Results for:
Species: Bjerkandera adusta

4-methoxybenzaldehyde

Mass-Spectra

Compound Details

Synonymous names
4-Methoxybenzaldehyde
123-11-5
P-ANISALDEHYDE
Anisic aldehyde
Anisaldehyde
p-Methoxybenzaldehyde
Aubepine
4-Anisaldehyde
Benzaldehyde, 4-methoxy-
p-Formylanisole
Crategine
Obepin
p-Anisic aldehyde
para-anisaldehyde
4-Methoxy-benzaldehyde
Formylanisole, p-
anisal
Caswell No. 051E
FEMA No. 2670
NSC 5590
CCRIS 821
4-methoxy benzaldehyde
MFCD00003385
para-methoxybenzaldehyde
p-Methoxybenzaldehyde (natural)
HSDB 2641
EINECS 204-602-6
UNII-9PA5V6656V
p-methoxy benzaldehyde
DTXSID2026997
AI3-00223
9PA5V6656V
NSC-5590
50984-52-6
p-Methoxybenzaldehyde-13C6
CHEMBL161598
DTXCID906997
CHEBI:28235
EC 204-602-6
P-ANISALDEHYDE (USP-RS)
P-ANISALDEHYDE [USP-RS]
p-Anisaldehyde,p-Methoxybenzaldhyde
CAS-123-11-5
MEPYRAMINE MALEATE IMPURITY P (EP IMPURITY)
MEPYRAMINE MALEATE IMPURITY P [EP IMPURITY]
anisaldehyd
Anis aldehyde
FEMA 2670
4-methoxybenzaldehye
4-methoxybezaldehyde
EINECS 256-891-3
Anisaldehyde (para)
P-Anisaldehyde,(S)
4-methoxylbenzaldehyde
p-Anisaldehyde, 8CI
4-methoxybenzylaldehyde
BRN 0471382
p-Anisaldehyde, 98%
p-Anisaldehyde, Reagent
benzaldehyde, 4-methoxy
para-methoxy benzaldehyde
4-(methyloxy)benzaldehyde
bmse010130
WLN: VHR DO1
ANISALDEHYDE [INCI]
SCHEMBL1100
P-ANISALDEHYDE [MI]
68894-36-0
MLS002152921
P-ANISALDEHYDE [HSDB]
p-Methoxybenzylidenemalonitrile
4-methoxybenzene carboxaldehyde
PARA- METHOXYBENZALDEHYDE
NSC5590
HMS3039F08
p-Anisaldehyde, analytical standard
P-METHOXYBENZALDEHYDE [FCC]
HY-Y0740
p-Anisaldehyde, natural, 98%, FG
P-METHOXYBENZALDEHYDE [FHFI]
Tox21_201943
Tox21_303331
AC7808
BDBM50139370
s5086
STL194068
AKOS000118814
CCG-214805
CS-W020189
MCULE-9537754812
p-Anisaldehyde (4-Methoxybenzaldehyde)
p-Anisaldehyde, for synthesis, 98.0%
NCGC00090807-01
NCGC00090807-02
NCGC00257076-01
NCGC00259492-01
p-Anisaldehyde, >=97.5%, FCC, FG
AC-10379
CS-11005
SMR001224521
SY001689
DB-012818
A0480
BENZALDEHYDE,4-METHOXY MFC8 H8 O2
NS00003331
EN300-16096
4-08-00-00252 (Beilstein Handbook Reference)
A805017
Q174937
Q-100105
Z53833125
F2190-0575
p-Anisaldehyde, primary pharmaceutical reference standard
p-Anisaldehyde, certified reference material, TraceCERT(R)
p-Anisaldehyde, United States Pharmacopeia (USP) Reference Standard
InChI=1/C8H8O2/c1-10-8-4-2-7(6-9)3-5-8/h2-6H,1H
Microorganism:

Yes

IUPAC name4-methoxybenzaldehyde
SMILESCOC1=CC=C(C=C1)C=O
InchiInChI=1S/C8H8O2/c1-10-8-4-2-7(6-9)3-5-8/h2-6H,1H3
FormulaC8H8O2
PubChem ID31244
Molweight136.15
LogP1.8
Atoms10
Bonds2
H-bond Acceptor2
H-bond Donor0
Chemical Classificationbenzenoids aromatic aldehydes aldehydes aromatic compounds benzaldehydes ethers
CHEBI-ID28235
Supernatural-IDSN0478525

mVOC Specific Details

Boiling Point
DegreeReference
255 °C peer reviewed
Volatilization
The Henry's Law constant for p-anisaldehyde is estimated as 1.4X10-5 atm-cu m/mole(SRC) derived from its vapor pressure, 3.29X10-2 mm Hg(1), and water solubility, 4.29X10+3 mg/L(2). This Henry's Law constant indicates that p-anisaldehyde is expected to volatilize 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 20 days(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 230 days(SRC). p-Anisaldehyde's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). p-Anisaldehyde has a vapor pressure of 3.29X10-2 mm Hg at 25 °C(1) and exists as a liquid under environmental conditions; therefore, p-anisaldehyde may volatilize from dry soil(SRC).
Soil Adsorption
The Koc of p-anisaldehyde is estimated as 53(SRC), using a log Kow of 1.76(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that p-anisaldehyde is expected to have high mobility in soil.
Vapor Pressure
PressureReference
1 MM HG @ 73 DEG CClayton, G. D. and F. E. Clayton (eds.). Patty's Industrial Hygiene and Toxicology: Volume 2A, 2B, 2C: Toxicology. 3rd ed. New York: John Wiley Sons, 1981-1982., p. 2663
MS-Links
1D-NMR-Links
Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaClitocybe OdoraNARapior et al. 2002
EukaryotaLentinellus CochleatusNARapior et al. 2002
EukaryotaDaedalea Juniperinan/aNAStotzky and Schenck 1976
EukaryotaTrametes SuaveolensNABirkinshaw et al. 1945
ProkaryotaPolyporus BenzoinusNABirkinshaw et al. 1952
EukaryotaBjerkandera AdustaNASpinnler at al. 1994
EukaryotaBjerkandera Adustan/aNALapadatescu et al. 2000
Lactobacillus PlantarumZhang et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaClitocybe Odorahydro-destillation, solvent extraction, GC-MSno
EukaryotaLentinellus Cochleatushydro-destillation, solvent extraction, GC-MSno
EukaryotaDaedalea Juniperinan/an/ano
EukaryotaTrametes Suaveolensno
ProkaryotaPolyporus Benzoinusno
EukaryotaBjerkandera Adustano
EukaryotaBjerkandera AdustaMinimal media plus glucose and L-phenylalanineExtraction with dichloromethane or with ethyl acetate, concentration under N2 stream /GC-MS.no
Lactobacillus PlantarumHabanero pepperGC–IMSno


3,4-dimethoxybenzaldehyde

Mass-Spectra

Compound Details

Synonymous names
3,4-Dimethoxybenzaldehyde
VERATRALDEHYDE
120-14-9
Veratric aldehyde
Methylvanillin
Benzaldehyde, 3,4-dimethoxy-
Vanillin methyl ether
Veratral
Veratrum aldehyde
Veratryl aldehyde
p-Veratric aldehyde
4-O-Methylvanillin
3,4-Dimethoxy benzaldehyde
3,4-Dimethoxybenzenecarbonal
Protocatechualdehyde dimethyl ether
Protocatechuic aldehyde dimethyl ether
3,4-DIMETHOXY-BENZALDEHYDE
Protocatechuecaldehyde dimethyl ether
MFCD00003363
NSC 24521
FEMA No. 3109
3, 4-Dimethoxybenzaldehyde
UI88P68JZD
DTXSID7026285
CHEBI:17098
NSC-8500
NSC-24521
Benzaldehyde, 3-methoxy-4-(methoxy-d3)-
Benzaldehyde,4-dimethoxy-
WLN: VHR CO1 DO1
DTXCID406285
Methyl vanillin
CAS-120-14-9
CCRIS 6285
EINECS 204-373-2
UNII-UI88P68JZD
BRN 0473899
veratrumald
ratryl aldehyde
Veratrumaldehyde
AI3-08099
FEMA 3109
3,4-dimethoxy
3,4dimethoxybenzaldehyde
3,4-dimethoxybenzaldehyde (veratraldehyde)
3,4-dimethoxybenzaldeyde
3,4 dimethoxybenzaldehyde
3,4-dimethoxybenzaidehyde
4,3-dimethoxybenzaldehyde
4,5-dimethoxybenzaldehyde
bmse010220
VERATRALDEHYDE [MI]
VERATRALDEHYDE [FCC]
SCHEMBL25202
VERATRALDEHYDE [FHFI]
Veratraldehyde, >=98%, FG
CHEMBL1088937
NSC8500
3,4-Dimethoxybenzaldehyde, 99%
HY-N1096
NSC24521
Tox21_201566
Tox21_303074
BBL010373
s3214
STK188425
AKOS000118989
CS-W019906
Dimethoxy-Benzaldehyde-O-Methylvanillin
MCULE-1202068347
NCGC00091642-01
NCGC00091642-02
NCGC00091642-03
NCGC00257217-01
NCGC00259115-01
AC-10201
AC-34441
AS-11996
SY004136
Benzaldehyde, 3,4-dimethoxy-veratraldehyde
Veratraldehyde (3,4-Dimethoxybenzaldehyde)
DB-014213
AM20050100
D0507
NS00013328
EN300-16145
C02201
AH-034/32845024
Q414395
W-108485
Z53837671
F2190-0618
VERAPAMIL HYDROCHLORIDE IMPURITY G [EP IMPURITY]
InChI=1/C9H10O3/c1-11-8-4-3-7(6-10)5-9(8)12-2/h3-6H,1-2H
Microorganism:

No

IUPAC name3,4-dimethoxybenzaldehyde
SMILESCOC1=C(C=C(C=C1)C=O)OC
InchiInChI=1S/C9H10O3/c1-11-8-4-3-7(6-10)5-9(8)12-2/h3-6H,1-2H3
FormulaC9H10O3
PubChem ID8419
Molweight166.17
LogP1.5
Atoms12
Bonds3
H-bond Acceptor3
H-bond Donor0
Chemical Classificationbenzenoids aromatic aldehydes aldehydes aromatic compounds benzaldehydes ethers
CHEBI-ID17098
Supernatural-IDSN0412195

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaBjerkandera Adustan/aNALapadatescu et al. 2000
EukaryotaBjerkandera AdustaNASpinnler at al. 1994
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaBjerkandera AdustaMinimal media plus glucose and L-phenylalanineExtraction with dichloromethane or with ethyl acetate, concentration under N2 stream /GC-MS.no
EukaryotaBjerkandera Adustano


Benzoic Acid

Mass-Spectra

Compound Details

Synonymous names
benzoic acid
65-85-0
Dracylic acid
benzenecarboxylic acid
Carboxybenzene
Benzeneformic acid
phenylformic acid
Benzenemethanoic acid
Phenylcarboxylic acid
benzoate
Retardex
Benzoesaeure GK
Benzoesaeure GV
Retarder BA
Tenn-Plas
Acide benzoique
Salvo liquid
Solvo powder
Benzoesaeure
Benzoic acid, tech.
Unisept BZA
HA 1 (acid)
Kyselina benzoova
Benzoic acid (natural)
HA 1
Benzoate (VAN)
Benzenemethonic acid
FEMA No. 2131
Vevovitall
Acido benzoico
Menno-florades
NSC 149
Benzoesaeure [German]
Caswell No. 081
Diacylic acid
Oracylic acid
Benzoicum acidum
CCRIS 1893
HSDB 704
Acide benzoique [French]
Acido benzoico [Italian]
E 210
Kyselina benzoova [Czech]
AI3-0310
AI3-03710
Diacylate
EPA Pesticide Chemical Code 009101
CHEBI:30746
Salvo powder
Acidum benzoicum
NSC-149
UNII-8SKN0B0MIM
E210
Salvo, liquid
Solvo, powder
8SKN0B0MIM
Benzoic acid (e 210)
EINECS 200-618-2
Tennplas
DTXSID6020143
Retarded BA
INS-210
Aromatic carboxylic acid
MFCD00002398
Benzoic acid [USP:JAN]
BENZOIC-4-D1 ACID
DTXCID80143
Benzoic acid-ring-UL-14C
INS NO.210
E-210
EC 200-618-2
Benzeneformate
Phenylformate
Benzenemethanoate
Phenylcarboxylate
Benzenecarboxylate
Benzoic acid 100 microg/mL in Acetone
Benzoic acid (USP:JAN)
BENZOIC ACID (II)
BENZOIC ACID [II]
Benzoic Acid 2000 microg/mL in Dichloromethane
BENZOIC ACID (MART.)
BENZOIC ACID [MART.]
BENZOIC ACID (USP-RS)
BENZOIC ACID [USP-RS]
BENZOIC ACID (EP MONOGRAPH)
BENZOIC ACID [EP MONOGRAPH]
BENZOIC ACID (USP MONOGRAPH)
BENZOIC ACID [USP MONOGRAPH]
Acid, Benzoic
Benzoic acid [USAN:JAN]
CAS-65-85-0
MFCD00002400
NSC7918
B A
Benzoic acid (TN)
phenylcarboxy
Dracylate
ProvitaCombat
benzoic aicd
benzoic-acid
benzoic_acid
bezoic acid
Aromatic acid
benzenecarboxylic
Benzoicum Ac
Eyelids Wipes
benzoic- acid
Provita Equiband
Retarder BAX
1gyx
1kqb
Rheumatism Diarrhea
Sodium benzoic acid
Benzoic Acid,(S)
CARBOXYLBENZENE
DIACYCLIC ACID
DRACYCLIC ACID
benzene carboxylic acid
760 - Preservatives
BENZOICACID-D5
ANTAZOLINE_met016
WLN: QVR
benzene-2-carboxylic acid
EUCATROPINE_met034
CYCLANDELATE_met022
BENZOIC ACID [MI]
Benzoic acid, ACS reagent
bmse000300
CHEMBL541
Epitope ID:139965
BENZOIC ACID [FCC]
BENZOIC ACID [JAN]
SCHEMBL1378
BENZOIC ACID [FHFI]
BENZOIC ACID [HSDB]
BENZOIC ACID [INCI]
SAMPL4, O1
TRIPELENNAMINE_met034
Benzoic acid (JP17/USP)
BENZOIC ACID [VANDF]
MLS002415717
27 - Preservatives in Cream
BIDD:ER0597
BENZOIC ACID [WHO-DD]
BENZOIC ACID [WHO-IP]
Benzoic acid, AR, >=99%
Benzoic acid, LR, >=99%
NSC149
31 - Preservatives in Mascara
BENZOICUM ACIDUM [HPUS]
FEMA 2131
Benzoic acid (7CI,8CI,9CI)
Benzoic acid, analytical standard
Benzoic acid, p.a., 99.5%
BENZOIC ACID [GREEN BOOK]
BDBM197302
Benzoic-2,3,4,5,6-d5 acid
HMS2092F18
HMS2267D03
HMS3652B03
Pharmakon1600-01503001
HY-N0216
Tox21_202403
Tox21_300180
NSC758203
s4161
STK301730
Benzoic acid, ReagentPlus(R), 99%
AKOS000119619
BS-3752
CCG-213088
DB03793
MCULE-4467353796
NSC-758203
ACIDUM BENZOICUM [WHO-IP LATIN]
Benzoic acid, >=99.5%, FCC, FG
USEPA/OPP Pesticide Code: 009101
Benzoic acid, ACS reagent, >=99.5%
NCGC00091886-01
NCGC00091886-02
NCGC00091886-03
NCGC00091886-05
NCGC00254112-01
NCGC00259952-01
TIAPROFENIC ACID IMPURITY D [EP]
Benzoic acid, USP, 99.5-100.5%
BP-30148
SMR001252220
SY009192
SY236257
Benzoic acid, tested according to Ph.Eur.
SBI-0206720.P001
Benzoic acid, SAJ first grade, >=99.5%
DB-029471
B0062
B2635
CS-0008257
NS00008785
SW219833-1
Benzoic acid, natural, >=99.5%, FCC, FG
Benzoic acid, SAJ special grade, >=99.5%
Benzoic acid, Vetec(TM) reagent grade, 98%
EN300-18007
2-BENZOYL-5-METHOXYBENZOQUINONE_met032
Benzoic acid, meets USP testing specifications
Benzoic acid, purified by sublimation, >=99%
C00180
C00539
D00038
D85168
MEFENAMIC ACID IMPURITY D [EP IMPURITY]
AB00949635_05
AB00949635_06
A835250
A934445
Benzoic Acid Zone Refined (number of passes:20)
Q191700
SR-05000001919
Benzoic acid, puriss. p.a., ACS reagent, 99.9%
SR-05000001919-1
0BE368DC-6DE6-4927-AECF-E4BB2968A4A0
GLYCOPYRRONIUM BROMIDE IMPURITY D [EP IMPURITY]
Melting point standard 121-123C, analytical standard
METRONIDAZOLE BENZOATE IMPURITY C [EP IMPURITY]
Z57127480
F2191-0092
HYDROUS BENZOYL PEROXIDE IMPURITY B [EP IMPURITY]
Benzoic acid, NIST(R) SRM(R) 39j, calorimetric standard
Benzoic acid, Standard for quantitative NMR, TraceCERT(R)
METHYLAMINOLEVULINATE HYDROCHLORIDE IMPURITY I [EP]
Benzoic acid, European Pharmacopoeia (EP) Reference Standard
Mettler-Toledo Calibration substance ME 18555, Benzoic acid
Benzoic acid, for calorimetrical determination (approx. 26460 J/g)
Benzoic acid, United States Pharmacopeia (USP) Reference Standard
InChI=1/C7H6O2/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H,8,9
SS Benzoic Acid, 2000 mug/mL in dichloromethane, analytical standard
Benzoic acid, Pharmaceutical Secondary Standard; Certified Reference Material
Benzoic acid, puriss. p.a., ACS reagent, reag. Ph. Eur., >=99.9% (alkalimetric)
14322-82-8
Benzoic acid, certified reference material for titrimetry, certified by BAM according to ISO 17025, >=99.5%
Benzoic acid, meets analytical specification of Ph. Eur., BP, USP, FCC, E210, 99.5-100.5% (alkalimetric)
Mettler-Toledo Calibration substance ME 18555, Benzoic acid, analytical standard, for the calibration of the thermosystem 900, traceable to primary standards (L
ScavengePore(TM) benzoic acid, macroporous, 40-70 mesh, extent of labeling: 0.5-1.5 mmol per g loading
Microorganism:

