Results for:
chemical Classification: Alkenes

Oct-3-en-2-one

Compound Details

Synonymous names
oct-3-en-2-one
Octenone
SCHEMBL230668
DTXSID1061867
DB-043671
NS00021738
Microorganism:

Yes

IUPAC nameoct-3-en-2-one
SMILESCCCCC=CC(=O)C
InchiInChI=1S/C8H14O/c1-3-4-5-6-7-8(2)9/h6-7H,3-5H2,1-2H3
FormulaC8H14O
PubChem ID15475
Molweight126.2
LogP2.3
Atoms9
Bonds4
H-bond Acceptor1
H-bond Donor0
Chemical Classificationalkenes ketones
Supernatural-IDSN0466503

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaFusarium VerticillioidesNAUsseglio et al. 2017
ProkaryotaPediococcus AcidilacticiMockus et al. 2024
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaFusarium VerticillioidesCzapek-dox agarSPME, GC-MSyes
ProkaryotaPediococcus Acidilacticilentils (Lens culinaris)SPME/ICP-MSno


2-methyl-5-prop-1-en-2-ylcyclohex-2-en-1-ol

Mass-Spectra

Compound Details

Synonymous names
CARVEOL
99-48-9
p-Mentha-6,8-dien-2-ol
p-Mentha-1,8-dien-6-ol
2-Methyl-5-(1-methylethenyl)-2-cyclohexen-1-ol
L-Carveol
(-)-Carveol
1-Methyl-4-isopropenyl-6-cyclohexen-2-ol
2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-ol
p-Mentha-1(6),8-dien-2-ol
2-methyl-5-prop-1-en-2-ylcyclohex-2-en-1-ol
5-Isopropenyl-2-methyl-2-cyclohexen-1-ol
2-Cyclohexen-1-ol, 2-methyl-5-(1-methylethenyl)-
5-isopropenyl-2-methylcyclohex-2-en-1-ol
2-Methyl-5-isopropenyl-2-cyclohexen-1-ol
NSC 68313
2-Methyl-5-(prop-1-en-2-yl)cyclohex-2-enol
6,8-p-Menthadien-2-ol
DTXSID3024736
CHEBI:23046
(Z)-Carveol
FEMA No. 2247
MFCD00062993
EINECS 202-757-4
2-Methyl-5(1-methylethenyl)cyclohex-2-ene-1-ol
2-Methyl-5-[1-methylethenyl]-2-cyclohexen-1-ol
(1S-trans)-2-Methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol
laevo-carveol
CCRIS 6219
p-Mentha-6,8-dien-2-ol (VAN)
BRN 1861032
a carveol
AI3-27596
MFCD00869995
laevo-(Z)-carveol
p-Mentha-6, l-
UPCMLD-DP073
Allyl 4-aminobutylcarbamate
SCHEMBL56868
2-06-00-00102 (Beilstein Handbook Reference)
L-p-mentha-6-8-dien-2-ol
DTXCID104736
GTPL6417
CHEMBL1385229
UPCMLD-DP073:001
FEMA 2247
NSC68313
Tox21_200175
NSC-68313
AKOS015915605
CS-W018086
HY-W017370
CAS-99-48-9
NCGC00091404-01
NCGC00091404-03
NCGC00091404-04
NCGC00257729-01
WLN: L6UTJ AQ B1 EY1 & U1
AS-66951
SY319013
1H-Imidazol-1-amine, 2-methyl-4-nitro-
DB-045454
DB-080605
NS00012077
2-Methyl-5-(1-propen-2-yl)-2-cyclohexenol
D77822
2-Cyclohexen-1-ol,2-methyl-5-(1-methylethenyl)-
Q2920205
20307-86-2
Microorganism:

No

IUPAC name2-methyl-5-prop-1-en-2-ylcyclohex-2-en-1-ol
SMILESCC1=CCC(CC1O)C(=C)C
InchiInChI=1S/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9-11H,1,5-6H2,2-3H3
FormulaC10H16O
PubChem ID7438
Molweight152.23
LogP2.1
Atoms11
Bonds1
H-bond Acceptor1
H-bond Donor1
Chemical Classificationalkenes alcohols terpenoids
CHEBI-ID23046
Supernatural-IDSN0020577

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


4-ethenyl-2-methoxyphenol

Compound Details

Synonymous names
2-Methoxy-4-vinylphenol
7786-61-0
4-vinylguaiacol
p-Vinylguaiacol
4-ETHENYL-2-METHOXYPHENOL
4-Hydroxy-3-methoxystyrene
Phenol, 4-ethenyl-2-methoxy-
o-methoxy-p-vinylphenol
para-vinylguaiacol
Guaiacol, 4-vinyl-
p-Vinyl guaiacol
4-vinyl-2-methoxyphenol
Phenol, 2-methoxy-4-vinyl-
4-Hydroxy-3-methoxyvinylbenzene
2-METHOXY-4-VINYL-PHENOL
FEMA No. 2675
3-Methoxy-4-hydroxystyrene
Varamol 106
CCRIS 548
CHEBI:42438
Vinylcatechol-O-methyl ether, P-
UNII-DA069CTH0O
EINECS 232-101-2
2M4VP
DA069CTH0O
Guaiacol, 4-vinyl
BRN 2044521
4-hydroxy-3-methoxyphenylethene
DTXSID7052529
2-(4-hydroxy-3-methoxyphenyl)ethene
2-Methoxy-4-ethenylphenol
Phenol, 2-methoxy-4-ethenyl
Phenol, 4-vinyl, 2-methoxy
CHEMBL1232595
DTXCID8031102
(4-Hydroxy-3-methoxyphenyl)ethene
3-06-00-04981 (Beilstein Handbook Reference)
4-vinyl guaiacol
EUG
Vinyl guaiacol
p-Vinyl guaicol
4-vinylguaiacole
4-Ethenylguaiacol
4-Vinyl-O-guaiacol
2-Methoxy-vinylphenol
31853-85-7
2-Metoxy-4-vinyl-phenol
bmse010071
4-ethenyl-2-methoxy-phenol
SCHEMBL54199
2-?Methoxy-?4-?vinylphenol
BCP27800
Tox21_304024
BDBM50548720
MFCD00015437
AKOS015890494
DB03514
FS-3782
HY-W019940
MCULE-4834642824
2-methoxy-4-vinylphenol (vinylguaiacol)
2-METHOXY-4-VINYLPHENOL [FHFI]
2-Methoxy-4-vinylphenol, >=98%, FG
NCGC00357234-01
Vinylguaiacol (4-vinyl-2-methoxyphenol)
BP-11167
PD006849
CAS-7786-61-0
2-Methoxy-4-vinylphenol (4-vinylguaiacol)
4-Vinyl-2-methoxyphenol (4-vinylguaiacol)
DB-003488
2-Methoxy-4-vinylphenol, analytical standard
4-Vinyl-2-methoxyphenol ( p-vinylguaiacol)
AM20041169
CS-0031749
NS00005168
C17883
EN300-1832370
A839253
Q4596898
W-104295
2-METHOXY-4-VINYLPHENOL (STABILIZED WITH TBC)
4M4
Microorganism:

