]cyclopropane-1,2-diyl}dibenzene
Microorganism:

Yes

IUPAC name[2-(benzenesulfinylmethyl)-3-phenylcyclopropyl]benzene
SMILESC1=CC=C(C=C1)C2C(C2C3=CC=CC=C3)CS(=O)C4=CC=CC=C4
InchiInChI=1S/C22H20OS/c23-24(19-14-8-3-9-15-19)16-20-21(17-10-4-1-5-11-17)22(20)18-12-6-2-7-13-18/h1-15,20-22H,16H2
FormulaC22H20OS
PubChem ID562543
Molweight332.5
LogP4.5
Atoms24
Bonds5
H-bond Acceptor2
H-bond Donor0
Chemical Classificationbenzenoids sulfoxides sulfur compounds aromatic compounds
CHEBI-ID84273
Supernatural-IDSN0236729

mVOC Specific Details

Solubility
1.06e-02 g/l
Literature: ALOGPS

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaPseudomonas Putidanablack pepper rootSheoran et al. 2015
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaPseudomonas PutidaLuria Bertani AgarSolvent extraction with hexane, GC/MSno


1-(2,4-dinitrophenyl)sulfinyl-2,4-dinitrobenzene

Compound Details

Synonymous names
Benzene, 1,1'-sulfinylbis[2,4-dinitro-
52427-27-7
2,2',4,4'-Tetranitrodiphenylsulfoxide
DTXSID30347596
LSKNYOCHCCPEJT-UHFFFAOYSA-N
AKOS003273028
1-[(2,4-Dinitrophenyl)sulfinyl]-2,4-dinitrobenzene #
Microorganism:

No

IUPAC name1-(2,4-dinitrophenyl)sulfinyl-2,4-dinitrobenzene
SMILESC1=CC(=C(C=C1[N+](=O)[O-])[N+](=O)[O-])S(=O)C2=C(C=C(C=C2)[N+](=O)[O-])[N+](=O)[O-]
InchiInChI=1S/C12H6N4O9S/c17-13(18)7-1-3-11(9(5-7)15(21)22)26(25)12-4-2-8(14(19)20)6-10(12)16(23)24/h1-6H
FormulaC12H6N4O9S
PubChem ID623449
Molweight382.26
LogP2
Atoms26
Bonds2
H-bond Acceptor10
H-bond Donor0
Chemical Classificationaromatic compounds benzenoids nitrogen compounds sulfoxides sulfur compounds

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
Aspergillus FlavusKate et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
Aspergillus Flavusinoculated potato samplesGC-MSno


2-methylsulfinyl-1,3-benzothiazole

Compound Details

Synonymous names
2-(methylsulfinyl)benzo[d]thiazole
3507-54-8
2-methylsulfinyl-1,3-benzothiazole
Benzothiazole, 2-(methylsulfinyl)-
2-(Methylsulfinyl)-1,3-benzothiazole
Benzothiazole, 2-(methylsulfinyl)- (7CI,8CI,9CI)
2-(Methylsulfinyl)benzothiazole
Maybridge3_004554
2-(methylsulphinyl)benzothiazole
SCHEMBL10928468
HMS1443O22
IDI1_015941
DB-274758
Microorganism:

No

IUPAC name2-methylsulfinyl-1,3-benzothiazole
SMILESCS(=O)C1=NC2=CC=CC=C2S1
InchiInChI=1S/C8H7NOS2/c1-12(10)8-9-6-4-2-3-5-7(6)11-8/h2-5H,1H3
FormulaC8H7NOS2
PubChem ID2824895
Molweight197.3
LogP1.7
Atoms12
Bonds1
H-bond Acceptor4
H-bond Donor0
Chemical Classificationaromatic compounds benzenoids heterocyclic compounds nitrogen compounds sulfoxides sulfur compounds thiazoles

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
Aspergillus FlavusKate et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
Aspergillus Flavusinoculated potato samplesGC-MSno