Yes

IUPAC namebenzoic acid
SMILESC1=CC=C(C=C1)C(=O)O
InchiInChI=1S/C7H6O2/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H,8,9)
FormulaC7H6O2
PubChem ID243
Molweight122.12
LogP1.9
Atoms9
Bonds1
H-bond Acceptor2
H-bond Donor1
Chemical Classificationbenzenoids aromatic compounds acids carboxylic acids
CHEBI-ID30746
Supernatural-IDSN0416870

mVOC Specific Details

Boiling Point
DegreeReference
249.2 °C peer reviewed
Volatilization
A pKa of 4.20(1) indicates benzoic acid will exist almost entirely in the ionized form at pH values of 5 to 9 and, therefore, volatilization from water or moist soil surfaces is not expected to be an important fate process. Benzoic acid is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 7.0X10-4 mm Hg at 25 deg C(2).
Literature: (1) Haynes WM, ed; CRC Handbook of Chemistry and Physics. 91st ed. Boca Raton, FL: CRC Press Inc., p 8-47 (2010) (2) McEachern DM, Sandoval O; J Phys E 6: 155-161 (1973)
Soil Adsorption
Koc of benzoic acid is estimated as 15(SRC), using a log Kow of 1.87(1) and a regression-derived equation(2). An experimental log Koc of 1.50 (Koc = 31) has been reported, test details not available(3). According to a classification scheme(4), these Koc values suggest that benzoic acid is expected to have very high mobility in soil. The pKa of benzoic acid is 4.20(5), indicating that this compound will exist in anion form in the environment and anions generally do not adsorb more strongly to organic carbon and clay than their neutral counterparts(6). Freundlich adsorption constants of 0.23, 0 and 0 were reported using Ersum sandy till (pH 4.7; 0.25% OC), Tirstrup melt water sand (pH 6.1; 0.09% OC) and Djursland clayey till (pH 7.6; 0.22% OC), respectively, at 6 deg C. Soils were collected in North Sealand and Djursland, Jutland(7). Benzoic acid displayed negligible adsorption when using a montmorillonite (Volclay bentonite, Upton WY) clay(8).
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. 29 (1995) (2) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.1. Nov, 2012. Available from, as of Aug 19, 2013: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (3) Schuurmann G et al; Environ Sci Technol 40: 7005-11 (2006) (4) Swann RL et al; Res Rev 85: 17-28 (1983) (5) Haynes WM, ed; CRC Handbook of Chemistry and Physics. 91st ed. Boca Raton, FL: CRC Press Inc., p 8-47 (2010) (6) Doucette WJ; pp. 141-188 in Handbook of Property Estimation Methods for Chemicals. Boethling RS, Mackay D, eds. Boca Raton, FL: Lewis Publ (2000) (7) Loekke H; Water Air Soil Pollut 22: 373-87 (1984) (8) Bailey GW et al; Soil Sci Soc Amer Proc 32: 222-34 (1968)
Vapor Pressure
PressureReference
7.0X10-4 mm Hg at 25 deg CMcEachern DM, Sandoval O; J Phys E 6: 155-61 (1973)
MS-Links
MS-MS Spectrum 1757 - Quattro_QQQ 25V Positive delivery=Flow_Injection analyzer=Triple_Quad
MS-MS Spectrum 5517 - EI-B (HITACHI M-80B) Positive
MS-MS Spectrum 1756 - Quattro_QQQ 10V Positive delivery=Flow_Injection analyzer=Triple_Quad
MS-MS Spectrum 5514 - EI-B (HITACHI RMU-7) Positive
MS-MS Spectrum 180881
MS-MS Spectrum 178562
MS-MS Spectrum 5521 - LC-ESI-QQ (API3000, Applied Biosystems) 40V Negative
MS-MS Spectrum 180880
MS-MS Spectrum 1758 - Quattro_QQQ 40V Positive delivery=Flow_Injection analyzer=Triple_Quad
MS-MS Spectrum 5516 - EI-B (HITACHI RMU-7M) Positive
MS-MS Spectrum 5515 - EI-B (HITACHI RMU-6E) Positive
MS-MS Spectrum 180879
MS-MS Spectrum 5519 - LC-ESI-QQ (API3000, Applied Biosystems) 20V Negative
MS-MS Spectrum 178561
MS-MS Spectrum 5518 - LC-ESI-QQ (API3000, Applied Biosystems) 10V Negative
MS-MS Spectrum 5520 - LC-ESI-QQ (API3000, Applied Biosystems) 30V Negative
MS-MS Spectrum 178560
1D-NMR-Links
Massbank-Links

Species emitting the compound
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaBacillus SubtilisLuria-Bertani (LB) agarHS / SPME / GC-MSno
EukaryotaBjerkandera AdustaMinimal media plus glucose and L-phenylalanineExtraction with dichloromethane or with ethyl acetate, concentration under N2 stream /GC-MS.no
ProkaryotaBacillus AmyloliquefaciensLBSPME-GC-MSno
ProkaryotaBacillus AtrophaeusLBSPME-GC-MSno
EukaryotaAgaricus BlazeinaHPLCyes
EukaryotaSparassis CrispanaHPLCyes
EukaryotaPhellinus LinteusnaHPLCyes
EukaryotaZygosaccharomyces RouxiiYPD mediumGC-MSno
ProkaryotaPeribacillus Sp.Schaeffer’s growth (SG) mediumHS-SPME-GC/MSno
ProkaryotaBacillus SubtilisTryptone soy broth (TSB)HPLCno
Bacillus Toyonensisbacteriological agar (BA, 15 g/L), gelatin peptone (GP, 5 g/L), and meat extract (ME, 3 g/L)GC–MSno
Bacillus Acidiproducensbacteriological agar (BA, 15 g/L), gelatin peptone (GP, 5 g/L), and meat extract (ME, 3 g/L)GC–MSno
Bacillus Cereusbacteriological agar (BA, 15 g/L), gelatin peptone (GP, 5 g/L), and meat extract (ME, 3 g/L)GC–MSno
Bacillus Safensisbacteriological agar (BA, 15 g/L), gelatin peptone (GP, 5 g/L), and meat extract (ME, 3 g/L)GC–MSno


Benzaldehyde

Mass-Spectra

Compound Details

Synonymous names
benzaldehyde
100-52-7
Benzoic aldehyde
Phenylmethanal
Benzenecarboxaldehyde
Benzenecarbonal
Benzenemethylal
Benzaldehyde FFC
Benzene carbaldehyde
Benzene carboxaldehyde
benzanoaldehyde
Benzylaldehyde
Benzoyl hydride
NCI-C56133
Benzoic acid aldehyde
FEMA No. 2127
Caswell No. 076
Phenylformaldehyde
Benzaldehyde (natural)
NSC 7917
Benzadehyde
Benzyaldehyde
CCRIS 2376
HSDB 388
NSC-7917
EINECS 202-860-4
UNII-TA269SD04T
Benzaldehyde-carbonyl-13C
Benzaldehyde [NF]
EPA Pesticide Chemical Code 008601
Benzaldehyde-formyl-d
TA269SD04T
Benzaldehyde-alpha-d1
DTXSID8039241
CHEBI:17169
AI3-09931
MFCD00003299
8013-76-1
Benzaldehyde, methyl-
CHEMBL15972
DTXCID90134
NSC7917
EC 202-860-4
Phenylmethanal benzenecarboxaldehyde
Benzaldehyde (NF)
NCGC00091819-01
NCGC00091819-02
BENZALDEHYDE (II)
BENZALDEHYDE [II]
BENZALDEHYDE (MART.)
BENZALDEHYDE [MART.]
benzaldehyd
Benzaldhyde
BENZALDEHYDE (USP IMPURITY)
BENZALDEHYDE [USP IMPURITY]
BDBM50139371
CAS-100-52-7
FENTANYL IMPURITY E (EP IMPURITY)
FENTANYL IMPURITY E [EP IMPURITY]
TRIBENOSIDE IMPURITY C (EP IMPURITY)
TRIBENOSIDE IMPURITY C [EP IMPURITY]
BENZYL ALCOHOL IMPURITY A (EP IMPURITY)
BENZYL ALCOHOL IMPURITY A [EP IMPURITY]
FENTANYL CITRATE IMPURITY E (EP IMPURITY)
FENTANYL CITRATE IMPURITY E [EP IMPURITY]
AMFETAMINE SULFATE IMPURITY D (EP IMPURITY)
AMFETAMINE SULFATE IMPURITY D [EP IMPURITY]
UN1990
BENZALKONIUM CHLORIDE IMPURITY B (EP IMPURITY)
BENZALKONIUM CHLORIDE IMPURITY B [EP IMPURITY]
GLYCOPYRRONIUM BROMIDE IMPURITY F (EP IMPURITY)
GLYCOPYRRONIUM BROMIDE IMPURITY F [EP IMPURITY]
HYDROUS BENZOYL PEROXIDE IMPURITY A (EP IMPURITY)
HYDROUS BENZOYL PEROXIDE IMPURITY A [EP IMPURITY]
benzaidehyde
benzaldehvde
benzaldehye
benzaldeyde
BENZOYLL PEROXIDE HYDROUS IMPURITY A (EP IMPURITY)
BENZOYLL PEROXIDE HYDROUS IMPURITY A [EP IMPURITY]
C7H6O
phenyl-methanone
Benzene methylal
Aromatic aldehyde
Benzoylwasserstoff
(phenyl)methanone
benzenecarbaldehyde
Benzaldehyde,(S)
PhCHO
Benzene carcaboxaldehyde
2vj1
WLN: VHR
BENZALDEHYDE [MI]
SCHEMBL573
BENZALDEHYDE [FCC]
BENZALDEHYDE [FHFI]
BENZALDEHYDE [HSDB]
BENZALDEHYDE [INCI]
BENZALDEHYDE [VANDF]
ghl.PD_Mitscher_leg0.170
BENZALDEHYDE [USP-RS]
Benzaldehyde, AR, >=99%
Benzaldehyde, LR, >=99%
BIDD:ER0249
BDBM60953
Benzaldehyde, analytical standard
Ald3-H_000012
Benzaldehyde, >=98%, FG, FCC
Ald3.1-H_000160
Ald3.1-H_000479
Ald3.1-H_000798
Tox21_113069
Tox21_113244
Tox21_200634
s5574
STL194067
Benzaldehyde, for synthesis, 95.0%
AKOS000119172
Benzaldehyde [UN1990] [Class 9]
CCG-266041
MCULE-7744113682
NA 1989
Benzaldehyde, purum, >=98.0% (GC)
Benzaldehyde, ReagentPlus(R), >=99%
NCGC00091819-03
NCGC00258188-01
PS-11959
Benzaldehyde, natural, >=98%, FCC, FG
DB-023673
B2379
Benzaldehyde, SAJ special grade, >=98.0%
NS00008510
Benzaldehyde, Vetec(TM) reagent grade, 98%
Benzaldehyde 1000 microg/mL in Dichloromethane
Benzaldehyde 2000 microg/mL in Dichloromethane
Benzaldehyde, puriss. p.a., >=99.0% (GC)
C00193
C00261
D02314
A800226
Q372524
SR-01000944375
Benzaldehyde, purified by redistillation, >=99.5%
SR-01000944375-1
F1294-0144
Flavor and Extract Manufacturers' Association No. 2127
InChI=1/C7H6O/c8-6-7-4-2-1-3-5-7/h1-6
Benzaldehyde, European Pharmacopoeia (EP) Reference Standard
Benzaldehyde, United States Pharmacopeia (USP) Reference Standard
Benzaldehyde, Pharmaceutical Secondary Standard; Certified Reference Material
Microorganism:

Yes

IUPAC namebenzaldehyde
SMILESC1=CC=C(C=C1)C=O
InchiInChI=1S/C7H6O/c8-6-7-4-2-1-3-5-7/h1-6H
FormulaC7H6O
PubChem ID240
Molweight106.12
LogP1.5
Atoms8
Bonds1
H-bond Acceptor1
H-bond Donor0
Chemical Classificationbenzenoids aldehydes aromatic compounds aromatic aldehydes benzaldehydes
CHEBI-ID17169
Supernatural-IDSN0135798