Yes

IUPAC name4-ethenyl-2-methoxyphenol
SMILESCOC1=C(C=CC(=C1)C=C)O
InchiInChI=1S/C9H10O2/c1-3-7-4-5-8(10)9(6-7)11-2/h3-6,10H,1H2,2H3
FormulaC9H10O2
PubChem ID332
Molweight150.17
LogP2.4
Atoms11
Bonds2
H-bond Acceptor2
H-bond Donor1
Chemical Classificationbenzenoids alkenes alcohols aromatic compounds ethers phenols
CHEBI-ID42438
Supernatural-IDSN0456029

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaLentilactobacillus BuchneriNANASquara et al. 2022
ProkaryotaLacticaseibacillus ParacaseiNANASquara et al. 2022
EukaryotaSaccharomyces EubayanusNANAMardones et al. 2022
EukaryotaSaccharomyces EubayanusNANAUrbina et al. 2020
EukaryotaPhytophthora CinnamomiN/APhytophthora cinnamomiQiu R et al. 2014
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaLentilactobacillus Buchnerimaize silageHS-SPME coupled with GC-TOF MSno
ProkaryotaLacticaseibacillus Paracaseimaize silageHS-SPME coupled with GC-TOF MSno
EukaryotaSaccharomyces EubayanusYPD agar media (yeast extract 1%, peptone 2%, glucose 2% and agar 2%)HS‐SPME‐GC‐MSno
EukaryotaSaccharomyces Eubayanusbeer wortHS-SPME-GC-MSno
EukaryotaPhytophthora CinnamomiV8 juice agarSPME/GC-MS/MSno


4-methylpent-3-en-2-one

Mass-Spectra

Compound Details

Synonymous names
MESITYL OXIDE
141-79-7
4-Methylpent-3-en-2-one
4-Methyl-3-penten-2-one
3-Penten-2-one, 4-methyl-
Methyl isobutenyl ketone
Isopropylideneacetone
Isobutenyl methyl ketone
Mesityloxid
Mesityloxyde
Ossido di mesitile
3-Isohexen-2-one
Isopropylidene acetone
Oxyde de mesityle
Acetone, isopropylidene-
Methyl 2-methyl-1-propenyl ketone
Methyl 2,2-dimethylvinyl ketone
2-Methyl-4-oxo-2-pentene
2-Methyl-2-pentenone-4
2,2-Dimethylvinyl methyl ketone
4-Metil-3-penten-2-one
4-Methyl-3-pentene-2-one
4-Methyl-3-penten-2-on
2-Methyl-2-penten-4-one
FEMA No. 3368
NSC 38717
4-Methyl-3-penten-2-one, 9CI
4-methyl-pent-3-en-2-one
DTXSID1029170
CHEBI:89993
(CH3)2C=CHC(=O)CH3
NSC-38717
77LAC84669
DTXCID209170
Mesityloxid [German]
Mesityloxyde [Dutch]
Caswell No. 547
FEMA Number 3368
Oxyde de mesityle [French]
CAS-141-79-7
Ossido di mesitile [Italian]
HSDB 1195
EINECS 205-502-5
4-Metil-3-penten-2-one [Italian]
UN1229
EPA Pesticide Chemical Code 052401
BRN 1361550
4-Methyl-3-penten-2-on [Dutch, German]
AI3-07702
UNII-77LAC84669
Mesityloxid(german)
MFCD00008900
Isopropylidene-Acetone
Mesityl oxide [UN1229] [Flammable liquid]
EC 205-502-5
2-methylpent-2-en-4-one
MESITYL OXIDE [MI]
1-Methylpent-2-en-4-one
MESITYL OXIDE [HSDB]
CHEMBL3185916
FEMA 3368
WLN: 1Y1 & U1V1
4-Methyl-3-penten-2-one, 90%
AMY23356
NSC38717
Tox21_202080
Tox21_303606
LMFA12000030
STL146350
Mesityl oxide, technical grade, 90%
AKOS000118892
MCULE-4922478422
UN 1229
NCGC00249161-01
NCGC00257514-01
NCGC00259629-01
4-Methyl-3-penten-2-one (mesityl oxide)
4-Methyl-3-penten-2-on(DUTCH, GERMAN)
4-METHYL-3-PENTENE-2-ONE [FHFI]
M0069
M1340
NS00006985
TEICOPLANIN IMPURITY A [EP IMPURITY]
3-PENTEN,2-ONE,4-METHYL MESITYLOXIDE
EN300-21333
Mesityl oxide [UN1229] [Flammable liquid]
3-PENTEN,2-ONE,4-METHYL MESITYLOXIDE
A807813
CILASTATIN SODIUM IMPURITY D [EP IMPURITY]
Q425668
Q-201356
4-Methyl-3-penten-2-one, analytical reference material
Mesityl oxide, 90%, remainder 4-methyl-4-penten-2-one
InChI=1/C6H10O/c1-5(2)4-6(3)7/h4H,1-3H
Mesityl oxide, European Pharmacopoeia (EP) Reference Standard
4-Methylpent-3-en-2-one; Mesityl oxide; Cilastatin Sodium Imp. D (EP)
Mesityl Oxide, Pharmaceutical Secondary Standard; Certified Reference Material
Mesityl oxide, suitable for neutral marker for measuring electroosmotic flow (EOF), ~98%
Microorganism:

Yes

IUPAC name4-methylpent-3-en-2-one
SMILESCC(=CC(=O)C)C
InchiInChI=1S/C6H10O/c1-5(2)4-6(3)7/h4H,1-3H3
FormulaC6H10O
PubChem ID8858
Molweight98.14
LogP1.4
Atoms7
Bonds1
H-bond Acceptor1
H-bond Donor0
Chemical Classificationalkenes aliphatic ketones ketones
CHEBI-ID89993
Supernatural-IDSN0345746

mVOC Specific Details

Boiling Point
DegreeReference
130 °C peer reviewed
Volatilization
The Henry's Law constant for mesityl oxide is estimated as 3.67X10-5 atm-cu m/mole(SRC) derived from its vapor pressure, 8.21 mm Hg(1), and water solubility, 28,900 mg/L(2). This Henry's Law constant indicates that mesityl oxide 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 17 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(3) is estimated as 11 days(SRC). Mesityl oxide's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of mesityl oxide from dry soil surfaces may exist(SRC) based upon its vapor pressure(1).
Literature: (1) Daubert TE, Danner DP; Physical & Thermodynamic Properties of Pure Chemicals Vol. 3 NY: Hemisphere Pub Corp (1989) (2) Yalkowsky SH, He Y; Handbook of Aqueous Solubility Data. CRC Press LLC, Boca Raton, FL. p. 285 (2003) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)
Soil Adsorption
The Koc of mesityl oxide is estimated as 15(SRC), using a water solubility of 28,900 mg/L(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that mesityl oxide is expected to have very high mobility in soil.
Literature: (1) Yalkowsky SH, He Y; Handbook of Aqueous Solubility Data. CRC Press LLC, Boca Raton, FL. p. 285 (2003) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 4-5 (1990) (3) Swann RL et al; Res Rev 85: 17-28 (1983)
Vapor Pressure
PressureReference
8.21 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
ProkaryotaPseudomonas AeruginosaNANADavis et al. 2020
ProkaryotaKlebsiella PneumoniaeNARees et al. 2017
ProkaryotaPseudomonas Aeruginosastimulate growth in Arabidopsis thaliana seedlings depending on inoculum concentrationavocado trees (Persea americana) rhizosphereGamboa-Becerra et al. 2022
ProkaryotaPseudomonas Sp.stimulate growth in Arabidopsis thaliana seedlings depending on inoculum concentrationavocado trees (Persea americana) rhizosphereGamboa-Becerra et al. 2022
ProkaryotaBacillus Sp.stimulate growth in Arabidopsis thaliana seedlings depending on inoculum concentrationavocado trees (Persea americana) rhizosphereGamboa-Becerra et al. 2022
ProkaryotaBrevibacillus Agristimulate growth in Arabidopsis thaliana seedlings depending on inoculum concentrationavocado trees (Persea americana) rhizosphereGamboa-Becerra et al. 2022
ProkaryotaAneurinibacillus Aneurinilyticusstimulate growth in Arabidopsis thaliana seedlings depending on inoculum concentrationavocado trees (Persea americana) rhizosphereGamboa-Becerra et al. 2022
ProkaryotaSerratia Liquefaciensstimulate growth in Arabidopsis thaliana seedlings depending on inoculum concentrationavocado trees (Persea americana) rhizosphereGamboa-Becerra et al. 2022
ProkaryotaStaphylococcus AureusLeibnitz Institute DSMZ-German Collection of Microorganisms and Cell Cultures GmbHFitzgerald et al. 2020
ProkaryotaPseudomonas AeruginosaLeibnitz 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
ProkaryotaStaphylococcus Epidermidisstrains were provided by Prof. O'Gara at NUI GalwayFitzgerald et al. 2020
ProkaryotaCollimonas Pratensisnarhizosphere of Marram grass in sandy dune soils, NetherlandsGarbeva et al. 2014
ProkaryotaCollimonas Pratensisn/aNAGarbeva et al. 2014
ProkaryotaStreptomyces Citreusn/aNASchulz and Dickschat 2007
EukaryotaLentinula EdodesGeng et al. 2024
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaPseudomonas AeruginosaLB brothSPME/GCxGC-MSno
ProkaryotaKlebsiella PneumoniaeLBSPME / GCxGC-TOFMSno
ProkaryotaPseudomonas AeruginosaLB mediaSPME/GC-MSno
ProkaryotaPseudomonas Sp.LB mediaSPME/GC-MSno
ProkaryotaBacillus Sp.LB mediaSPME/GC-MSno
ProkaryotaBrevibacillus AgriLB mediaSPME/GC-MSno
ProkaryotaAneurinibacillus AneurinilyticusLB mediaSPME/GC-MSno
ProkaryotaSerratia LiquefaciensLB mediaSPME/GC-MSno
ProkaryotaStaphylococcus AureusTSB mediaHS-SPME/GC-MSno
ProkaryotaPseudomonas AeruginosaTSB mediaHS-SPME/GC-MSno
ProkaryotaEscherichia ColiTSB mediaHS-SPME/GC-MSno
ProkaryotaStaphylococcus EpidermidisTSB mediaHS-SPME/GC-MSno
ProkaryotaCollimonas Pratensissand containing artificial root exudatesGC/MSno
ProkaryotaCollimonas PratensisHeadspace trapping/GC-MSno
ProkaryotaStreptomyces Citreusn/an/ano
EukaryotaLentinula EdodesJiuqu (traditional wheat Qu)GC-IMSno