mVOC Specific Details

Boiling Point
DegreeReference
178.7 °C peer reviewed
Volatilization
The Henry's Law constant for benzaldehyde is 2.67X10-5 atm-cu m/mole(1). This Henry's Law constant indicates that benzaldehyde 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 1.5 days (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 14 days(SRC). Benzaldehyde's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Benzaldehyde is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 1.27 mm Hg at 25 deg C(3).
Literature: (1) Betterton EA, Hoffmann MR; Environ Sci Technol 22: 1415-8 (1988) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Ambrose D et al; J Chem Therm 7: 1143-57 (1975)
Soil Adsorption
Using a structure estimation method based on molecular connectivity indices(1), the Koc of benzaldehyde can be estimated to be 11(SRC). According to a classification scheme(2), this estimated Koc value suggests that benzaldehyde is expected to have very high mobility in soil.
Literature: (1) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.1. Nov, 2012. Available from, as of May 30, 2016: http://www2.epa.gov/tsca-screening-tools/ (2) Swann RL et al; Res Rev 85: 17-28 (1983)
Vapor Pressure
PressureReference
1.27 mm Hg at 25 deg CAmbrose D et al; J Chem Therm 7: 1143-57 (1975)
MS-Links
1D-NMR-Links
Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaEscherichia ColiNANAAhmed et al. 2023
ProkaryotaEscherichia ColiNANAHewett et al. 2020
EukaryotaAspergillus NigerNANACosta et al. 2016
EukaryotaCandida AlbicansNANACosta et al. 2016
EukaryotaPenicillium ChrysogenumNANACosta et al. 2016
ProkaryotaStreptococcus PneumoniaeNANAMellors et al. 2018
ProkaryotaStaphylococcus AureusNANAFilipiak et al. 2012
EukaryotaAgaricus EssetteiNARapior et al. 2002
EukaryotaCandida AlbicansNAKarami et al. 2017
ProkaryotaEscherichia ColiNAKarami et al. 2017
ProkaryotaStaphylococcus AureusNAKarami et al. 2017
ProkaryotaBacillus SubtilisNAGao et al. 2018
EukaryotaFusarium CulmorumNASchmidt et al. 2018
EukaryotaHypoxylon InvadensNADickschat et al. 2018
EukaryotaFusarium Acuminatumroots of two species of the Brassicaceae family Microthlaspi perfoliatum and Microthlaspi erraticumSchenkel et al. 2018
EukaryotaFusarium Oxysporumroots of two species of the Brassicaceae family Microthlaspi perfoliatum and Microthlaspi erraticumSchenkel et al. 2018
EukaryotaPolyporus TuberasterNAKawabe et al. 1994
ProkaryotaBacillus Subtilisantibacterial activity against growth of Ralstonia solanacearumPlant Bacteriology Lab, Division of Plant Pathology, Indian Council of Agricultural Research - Indian Agricultural Research Institute, New DelhiKashyap et al. 2022
ProkaryotaPseudomonas Fluorescensantibacterial activity against growth of Ralstonia solanacearumPlant Bacteriology Lab, Division of Plant Pathology, Indian Council of Agricultural Research - Indian Agricultural Research Institute, New DelhiKashyap et al. 2022
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
ProkaryotaBacillus Amyloliquefacienscommercial strainHeenan-Daly et al. 2021
ProkaryotaBacillus Toyonensisstimulate growth of Solanum tuberosumisolate from Irish potato soilsHeenan-Daly et al. 2021
ProkaryotaSerratia Myotisisolate from Irish potato soilsHeenan-Daly 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
ProkaryotaEscherichia ColiLeibnitz Institute DSMZ-German Collection of Microorganisms and Cell Cultures GmbHFitzgerald 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 Velezensisinhibite the growth of Botrytis cinerea VG1, Monilinia fructicola VG 104, Monilinia laxa VG 105, Penicillium digitatum VG 20, Penicillium expansum CECT 20140, Penicillium italicum VG 101NACalvo et al. 2020
ProkaryotaStaphylococcus EpidermidisAmerican Type Culture CollectionJenkins and Bean 2020
ProkaryotaErwinia Amylovoraenhances Arabidopsis thaliana shoot and root growthbacterial collection of the LabParmagnani et al. 2023
ProkaryotaLactobacillus Plantarumn/aNASchulz and Dickschat 2007
ProkaryotaPseudomonas Fluorescensn/aNAFernando et al. 2005
ProkaryotaPseudomonas Corrugatan/aNAFernando et al. 2005
ProkaryotaPseudomonas Chlororaphisn/aNAFernando et al. 2005
ProkaryotaPseudomonas Aurantiacan/aNAFernando 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
ProkaryotaBacillus SimplexReduction of movement or death of Panagrelleus redivivus and Bursaphelenchus xylophilus.NAGu et al. 2007
ProkaryotaBacillus SubtilisReduction of movement or death of Panagrelleus redivivus and Bursaphelenchus xylophilus.NAGu et al. 2007
ProkaryotaBacillus WeihenstephanensisReduction of movement or death of Panagrelleus redivivus and Bursaphelenchus xylophilus.NAGu et al. 2007
ProkaryotaMicrobacterium OxydansReduction of movement or death of Panagrelleus redivivus and Bursaphelenchus xylophilus.NAGu et al. 2007
ProkaryotaStreptomyces LateritiusReduction of movement or death of Panagrelleus redivivus and Bursaphelenchus xylophilus.NAGu et al. 2007
ProkaryotaSerratia MarcescensReduction of movement or death of Panagrelleus redivivus and Bursaphelenchus xylophilus.NAGu et al. 2007
ProkaryotaCytophaga-Flavobacterium-Bacteroidesn/aNADickschat et al. 2005_3
ProkaryotaOctadecabacter Sp.n/aNADickschat et al. 2005_3
ProkaryotaStigmatella Aurantiacan/aNADickschat et al. 2005_5
ProkaryotaLactobacillus Casein/aNATracey and Britz 1989
ProkaryotaLactobacillus Plantarumn/aNATracey and Britz 1989
ProkaryotaPediococcus Damnosusn/aNATracey and Britz 1989
ProkaryotaLeuconostoc Cremorisn/aNATracey and Britz 1989
ProkaryotaLeuconostoc Dextranicumn/aNATracey and Britz 1989
ProkaryotaLactococcus Lactisn/aNATracey and Britz 1989
ProkaryotaLeuconostoc Mesenteroidesn/aNATracey and Britz 1989
ProkaryotaLeuconostoc Paramesenteroidesn/aNATracey and Britz 1989
ProkaryotaOenococcus Oenin/aNATracey and Britz 1989
EukaryotaFusarium Graminearumn/aNABusko et al. 2014
EukaryotaTuber Mesentericumn/aFortywoodland of the Basilicata regionMauriello et al. 2004
EukaryotaTuber Excavatumn/aFortywoodland of the Basilicata regionMauriello et al. 2004
EukaryotaTuber Aestivumn/aFortywoodland of the Basilicata regionMauriello et al. 2004
EukaryotaTuber Panniferumn/aFortywoodland of the Basilicata regionMauriello et al. 2004
EukaryotaTuber Melanosporumn/aAgricultural Centre of Castilla and León Community (Monasterio de la Santa Espina, Valladolid, Spain) and Navaleno (Soria, Spain).Diaz et al. 2003
EukaryotaBjerkandera Adustan/aNALapadatescu et al. 2000
ProkaryotaBacillus Subtilisn/aNALee et al. 2012
EukaryotaAscocoryne Sarcoidesn/aNAMallette et al.  2012
EukaryotaTrichoderma Viriden/aNAWheatley et al. 1997
ProkaryotaBurkholderia Sp.bacterial interationsrhizosphere and bulk soil of Carex arenariaTyc et al. 2017
ProkaryotaPaenibacillus Sp.bacterial interationsrhizosphere and bulk soil of Carex arenariaTyc et al. 2017
ProkaryotaBacillus AmyloliquefaciensAgriculture University of Nanjing, ChinaTahir et al. 2017
ProkaryotaCitrobacter FreundiiAmerican Type Culture Collection Robacker and Bartelt 1997
ProkaryotaKlebsiella PneumoniaeAmerican Type Culture Collection Robacker and Bartelt 1997
EukaryotaPleurotus OstreatusNABeltran-Garcia et al. 1997
EukaryotaFomes FomentariusNAFäldt et al. 1999
EukaryotaPenicillium Sp.NATakeuchi et al. 2012
EukaryotaFusarium Sp.NATakeuchi et al. 2012
EukaryotaBotrytis Sp.NAKikuchi et al. 1983
EukaryotaAspergillus Sp.NATakeuchi et al. 2012
ProkaryotaThermomonospora FuscanasoilWilkins 1996
ProkaryotaPseudomonas Fluorescenspromotes volatile oil accumulation, activating plant defensefrom geo-authentic Atractylodes lanceaZhou et al. 2016
ProkaryotaPseudomonas Veroniinarhizosphere of field-grown potato plantsHunziker et al. 2015
ProkaryotaPseudomonas Syringaenaphyllosphere of field-grown potato plantsHunziker et al. 2015
ProkaryotaPseudomonas Jesseniinaphyllosphere of field-grown potato plantsHunziker et al. 2015
ProkaryotaLactobacillus HelveticusnayoghurtPogačić et al. 2016
ProkaryotaPedobacter Sp.narhizosphere of Marram grass in sandy dune soils, NetherlandsGarbeva et al. 2014
ProkaryotaChryseobacterium Sp.nanaTyc et al. 2015
ProkaryotaTsukamurella Sp.nanaTyc et al. 2015
ProkaryotaJanthinobacterium Sp.nanaTyc et al. 2015
EukaryotaPiptoporus BetulinusnaSachsenwald near HamburgRösecke et al. 2000
EukaryotaFomitopsis PinicolanaGermanyRösecke et al. 2000
EukaryotaTrametes Suaveolensnanear Zachersmühle, Göppingen, southern GermanyRösecke et al. 2000
EukaryotaPleurotus EryngiinanaUsami et al. 2014
EukaryotaPleurotus CystidiosusnanaUsami et al. 2014
ProkaryotaStreptococcus PneumoniaeclinicPreti et al. 2009
ProkaryotaHaemophilus InfluenzaeclinicPreti et al. 2009
ProkaryotaBranhamella CatarrhalisclinicPreti et al. 2009
EukaryotaBjerkandera AdustaNASpinnler at al. 1994
EukaryotaTuber MelanosporumNoneT. melanosporum, T. borchii were collected from northern Italy (Piedmont) and T. indicum from Yunnan and Sichuan Provinces (China). Splivallo et al. 2007b
EukaryotaTuber IndicumNoneT. melanosporum, T. borchii were collected from northern Italy (Piedmont) and T. indicum from Yunnan and Sichuan Provinces (China). Splivallo et al. 2007b
ProkaryotaLentilactobacillus BuchneriNANASquara et al. 2022
ProkaryotaLacticaseibacillus ParacaseiNANASquara et al. 2022
EukaryotaMetschnikowia PulcherrimaNANALjunggren et al. 2019
EukaryotaMetschnikowia FructicolaNANALjunggren et al. 2019
EukaryotaZygosaccharomyces RouxiiNANAPei et al. 2022
EukaryotaSaccharomyces CerevisiaeNANAHarris et al. 2021
EukaryotaAureobasidium PullulansNANAMozūraitis et al. 2022
EukaryotaCryptococcus WieringaeNANAMozūraitis et al. 2022
EukaryotaHanseniaspora UvarumNANAMozūraitis et al. 2022
EukaryotaPichia KudriavzeviiNANAMozūraitis et al. 2022
EukaryotaPichia FermentansNANAMozūraitis et al. 2022
EukaryotaPichia KluyveriNANAMozūraitis et al. 2022
EukaryotaPichia MembranifaciensNANAMozūraitis et al. 2022
EukaryotaSaccharomyces ParadoxusNANAMozūraitis et al. 2022
EukaryotaTorulaspora DelbrueckiiNANAMozūraitis et al. 2022
EukaryotaPichia AnomalaNANAMozūraitis et al. 2022
EukaryotaMetschnikowia PulcherrimaNANAMozūraitis et al. 2022
ProkaryotaStaphylococcus EquorumNANAToral et al. 2021
ProkaryotaBacillus AtrophaeusNANAToral et al. 2021
ProkaryotaPeribacillus Sp.NANAToral et al. 2021
ProkaryotaPseudomonas SegetisNANAToral et al. 2021
ProkaryotaBacillus VelezensisNANAToral et al. 2021
ProkaryotaPsychrobacillus VulpisNANAToral et al. 2021
EukaryotaWickerhamomyces AnomalusNANAShi et al. 2022
ProkaryotaBacillus SubtilisNANALee et al. 2023
EukaryotaSaccharomyces EubayanusNANAUrbina et al. 2020
EukaryotaMeyerozyma GuilliermondiiNANAZhao et al. 2022
EukaryotaSaccharomyces CerevisiaeNANAZhao et al. 2022
EukaryotaSaccharomycopsis ViniNANAZhao et al. 2022
EukaryotaSaturnispora DiversaNANAZhao et al. 2022
EukaryotaWickerhamomyces AnomalusNANAZhao et al. 2022
Meyerozyma GuilliermondiiXiong et al. 2023
Lentinula EdodesGeng et al. 2024
Lactiplantibacillus PlantarumChen et al. 2023
Bacillus ThuringiensisKoilybayeva et al. 2023
Bacillus AcidiproducensKoilybayeva et al. 2023
Bacillus CereusKoilybayeva et al. 2023
Bacillus SafensisKoilybayeva et al. 2023
Lactobacillus PlantarumMa et al. 2023
Citrobacter FreundiiTallon et al. 2023
Enterobacter AgglomeransTallon et al. 2023
Enterobacter CloacaeTallon et al. 2023
Klebsiella OxytocaTallon et al. 2023
Saccharomyces CerevisiaePeng et al. 2023
Staphylococcus AureusWang et al. 2023
Pediococcus AcidilacticiMockus et al. 2024
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaEscherichia ColiNBTD/GC-MSno
ProkaryotaEscherichia ColiLBSPME/GC-MSno
EukaryotaAspergillus NigerYeast Glucose ChloramphenicolSPME/GCxGC-MSno
EukaryotaCandida AlbicansYeast Glucose ChloramphenicolSPME/GCxGC-MSno
EukaryotaPenicillium ChrysogenumYeast Glucose ChloramphenicolSPME/GCxGC-MSno
ProkaryotaStreptococcus PneumoniaeModified Lacks MediaSPME/GCxGC-MSno
ProkaryotaStaphylococcus Aureustryptic soy brothTD/GC-MSno
EukaryotaAgaricus Essetteihydro-destillation, solvent extraction, GC-MSno
EukaryotaCandida AlbicansMueller Hinton broth (MB), tryptic soy broth (TSB)SPME, DVB/CAR/PDMS, GC-MSno
ProkaryotaEscherichia ColiMueller Hinton broth (MB), tryptic soy broth (TSB)SPME, DVB/CAR/PDMS, GC-MSno
ProkaryotaStaphylococcus AureusMueller Hinton broth (MB), tryptic soy broth (TSB)SPME, DVB/CAR/PDMS, GC-MSno
ProkaryotaBacillus SubtilisLuria-Bertani (LB) agarHS / SPME / GC-MSno
EukaryotaFusarium CulmorumKing`s B agarUPLC-MSno
EukaryotaHypoxylon InvadensYMG mediumCSLA-GCMSyes
EukaryotaFusarium AcuminatumMalt extractSPME, GC-MSyes
EukaryotaFusarium OxysporumMalt extractSPME, GC-MSyes
EukaryotaPolyporus TuberasterPGYGC-MSno
ProkaryotaBacillus SubtilisLB agarGC-MSno
ProkaryotaPseudomonas FluorescensLB agarGC-MSno
ProkaryotaPseudomonas Sp.LB mediaHS-SPME/GC-MSyes
ProkaryotaBacillus AmyloliquefaciensTSB mediaSPME/GC-MSno
ProkaryotaBacillus ToyonensisTSB media, MR-VP (Methyl Red-Vogos Proskeur) mediaSPME/GC-MSno
ProkaryotaSerratia MyotisTSB mediaSPME/GC-MSno
EukaryotaCandida AlbicansYGC mediaHS-SPME/GC-GC-ToFMSno
EukaryotaCandida GlabrataYGC mediaHS-SPME/GC-GC-ToFMSno
EukaryotaCandida TropicalisYGC mediaHS-SPME/GC-GC-ToFMSno
ProkaryotaEscherichia ColiTSB mediaHS-SPME/GC-MSno
ProkaryotaPaenibacillus PolymyxaLB agar and M49 (minimal) mediaSPME/GC-MSyes
ProkaryotaStenotrophomonas MaltophiliaNA mediaGC-MSno
ProkaryotaBacillus VelezensisMOLP mediaSPME/GC-MSyes
ProkaryotaStaphylococcus EpidermidisMHB mediaHS-SPME/GC×GC-TOFMSno
ProkaryotaErwinia AmylovoraSBSE/GC-MSno
ProkaryotaLactobacillus Plantarumn/an/ano
ProkaryotaPseudomonas Fluorescensn/an/ano
ProkaryotaPseudomonas Corrugatan/an/ano
ProkaryotaPseudomonas Chlororaphisn/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
ProkaryotaBacillus Simplexn/an/ano
ProkaryotaBacillus Subtilisn/an/ano
ProkaryotaBacillus Weihenstephanensisn/an/ano
ProkaryotaMicrobacterium Oxydansn/an/ano
ProkaryotaStreptomyces Lateritiusn/an/ano
ProkaryotaSerratia Marcescensn/an/ano
ProkaryotaCytophaga-Flavobacterium-Bacteroidesn/an/ano
ProkaryotaOctadecabacter Sp.n/an/ano
ProkaryotaStigmatella Aurantiacan/an/ano
ProkaryotaLactobacillus Casein/an/ano
ProkaryotaPediococcus Damnosusn/an/ano
ProkaryotaLeuconostoc Cremorisn/an/ano
ProkaryotaLeuconostoc Dextranicumn/an/ano
ProkaryotaLactococcus Lactisn/an/ano
ProkaryotaLeuconostoc Mesenteroidesn/an/ano
ProkaryotaLeuconostoc Paramesenteroidesn/an/ano
ProkaryotaOenococcus Oenin/an/ano
EukaryotaFusarium Graminearumyeast extract sucrose agarSPME/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 Panniferumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)no
EukaryotaTuber Melanosporumn/an/ano
EukaryotaBjerkandera AdustaMinimal media plus glucose and L-phenylalanineExtraction with dichloromethane or with ethyl acetate, concentration under N2 stream /GC-MS.no
ProkaryotaBacillus SubtilisTryptic soy agarSPME coupled with GC-MSno
EukaryotaAscocoryne SarcoidesMinimal mediumPTR-MS and SPME GC-MSno
EukaryotaTrichoderma VirideMalt extractGC/MSno
ProkaryotaBurkholderia Sp.TSBAGC-Q-TOFno
ProkaryotaPaenibacillus Sp.TSBAGC-Q-TOFno
ProkaryotaBacillus AmyloliquefaciensLBSPME-GC-MSno
ProkaryotaCitrobacter Freundiitryptic soy broth SPME, GC-MSyes
ProkaryotaKlebsiella Pneumoniaetryptic soy broth SPME, GC-MSyes
EukaryotaPleurotus Ostreatusno
EukaryotaFomes Fomentariusno
EukaryotaPenicillium Sp.no
EukaryotaFusarium Sp.no
EukaryotaBotrytis Sp.no
EukaryotaAspergillus Sp.no
ProkaryotaThermomonospora FuscaNutrient agar CM3GC/MSno
ProkaryotaPseudomonas FluorescensMS rooting agarGC/MS + comparison to NISTno
ProkaryotaPseudomonas VeroniiLB mediumGC/MSyes
ProkaryotaPseudomonas SyringaeLB mediumGC/MSyes
ProkaryotaPseudomonas JesseniiLB mediumGC/MSyes
ProkaryotaLactobacillus Helveticuscurd-based broth mediumGC/MSyes
ProkaryotaPedobacter Sp.sand containing artificial root exudatesGC/MSno
ProkaryotaChryseobacterium Sp.Tryptic soy broth agarGC/MS-Q-TOFno
ProkaryotaTsukamurella Sp.Tryptic soy broth agarGC/MS-Q-TOFno
ProkaryotaJanthinobacterium Sp.Tryptic soy broth agarGC/MS-Q-TOFno
EukaryotaPiptoporus BetulinusnaGC/MSno
EukaryotaFomitopsis PinicolanaGC/MSno
EukaryotaTrametes SuaveolensnaGC/MSno
EukaryotaPleurotus EryngiinaGC/MS, GC-O, AEDAno
EukaryotaPleurotus CystidiosusnaGC/MS, GC-O, AEDAno
ProkaryotaStreptococcus PneumoniaeBlood agar/chocolate blood agaHS-SPME/GC-MS no
ProkaryotaHaemophilus InfluenzaeBlood agar/chocolate blood agaHS-SPME/GC-MS no
ProkaryotaBranhamella CatarrhalisBlood agar/chocolate blood agaHS-SPME/GC-MS no
EukaryotaBjerkandera Adustano
EukaryotaTuber MelanosporumNoneNoneyes
EukaryotaTuber IndicumNoneNoneyes
ProkaryotaLentilactobacillus Buchnerimaize silageHS-SPME coupled with GC-TOF MSno
ProkaryotaLacticaseibacillus Paracaseimaize silageHS-SPME coupled with GC-TOF MSno
EukaryotaMetschnikowia Pulcherrimaliquid YPD mediumGC-MSno
EukaryotaMetschnikowia Fructicolaliquid YPD mediumGC-MSno
EukaryotaZygosaccharomyces RouxiiYPD mediumGC-MSno
EukaryotaSaccharomyces Cerevisiaemalt extract brothHS-SPME with GC-MSno
EukaryotaAureobasidium PullulansYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaCryptococcus WieringaeYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaHanseniaspora UvarumYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaPichia KudriavzeviiYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaPichia FermentansYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaPichia KluyveriYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaPichia MembranifaciensYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaSaccharomyces ParadoxusYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaTorulaspora DelbrueckiiYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaPichia AnomalaYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaMetschnikowia PulcherrimaYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
ProkaryotaStaphylococcus EquorumMOLPHS-SPME-GC/MSno
ProkaryotaStaphylococcus EquorumSchaeffer’s growth (SG) mediumHS-SPME-GC/MSno
ProkaryotaBacillus AtrophaeusMOLPHS-SPME-GC/MSno
ProkaryotaBacillus AtrophaeusSchaeffer’s growth (SG) mediumHS-SPME-GC/MSno
ProkaryotaBacillus Atrophaeustryptic soy agar (TSA, Panreac Applichem) mediumHS-SPME-GC/MSno
ProkaryotaPeribacillus Sp.MOLPHS-SPME-GC/MSno
ProkaryotaPeribacillus Sp.Schaeffer’s growth (SG) mediumHS-SPME-GC/MSno
ProkaryotaPeribacillus Sp.tryptic soy agar (TSA, Panreac Applichem) mediumHS-SPME-GC/MSno
ProkaryotaPseudomonas SegetisMOLPHS-SPME-GC/MSno
ProkaryotaBacillus VelezensisMOLPHS-SPME-GC/MSno
ProkaryotaBacillus VelezensisSchaeffer’s growth (SG) mediumHS-SPME-GC/MSno
ProkaryotaPsychrobacillus VulpisMOLPHS-SPME-GC/MSno
ProkaryotaPsychrobacillus VulpisSchaeffer’s growth (SG) mediumHS-SPME-GC/MSno
EukaryotaWickerhamomyces Anomalusmedium consisted of glucose (20 g/l), peptone (5 g/l), agar (20 g/l) and amoxicillin (1 g/l)SPME with GC-MSno
EukaryotaWickerhamomyces Anomalussolid-state fermentation starter culture DaquSPME coupled with GC-MSno
ProkaryotaBacillus SubtilisTryptone soy broth (TSB)HPLCno
EukaryotaSaccharomyces Eubayanusbeer wortHS-SPME-GC-MSno
EukaryotaMeyerozyma Guilliermondiisynthetic grape juiceHS-SPMEno
EukaryotaSaccharomyces Cerevisiaesynthetic grape juiceHS-SPMEno
EukaryotaSaccharomycopsis Vinisynthetic grape juiceHS-SPMEno
EukaryotaSaturnispora Diversasynthetic grape juiceHS-SPMEno
EukaryotaWickerhamomyces Anomalussynthetic grape juiceHS-SPMEno
Meyerozyma GuilliermondiiYEPD, 10 g/L yeast extrac, 20 g/L peptone, 20 g dextroseGC-MS and GC-IMSno
Lentinula EdodesJiuqu (traditional wheat Qu)GC-IMSno
Lactiplantibacillus Plantarumfermentation of ginkgo kernel juiceGC-IMSno
Bacillus Thuringiensisbacteriological agar (BA, 15 g/L), gelatin peptone (GP, 5 g/L), and meat extract (ME, 3 g/L)GC–MSno
Bacillus Acidiproducensbacteriological agar (BA, 15 g/L), gelatin peptone (GP, 5 g/L), and meat extract (ME, 3 g/L)GC–MSno
Bacillus Cereusbacteriological agar (BA, 15 g/L), gelatin peptone (GP, 5 g/L), and meat extract (ME, 3 g/L)GC–MSno
Bacillus Safensisbacteriological agar (BA, 15 g/L), gelatin peptone (GP, 5 g/L), and meat extract (ME, 3 g/L)GC–MSno
Lactobacillus Plantarumtuna cooking liquidHS-SPME-GC/MSno
Citrobacter Freundiitryptone soya broth (TSB) mediaTenax/GC/MSno
Enterobacter Agglomeranstryptone soya broth (TSB) mediaTenax/GC/MSno
Enterobacter Cloacaetryptone soya broth (TSB) mediaTenax/GC/MSno
Klebsiella Oxytocatryptone soya broth (TSB) mediaTenax/GC/MSno
Saccharomyces Cerevisiaesea buckthorn juiceHS-SPME-GC–MS/UHPLC–MSno
Staphylococcus Aureusraw Shiyang chickenHS-GC-IMS/HS-SPME-GC-MSno
Pediococcus Acidilacticilentils (Lens culinaris)SPME/ICP-MSno


2-butylfuran

Mass-Spectra

Compound Details

Synonymous names
2-BUTYLFURAN
4466-24-4
2-n-Butylfuran
Furan, 2-butyl-
2-butyl furan
2-n-Butyl furan
81JV9ZYK0D
MFCD00047071
2-n-Butylfuran; Furan, 2-butyl-
2-butyl-furan
UNII-81JV9ZYK0D
EINECS 224-732-7
2-Butylfuran, AldrichCPR
2-BUTYLFURAN [FHFI]
SCHEMBL256700
DTXSID8073340
FEMA NO. 4081
CHEBI:89750
NWZIYQNUCXUJJJ-UHFFFAOYSA-
AKOS025396869
PS-4850
SB60946
SY048490
2-Butylfuran 100 microg/mL in Acetonitrile
B2412
CS-0152344
NS00022199
2-Butylfuran 1000 microg/mL in Acetonitrile
D88935
EN300-7396471
Q27161938
InChI=1/C8H12O/c1-2-3-5-8-6-4-7-9-8/h4,6-7H,2-3,5H2,1H3
Microorganism:

Yes

IUPAC name2-butylfuran
SMILESCCCCC1=CC=CO1
InchiInChI=1S/C8H12O/c1-2-3-5-8-6-4-7-9-8/h4,6-7H,2-3,5H2,1H3
FormulaC8H12O
PubChem ID20534
Molweight124.18
LogP3.1
Atoms9
Bonds3
H-bond Acceptor1
H-bond Donor0
Chemical Classificationaromatic compounds ethers heterocyclic compounds furan derivatives
CHEBI-ID89750
Supernatural-IDSN0257523

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaPseudomonas AeruginosaNANADavis et al. 2020
EukaryotaAspergillus Flavusn/aNABeck et al. 2012
EukaryotaAspergillus Parasiticusn/aNABeck et al. 2012
EukaryotaAspergillus Nigern/aNABeck et al. 2012
EukaryotaPenicillium Glabrumn/aNABeck et al. 2012
EukaryotaRhizopus Stolonifern/aNABeck et al. 2012
EukaryotaBjerkandera AdustaNAZiegenbein et al. 2010
EukaryotaXylaria Sp.naHaematoxylon brasiletto, Morelos, MexicoSánchez-Ortiz et al. 2016
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaPseudomonas AeruginosaLB brothSPME/GCxGC-MSno
EukaryotaAspergillus Flavuspotato dextrose agar and Polyunsaturated Fatty AcidsSPME/ GC-MSno
EukaryotaAspergillus Parasiticuspotato dextrose agar and Polyunsaturated Fatty AcidsSPME/ GC-MSno
EukaryotaAspergillus Nigerpotato dextrose agar and Polyunsaturated Fatty AcidsSPME/ GC-MSno
EukaryotaPenicillium Glabrumpotato dextrose agar and Polyunsaturated Fatty AcidsSPME/ GC-MSno
EukaryotaRhizopus Stoloniferpotato dextrose agar and Polyunsaturated Fatty AcidsSPME/ GC-MSno
EukaryotaBjerkandera Adustano
EukaryotaXylaria Sp.PDA mediumSPME-GC/MSyes


1-phenylethanone

Mass-Spectra

Compound Details

Synonymous names
ACETOPHENONE
98-86-2
1-Phenylethanone
Methyl phenyl ketone
Phenyl methyl ketone
Acetylbenzene
Ethanone, 1-phenyl-
Hypnone
Benzoyl methide
Acetophenon
Acetylbenzol
1-phenylethan-1-one
1-Phenyl-1-ethanone
Benzoylmethide
Acetofenon
Benzene, acetyl-
Ketone, methyl phenyl
Phenylethanone
Hypnon
USAF EK-496
methylphenylketone
phenylmethylketone
RCRA waste number U004
1-phenyl-ethanone
Acetofenon [Czech]
Dymex
NSC 7635
FEMA No. 2009
FEMA Number 2009
CCRIS 1341
HSDB 969
AI3-00575
RCRA waste no. U004
EINECS 202-708-7
UNII-RK493WHV10
RK493WHV10
DTXSID6021828
CHEBI:27632
Ketone, methyl phenyl-
NSC-7635
Acetophenone-alpha-13C
Acetophenone-1,2-13C2
CHEMBL274467
DTXCID501828
EC 202-708-7
Ethanone-2,2,2-d3, 1-(phenyl-d5)-
ACETOPHENONE (II)
ACETOPHENONE [II]
Acetofenona
CAS-98-86-2
MFCD00064447
AC0
(2,2,2,-2H3)ACETOPHENONE
aceto phenone
aceto-phenone
acetyl-benzen
Acetyl-Benzene
alpha-Acetophenone
Ethanone,1-phenyl
methyl-phenyl ketone
Methyl phenyl-Ketone
nchem.180-comp5
Benzoyl methide hypnone
1-Phenylethanone, 9CI
ACETOPHENONE [MI]
SCHEMBL737
ACETOPHENONE [FCC]
bmse000286
ACETOPHENONE [FHFI]
ACETOPHENONE [HSDB]
ACETOPHENONE [INCI]
WLN: 1VR
Acetophenone, >=98%, FG
SCHEMBL8170205
1-Phenylethanone (acetophenone)
SCHEMBL13341485
Acetophenone, analytical standard
FEMA 2009
NSC7635
Acetophenone, >=98.0% (GC)
Acetophenone, natural, 98%, FG
HY-Y0989
STR00017
Tox21_202422
Tox21_300343
Acetophenone, ReagentPlus(R), 99%
BDBM50236986
c0117
MFCD00008724
s5528
AKOS000119011
CCG-266074
DB04619
MCULE-4710225344
USEPA/OPP Pesticide Code: 129033
NCGC00248000-01
NCGC00248000-02
NCGC00254370-01
NCGC00259971-01
SY073923
DB-044220
A0061
CS-0015982
NS00010659
EN300-18050
Acetophenone, puriss. p.a., >=99.0% (GC)
C07113
D71016
A854783
Q375112
J-519533
Z57127548
Acetophenone, TraceCERT(R), certified reference material
InChI=1/C8H8O/c1-7(9)8-5-3-2-4-6-8/h2-6H,1H
Microorganism:

Yes

IUPAC name1-phenylethanone
SMILESCC(=O)C1=CC=CC=C1
InchiInChI=1S/C8H8O/c1-7(9)8-5-3-2-4-6-8/h2-6H,1H3
FormulaC8H8O
PubChem ID7410
Molweight120.15
LogP1.6
Atoms9
Bonds1
H-bond Acceptor1
H-bond Donor0
Chemical Classificationaromatic compounds aromatic ketones ketones benzenoids
CHEBI-ID27632
Supernatural-IDSN0197388

mVOC Specific Details

Boiling Point
DegreeReference
202.1 °C peer reviewed
Volatilization
The Henry's Law constant for acetophenone was measured as 1.04X10-5 atm-cu m/mole(1). This Henry's Law constant indicates that acetophenone 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 61 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 32 days(SRC). Acetophenone's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Acetophenone is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 0.397 mm Hg(3).
Literature: (1) Betterton EA et al; Atmos Environ 25A: 1473-77 (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 acetophenone was measured as 10, using an agricultural soil obtained from Northeastern China(1). According to a classification scheme(2), this Koc value suggests that acetophenone is expected to have very high mobility in soil(SRC).
Literature: (1) Ding Y, Wang L; Toxicol Environ Chem 78: 1-9 (2000) (2) Swann RL et al; Res Rev 85: 17-28 (1983)
Literature: #The experimental and estimated log Koc for acetophenone in several soils and sediments ranged from 1.34-2.43(1-6,8). These values are indicative of medium to high mobility in soil and low adsorption to sediments(7).
Literature: (1) Bahnick DA, Doucette WJ; Chemosphere 17: 1703-15 (1988) (2) Sabljic A; Enviorn Sci Technol 21: 358-66 (1987) (3) Banwart WL et al; J Environ Sci Health B15: 165-79 (1980) (4) Hodson J, Williams NA; Chemosphere 17: 67-77 (1988) (5) Gerstl Z, Mingelgrin U; J Environ Sci Health B19: 297-312 (1984) (6) Khan A et al; Soil Sci 128: 297-302 (1979) (7) Swann RL et al; Res Rev 85: 17-28 (1983) (8) Southworth GR, Keller JL; Water Air Soil Poll 28: 239-48 (1986)
Vapor Pressure
PressureReference
0.397 mm Hg @ 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
ProkaryotaEscherichia ColiNANAHewett et al. 2020
ProkaryotaPseudomonas AeruginosaNANABean et al. 2016
ProkaryotaPseudomonas AeruginosaNANABean et al. 2012
ProkaryotaEscherichia ColiNANADixon et al. 2022
ProkaryotaAcinetobacter RadioresistensNATimm et al. 2018
ProkaryotaBrevibacterium EpidermidisNATimm et al. 2018
ProkaryotaCorynebacterium XerosisNATimm et al. 2018
ProkaryotaPseudomonas AeruginosaNATimm et al. 2018
ProkaryotaRhodococcus ErythropolisNATimm et al. 2018
ProkaryotaStaphylococcus EpidermidisNATimm et al. 2018
EukaryotaHypoxylon InvadensNADickschat et al. 2018
ProkaryotaBacillus SubtilisZhang et al. 2021
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 Protegensinhibite the growth of Heterobasidion abietinum 10 and several fungi of different species (Basidiomycete, Ascomycete, Oomycota, Zygomycota)NAPrigigallo et al. 2021
EukaryotaMortierella Isabellinamor horizon of a spruce forest soil southeastern SwedenBengtsson et al. 1991
ProkaryotaCytophaga-Flavobacterium-Bacteroidesn/aNADickschat et al. 2005_3
ProkaryotaStigmatella Aurantiacan/aNADickschat et al. 2005_5
ProkaryotaBurkholderia Ambifarian/aBurkholderia ambifaria LMG 17828 from root, LMG 19182 from rhizosphere and LMG 19467 from clinical.Groenhagen et al. 2013
ProkaryotaXanthomonas Campestrisn/aNAWeise et al. 2012
EukaryotaBjerkandera Adustan/aNALapadatescu et al. 2000
ProkaryotaStenotrophomonas MaltophiliaclinicPreti et al. 2009
EukaryotaAspergillus ClavatusNASeifert and King 1982
EukaryotaMortierella IsabellinaNABengtsson et al. 1991
EukaryotaVerticillium BulbillosumNABengtsson et al. 1991
ProkaryotaPseudochrobactrum SaccharolyticumNematicidal activitycow dungXU et al. 2015
ProkaryotaArthrobacter NicotianaeNematicidal activitycow dungXU et al. 2015
ProkaryotaAchromobacter XylosoxidansNematicidal activitycow dungXU et al. 2015
ProkaryotaPseudomonas Vranovensisnarhizosphere of field-grown potato plantsHunziker et al. 2015
ProkaryotaPseudomonas Veroniinarhizosphere of field-grown potato plantsHunziker et al. 2015
ProkaryotaPseudomonas Chlororaphisnarhizosphere of field-grown potato plantsHunziker et al. 2015
ProkaryotaPseudomonas Frederiksbergensisnaphyllosphere of field-grown potato plantsHunziker et al. 2015
ProkaryotaPseudomonas Syringaenaphyllosphere of field-grown potato plantsHunziker et al. 2015
ProkaryotaPseudomonas Jesseniinaphyllosphere of field-grown potato plantsHunziker et al. 2015
ProkaryotaProteus VulgarisnanaSu et al. 2016
ProkaryotaProvidencia RettgerinanaSu et al. 2016
ProkaryotaPseudochrobactrum AsaccharolyticumnanaSu et al. 2016
EukaryotaTrametes Suaveolensnanear Zachersmühle, Göppingen, southern GermanyRösecke et al. 2000
EukaryotaPleurotus EryngiinanaUsami et al. 2014
EukaryotaPleurotus CystidiosusnanaUsami et al. 2014
ProkaryotaBacillus SimplexReduction of movement or death of Panagrelleus redivivus and Bursaphelenchus xylophilus.NAGu et al. 2007
ProkaryotaBacillus SubtilisReduction of movement or death of Panagrelleus redivivus and Bursaphelenchus xylophilus.NAGu et al. 2007
ProkaryotaBacillus WeihenstephanensisReduction of movement or death of Panagrelleus redivivus and Bursaphelenchus xylophilus.NAGu et al. 2007
ProkaryotaMicrobacterium OxydansReduction of movement or death of Panagrelleus redivivus and Bursaphelenchus xylophilus.NAGu et al. 2007
ProkaryotaStenotrophomonas MaltophiliaReduction of movement or death of Panagrelleus redivivus and Bursaphelenchus xylophilus.NAGu et al. 2007
ProkaryotaStreptomyces LateritiusReduction of movement or death of Panagrelleus redivivus and Bursaphelenchus xylophilus.NAGu et al. 2007
ProkaryotaSerratia MarcescensReduction of movement or death of Panagrelleus redivivus and Bursaphelenchus xylophilus.NAGu et al. 2007
EukaryotaCladosporium CladosporioidesNAHedlund et al. 1995
EukaryotaCladosporium HerbarumNAHedlund et al. 1995
EukaryotaPenicillium SpinulosumNAHedlund et al. 1995
EukaryotaTuber BorchiiNoneT. melanosporum, T. borchii were collected from northern Italy (Piedmont) and T. indicum from Yunnan and Sichuan Provinces (China). Splivallo et al. 2007b
EukaryotaTuber MelanosporumNoneT. melanosporum, T. borchii were collected from northern Italy (Piedmont) and T. indicum from Yunnan and Sichuan Provinces (China). Splivallo et al. 2007b
ProkaryotaLentilactobacillus BuchneriNANASquara et al. 2022
EukaryotaZygosaccharomyces RouxiiNANAPei et al. 2022
EukaryotaAureobasidium PullulansNANAMozūraitis et al. 2022
EukaryotaCryptococcus WieringaeNANAMozūraitis et al. 2022
EukaryotaHanseniaspora UvarumNANAMozūraitis et al. 2022
EukaryotaPichia KudriavzeviiNANAMozūraitis et al. 2022
EukaryotaPichia FermentansNANAMozūraitis et al. 2022
EukaryotaPichia KluyveriNANAMozūraitis et al. 2022
EukaryotaPichia MembranifaciensNANAMozūraitis et al. 2022
EukaryotaSaccharomyces ParadoxusNANAMozūraitis et al. 2022
EukaryotaTorulaspora DelbrueckiiNANAMozūraitis et al. 2022
EukaryotaPichia AnomalaNANAMozūraitis et al. 2022
EukaryotaMetschnikowia PulcherrimaNANAMozūraitis et al. 2022
ProkaryotaStaphylococcus EquorumNANAToral et al. 2021
ProkaryotaPeribacillus Sp.NANAToral et al. 2021
ProkaryotaBacillus VelezensisNANAToral et al. 2021
ProkaryotaBacillus SubtilisNANALee et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaEscherichia ColiLBSPME/GC-MSno
ProkaryotaPseudomonas AeruginosaLB-LennoxSPME/GC-MSno
ProkaryotaPseudomonas Aeruginosalysogeny brothSPME/GCxGC-MSno
ProkaryotaEscherichia ColiLBTD/GC-MSno
ProkaryotaAcinetobacter RadioresistensMOPS glucoseSPME, GC-MSno
ProkaryotaAcinetobacter RadioresistensTSASPME, GC-MSno
ProkaryotaBrevibacterium EpidermidisTSASPME, GC-MSno
ProkaryotaCorynebacterium XerosisTSASPME, GC-MSno
ProkaryotaPseudomonas AeruginosaTSASPME, GC-MSno
ProkaryotaRhodococcus ErythropolisTSASPME, GC-MSno
ProkaryotaStaphylococcus EpidermidisMOPS glucose+EZSPME, GC-MSno
ProkaryotaStaphylococcus EpidermidisTSASPME, GC-MSno
ProkaryotaStaphylococcus EpidermidisMOPS glucoseSPME, GC-MSno
EukaryotaHypoxylon InvadensYMG mediumCSLA-GCMSyes
ProkaryotaBacillus SubtilisLB mediaHS-SPME/GC-MSno
ProkaryotaPseudomonas Sp.DYGS mediaHS-SPME/GC-MSno
ProkaryotaPseudomonas ProtegensLB agar/PD agarGC-MSyes
EukaryotaMortierella Isabellinamalt extact agardiethyl extraction, GC-MSno
ProkaryotaCytophaga-Flavobacterium-Bacteroidesn/an/ano
ProkaryotaStigmatella Aurantiacan/an/ano
ProkaryotaBurkholderia AmbifariaLuria-Bertani medium, Malt Extractn/ano
ProkaryotaXanthomonas CampestrisNBIIClosed airflow-system/GC-MS and PTR-MSno
EukaryotaBjerkandera AdustaMinimal media plus glucose and L-phenylalanineExtraction with dichloromethane or with ethyl acetate, concentration under N2 stream /GC-MS.no
ProkaryotaStenotrophomonas MaltophiliaBlood agar/chocolate blood agaHS-SPME/GC-MS no
EukaryotaAspergillus Clavatusno
EukaryotaMortierella Isabellinano
EukaryotaVerticillium Bulbillosumno
ProkaryotaPseudochrobactrum SaccharolyticumLB liquidSPME-GC/MSno
ProkaryotaArthrobacter NicotianaeLB liquidSPME-GC/MSno
ProkaryotaAchromobacter XylosoxidansLB liquidSPME-GC/MSno
ProkaryotaPseudomonas VranovensisLB mediumGC/MSyes
ProkaryotaPseudomonas VeroniiLB mediumGC/MSyes
ProkaryotaPseudomonas ChlororaphisLB mediumGC/MSyes
ProkaryotaPseudomonas FrederiksbergensisLB mediumGC/MSyes
ProkaryotaPseudomonas SyringaeLB mediumGC/MSyes
ProkaryotaPseudomonas JesseniiLB mediumGC/MSyes
ProkaryotaProteus VulgarisLB mediumSPME-GC/MSno
ProkaryotaProvidencia RettgeriLB mediumSPME-GC/MSno
ProkaryotaPseudochrobactrum AsaccharolyticumLB mediumSPME-GC/MSno
EukaryotaTrametes SuaveolensnaGC/MSno
EukaryotaPleurotus EryngiinaGC/MS, GC-O, AEDAno
EukaryotaPleurotus CystidiosusnaGC/MS, GC-O, AEDAno
ProkaryotaBacillus Simplexn/an/ano
ProkaryotaBacillus Subtilisn/an/ano
ProkaryotaBacillus Weihenstephanensisn/an/ano
ProkaryotaMicrobacterium Oxydansn/an/ano
ProkaryotaStenotrophomonas Maltophilian/an/ano
ProkaryotaStreptomyces Lateritiusn/an/ano
ProkaryotaSerratia Marcescensn/an/ano
EukaryotaCladosporium CladosporioidesGC-MSno
EukaryotaCladosporium HerbarumGC-MSno
EukaryotaPenicillium SpinulosumGC-MSno
EukaryotaTuber BorchiiNoneNoneyes
EukaryotaTuber MelanosporumNoneNoneyes
ProkaryotaLentilactobacillus Buchnerimaize silageHS-SPME coupled with GC-TOF MSno
EukaryotaZygosaccharomyces RouxiiYPD mediumGC-MSno
EukaryotaAureobasidium PullulansYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaCryptococcus WieringaeYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaHanseniaspora UvarumYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaPichia KudriavzeviiYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaPichia FermentansYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaPichia KluyveriYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaPichia MembranifaciensYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaSaccharomyces ParadoxusYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaTorulaspora DelbrueckiiYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaPichia AnomalaYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaMetschnikowia PulcherrimaYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
ProkaryotaStaphylococcus EquorumMOLPHS-SPME-GC/MSno
ProkaryotaPeribacillus Sp.MOLPHS-SPME-GC/MSno
ProkaryotaBacillus VelezensisMOLPHS-SPME-GC/MSno
ProkaryotaBacillus SubtilisTryptone soy broth (TSB)HPLCno