Undec-10-enoic Acid

Compound Details

Synonymous names
undecylenic acid
10-UNDECENOIC ACID
Undec-10-enoic acid
112-38-9
Undecenoic acid
Desenex
10-Hendecenoic acid
Renselin
Sevinon
Declid
10-Undecylenic acid
9-Undecylenic acid
Undecyl-10-enic acid
FEMA No. 3247
undecylenate
Kyselina undecylenova
Caswell No. 901
UNDECEN-10-ACID-1
Undecenoic acid, omega-
Undecylenic acid [JAN]
Hendecenoic acid, omega-
omega-undecenoic acid
NSC 2013
omega-hendecenoic acid
10-Henedecenoic acid
CHEBI:35045
undecelinic acid
10-Hendecenoic
10-Undecensaeure
NSC-2013
EINECS 203-965-8
n-Undecylenic acid
UNII-K3D86KJ24N
Undecen-10-saeure
Cruex
EPA Pesticide Chemical Code 085501
BRN 1762631
K3D86KJ24N
Cruex (TN)
Kyselina 9-decen-1-karboxylova
acide 10-undecylique
acido 10-undecenoico
1333-28-4
DTXSID8035001
acide 10-undecanoique
AI3-02065
NSC2013
MFCD00004442
Undecylenic acid (JAN/USP)
Undecylenic acid [USP:JAN]
DTXCID6015001
EC 203-965-8
4-02-00-01612 (Beilstein Handbook Reference)
Undesine
C11:1n-1
NCGC00159425-02
NCGC00159425-04
Undecylenic acid (USP:JAN)
UNDECYLENIC ACID (II)
UNDECYLENIC ACID [II]
UNDECENOIC ACID (MART.)
UNDECENOIC ACID [MART.]
Undecenoicacid
UNDECYLENIC ACID (USP-RS)
UNDECYLENIC ACID [USP-RS]
UNDECYLENIC ACID (EP MONOGRAPH)
UNDECYLENIC ACID [EP MONOGRAPH]
UNDECYLENIC ACID (USP MONOGRAPH)
UNDECYLENIC ACID [USP MONOGRAPH]
96451-28-4
CAS-112-38-9
Kyselina undecylenova [Czech]
10-Undecenoic acid, 98%
Kyselina 9-decen-1-karboxylova [Czech]
Desinex
Micocilen
Tobcharm
HongocuraM
HongocuraS
Antifungal Pen
undecylenic-acid
Remedy Nails
Anti-Fungal Pen
Rite Aid Fungal
Undecylenenic acid
MicocilenAntifungal
Topcare Antifungal
Antifungal Solution
Diabetic Antifungal
Anti-Fungal Liquid
Fungicure LiquidGel
10-Undecenic acid
Antifungal Nail Pen
EINECS 215-583-9
EmoniNail Antifungal
Hongocura Pinceladas
n-UNDECYLENIC ACID (10-1)
Zinc Undecylenate (undecylenic acid)
Anti-Fungal PenCVS
10-undeceneoic acid
Flexitol Anti Fungal
TERPENICOL
Zeta Clear Antifungal
NU CALMAR
HC Max Hongo CuraMS
Undecylenic Acid Liquid
Undecylenic acid, USAN
FungicureMaximum Strength
Premier Value Antifungal
FUNGWAY Fungus Clearing
Anti-Fungal Nail Solution
Good Neighbor Anti-Fungal
Tineacide Physician Formula
Fiore Rx Antifungal ProPen
Sally HansenNo More Fungus
Hongo KillerNail and Fungus
NCIOpen2_002642
UNDECYLENATE [VANDF]
WLN: QV9U1
Direct Naturals Fungus Clear
SCHEMBL17827
UNDECYLENIC ACID [MI]
Pinceladas Para Hongos Navarro
Maximum Strength Antifungal Pen
Diabetic Antifungal Professional
UNDECYLENIC ACID [INCI]
CHEMBL1276010
Myco Nail A Antifungal Solution
UNDECYLENIC ACID [VANDF]
FEMA 3247
Undecylenic acid, >=95%, FG
Undecylenic acid, >=96%, FG
TopCare AntifungalMaximum Strength
UNDECYLENIC ACID [WHO-DD]
HMS2093L21
Pharmakon1600-01505468
Fungicure Anti-Fungal Liquid 25%
Human Science Antifungal Foot Care
10-UNDECENOIC ACID [FHFI]
HY-B0914
PURESKIN FUNGAL NAIL RENEWAL
Tox21_111657
Tox21_300383
BBL027462
BDBM50248304
Fungi Nail Toe and Foot Anti-Fungal
LMFA01030036
NSC759153
Pinceladas Goyescas OriginalFungicide
s9452
STK801548
Dermaced Maximum Strength Anti-Fungal
FUNGINIX ANTI-FUNGAL TREATMENT
maximum strengthantifungal nail liquid
AKOS009031595
Tox21_111657_1
CCG-213461
DB11117
ELON Dual Defense Anti Fungal Formula
MCULE-7928135942
NSC-759153
PB48616
Undecylenic acid; Undec-10-enoic acid
10-Undecenoic acid, analytical standard
Premier Value AntifungalMaximum Strength
Botanimedix OnychoRX Antifungal Nail Gel
ETERNAL SPIRIT BEAUTY FUNGI FRESH
NCGC00159425-03
NCGC00159425-05
NCGC00159425-09
NCGC00254296-01
Undecylenic acid, natural, >=97%, FG
FLUSH Maximum Strength Antifungal formula
NCI60_001670
SBI-0206806.P001
SBI-0206806.P002
CVS Maximum Strength Anti-Fungal Pen 25%
Maximum Strength Antifungal Liquid Solution
Nutra Nail FUNGI FREE Antifungal Treatment
CVS PharmacyAnti-fungal Pen Maximum Strength
NS00009009
U0007
EN300-20666
Fiore Rx Coral Sorbet Antifungal Nail Polish
Pinceladas Goyescas OriginalBrush on Fungicide
10-Undecenoic acid, purum, >=97.0% (GC)
D02159
P19683
AB00630892_02
CVS MAXIMUM STRENGTH ANTI FUNGAL PEN 25
Fiore Rx CranApple Crush Antifungal Nail Polish
Fiore Rx Pixie Dust Pink Antifungal Nail Polish
Fiore Rx Antifungal Nail Lacquer Red Velvet Cake
Fiore Rx Rock Candy Clear Antifungal Nail Lacquer
Q420346
SR-05000002050
10-Undecenoic acid, Vetec(TM) reagent grade, 98%
Fiore Rx Almond Milk Matte Antifungal Nail Lacquer
Fiore Rx Eggplant My Garden Antifungal Nail Polish
Fiore Rx Pink Peppermint Pie Antifungal Nail Polish
RIte AidMaximum Strength Foot Care Anti-fungal Pen
SR-05000002050-1
W-200840
F0001-0258
Z104479700
CVS PharmacyMaximum Strength Antifungal Liquid with Aloe and Vitamin E
Undecylenic acid, United States Pharmacopeia (USP) Reference Standard
10-Undecenoic acid, puriss., meets analytical specification of Ph. Eur., BP, USP, 98-100.5%
InChI=1/C11H20O2/c1-2-3-4-5-6-7-8-9-10-11(12)13/h2H,1,3-10H2,(H,12,13
Microorganism:

Yes

IUPAC nameundec-10-enoic acid
SMILESC=CCCCCCCCCC(=O)O
InchiInChI=1S/C11H20O2/c1-2-3-4-5-6-7-8-9-10-11(12)13/h2H,1,3-10H2,(H,12,13)
FormulaC11H20O2
PubChem ID5634
Molweight184.27
LogP3.9
Atoms13
Bonds9
H-bond Acceptor2
H-bond Donor1
Chemical Classificationalkenes organic acids carboxylic acids
CHEBI-ID39448
Supernatural-IDSN0093708

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


2,6,6-trimethylcyclohexene-1-carbaldehyde

Mass-Spectra

Compound Details

Synonymous names
beta-Cyclocitral
432-25-7
b-cyclocitral
2,6,6-Trimethylcyclohexene-1-carbaldehyde
2,6,6-trimethylcyclohex-1-ene-1-carbaldehyde
1-Cyclohexene-1-carboxaldehyde, 2,6,6-trimethyl-
.beta.-Cyclocitral
2,6,6-TRIMETHYL-1-CYCLOHEXENE-1-CARBOXALDEHYDE
CYCLOCITRAL
2,6,6-trimethylcyclohex-1-enecarbaldehyde
alpha(beta)-Cyclocitral
2,6,6-Trimethylcyclohexenecarbaldehyde
1-Formyl-2,6,6-trimethyl-1-cyclohexene
beta -cyclocitral
Cyclohexenecarboxaldehyde, 2,6,6-trimethyl-
MFCD00079078
52844-21-0
DTXSID7047142
CHEBI:53177
2,6,6-Trimethyl-1-cyclohexen-1-carboxaldehyde
77Y0U2X29G
2,6,6-trimethyl-cyclohexene-1-carboxaldehyde
2,6,6-Trimethyl-1-cyclohexene-1-carbaldehyde
UNII-77Y0U2X29G
beta cyclocitral
beta-cyclocitrol
beta-Cyclocitral, Technical Grade
EINECS 207-081-3
AI3-37227
2,6,6-Trimethyl-1-cyclohexenecarboxaldehyde
UNII-GLL5338RMI
beta-Cyclocitral, >=95%
GLL5338RMI
CYCLOCITRAL, .BETA.-
SCHEMBL309759
b-Cyclocitral, Technical Grade
CHEMBL1952257
DTXCID5027142
?-Cyclocitral, Technical Grade
EINECS 258-219-4
Tox21_302524
beta-Cyclocitral, analytical standard
AKOS022504751
CS-W010947
HY-W010231
MCULE-7819289735
FEMA NO. 3639, .BETA.-
NCGC00256741-01
AS-56746
CAS-432-25-7
SY029933
2,6,6-Trimethyl-1-cyclohexenecarbaldehyde
2,6,6-Trimethyl-Cyclohexenecarboxaldehyde
2,6,6-trimethyl-cyclohexene-1-carbaldehyde
DB-302496
NS00013267
C20425
EN300-180215
F14917
2,6,6-Trimethyl-1-cyclohexene-1-carbaldehyde #
W-202757
Q27124011
Z1255386953
Pentadeuterio-beta-cyclocitral;1-Formyl-2,6,6-trimethyl-1-cyclohexene
InChI=1/C10H16O/c1-8-5-4-6-10(2,3)9(8)7-11/h7H,4-6H2,1-3H
Microorganism:

Yes

IUPAC name2,6,6-trimethylcyclohexene-1-carbaldehyde
SMILESCC1=C(C(CCC1)(C)C)C=O
InchiInChI=1S/C10H16O/c1-8-5-4-6-10(2,3)9(8)7-11/h7H,4-6H2,1-3H3
FormulaC10H16O
PubChem ID9895
Molweight152.23
LogP2.4
Atoms11
Bonds1
H-bond Acceptor1
H-bond Donor0
Chemical Classificationalkenes aldehydes ketones terpenoids
CHEBI-ID53177
Supernatural-IDSN0231223

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaCalothrix Sp.n/aNASchulz and Dickschat 2007
ProkaryotaPlectonema Sp.n/aNASchulz and Dickschat 2007
ProkaryotaCyanobacteria Sp.n/aNAHoeckelmann et al. 2004
ProkaryotaCalothrix Parietinan/aNAHoeckelmann et al. 2004
ProkaryotaPlectonema Notatumn/aNAHoeckelmann et al. 2004
ProkaryotaPlectonema Sp.n/aNAHoeckelmann et al. 2004
ProkaryotaRivularia Sp.n/aNAHoeckelmann et al. 2004
ProkaryotaRivularia Sp./Calothrix Parietinan/aNAHoeckelmann et al. 2004
ProkaryotaPhormidium Sp.n/aNAHoeckelmann et al. 2004
ProkaryotaLentilactobacillus BuchneriNANASquara et al. 2022
ProkaryotaLacticaseibacillus ParacaseiNANASquara et al. 2022
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaCalothrix Sp.n/an/ano
ProkaryotaPlectonema Sp.n/an/ano
ProkaryotaCyanobacteria Sp.n/an/ano
ProkaryotaCalothrix Parietinan/an/ano
ProkaryotaPlectonema Notatumn/an/ano
ProkaryotaRivularia Sp.n/an/ano
ProkaryotaRivularia Sp./Calothrix Parietinan/an/ano
ProkaryotaPhormidium Sp.n/an/ano
ProkaryotaLentilactobacillus Buchnerimaize silageHS-SPME coupled with GC-TOF MSno
ProkaryotaLacticaseibacillus Paracaseimaize silageHS-SPME coupled with GC-TOF MSno


Prop-2-enoic Acid

Mass-Spectra

Compound Details

Synonymous names
ACRYLIC ACID
2-Propenoic acid
79-10-7
prop-2-enoic acid
Vinylformic acid
Propenoic acid
Acroleic acid
Ethylenecarboxylic acid
Propene acid
ACRYLATE
Propenoate
Glacial acrylic acid
9003-01-4
Kyselina akrylova
Acrylic acid, glacial
RCRA waste number U008
Acide acrylique
Acido acrilio
Caswell No. 009A
Carbopol 934p
Viscalex HV 30
NSC 4765
CCRIS 737
Acrylic resin
HSDB 1421
UNII-J94PBK7X8S
EINECS 201-177-9
J94PBK7X8S
Carbopol 940
BRN 0635743
ACRLYLIC ACID
DTXSID0039229
CHEBI:18308
AI3-15717
NSC-4765
DTXCID8028
Aron
Antiprex A
Versicol E9
NSC4765
EC 201-177-9
Acrylic acid resin
ACRYLIC ACID (13C3)
Acrysol ase-75
C3:1n-1
Versicol E 7
Versicol E15
4-02-00-01455 (Beilstein Handbook Reference)
Acrysol A 1
Acrysol A 3
Acrysol A 5
Acrysol A-1
Acrysol AC 5
Carbopol 960
Carboset 515
Primal Ase 60
Revacryl A191
Versicol K 11
Versicol S 25
Dispex C40
Acrysol WS-24
Cyguard 266
Joncryl 678
Jurimer AC 10H
Jurimer AC 10P
Nalfloc 636
Good-rite K 37
Revacryl A 191
Junlon 110
Viscon 103
Good-rite K 702
Good-rite K 732
Good-rite WS 801
NCGC00166246-01
Poly(acrylic acid), 25% soln in water
Synthemul 90-588
Aron A 10H
Carboset Resin No. 515
ACRYLIC ACID (IARC)
ACRYLIC ACID [IARC]
OLD 01
PA 11M
PAA-25
Carbopol
P 11H
P-11H
WS 24
Acido acrilio [Spanish]
Acide acrylique [French]
WS 801
Kyselina akrylova [Czech]
R968
UN2218
RCRA waste no. U008
allenediol
Acrysol lmw-20X
XPA
Aqueous acrylic acid
25987-55-7
Dow Latex 354
Ethene carboxylic acid
Acrylic acid, inhibited
CH2=CHCOOH
(stabilized with MEHQ)
Carbomer 934 (NF)
Carbomer 940 (NF)
Carbomer 941 (NF)
Carbopol 910 (TN)
Carbopol 934 (TN)
Carbopol 940 (TN)
Carbopol 941 (TN)
Carbomer 934P (NF)
Carbopol 934P (TN)
Carbomer 910 (USAN)
ACRYLIC ACID [MI]
Carbomer 1342 (NF)
Carbopol 1342 (TN)
ACRYLIC ACID [HSDB]
ACRYLIC ACID [INCI]
WLN: QV1U1
average Mv ~450,000
UN 2218 (Salt/Mix)
Acrylic acid, p.a., 99%
CHEMBL1213529
STR00040
Tox21_112372
LMFA01030193
MFCD00004367
NSC106034
NSC106035
NSC106036
NSC106037
NSC112122
NSC112123
NSC114472
NSC165257
NSC226569
STL281870
AKOS000118799
DB02579
MCULE-9352227082
NSC-106034
NSC-106035
NSC-106036
NSC-106037
NSC-112122
NSC-112123
NSC-114472
NSC-165257
NSC-226569
CAS-79-10-7
BP-30259
DB-220116
DB-251641
A0141
NS00001146
EN300-17959
C00511
C19501
D03392
D03393
D03394
D03395
D03396
D03397
Acrylic Acid contains 200ppm MEHQ as inhibitor
Acrylic acid, inhibited [UN2218] [Corrosive]
A830860
Q324628
Z57127944
F0001-2070
InChI=1/C3H4O2/c1-2-3(4)5/h2H,1H2,(H,4,5
Acrylic acid, anhydrous, contains 200 ppm MEHQ as inhibitor, 99%
Acrylic acid, SAJ first grade, >=97.0%, contains 190-210 ppm MEHQ as stabilizer
1204391-75-2
55927-87-2
9063-87-0
Microorganism:

Yes

IUPAC nameprop-2-enoic acid
SMILESC=CC(=O)O
InchiInChI=1S/C3H4O2/c1-2-3(4)5/h2H,1H2,(H,4,5)
FormulaC3H4O2
PubChem ID6581
Molweight72.06
LogP0.3
Atoms5
Bonds1
H-bond Acceptor2
H-bond Donor1
Chemical Classificationalkenes acids carboxylic acids organic acids
CHEBI-ID18308
Supernatural-IDSN0246839

mVOC Specific Details

Boiling Point
DegreeReference
142 °C peer reviewed
Volatilization
A pKa of 4.26(1) indicates acrylic acid will exist almost entirely in the anion form at pH values of 5 to 9 and therefore volatilization from water surfaces and moist soil is not expected to be an important fate process(2). The potential for volatilization of acrylic acid from dry soil surfaces may exist(SRC) based upon a vapor pressure of 3.97 mm Hg(3).
Literature: (1) Riddick JA et al; Organic Solvents: Physical Properties and Methods of Purification. Techniques of Chemistry. 4th ed. New York, NY: Wiley-Interscience (1986) (2) Doucette WJ; pp. 141-188 in Handbook of Property Estimation Methods for Chemicals. Boethling RS, Mackay D, eds, Boca Raton, FL: Lewis Publ (2000) (3) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals: Data Compilation. Design Inst Phys Prop Data, Amer Inst Chem Eng New York, NY: Hemisphere Pub Corp 5 Vol (1987)
Soil Adsorption
Koc values for acrylic acid have been reported as 6 in Washington clay/loam (29% sand, 42% silt, 29% clay, 3.39% organic carbon, pH 6.0), 9 in Canfield loam (45% sand, 42% silt, 13% clay, 4.58% organic carbon, pH 6.1), 29 in Ellsworth loam (35% sand, 40% silt, 25% clay, 1.42% organic carbon, pH 7.2), 137 in Tyner loamy sand (79% sand, 14% silt, 7% clay, 0.46% organic carbon, pH 5.2), and 33 in sandy loam sediment (53% sand, 28% silt, 19% clay, 1.23% organic carbon, pH 7.5)(1) According to a classification scheme(2), these Koc values suggest that acrylic acid is expected to have very high to high mobility in soil. The pKa of acrylic acid is 4.26(3), indicating that this compound will exist almost entirely in anion form in the environment and anions generally do not adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts(4).
Literature: (1) Staples CA et al; Chemosphere 40: 29-38 (2000) (2) Swann RL et al; Res Rev 85: 17-28 (1983) (3) Riddick JA et al; Organic Solvents: Physical Properties and Methods of Purification. Techniques of Chemistry. 4th ed. New York, NY: Wiley-Interscience (1986) (4) Doucette WJ; pp. 141-188 in Handbook of Property Estimation Methods for Chemicals. Boethling RS, Mackay D, eds. Boca Raton, FL: Lewis Publ (2000)
Vapor Pressure
PressureReference
3.97 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
Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaTuber Aestivumn/aAgricultural Centre of Castilla and León Community (Monasterio de la Santa Espina, Valladolid, Spain) and Navaleno (Soria, Spain).Diaz et al. 2003
ProkaryotaClostridium Sp.n/aNAStotzky and Schenck 1976
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaTuber Aestivumn/an/ano
ProkaryotaClostridium Sp.n/an/ano


2,5,8,11-tetramethyldodec-2-ene

Compound Details

Synonymous names
Tetraisobutylene
2,5,8,11-tetramethyldodec-2-ene
Tetraisobutylen
1-Propene,2-methyl-,tetramer
AKOS015914157
Microorganism:

Yes

IUPAC name2,5,8,11-tetramethyldodec-2-ene
SMILESCC(C)CCC(C)CCC(C)CC=C(C)C
InchiInChI=1S/C16H32/c1-13(2)7-9-15(5)11-12-16(6)10-8-14(3)4/h7,14-16H,8-12H2,1-6H3
FormulaC16H32
PubChem ID56846471
Molweight224.42
LogP7.3
Atoms16
Bonds8
H-bond Acceptor0
H-bond Donor0
Chemical Classificationalkenes unsaturated hydrocarbons

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaErwinia Amylovoraenhances Arabidopsis thaliana shoot and root growthbacterial collection of the LabParmagnani et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaErwinia AmylovoraSBSE/GC-MSno


(E)-3-methylnon-2-ene

Compound Details

Synonymous names
(E)-3-methylnon-2-ene
2-Nonene, 3-methyl-, (E)-
17003-99-5
(E)-3-Methyl-2-nonene
3-methyl-2-nonene
(2E)-3-Methyl-2-nonene #
Microorganism:

Yes

IUPAC name(E)-3-methylnon-2-ene
SMILESCCCCCCC(=CC)C
InchiInChI=1S/C10H20/c1-4-6-7-8-9-10(3)5-2/h5H,4,6-9H2,1-3H3/b10-5+
FormulaC10H20
PubChem ID5366150
Molweight140.27
LogP4.9
Atoms10
Bonds5
H-bond Acceptor0
H-bond Donor0
Chemical Classificationalkenes unsaturated hydrocarbons