(3,4-dimethoxyphenyl)methanol

Mass-Spectra

Compound Details

Synonymous names
3,4-Dimethoxybenzyl alcohol
93-03-8
(3,4-Dimethoxyphenyl)methanol
VERATRYL ALCOHOL
Benzenemethanol, 3,4-dimethoxy-
3,4-Dimethoxyphenylmethyl alcohol
veratrole alcohol
3,4-dimethoxybenzenemethanol
MFCD00004638
dimethoxybenzyl alcohol
NSC 6317
3,4-dimethoxy-benzyl alcohol
MB4T4A711H
NSC-6317
3,4-Dimethoxybenzylalcohol
UNII-MB4T4A711H
VOH
EINECS 202-212-0
VERATRALCOHOL
AI3-24181
3,4dimethoxybenzyl alcohol
bmse010029
3,4-Dimethoxybenzyl alcohol (Veratryl alcohol)
Benzenemethanol,4-dimethoxy-
SCHEMBL119395
3,4-Diamethoxybenzyl Methanol
VERATRYL ALCOHOL [INCI]
(3,4-dimethoxyphenyl)-methanol
DTXSID1059076
CHEBI:62150
NSC6317
(3,4-Dimethoxyphenyl)methanol #
[3,4-bis(methyloxy)phenyl]methanol
3,4-Dimethoxybenzyl alcohol, 96%
BBL027469
s3213
STL373549
DIMETHOXYBENZYL ALCOHOL [INCI]
AKOS000119346
AM81461
MCULE-1479539782
SY001541
DB-057359
HY-107858
CS-0030741
NS00039520
V0020
EN300-20192
A25060
C21420
(3,4-Dimethoxyphenyl)methanol, Veratryl alcohol
Q410698
J-511214
Q27160083
F0001-2235
VERAPAMIL HYDROCHLORIDE IMPURITY E [EP IMPURITY]
Z104477212
3,4-dimethoxy-benzenemethano;3,4-dimethoxy-Benzenemethanol;(3,4-Dimethoxyphenyl)methanol
Microorganism:

No

IUPAC name(3,4-dimethoxyphenyl)methanol
SMILESCOC1=C(C=C(C=C1)CO)OC
InchiInChI=1S/C9H12O3/c1-11-8-4-3-7(6-10)5-9(8)12-2/h3-5,10H,6H2,1-2H3
FormulaC9H12O3
PubChem ID7118
Molweight168.19
LogP0.6
Atoms12
Bonds3
H-bond Acceptor3
H-bond Donor1
Chemical Classificationaromatic compounds aromatic alcohols alcohols benzenoids ethers
CHEBI-ID62150
Supernatural-IDSN0263079

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaBjerkandera Adustan/aNALapadatescu et al. 2000
EukaryotaBjerkandera AdustaNASpinnler at al. 1994
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaBjerkandera AdustaMinimal media plus glucose and L-phenylalanineExtraction with dichloromethane or with ethyl acetate, concentration under N2 stream /GC-MS.no
EukaryotaBjerkandera Adustano


(4-methoxyphenyl)methanol

Mass-Spectra

Compound Details

Synonymous names
4-METHOXYBENZYL ALCOHOL
105-13-5
(4-Methoxyphenyl)methanol
Anisyl alcohol
Anise alcohol
p-Methoxybenzyl alcohol
p-Anisyl alcohol
Benzenemethanol, 4-methoxy-
Anisic alcohol
p-Anisol alcohol
4-Methoxybenzenemethanol
Benzyl alcohol, p-methoxy-
Anis alcohol
4-Methoxybenzylalcohol
FEMA No. 2099
4-Anisylalcohol
NSC 2151
p-methoxy-benzyl alcohol
MFCD00004653
4-Methoxybenzyl-d2Alcohol
(4-methoxyphenyl)-methanol
(4-Methoxy-phenyl)-methanol
7N6XGV3U49
DTXSID6044357
NSC-2151
Anisalcohol, p-
[4-(methyloxy)phenyl]methanol
Anisyl alcohol (natural)
(4-(METHYLOXY)PHENYL)METHANOL
CCRIS 5111
4-METHOXY-[7-13C]-BENZYL ALCOHOL
EINECS 203-273-6
METHOXYBENZYLALCOHOL
BRN 0636654
UNII-7N6XGV3U49
Anisalkohol
p-anisalcohol
AI3-01170
ar-anisyl alcohol
JandaJel(TM)-Wang
p-methoxybenzylalcohol
4-methoxyphenylmethanol
4-methoxy-benzylalcohol
4-methoxylbenzyl alcohol
4-methyoxybenzyl alcohol
4-methoxy-benzenemethanol
4-methoxy-benzyl alcohol
4-(Hydroxymethyl)anisole
para-methoxybenzyl alcohol
bmse010025
EC 203-273-6
ANISE ALCOHOL [MI]
DSSTox_CID_24357
DSSTox_RID_82376
4-methoxyphenylmethyl alcohol
DSSTox_GSID_47486
SCHEMBL27329
WLN: Q1R DO1
(4-Methoxyphenyl)methanol #
ANISE ALCOHOL [INCI]
ANISYL ALCOHOL [FCC]
4-06-00-05909 (Beilstein Handbook Reference)
ANISYL ALCOHOL [FHFI]
4-Methoxybenzyl alcohol, 98%
CHEMBL294431
DTXCID4024357
FEMA 2099
PARA METHOXYBENZYL ALCOHOL
NSC2151
1-methoxy-4-hydroxymethyl-benzene
CHEBI:193647
BENZENEMETHANOL,AR-METHOXY-
BCP26725
STR00774
Tox21_301115
Tox21_302521
BBL027471
STL146342
Anisyl alcohol, >=98%, FCC, FG
AKOS000249369
Anisyl alcohol, natural, >=98%, FG
CS-W016493
MCULE-6123978072
PB47798
PS-4037
NCGC00248292-01
NCGC00255015-01
NCGC00256684-01
CAS-105-13-5
CAS-1331-81-3
DB-003500
4-Methoxybenzyl alcohol, analytical standard
AM20020146
M0107
NS00009442
EN300-16200
A15090
Anisyl alcohol 1000 microg/mL in Acetonitrile
D77792
Q548873
J-501422
Z54603098
F0001-0102
InChI=1/C8H10O2/c1-10-8-4-2-7(6-9)3-5-8/h2-5,9H,6H2,1H
JandaJel(TM)-Wang, 100-200 mesh, extent of labeling: 1.0 mmol/g loading, 2 % cross-linked
Microorganism:

Yes

IUPAC name(4-methoxyphenyl)methanol
SMILESCOC1=CC=C(C=C1)CO
InchiInChI=1S/C8H10O2/c1-10-8-4-2-7(6-9)3-5-8/h2-5,9H,6H2,1H3
FormulaC8H10O2
PubChem ID7738
Molweight138.16
LogP1.1
Atoms10
Bonds2
H-bond Acceptor2
H-bond Donor1
Chemical Classificationaromatic compounds alcohols ethers aromatic alcohols benzenoids
CHEBI-ID193647
Supernatural-IDSN0234060

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaBacillus Subtilisantifungal activity against Alternaria solaniisolate from rhizosphere of potato in Shandong and Hebei Province in ChinaZhang et al. 2020
EukaryotaBjerkandera AdustaNASpinnler at al. 1994
EukaryotaBjerkandera Adustan/aNALapadatescu et al. 2000
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaBacillus SubtilisLB mediaHS-SPME/GC-MSyes
EukaryotaBjerkandera Adustano
EukaryotaBjerkandera AdustaMinimal media plus glucose and L-phenylalanineExtraction with dichloromethane or with ethyl acetate, concentration under N2 stream /GC-MS.no


Phenylmethanol

Mass-Spectra

Compound Details

Synonymous names
benzyl alcohol
phenylmethanol
benzenemethanol
100-51-6
phenylcarbinol
benzylalcohol
Benzoyl alcohol
Benzenecarbinol
alpha-Toluenol
Phenylmethyl alcohol
Hydroxytoluene
(Hydroxymethyl)benzene
Phenolcarbinol
Benzal alcohol
benzylic alcohol
Alcool benzylique
Benzylicum
Methanol, phenyl-
Phenylcarbinolum
alpha-hydroxytoluene
Euxyl K 100
hydroxymethylbenzene
Bentalol
Ulesfia
Phenyl Methanol
Phenyl-Methanol
66072-40-0
BENZYL-ALCOHOL
Caswell No. 081F
alcoholum benzylicum
Benzyl alcohol (natural)
FEMA No. 2137
Benzylalkohol
Alcohol,benzyl
NCI-C06111
.alpha.-Hydroxytoluene
Alcool benzilico
Aromatic alcohol
Alcohol, Benzyl
Alcohol bencilico
.alpha.-Toluenol
Alcool benzilico [DCIT]
Itch-X
NSC 8044
HSDB 46
benzenmethanol
Benzalalcohol
Benzalcohol
CCRIS 2081
Aromatic primary alcohol
Alcoolbenzylique
Alcool benzylique [INN-French]
Benzyl alkohol
Alcohol bencilico [INN-Spanish]
Methanol benzene
Alcoholum benzylicum [INN-Latin]
UNII-LKG8494WBH
Alcohol benzylicus
NSC-8044
EINECS 202-859-9
BnOH
LKG8494WBH
EPA Pesticide Chemical Code 009502
BRN 0878307
Sunmorl BK 20
DTXSID5020152
CHEBI:17987
INS NO.1519
AI3-01680
INS-1519
MFCD00004599
Hydroxymethyl resin (100-200 mesh)
TOLUENE,ALPHA-HYDROXY
DTXCID70152
Benzyl alcohol (Benzenemethanol)
benzyl alcohol (ring-13c6)
E-1519
EC 202-859-9
4-06-00-02222 (Beilstein Handbook Reference)
185532-71-2
NCGC00091865-01
BENZYL-ALPHA,ALPHA-D2 ALCOHOL
BENZYL ALCOHOL (II)
BENZYL ALCOHOL [II]
MBN
BENZYL ALCOHOL (MART.)
BENZYL ALCOHOL [MART.]
Alcool benzylique (INN-French)
BENZYL ALCOHOL (USP-RS)
BENZYL ALCOHOL [USP-RS]
Alcohol bencilico (INN-Spanish)
Alcoholum benzylicum (INN-Latin)
BENZYL ALCOHOL (EP MONOGRAPH)
BENZYL ALCOHOL [EP MONOGRAPH]
phenylmethan-1-ol
CAS-100-51-6
Ulesfia (TN)
201740-95-6
Benzyl alcohol [USAN:INN:JAN]
enzylalcohol
Protocoxil
phenyl carbinol
benzene-methanol
Benzyl Alcohole
a-Hydroxytoluene
a-Toluenol
Alcohol benzilico
Benzyl alcohol [INN:JAN:NF]
Hydroxymethyl resin (200-400 mesh)
PhCH2OH
Bn-OH
SCHEMBL147
Benzyl alcohol, ACS grade
bmse000407
C6H5CH2OH
CHEMBL720
WLN: Q1R
BENZYL ALCOHOL [MI]
Benzyl alcohol (JP15/NF)
BENZYL ALCOHOL [FCC]
BENZYL ALCOHOL [INN]
BENZYL ALCOHOL [JAN]
BENZYL ALCOHOL [FHFI]
BENZYL ALCOHOL [HSDB]
BENZYL ALCOHOL [INCI]
BIDD:ER0248
ALCOHOL,BENZYL [VANDF]
BENZYL ALCOHOL [VANDF]
ZilactinEarly Relief Cold Sore
TB 13G
Benzyl alcohol, LR, >=99%
BENZYL ALCOHOL [WHO-DD]
BENZYL ALCOHOL [WHO-IP]
BDBM16418
NSC8044
Benzyl alcohol (JP17/NF/INN)
HMS3264B16
HMS3885F10
Pharmakon1600-01502555
Benzyl alcohol, analytical standard
Benzyl alcohol, AR, >=99.5%
HY-B0892
Benzyl alcohol, anhydrous, 99.8%
Tox21_111172
Tox21_202447
Tox21_300044
BBL011938
BENZYL ALCOHOL [ORANGE BOOK]
NSC760098
s4600
STL163453
Benzyl alcohol, >=99%, FCC, FG
AKOS000119907
Benzyl alcohol, natural, >=98%, FG
CCG-213843
DB06770
MCULE-6011707909
NSC-760098
USEPA/OPP Pesticide Code: 009502
NCGC00091865-02
NCGC00091865-03
NCGC00091865-04
NCGC00254154-01
NCGC00259996-01
ALCOHOL BENZYLICUS [WHO-IP LATIN]
Benzyl alcohol, ACS reagent, >=99.0%
Benzyl alcohol, ReagentPlus(R), >=99%
Benzyl alcohol, USP, 98.0-100.5%
B2378
Benzyl alcohol, tested according to Ph.Eur.
Benzylalcohol 100 microg/mL in Acetonitrile
E1519
NS00009775
Benzyl alcohol, p.a., ACS reagent, 99.0%
Benzyl alcohol, SAJ first grade, >=98.5%
EN300-20016
Benzyl alcohol, SAJ special grade, >=99.0%
Benzyl alcohol, Vetec(TM) reagent grade, 98%
C00556
C03485
D00077
D70182
Q52353
AB01563201_01
A800221
SR-01000872610
J-000153
SR-01000872610-3
BENZALKONIUM CHLORIDE IMPURITY A [EP IMPURITY]
F0001-0019
Z104476418
3762963D-6C2A-4BFF-AD94-3180E51BCA68
Benzyl alcohol, certified reference material, TraceCERT(R)
Benzyl alcohol, European Pharmacopoeia (EP) Reference Standard
Benzyl alcohol, puriss. p.a., ACS reagent, >=99.0% (GC)
Benzyl alcohol, United States Pharmacopeia (USP) Reference Standard
InChI=1/C7H8O/c8-6-7-4-2-1-3-5-7/h1-5,8H,6H
Benzyl alcohol, Pharmaceutical Secondary Standard; Certified Reference Material
Benzyl alcohol, puriss., meets analytical specification of Ph.??Eur., BP, NF, 99-100.5% (GC)
StratoSpheres(TM) PL-HMS (Hydroxymethylstyrene) resin, 50-100 mesh, extent of labeling: 2.0 mmol loading, 1 % cross-linked
Microorganism:

Yes

IUPAC namephenylmethanol
SMILESC1=CC=C(C=C1)CO
InchiInChI=1S/C7H8O/c8-6-7-4-2-1-3-5-7/h1-5,8H,6H2
FormulaC7H8O
PubChem ID244
Molweight108.14
LogP1.1
Atoms8
Bonds1
H-bond Acceptor1
H-bond Donor1
Chemical Classificationaromatic compounds aromatic alcohols alcohols benzenoids
CHEBI-ID17987
Supernatural-IDSN0420832

mVOC Specific Details

Boiling Point
DegreeReference
205.3 °C peer reviewed
Volatilization
The Henry's Law constant for benzyl alcohol is 3.37X10-7 atm cu m/mole(1). This Henry's Law constant indicates that benzyl alcohol is expected to be essentially nonvolatile from water and moist soil 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 113 days(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 825 days(SRC). Benzyl alcohol's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Benzyl alcohol is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 9.4X10-2 mm Hg(3).
Literature: (1) Abraham MH et al; J Pharm Sci 83: 1085-100 (1994) (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
Experimental Koc values for benzyl alcohol were <5 for three different soils; Apison (0.11% organic carbon), Fullerton (0.06% organic carbon), and Dormont (1.2% organic carbon)(1). An experimental Koc of 15 was determined for benzyl alcohol on a red-brown Australian soil (1.09% organic carbon)(2,3). A log Koc of 1.43 has also been reported(4). According to a classification scheme(5), these Koc values suggest that benzyl alcohol is expected to have very high mobility in soil.
Literature: (1) Southworth GR, Keller JL; Water Air Soil Poll 28: 239-48 (1986) (2) Briggs GG; Aust J Soil Res 19: 61-8 (1981) (3) Briggs GG; J Agric Food Chem 29: 1050-9 (1981) (4) Xu F et al; J Environ Qual 30: 1618-23 (2001) (5) Swann RL et al; Res Rev 85: 17-28 (1983)
Vapor Pressure
PressureReference
0.094 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
EukaryotaCandida AlbicansNANAFitzgerald et al. 2022
EukaryotaCandida ParapsilosisNANAFitzgerald et al. 2022
ProkaryotaEscherichia ColiNANAHewett et al. 2020
ProkaryotaEscherichia ColiNANADevaraj et al. 2018
ProkaryotaEscherichia ColiNANADixon et al. 2022
EukaryotaAgaricus EssetteiNARapior et al. 2002
EukaryotaPolyporus Tuberasterculture collection Takara Shuzo Food Research LaboratoriesKawabe et al. 1994
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 Amyloliquefaciensantifungal 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
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
ProkaryotaStaphylococcus AureusLeibnitz Institute DSMZ-German Collection of Microorganisms and Cell Cultures GmbHFitzgerald et al. 2020
ProkaryotaEscherichia ColiLeibnitz Institute DSMZ-German Collection of Microorganisms and Cell Cultures GmbHFitzgerald et al. 2020
EukaryotaChaetomium IndicumNAMoisan et al. 2021
ProkaryotaEscherichia ColiSwedish Institute for Communicable Disease Control (SMI), Stockholm, SwedenSousa et al. 2023
ProkaryotaBacillus Subtilispromote biomass production of Arabidopsis thalianarhizosphere of Haloxylon ammodendronHe et al. 2023
EukaryotaMetschnikowia Reukaufiiinhibitory and promoting effects on the growth of different microorganismsisolate from Aconitum piepunense, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
ProkaryotaLactobacillus Casein/aNATracey and Britz 1989
ProkaryotaLactobacillus Plantarumn/aNATracey and Britz 1989
ProkaryotaPediococcus Damnosusn/aNATracey and Britz 1989
ProkaryotaLeuconostoc Cremorisn/aNATracey and Britz 1989
ProkaryotaLeuconostoc Dextranicumn/aNATracey and Britz 1989
ProkaryotaLactococcus Lactisn/aNATracey and Britz 1989
ProkaryotaLeuconostoc Mesenteroidesn/aNATracey and Britz 1989
ProkaryotaLeuconostoc Paramesenteroidesn/aNATracey and Britz 1989
ProkaryotaOenococcus Oenin/aNATracey and Britz 1989
ProkaryotaMyxobacterium Sp.n/aNASchulz and Dickschat 2007
ProkaryotaStreptomyces Sp.n/aNASchulz and Dickschat 2007
ProkaryotaCytophaga-Flavobacteria-Bacteroides Groupn/aNASchulz and Dickschat 2007
EukaryotaPhellinus Sp.n/aNAStotzky and Schenck 1976
ProkaryotaStreptomyces Sp.n/aNADickschat et al. 2005_2
ProkaryotaChondromyces Crocatusn/aNASchulz et al. 2004
ProkaryotaCytophaga-Flavobacterium-Bacteroidesn/aNADickschat et al. 2005_3
ProkaryotaNannocystis Exedensn/aNADickschat et al. 2007
ProkaryotaStigmatella Aurantiacan/aNADickschat et al. 2005_5
EukaryotaBjerkandera Adustan/aNALapadatescu et al. 2000
EukaryotaAscocoryne Sarcoidesn/aNAMallette et al.  2012
ProkaryotaPseudomonas Syringaenaphyllosphere of field-grown potato plantsHunziker et al. 2015
ProkaryotaPropionibacterium Acidifaciens as a biomarker for a breath test for detection of cariesNAHertel et al. 2016
ProkaryotaXanthomonas Campestrisn/aNAWeise et al. 2012
ProkaryotaStreptococcus PneumoniaeclinicPreti et al. 2009
ProkaryotaBranhamella CatarrhalisclinicPreti et al. 2009
EukaryotaBjerkandera AdustaNASpinnler at al. 1994
EukaryotaPleurotus EryngiinanaUsami et al. 2014
EukaryotaPleurotus CystidiosusnanaUsami et al. 2014
ProkaryotaHaemophilus InfluenzaeclinicPreti et al. 2009
ProkaryotaBacillus Cereusn/aNABlom et al. 2011
ProkaryotaBurkholderia Andropogonisn/aNABlom et al. 2011
ProkaryotaCellulomonas Udan/aNABlom et al. 2011
ProkaryotaEscherichia Colin/aNABlom et al. 2011
ProkaryotaPseudomonas Chlororaphisn/aNABlom et al. 2011
ProkaryotaPseudomonas Fluorescensn/aNABlom et al. 2011
ProkaryotaPseudomonas Putidan/aNABlom et al. 2011
ProkaryotaSerratia Entomophilan/aNABlom et al. 2011
ProkaryotaSerratia Marcescensn/aNABlom et al. 2011
ProkaryotaSerratia Plymuthican/aNABlom et al. 2011
ProkaryotaSerratia Proteamaculansn/aNABlom et al. 2011
ProkaryotaBurkholderia Caribensisn/aNABlom et al. 2011
ProkaryotaBurkholderia Caryophyllin/aNABlom et al. 2011
ProkaryotaBurkholderia Fungorumn/aNABlom et al. 2011
ProkaryotaBurkholderia Gladiolin/aNABlom et al. 2011
ProkaryotaBurkholderia Glumaen/aNABlom et al. 2011
ProkaryotaBurkholderia Graminisn/aNABlom et al. 2011
ProkaryotaBurkholderia Hospitan/aNABlom et al. 2011
ProkaryotaBurkholderia Kururiensisn/aNABlom et al. 2011
ProkaryotaBurkholderia Phenaziniumn/aNABlom et al. 2011
ProkaryotaBurkholderia Phytofirmansn/aNABlom et al. 2011
ProkaryotaBurkholderia Pyrrocinian/aNABlom et al. 2011
ProkaryotaBurkholderia Saccharin/aNABlom et al. 2011
EukaryotaTuber BorchiiNoneT. melanosporum, T. borchii were collected from northern Italy (Piedmont) and T. indicum from Yunnan and Sichuan Provinces (China). Splivallo et al. 2007b
EukaryotaTuber MelanosporumNoneT. melanosporum, T. borchii were collected from northern Italy (Piedmont) and T. indicum from Yunnan and Sichuan Provinces (China). Splivallo et al. 2007b
EukaryotaTuber IndicumNoneT. melanosporum, T. borchii were collected from northern Italy (Piedmont) and T. indicum from Yunnan and Sichuan Provinces (China). Splivallo et al. 2007b
ProkaryotaLentilactobacillus BuchneriNANASquara et al. 2022
ProkaryotaLacticaseibacillus ParacaseiNANASquara et al. 2022
EukaryotaZygosaccharomyces RouxiiNANAPei et al. 2022
EukaryotaSaccharomyces CerevisiaeNANAHarris et al. 2021
ProkaryotaSerratia Sp.NANAAlmeida et al. 2022
ProkaryotaEnterobacter Sp.NANAAlmeida et al. 2022
ProkaryotaEscherichia ColiNANAAlmeida et al. 2022
EukaryotaCryptococcus WieringaeNANAMozūraitis et al. 2022
EukaryotaHanseniaspora UvarumNANAMozūraitis et al. 2022
EukaryotaPichia KudriavzeviiNANAMozūraitis et al. 2022
EukaryotaPichia FermentansNANAMozūraitis et al. 2022
EukaryotaPichia KluyveriNANAMozūraitis et al. 2022
EukaryotaPichia MembranifaciensNANAMozūraitis et al. 2022
EukaryotaSaccharomyces ParadoxusNANAMozūraitis et al. 2022
EukaryotaTorulaspora DelbrueckiiNANAMozūraitis et al. 2022
EukaryotaPichia AnomalaNANAMozūraitis et al. 2022
EukaryotaMetschnikowia PulcherrimaNANAMozūraitis et al. 2022
ProkaryotaLactobacillus PlantarumNANAZhang et al. 2022
EukaryotaSaccharomycopsis ViniNANAZhao et al. 2022
EukaryotaSaturnispora DiversaNANAZhao et al. 2022
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaCandida AlbicansYPDSPME/GC-MSno
EukaryotaCandida AlbicansTSBSPME/GC-MSno
EukaryotaCandida ParapsilosisYPDSPME/GC-MSno
EukaryotaCandida ParapsilosisTSBSPME/GC-MSno
ProkaryotaEscherichia ColiLBSPME/GC-MSno
ProkaryotaEscherichia ColiTSATD/GC-MSno
ProkaryotaEscherichia ColiLBTD/GC-MSno
EukaryotaAgaricus Essetteihydro-destillation, solvent extraction, GC-MSno
EukaryotaPolyporus TuberasterPGYGC-MSno
ProkaryotaBacillus MuralisNA mediaSPME/GC-MSno
ProkaryotaNovosphingobium LindaniclasticumNA mediaSPME/GC-MSno
ProkaryotaBacillus SubtilisNA mediaSPME/GC-MSno
ProkaryotaBacillus AmyloliquefaciensNA mediaSPME/GC-MSno
ProkaryotaBacillus MegateriumNA mediaSPME/GC-MSno
ProkaryotaPseudomonas Sp.LB media, DYGS mediaHS-SPME/GC-MSno
ProkaryotaPseudomonas Sp.LB mediaHS-SPME/GC-MSno
ProkaryotaStaphylococcus AureusTSB mediaHS-SPME/GC-MSno
ProkaryotaEscherichia ColiTSB mediaHS-SPME/GC-MSno
EukaryotaChaetomium Indicum1/5th PDA mediumGC-MSno
ProkaryotaEscherichia ColiLB media, rocket lysate, spinach lysateHS-SPME/GC-MSno
ProkaryotaBacillus Subtilis1/2 MS mediaSPME/GC-MSyes
EukaryotaMetschnikowia Reukaufiiartificial nectar mediaGC-MSno
ProkaryotaLactobacillus Casein/an/ano
ProkaryotaLactobacillus Plantarumn/an/ano
ProkaryotaPediococcus Damnosusn/an/ano
ProkaryotaLeuconostoc Cremorisn/an/ano
ProkaryotaLeuconostoc Dextranicumn/an/ano
ProkaryotaLactococcus Lactisn/an/ano
ProkaryotaLeuconostoc Mesenteroidesn/an/ano
ProkaryotaLeuconostoc Paramesenteroidesn/an/ano
ProkaryotaOenococcus Oenin/an/ano
ProkaryotaMyxobacterium Sp.n/an/ano
ProkaryotaStreptomyces Sp.n/an/ano
ProkaryotaCytophaga-Flavobacteria-Bacteroides Groupn/an/ano
EukaryotaPhellinus Sp.n/an/ano
ProkaryotaChondromyces Crocatusn/an/ano
ProkaryotaCytophaga-Flavobacterium-Bacteroidesn/an/ano
ProkaryotaNannocystis Exedensn/an/ano
ProkaryotaStigmatella Aurantiacan/an/ano
EukaryotaBjerkandera AdustaMinimal media plus glucose and L-phenylalanineExtraction with dichloromethane or with ethyl acetate, concentration under N2 stream /GC-MS.no
EukaryotaAscocoryne SarcoidesMinimal mediumPTR-MS and SPME GC-MSno
ProkaryotaPseudomonas SyringaeLB mediumGC/MSyes
ProkaryotaPropionibacterium AcidifaciensBrain-Heart-Infusion agarTenax-trap/GC-MSno
ProkaryotaXanthomonas CampestrisNBIIClosed airflow-system/GC-MS and PTR-MSno
ProkaryotaStreptococcus PneumoniaeBlood agar/chocolate blood agaHS-SPME/GC-MS no
ProkaryotaBranhamella CatarrhalisBlood agar/chocolate blood agaHS-SPME/GC-MS no
EukaryotaBjerkandera Adustano
EukaryotaPleurotus EryngiinaGC/MS, GC-O, AEDAno
EukaryotaPleurotus CystidiosusnaGC/MS, GC-O, AEDAno
ProkaryotaHaemophilus InfluenzaeBlood agar/chocolate blood agaHS-SPME/GC-MS no
ProkaryotaBacillus CereusLBHeadspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
ProkaryotaBurkholderia AndropogonisLB, MR-VP, MS and AngleHeadspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
ProkaryotaCellulomonas UdaLB and MS Headspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
ProkaryotaEscherichia ColiLB, MR-VP and MS Headspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
ProkaryotaPseudomonas ChlororaphisLB, MR-VP and MS Headspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
ProkaryotaPseudomonas FluorescensLBHeadspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
ProkaryotaPseudomonas PutidaLB and MS Headspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
ProkaryotaSerratia EntomophilaMS Headspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
ProkaryotaSerratia MarcescensMS Headspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
ProkaryotaSerratia PlymuthicaMS Headspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
ProkaryotaSerratia ProteamaculansLB, MR-VP and MS Headspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
ProkaryotaBurkholderia CaribensisLBHeadspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
ProkaryotaBurkholderia CaryophylliLB and MS Headspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
ProkaryotaBurkholderia FungorumLBHeadspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
ProkaryotaBurkholderia GladioliLB, MR-VP, MS and AngleHeadspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
ProkaryotaBurkholderia GlumaeLB and MR-VPHeadspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
ProkaryotaBurkholderia GraminisLB and MR-VPHeadspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
ProkaryotaBurkholderia HospitaLB and MR-VPHeadspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
ProkaryotaBurkholderia KururiensisMR-VPHeadspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
ProkaryotaBurkholderia PhenaziniumLB and MR-VPHeadspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
ProkaryotaBurkholderia PhytofirmansLB, MR-VP, MS and AngleHeadspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
ProkaryotaBurkholderia PyrrociniaLBHeadspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
ProkaryotaBurkholderia SacchariLB, MR-VP and MSHeadspace air was trapped in glass Gerstel TDS tubes and analysed by gas chromatography with mass selective detection (GC-MSD)no
EukaryotaTuber BorchiiNoneNoneyes
EukaryotaTuber MelanosporumNoneNoneyes
EukaryotaTuber IndicumNoneNoneyes
ProkaryotaLentilactobacillus Buchnerimaize silageHS-SPME coupled with GC-TOF MSno
ProkaryotaLacticaseibacillus Paracaseimaize silageHS-SPME coupled with GC-TOF MSno
EukaryotaZygosaccharomyces RouxiiYPD mediumGC-MSno
EukaryotaSaccharomyces Cerevisiaemalt extract brothHS-SPME with GC-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
EukaryotaCryptococcus WieringaeYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaHanseniaspora UvarumYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaPichia KudriavzeviiYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaPichia FermentansYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaPichia KluyveriYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaPichia MembranifaciensYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaSaccharomyces ParadoxusYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaTorulaspora DelbrueckiiYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaPichia AnomalaYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
EukaryotaMetschnikowia PulcherrimaYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
ProkaryotaLactobacillus Plantarumchickpea milkUHPLC/MSno
EukaryotaSaccharomycopsis Vinisynthetic grape juiceHS-SPMEno
EukaryotaSaturnispora Diversasynthetic grape juiceHS-SPMEno