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaSaccharomyces CerevisiaeNANAHarris et al. 2021
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaSaccharomyces Cerevisiaemalt extract brothHS-SPME with GC-MSno


(E)-2,2,4,6,6-pentamethylhept-3-ene

Mass-Spectra

Compound Details

Synonymous names
123-48-8
3-Heptene, 2,2,4,6,6-pentamethyl-
2,2,4,6,6-PENTAMETHYL-3-HEPTENE
(E)-2,2,4,6,6-pentamethylhept-3-ene
2,2,4,6,6-Pentamethylhept-3-ene
2,2,4,6,6-Pentamethylhept-3-ene, (E)-
2,2,4,6,6-Pentamethylheptene-3
02S68B714V
trans-2,2,4,6,6-Pentamethyl-3-heptene
3-Heptene, 2,2,4,6,6-pentamethyl-, (E)-
3-Heptene, 2,2,4,6,6-pentamethyl-, (3E)-
(3E)-2,2,4,6,6-PENTAMETHYLHEPT-3-ENE
27656-49-1
HSDB 5599
UNII-93OVL3281U
EINECS 204-631-4
UNII-02S68B714V
93OVL3281U
2,2,4,6,6-Pentamethyl-3-heptene,c&t
(3E)-2,2,4,6,6-Pentamethyl-3-heptene #
W-109460
Q27231549
InChI=1/C12H24/c1-10(8-11(2,3)4)9-12(5,6)7/h8H,9H2,1-7H3/b10-8
Microorganism:

No

IUPAC name(E)-2,2,4,6,6-pentamethylhept-3-ene
SMILESCC(=CC(C)(C)C)CC(C)(C)C
InchiInChI=1S/C12H24/c1-10(8-11(2,3)4)9-12(5,6)7/h8H,9H2,1-7H3/b10-8+
FormulaC12H24
PubChem ID5365103
Molweight168.32
LogP5.2
Atoms12
Bonds3
H-bond Acceptor0
H-bond Donor0
Chemical Classificationalkenes unsaturated hydrocarbons

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaTrichoderma Pseudokoningiin/aNAWheatley et al. 1997
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaTrichoderma PseudokoningiiMalt extract/Low mediumGC/MSno


(Z)-6-methyldec-2-ene

Compound Details

Synonymous names
2-Decene, 6-methyl-, (Z)-
(2Z)-6-Methyl-2-decene #
LWBAWMILIWHSPF-XQRVVYSFSA-N
Microorganism:

Yes

IUPAC name(Z)-6-methyldec-2-ene
SMILESCCCCC(C)CCC=CC
InchiInChI=1S/C11H22/c1-4-6-8-10-11(3)9-7-5-2/h4,6,11H,5,7-10H2,1-3H3/b6-4-
FormulaC11H22
PubChem ID5364865
Molweight154.29
LogP5.1
Atoms11
Bonds6
H-bond Acceptor0
H-bond Donor0
Chemical Classificationalkenes unsaturated hydrocarbons

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaSaccharomyces CerevisiaeNANAHarris et al. 2021
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaSaccharomyces Cerevisiaemalt extract brothHS-SPME with GC-MSno


(Z)-8-methyldec-2-ene

Compound Details

Synonymous names
(Z)-8-methyldec-2-ene
(Z)-8-Methyl-2-decene
2-Decene, 8-methyl-, (Z)-
(2Z)-8-Methyl-2-decene #
CHEBI:229413
DUBPNDBMNWVPTM-XQRVVYSFSA-N
Microorganism:

Yes

IUPAC name(Z)-8-methyldec-2-ene
SMILESCCC(C)CCCCC=CC
InchiInChI=1S/C11H22/c1-4-6-7-8-9-10-11(3)5-2/h4,6,11H,5,7-10H2,1-3H3/b6-4-
FormulaC11H22
PubChem ID5364689
Molweight154.29
LogP5.1
Atoms11
Bonds6
H-bond Acceptor0
H-bond Donor0
Chemical Classificationalkenes unsaturated hydrocarbons
CHEBI-ID229413

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaSaccharomyces CerevisiaeNANAHarris et al. 2021
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaSaccharomyces Cerevisiaemalt extract brothHS-SPME with GC-MSno


(E)-octadec-9-ene

Compound Details

Synonymous names
9-Octadecene
(E)-octadec-9-ene
5557-31-3
9-Octadecene, (E)-
(9E)-9-Octadecene
trans-9-Octadecene
(E)-9-Octadecene
octadec-9-ene
trans-octadec-9-ene
7206-25-9
9-Octadecene, (9E)-
3K7K2NDB3U
(9E)-octadec-9-ene
UNII-3K7K2NDB3U
CHEBI:37605
CHEBI:37607
DTXSID10880855
LMFA11000563
NS00096306
Q27117203
Q27117204
Microorganism:

Yes

IUPAC name(E)-octadec-9-ene
SMILESCCCCCCCCC=CCCCCCCCC
InchiInChI=1S/C18H36/c1-3-5-7-9-11-13-15-17-18-16-14-12-10-8-6-4-2/h17-18H,3-16H2,1-2H3/b18-17+
FormulaC18H36
PubChem ID5364599
Molweight252.5
LogP9
Atoms18
Bonds14
H-bond Acceptor0
H-bond Donor0
Chemical Classificationalkenes unsaturated hydrocarbons
CHEBI-ID37607
Supernatural-IDSN0134253-01

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaCarnobacterium Divergensn/aNAErcolini et al. 2009
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaCarnobacterium Divergensn/an/ano


(E)-octadec-5-ene

Compound Details

Synonymous names
5-Octadecene
(E)-5-Octadecene
5-Octadecene, (E)-
(5E)-5-Octadecene
7206-21-5
18899-24-6
(E)-5-Octadec-5-ene
trans-5-Octadecene
DTXSID70880871
YIYQJOMDMPTKEL-PKNBQFBNSA-N
HY-24574
CS-0373964
NS00095943
Microorganism:

Yes

IUPAC name(E)-octadec-5-ene
SMILESCCCCCCCCCCCCC=CCCCC
InchiInChI=1S/C18H36/c1-3-5-7-9-11-13-15-17-18-16-14-12-10-8-6-4-2/h9,11H,3-8,10,12-18H2,1-2H3/b11-9+
FormulaC18H36
PubChem ID5364598
Molweight252.5
LogP9
Atoms18
Bonds14
H-bond Acceptor0
H-bond Donor0
Chemical Classificationalkenes unsaturated hydrocarbons
Supernatural-IDSN0451704-01