3-chloro-4-methoxybenzaldehyde

Compound Details

Synonymous names
3-Chloro-4-methoxybenzaldehyde
4903-09-7
3-Chloro-p-anisaldehyde
3-Chloroanisaldehyde
Benzaldehyde, 3-chloro-4-methoxy-
3-Chloro-anisaldehyde
3-Chloro-4-methoxybenzenecarbaldehyde
3-Chloro-4-methoxy-benzaldehyde
MFCD00016601
SCHEMBL335717
DTXSID50197671
CHEBI:200810
EINECS 225-532-2
CL8902
STK198720
3-Chloro-4-methoxybenzaldehyde, 97%
AKOS000295169
AM83075
CS-W004738
MCULE-6598481701
SY004242
C1797
NS00044499
EN300-85152
A23104
A827643
12W-0807
J-512240
Z57313891
Microorganism:

No

IUPAC name3-chloro-4-methoxybenzaldehyde
SMILESCOC1=C(C=C(C=C1)C=O)Cl
InchiInChI=1S/C8H7ClO2/c1-11-8-3-2-6(5-10)4-7(8)9/h2-5H,1H3
FormulaC8H7ClO2
PubChem ID78619
Molweight170.59
LogP2.2
Atoms11
Bonds2
H-bond Acceptor2
H-bond Donor0
Chemical Classificationaromatic aldehydes ethers aldehydes chlorides benzaldehydes halogenated compounds
CHEBI-ID200810
Supernatural-IDSN0423704

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAnthracophyllum DiscolorNASchalchli et al. 2015
EukaryotaBjerkandera AdustaNASpinnler at al. 1994
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAnthracophyllum Discolorno
EukaryotaBjerkandera Adustano


3,5-dichloro-4-methoxybenzaldehyde

Compound Details

Synonymous names
3,5-dichloro-4-methoxybenzaldehyde
41727-58-6
3,5-Dichloro-anisaldehyde
MFCD04070684
Benzaldehyde, 3,5-dichloro-4-methoxy-
SCHEMBL2391793
CHEBI:214425
LEEKELDJRCUBEM-UHFFFAOYSA-N
STK188427
AKOS000290660
MCULE-5459456675
AS-49512
SY029667
CS-0061916
I11115
Microorganism:

No

IUPAC name3,5-dichloro-4-methoxybenzaldehyde
SMILESCOC1=C(C=C(C=C1Cl)C=O)Cl
InchiInChI=1S/C8H6Cl2O2/c1-12-8-6(9)2-5(4-11)3-7(8)10/h2-4H,1H3
FormulaC8H6Cl2O2
PubChem ID883207
Molweight205.03
LogP2.9
Atoms12
Bonds2
H-bond Acceptor2
H-bond Donor0
Chemical Classificationaromatic aldehydes ethers aldehydes benzenoids halogenated compounds aromatic compounds benzaldehydes chlorides
CHEBI-ID214425
Supernatural-IDSN0203027

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAnthracophyllum DiscolorNASchalchli et al. 2015
EukaryotaBjerkandera AdustaNASpinnler at al. 1994
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAnthracophyllum Discolorno
EukaryotaBjerkandera Adustano


4-(hydroxymethyl)phenol

Mass-Spectra

Compound Details

Synonymous names
4-hydroxybenzyl alcohol
623-05-2
4-(Hydroxymethyl)phenol
p-Hydroxybenzyl alcohol
p-Methylolphenol
4-Methylolphenol
4-Hydroxybenzenemethanol
Benzenemethanol, 4-hydroxy-
4-Hydroxybenzylalcohol
p-(Hydroxymethyl)phenol
Benzyl alcohol, p-hydroxy-
Gastrodigenin
alpha-Hydroxy-p-cresol
MFCD00004658
Parahydroxybenzyl Alcohol
.alpha.-Hydroxy-p-cresol
1A3AH1FP1B
CHEMBL202132
CHEBI:67410
NSC-227926
4-Hydroxymethyl-phenol
CCRIS 5114
p-hydroxy benzyl alcohol
EINECS 210-768-0
(4-Hydroxyphenyl)methanol
UNII-1A3AH1FP1B
NSC 227926
a-hydroxy-p-cresol
4-hydroxymethylphenol
p-Hydroxybenzyl alcoho
4-hydroxymethyl phenol
4-hydroxybenzyl-alcohol
4-Hydroxy-benzylalcohol
4-Hydroxyphenyl methanol
p-hydroxy-Benzyl alcohol
4-Hydroxyphenyl Carbinol
4-hydroxy benzyl alcohol
4-hydroxy-benzyl alcohol
4HBA
B4-hydroxy-enzenemethanol
para-hydroxybenzyl alcohol
4-hydroxyl-benzyl alcohol
bmse000623
bmse010028
EC 210-768-0
SCHEMBL62690
4-Hydroxybenzyl alcohol, 99%
DTXSID8073920
FEMA NO. 3987
HMS3885O08
BCP27109
Benzyl alcohol, p-hydroxy- (8CI)
HY-Y0892
STR00674
HYDROXYBENZYL ALCOHOL [INCI]
BDBM50177408
Benzenemethanol, 4-hydroxy- (9CI)
NSC227926
s3857
STL284640
AKOS000121529
4-HYDROXYBENZYL ALCOHOL [FHFI]
4-Hydroxybenzyl alcohol, >=98%, FG
CCG-266090
CS-W019891
MCULE-8377025602
PS-3494
AC-24727
SY003753
4-(hydroxymethyl)phenol (ACD/Name 4.0)
DB-003490
4-Hydroxybenzyl alcohol, analytical standard
AM20050567
H0224
NS00005609
EN300-21091
A15709
C17467
C93495
Q-200481
Q5526828
F0001-1668
Z104490108
4-(Hydroxymethyl)phenol;p-Hydroxybenzyl alcohol;p-Methylolphenol
InChI=1/C7H8O2/c8-5-6-1-3-7(9)4-2-6/h1-4,8-9H,5H
Microorganism:

No

IUPAC name4-(hydroxymethyl)phenol
SMILESC1=CC(=CC=C1CO)O
InchiInChI=1S/C7H8O2/c8-5-6-1-3-7(9)4-2-6/h1-4,8-9H,5H2
FormulaC7H8O2
PubChem ID125
Molweight124.14
LogP0.2
Atoms9
Bonds1
H-bond Acceptor2
H-bond Donor2
Chemical Classificationaromatic alcohols alcohols phenols aromatic compounds benzenoids
CHEBI-ID67410
Supernatural-IDSN0036507

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaBjerkandera Adustan/aNALapadatescu et al. 2000
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaBjerkandera AdustaMinimal media plus glucose and L-phenylalanineExtraction with dichloromethane or with ethyl acetate, concentration under N2 stream /GC-MS.no


2-hydroxy-3-phenylpropanoic Acid

Mass-Spectra

Compound Details

Synonymous names
DL-3-Phenyllactic acid
828-01-3
2-Hydroxy-3-phenylpropanoic acid
3-Phenyllactic acid
DL-beta-Phenyllactic acid
2-Hydroxy-3-phenylpropionic acid
2-hydroxy-3-phenyl-propionic acid
156-05-8
DL-Phenyllactic acid
beta-Phenyllactic acid
Ba 2653
Benzenepropanoic acid, alpha-hydroxy-
SC6T4O59BK
DL-.beta.-Phenyllactic acid
(RS)-2-Hydroxy-3-phenyl-propionic acid
CHEBI:25998
NSC-2627
MFCD00065928
b-phenyllactic acid
(+/-)-2-Hydroxy-3-phenylpropanoic acid
D-(+)-Phenyllactic acid
(+-)-3-Phenyllactic acid
Benzenepropanoic acid, a-hydroxy-
DL-b-Phenyllactic acid
DL-alpha-Hydroxycinnamic acid
b-Phenyllactate
Lactic acid, 3-phenyl-, DL-
beta-Phenyllactate
2-hydroxy-3-phenyl-propanoic acid
DL-b-Phenyllactate
NSC 2627
EINECS 212-580-4
DL-3-Phenyllactate
Benzyl-glycolic Acid
DL-beta-Phenyllactate
Benzenepropanoic acid, .alpha.-hydroxy-
DL--Phenyllactic acid
beta-phenyl lactic acid
(+/-)-2-Hydroxy-3-phenylpropionic acid
AI3-50440
a-Hydroxybenzenepropanoate
Lactic acid, 3-phenyl-
(1)-3-Phenyllactic acid
UNII-SC6T4O59BK
alpha-Hydroxybenzenepropanoate
SCHEMBL57558
2-Hydroxy-3-phenylpropionate
3-Phenyl-2-hydroxypropanoate
a-Hydroxybenzenepropanoic acid
(+/-)-3-Phenyllactic acid
(A+/-)-3-Phenyllactic acid
3-PHENYL-DL-LACTIC ACID
CHEMBL1778420
DL-.alpha.-Hydroxycinnamic acid
DL-2-Hydroxy-3-phenylpropionate
3-Phenyl-2-hydroxypropanoic acid
3-Phenyl-2-hydroxypropionic acid
alpha-Hydroxybenzenepropanoic acid
DTXSID30862436
NSC2627
DL-3-Phenyllactic acid, >=98%
2-Hydroxy-3-phenylpropanoic acid #
AC1610
DL-2-Hydroxy-3-phenylpropionic acid
AKOS009103896
CS-W017878
HY-W017162
MCULE-9508817950
(2rs)-2-hydroxy-3-phenylpropanoic acid
(RS)-2-hydroxy-3-phenyl propanoic acid
AS-19567
SY020879
SY021341
SY036063
DB-011663
DB-056660
AM20060840
NS00079831
EN300-124810
Benzenepropanoic acid, .alpha.-hydroxy-, (S)-
A840451
W-203882
Q10395585
8C1DB5C8-C19C-4963-8F3E-B683EAB4B04F
F9995-2643
Z788000648
(R)-3-Phenyllactic acid; (R)-2-Hydroxy-3-phenylpropionic acid
Microorganism:

No

IUPAC name2-hydroxy-3-phenylpropanoic acid
SMILESC1=CC=C(C=C1)CC(C(=O)O)O
InchiInChI=1S/C9H10O3/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8,10H,6H2,(H,11,12)
FormulaC9H10O3
PubChem ID3848
Molweight166.17
LogP1.1
Atoms12
Bonds3
H-bond Acceptor3
H-bond Donor2
Chemical Classificationaromatic alcohols acids benzenoids carboxylic acids aromatic compounds organic acids
CHEBI-ID25998
Supernatural-IDSN0396180

mVOC Specific Details

MS-Links
MS-MS Spectrum 201700
MS-MS Spectrum 16329
MS-MS Spectrum 201698
MS-MS Spectrum 4663 - LC-ESI-QQ (API3000, Applied Biosystems) 50V Negative
MS-MS Spectrum 4660 - LC-ESI-QQ (API3000, Applied Biosystems) 20V Negative
MS-MS Spectrum 9658
MS-MS Spectrum 1107 - Quattro_QQQ 10V Positive delivery=Flow_Injection analyzer=Triple_Quad
MS-MS Spectrum 201699
MS-MS Spectrum 4662 - LC-ESI-QQ (API3000, Applied Biosystems) 40V Negative
MS-MS Spectrum 9656
MS-MS Spectrum 4659 - LC-ESI-QQ (API3000, Applied Biosystems) 10V Negative
MS-MS Spectrum 9657
MS-MS Spectrum 4661 - LC-ESI-QQ (API3000, Applied Biosystems) 30V Negative
MS-MS Spectrum 1109 - Quattro_QQQ 40V Positive delivery=Flow_Injection analyzer=Triple_Quad
MS-MS Spectrum 1108 - Quattro_QQQ 25V Positive delivery=Flow_Injection analyzer=Triple_Quad
MS-MS Spectrum 16328
MS-MS Spectrum 16330
MS-Links
Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaBjerkandera Adustan/aNASchulz and Dickschat 2007
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaBjerkandera Adustan/an/ano


(E)-3-phenylprop-2-enoic Acid

Mass-Spectra

Compound Details

Synonymous names
CINNAMIC ACID
TRANS-CINNAMIC ACID
140-10-3
621-82-9
3-Phenylacrylic acid
(E)-Cinnamic acid
trans-3-Phenylacrylic acid
Phenylacrylic acid
(E)-3-phenylprop-2-enoic acid
Zimtsaeure
E-Cinnamic Acid
3-Phenylpropenoic acid
trans-Cinnamate
2-Propenoic acid, 3-phenyl-, (2E)-
(2E)-3-phenylprop-2-enoic acid
3-phenylprop-2-enoic acid
Cinnamic acid, (E)-
Cinnamylic acid
trans-beta-Carboxystyrene
(2E)-3-Phenyl-2-propenoic acid
beta-Phenylacrylic acid
(E)-cinnamate
Benzeneacrylic acid
trans-3-Phenyl-2-propenoic acid
3-Phenyl-2-propenoic acid
Benzenepropenoic acid
FEMA No. 2288
CCRIS 3190
2-Propenoic acid, 3-phenyl-, (E)-
(E)-3-Phenyl-2-propenoic acid
t-Cinnamic acid
EINECS 205-398-1
MFCD00004369
NSC 44010
Benzylideneacetic acid
UNII-U14A832J8D
BRN 1905952
CINNAMIC ACIDUM
AI3-23709
Cinnamic acid, trans-
Kyselina skoricove
PhCH=CHCO2H
Acidum cinnamylicum
U14A832J8D
(2E)-2-Phenyl-2-propenoic acid
PHENYLETHYLENECARBOXYLIC ACID
NSC-9189
NSC-44010
Cinnamic acid(only trans)
NSC-623441
Heparin, lithium salt
(2E)-3-phenylacrylic acid
CHEMBL27246
Cinnamic acid (natural)
DTXSID5022489
CHEBI:27386
CHEBI:35697
NSC 9189
cinnamate
4-09-00-02002 (Beilstein Handbook Reference)
NCGC00165979-01
352431-48-2
EINECS 210-708-3
BRN 0507757
AI3-00891
CINNAMIC ACID (MART.)
CINNAMIC ACID [MART.]
DTXCID002489
CINNAMIC ACID (USP-RS)
CINNAMIC ACID [USP-RS]
(E)-3-phenylprop-2-enoate
CAS-140-10-3
.beta.-Phenylacrylic acid
343338-31-8
(E)-3-Phenylacrylic acid
DTXSID40110056
trans-Zimtsaeure
NSC 623441
trans cinnamic acid
cinnamic acid, (trans)-(E)-isomer
5-Thiazolamine?HCl
b-Phenylacrylic acid
Cinnamic acid, E-
Cinnamic Acid Natural
Cinnamic Acid1511
trans-b-Carboxystyrene
Cinnamicacid(onlytrans)
trans-3-Phenylacrylate
(E)-3-Phenylacrylate
E-3-phenylpropenoic acid
Trans-Cinnamic Acid,(S)
bmse000124
CINNAMIC ACID [MI]
SCHEMBL1332
trans-.beta.-Carboxystyrene
trans-Cinnamic acid, 97%
trans-Cinnamic acid, 99%
WLN: QV1U1R
(E)-3-phenyl-acrylic acid
3-phenyl-2E-propenoic acid
CINNAMIC ACID [FCC]
Zimtsaeure | trans-Cinnamate
CINNAMIC ACID [FHFI]
CINNAMIC ACID [INCI]
trans-3-Phenyl-2-propenoate
BIDD:ER0586
tert-.beta.-Phenylacrylic acid
trans-Cinnamic acid, >=99%
(2E)-2-Phenyl-2-propenoate
(2E)-3-Phenyl-2-propenoate
GTPL3203
CINNAMIC ACID [WHO-DD]
DTXCID9065316
BDBM16430
HY-N0610A
NSC9189
NSC44010
STR00363
trans-Cinnamic acid, >=99%, FG
Tox21_112279
Tox21_302137
BBL036895
NSC623441
s3677
STK286093
AKOS000118871
CCG-214473
CS-W020005
trans-Cinnamic acid, analytical standard
NCGC00165979-04
NCGC00165979-06
NCGC00255114-01
1ST40140
AC-34658
AS-75479
BP-20203
3-Phenylacrylic acid; -Phenylacrylic acid
DB-003797
DB-215130
C3412
NS00001286
EN300-19599
trans-Cinnamic acid, purum, >=99.0% (T)
C00423
D70605
EN300-306004
AB00374254-03
trans-cinnamic acid (trans-3-phenylacrylic acid)
trans-Cinnamic Acid [Matrix for MALDI-TOF/MS]
A833631
Q164785
SR-05000002380
trans-Cinnamic acid, natural, >=99%, FCC, FG
Q-100150
SR-05000002380-1
W-105037
F2191-0134
trans-Cinnamic Acid Zone Refined (number of passes:40)
trans-Cinnamic acid; Phenylacrylic acid;Cinnamylic acid
Z104474406
1BE36587-A165-4142-9340-18FFE3E03426
CINNAMIC ACID (CONSTITUENT OF CINNAMOMUM VERUM BARK) [DSC]
Cinnamic acid, United States Pharmacopeia (USP) Reference Standard
TRANS-CINNAMIC ACID (CONSTITUENT OF CINNAMOMUM CASSIA BARK) [DSC]
InChI=1/C9H8O2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-7H,(H,10,11)/b7-6
Microorganism:

Yes

IUPAC name(E)-3-phenylprop-2-enoic acid
SMILESC1=CC=C(C=C1)C=CC(=O)O
InchiInChI=1S/C9H8O2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-7H,(H,10,11)/b7-6+
FormulaC9H8O2
PubChem ID444539
Molweight148.16
LogP2.1
Atoms11
Bonds2
H-bond Acceptor2
H-bond Donor1
Chemical Classificationacids benzenoids carboxylic acids aromatic compounds organic acids
CHEBI-ID27386
Supernatural-IDSN0406189-02

mVOC Specific Details

Boiling Point
DegreeReference
298 median
MS-Links
MS-MS Spectrum 179668
MS-MS Spectrum 201728
MS-MS Spectrum 4932 - LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) Negative
MS-MS Spectrum 4925 - LC-ESI-QQ (API3000, Applied Biosystems) 20V Negative
MS-MS Spectrum 4926 - LC-ESI-QQ (API3000, Applied Biosystems) 30V Negative
MS-MS Spectrum 182001
MS-MS Spectrum 1325 - Quattro_QQQ 25V Positive delivery=Flow_Injection analyzer=Triple_Quad
MS-MS Spectrum 179667
MS-MS Spectrum 182003
MS-MS Spectrum 4924 - LC-ESI-QQ (API3000, Applied Biosystems) 10V Negative
MS-MS Spectrum 1324 - Quattro_QQQ 10V Positive delivery=Flow_Injection analyzer=Triple_Quad
MS-MS Spectrum 4927 - LC-ESI-QQ (API3000, Applied Biosystems) 40V Negative
MS-MS Spectrum 4928 - LC-ESI-QQ (API3000, Applied Biosystems) 50V Negative
MS-MS Spectrum 201727
MS-MS Spectrum 201729
MS-MS Spectrum 4931 - LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) Positive
MS-MS Spectrum 179669
MS-MS Spectrum 182002
MS-MS Spectrum 1326 - Quattro_QQQ 40V Positive delivery=Flow_Injection analyzer=Triple_Quad
1D-NMR-Links
Massbank-Links
Massbank Spectrum MSBNK-Antwerp_Univ-METOX_N109828_B8BB
Massbank Spectrum MSBNK-BGC_Munich-RP018301
Massbank Spectrum MSBNK-BGC_Munich-RP018302
Massbank Spectrum MSBNK-BGC_Munich-RP018303
Massbank Spectrum MSBNK-BGC_Munich-RP018311
Massbank Spectrum MSBNK-BGC_Munich-RP018312
Massbank Spectrum MSBNK-Kazusa-KZ000090
Massbank Spectrum MSBNK-Keio_Univ-KO000401
Massbank Spectrum MSBNK-Keio_Univ-KO000402
Massbank Spectrum MSBNK-Keio_Univ-KO000403
Massbank Spectrum MSBNK-Keio_Univ-KO000404
Massbank Spectrum MSBNK-Keio_Univ-KO000405
Massbank Spectrum MSBNK-RIKEN-PR010191
Massbank Spectrum MSBNK-RIKEN-PR100060
Massbank Spectrum MSBNK-RIKEN-PR100513
Massbank Spectrum MSBNK-RIKEN-PR303321
Massbank Spectrum MSBNK-RIKEN-PR303323
Massbank Spectrum MSBNK-RIKEN-PR303325
Massbank Spectrum MSBNK-RIKEN-PR303328
Massbank Spectrum MSBNK-RIKEN-PR303330
Massbank Spectrum MSBNK-RIKEN-PR303332
Massbank Spectrum MSBNK-RIKEN-PR303335
Massbank Spectrum MSBNK-RIKEN-PR303337
Massbank Spectrum MSBNK-RIKEN-PR303339

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaBjerkandera Adustan/aNASchulz and Dickschat 2007
ProkaryotaStereum SubpileatumNABirkinshaw et al. 1957
EukaryotaGanoderma Lucidumnanortheast PortugalHeleno et al. 2012
EukaryotaAgaricus Bisporusnanortheast PortugalReis et al. 2012
EukaryotaPleurotus Ostreatusnanortheast PortugalReis et al. 2012
EukaryotaPleurotus Eryngiinanortheast PortugalReis et al. 2012
EukaryotaLentinula Edodesnanortheast PortugalReis et al. 2012
EukaryotaAgaricus BlazeinaKoreaKim et al. 2008
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaBjerkandera Adustan/an/ano
ProkaryotaStereum Subpileatumno
EukaryotaGanoderma Lucidumsolid MMN culture medium, liquid MMN culture medium, PDA culture mediumHPLC-DAD-MSyes
EukaryotaAgaricus BisporusMMN-mediumHPLC/PADyes
EukaryotaPleurotus OstreatusMMN-mediumHPLC/PADyes
EukaryotaPleurotus EryngiiMMN-mediumHPLC/PADyes
EukaryotaLentinula EdodesMMN-mediumHPLC/PADyes
EukaryotaAgaricus BlazeinaHPLCyes


2-oxo-3-phenylpropanoic Acid

Compound Details

Synonymous names
phenylpyruvic acid
156-06-9
2-Oxo-3-phenylpropanoic acid
3-Phenylpyruvic acid
phenylpyruvate
Pyruvic acid, phenyl-
beta-Phenylpyruvic acid
Phenyl pyruvic acid
Benzenepropanoic acid, alpha-oxo-
Phenylpyroracemic acid
3-Phenyl-2-oxopropanoic acid
2-OXO-3-PHENYLPROPIONIC ACID
keto-phenylpyruvic acid
3-phenyl-2-oxopropanoate
alpha-ketohydrocinnamic acid
Benzenepropanoic acid, .alpha.-oxo-
2-oxo-3-phenyl-propanoic acid
CHEBI:30851
MFCD00002589
.beta.-Phenylpyruvic acid
2-oxo-3-phenyl-propionic acid
DTXSID1042281
X7CO62M413
b-phenylpyruvic acid
PPY
alpha-Keto-DL-phenylalanine
2-Oxo-3-phenylpropanic acid
UNII-X7CO62M413
b-Phenylpyruvate
Phenylpyroracemate
4kif
beta-Phenylpyruvate
phenyl-pyruvic acid
EINECS 205-847-1
a-hydroxycinnamic acid
Phenylbrenztraubensaeure
3-Phenyl-pyruvic acid
alpha-Ketohydrocinnamate
starbld0007879
a-Oxobenzenepropanoic Acid
Phenylpyruvic acid, 98%
SCHEMBL43235
alpha-oxo-benzenepropanoic acid
ALPHA-KETO-PHENYLALANINE
a-Oxobenzenepropanoic acid, 9CI
CHEMBL1162488
DTXCID9022281
FEMA NO. 3892
FEMA 3892
PHENYLPYRUVIC ACID [WHO-DD]
Tox21_301362
BDBM50167651
s6131
AKOS000161798
3-PHENYL-2-OXO PROPIONIC ACID
CS-W013246
DB03884
HY-W012530
MCULE-9935480822
Phenylpyruvic acid, analytical standard
.ALPHA.-OXOBENZENEPROPANOIC ACID
NCGC00255726-01
CAS-156-06-9
SY040637
2-Hydroxy-3-phenyl-2-propenoic acid, 9CI
AC-116009
DB-043302
DB-315591
Phenylpyruvic acid, purum, >=98.0% (T)
2-OXO-3-PHENYLPROPIONIC ACID [FHFI]
NS00003384
P0154
EN300-49247
C00166
D91915
1R-0191
A883597
Q425030
SR-01000580517
Q-201562
SR-01000580517-1
7D5F143E-52E8-4FBB-87F1-0D4F96B4CA60
Z285151774
Microorganism:

Yes

IUPAC name2-oxo-3-phenylpropanoic acid
SMILESC1=CC=C(C=C1)CC(=O)C(=O)O
InchiInChI=1S/C9H8O3/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5H,6H2,(H,11,12)
FormulaC9H8O3
PubChem ID997
Molweight164.16
LogP1.3
Atoms12
Bonds3
H-bond Acceptor3
H-bond Donor1
Chemical Classificationacids benzenoids carboxylic acids ketones aromatic compounds organic acids
CHEBI-ID30851
Supernatural-IDSN0035060

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaLactococcus Sp.n/aNASchulz and Dickschat 2007
ProkaryotaLactobacillus Plantarumn/aNASchulz and Dickschat 2007
EukaryotaBjerkandera Adustan/aNASchulz and Dickschat 2007
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaLactococcus Sp.n/an/ano
ProkaryotaLactobacillus Plantarumn/an/ano
EukaryotaBjerkandera Adustan/an/ano


4-hydroxybenzaldehyde

Mass-Spectra

Compound Details

Synonymous names
4-hydroxybenzaldehyde
p-Hydroxybenzaldehyde
123-08-0
4-Formylphenol
p-Formylphenol
Benzaldehyde, 4-hydroxy-
p-Oxybenzaldehyde
Parahydroxybenzaldehyde
4-Hydroxy benzaldehyde
Benzaldehyde, p-hydroxy-
4-HYDROXY-BENZALDEHYDE
USAF M-6
MFCD00006939
NSC 2127
p-Hydroxy-benzaldehyde
Para-Hydroxybenzaldehyde
4-Hydroxybenzenecarbonal
4-Hydroxybenzaldehyde-d5
CHEMBL14193
65581-83-1
CHEBI:17597
NSC-2127
O1738X3Y38
4-formyl phenol
EINECS 204-599-1
BRN 0471352
AI3-15366
CCRIS 8911
PARA-HYDROXY BENZALDEHYDE
4-formyl-phenol
UNII-O1738X3Y38
4hydroxybenzaldehyde
p-hydroxibezaldehyde
p-hydroxybenzaldehye
4-Hydroxybenzaldehyde; Bisoprolol Fumarate Imp. S (EP); Bisoprolol Imp. S (EP); Bisoprolol Fumarate Impurity S; Bisoprolol Impurity S
4-hydoxybenzaldehyde
4-hydroxybenzaldehyd
4-hydroxybezaldehyde
4-Hydroxybenzaldehye
4-hydroxibenzaldehyde
4-hydroxylbenzaldehyde
p-hydroxy benzaldehyde
4--hydroxybenzaldehyde
p-hydroxyl benzaldehyde
4-hydroxyl benzaldehyde
4-hydroxy- benzaldehyde
PYRILAMINE_met038
WLN: VHR DQ
bmse000259
bmse000582
bmse010005
SCHEMBL37193
4-Hydroxybenzaldehyde, 98%
4-08-00-00251 (Beilstein Handbook Reference)
BIDD:ER0339
p-Hydroxybenzaldehyde, Pract.
4-Hydroxybenzaldehyde, >=97%
DTXSID8059552
FEMA NO. 3984
HYDROXYBENZALDEHYDE [INCI]
NSC2127
1k03
P-HYDROXYBENZALDEHYDE [MI]
BCP26952
CS-D1179
HY-Y0313
STR00705
4-HYDROXYBENZALDEHYDE [FHFI]
4-Hydroxybenzaldehyde, >=97%, FG
BDBM50177411
BR1235
s6008
STK188428
AKOS000119184
AC-2984
AM10667
DB03560
MCULE-3788300475
PS-3635
NCGC00188243-01
NCGC00188243-02
4-Hydroxybenzaldehyde, analytical standard
BP-30158
SY003489
4-Hydroxybenzaldehyde, >=95.0% (HPLC)
DB-003763
H0198
NS00014566
EN300-18030
A15180
C00633
H-3800
AB-131/40191192
BISOPROLOL FUMARATE IMPURITY S [EP IMPURITY]
Q1953888
4-Hydroxybenzaldehyde, Vetec(TM) reagent grade, 95%
Z57127520
F2190-0635
InChI=1/C7H6O2/c8-5-6-1-3-7(9)4-2-6/h1-5,9
p-Hydroxybenzaldehyde;4-Formylphenol;p-Formylphenol;Bisoprolol Fumarate EP Impurity S
Microorganism:

Yes

IUPAC name4-hydroxybenzaldehyde
SMILESC1=CC(=CC=C1C=O)O
InchiInChI=1S/C7H6O2/c8-5-6-1-3-7(9)4-2-6/h1-5,9H
FormulaC7H6O2
PubChem ID126
Molweight122.12
LogP1.4
Atoms9
Bonds1
H-bond Acceptor2
H-bond Donor1
Chemical Classificationbenzenoids benzaldehydes alcohols phenols aldehydes aromatic aldehydes aromatic compounds
CHEBI-ID17597
Supernatural-IDSN0324542

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaBacillus SubtilissoilChen et al. 2008
EukaryotaBjerkandera Adustan/aNALapadatescu et al. 2000
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaBacillus SubtilisLuria-Bertani (LB)activated charcoral trapno
EukaryotaBjerkandera Adustan/aThe culture media were extracted with dichloromethane or with ethyl acetate. The solutions were dried over anhydrous sodium sulfate, and concentrated under N2 stream. The concentrates were analyzed by gas chromatography (GC)-mass spectrometry (MS)no


(3,5-dichloro-4-methoxyphenyl)methanol

Compound Details

Synonymous names
(3,5-dichloro-4-methoxyphenyl)methanol
4892-23-3
3,5-Dichloro-4-methoxybenzyl alcohol
3,5-Dichloro-anisyl alcohol
3,5-dichloro-p-anisyl alcohol
SCHEMBL2388964
CHEBI:204868
HMS1589F17
MFCD03997279
AKOS022959314
DA-24625
CS-0194414
E89717
Microorganism:

No

IUPAC name(3,5-dichloro-4-methoxyphenyl)methanol
SMILESCOC1=C(C=C(C=C1Cl)CO)Cl
InchiInChI=1S/C8H8Cl2O2/c1-12-8-6(9)2-5(4-11)3-7(8)10/h2-3,11H,4H2,1H3
FormulaC8H8Cl2O2
PubChem ID893589
Molweight207.05
LogP2.3
Atoms12
Bonds2
H-bond Acceptor2
H-bond Donor1
Chemical Classificationalcohols benzenoids ethers halogenated compounds
CHEBI-ID204868
Supernatural-IDSN0165186

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaBjerkandera AdustaNASpinnler at al. 1994
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaBjerkandera Adustano


Non-1-en-3-ol

Mass-Spectra

Compound Details

Synonymous names
1-Nonen-3-ol
21964-44-3
Non-1-en-3-ol
Hexylvinylcarbinol
1-Vinylheptanol
delta1-nonen-3-ol
nonene-1-ol-3
1-Nonene-3-ol
3-Hydroxy-1-nonene
Hexyl vinyl carbinol
0GKA6U7Q9G
NSC 102782
NSC-102782
NSC102782
1-Nonen-3 ol
UNII-0GKA6U7Q9G
SCHEMBL148996
DWUPJMHAPOQKGJ-UHFFFAOYSA-
DTXSID30865023
CHEBI:179597
WAA96444
EINECS 244-686-1
LMFA05000504
MFCD00021953
(+/-)-1-NONEN-3-OL
AKOS009156593
1-NONEN-3-OL, (+/-)-
CS-0449661
N0451
NS00013041
D91710
J-014376
Q27236759
(4-DIMETHYLAMINO-PHENYL)-PHOSPHONICACIDDIETHYLESTER
InChI=1/C9H18O/c1-3-5-6-7-8-9(10)4-2/h4,9-10H,2-3,5-8H2,1H3
Microorganism:

Yes

IUPAC namenon-1-en-3-ol
SMILESCCCCCCC(C=C)O
InchiInChI=1S/C9H18O/c1-3-5-6-7-8-9(10)4-2/h4,9-10H,2-3,5-8H2,1H3
FormulaC9H18O
PubChem ID89560
Molweight142.24
LogP3.1
Atoms10
Bonds6
H-bond Acceptor1
H-bond Donor1
Chemical Classificationalcohols
CHEBI-ID179597
Supernatural-IDSN0077614

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaSerratia Proteamaculansn/aNAErcolini et al. 2009
ProkaryotaCarnobacterium Divergensn/aNAErcolini et al. 2009
ProkaryotaPseudomonas Fragin/aNAErcolini et al. 2009
EukaryotaSpongiporus Leucomallellusnasaprophytic mostly on wet, old pinesCampos Ziegenbein et al. 2006
EukaryotaBjerkandera AdustaNAThakeow et al. 2008
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaSerratia Proteamaculansn/an/ano
ProkaryotaCarnobacterium Divergensn/an/ano
ProkaryotaPseudomonas Fragin/an/ano
EukaryotaSpongiporus LeucomallellusnaGC/MSno
EukaryotaBjerkandera Adustano