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaCarnobacterium Divergensn/aNAErcolini et al. 2009
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaCarnobacterium Divergensn/an/ano


(E)-dec-2-ene

Compound Details

Synonymous names
2-Decene, (E)-
(E)-dec-2-ene
2-DECENE
(E)-2-Decene
25339-53-1
20063-97-2
2-Decene, (2E)-
(2E)-2-Decene
(2E)-2-Decene #
HSDB 5129
DTXSID70891927
EINECS 246-870-7
AKOS006229084
NSC 102790
(E)-2-C10H20
NS00009277
EC 246-870-7
Q63396272
Microorganism:

Yes

IUPAC name(E)-dec-2-ene
SMILESCCCCCCCC=CC
InchiInChI=1S/C10H20/c1-3-5-7-9-10-8-6-4-2/h3,5H,4,6-10H2,1-2H3/b5-3+
FormulaC10H20
PubChem ID5364559
Molweight140.27
LogP5.4
Atoms10
Bonds6
H-bond Acceptor0
H-bond Donor0
Chemical Classificationalkenes unsaturated hydrocarbons

mVOC Specific Details

Boiling Point
DegreeReference
170.6 °C peer reviewed
Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaPseudomonas Fragin/aNAErcolini et al. 2009
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaPseudomonas Fragin/an/ano


(Z)-hexadec-3-ene

Compound Details

Synonymous names
3-Hexadecene, (Z)-
cis-3-Hexadecene
3-Hexadecene, (3Z)-
(Z)-3-Hexadecene
(3Z)-3-Hexadecene
UNII-U767201ISR
34303-81-6
U767201ISR
Q27290783
Microorganism:

Yes

IUPAC name(Z)-hexadec-3-ene
SMILESCCCCCCCCCCCCC=CCC
InchiInChI=1S/C16H32/c1-3-5-7-9-11-13-15-16-14-12-10-8-6-4-2/h5,7H,3-4,6,8-16H2,1-2H3/b7-5-
FormulaC16H32
PubChem ID5364494
Molweight224.42
LogP7.9
Atoms16
Bonds12
H-bond Acceptor0
H-bond Donor0
Chemical Classificationalkenes unsaturated hydrocarbons
Supernatural-IDSN0306741-01

mVOC Specific Details


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


(Z)-non-2-ene

Compound Details

Synonymous names
cis-2-Nonene
6434-77-1
(Z)-non-2-ene
(2Z)-2-Nonene
(Z)-2-Nonene
2-Nonene, (Z)-
2-Nonene, (2Z)-
(2Z)-non-2-ene
UME13MDO8T
(Z)-2-C9H18
beta-cis-Nonene
UNII-UME13MDO8T
.BETA.-CIS-NONENE
DTXSID801025641
MFCD00067492
DB-220273
Q27291145
InChI=1/C9H18/c1-3-5-7-9-8-6-4-2/h3,5H,4,6-9H2,1-2H3/b5-3
Microorganism:

Yes

IUPAC name(Z)-non-2-ene
SMILESCCCCCCC=CC
InchiInChI=1S/C9H18/c1-3-5-7-9-8-6-4-2/h3,5H,4,6-9H2,1-2H3/b5-3-
FormulaC9H18
PubChem ID5364455
Molweight126.24
LogP4.8
Atoms9
Bonds5
H-bond Acceptor0
H-bond Donor0
Chemical Classificationalkenes unsaturated hydrocarbons

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaSaccharomyces CerevisiaeNANAHarris et al. 2021
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaSaccharomyces Cerevisiaemalt extract brothHS-SPME with GC-MSno


(E)-undec-2-ene

Compound Details

Synonymous names
2-Undecene, (E)-
(E)-2-Undecene
2-Undecene, (2E)-
trans-2-Undecene
2-Undecene
693-61-8
4JH4KV7M4K
28761-27-5
UNII-4JH4KV7M4K
HSDB 5176
2244-02-2
(2E)-2-Undecene
(2E)-2-Undecene #
UNII-FH2735S2NU
.BETA.-TRANS-UNDECENE
(E)- and (Z)-2-Undecene
FH2735S2NU
DTXSID10876612
EINECS 249-202-2
NSC158677
NSC-158677
Q27259757
Microorganism:

Yes

IUPAC name(E)-undec-2-ene
SMILESCCCCCCCCC=CC
InchiInChI=1S/C11H22/c1-3-5-7-9-11-10-8-6-4-2/h3,5H,4,6-11H2,1-2H3/b5-3+
FormulaC11H22
PubChem ID5364452
Molweight154.29
LogP5.9
Atoms11
Bonds7
H-bond Acceptor0
H-bond Donor0
Chemical Classificationalkenes unsaturated hydrocarbons
Supernatural-IDSN0170818-01

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaSaccharomyces CerevisiaeNANAHarris et al. 2021
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaSaccharomyces Cerevisiaemalt extract brothHS-SPME with GC-MSno


(Z)-dec-2-ene

Compound Details

Synonymous names
cis-2-Decene
20348-51-0
(Z)-dec-2-ene
(Z)-2-Decene
2-Decene, (Z)-
(2Z)-2-Decene
(2Z)-2-Decene #
DTXSID50891925
MFCD00048946
NSC102790
(Z)-C10H20
NSC-102790
CS-0449480
D2161
T70533
J-013232
Microorganism:

Yes

IUPAC name(Z)-dec-2-ene
SMILESCCCCCCCC=CC
InchiInChI=1S/C10H20/c1-3-5-7-9-10-8-6-4-2/h3,5H,4,6-10H2,1-2H3/b5-3-
FormulaC10H20
PubChem ID5364451
Molweight140.27
LogP5.4
Atoms10
Bonds6
H-bond Acceptor0
H-bond Donor0
Chemical Classificationalkenes unsaturated hydrocarbons

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaSaccharomyces CerevisiaeNANAHarris et al. 2021
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaSaccharomyces Cerevisiaemalt extract brothHS-SPME with GC-MSno


(E)-dodec-4-ene

Mass-Spectra

Compound Details

Synonymous names
4-Dodecene
trans-4-dodecene
4-Dodecene, (E)-
(E)-dodec-4-ene
2030-84-4
(4E)-4-Dodecene
(E)-4-Dodecene
7206-15-7
DTXSID80880822
PHCKFVVLVZFFLU-VQHVLOKHSA-N
NS00095967
Microorganism:

No

IUPAC name(E)-dodec-4-ene
SMILESCCCCCCCC=CCCC
InchiInChI=1S/C12H24/c1-3-5-7-9-11-12-10-8-6-4-2/h7,9H,3-6,8,10-12H2,1-2H3/b9-7+
FormulaC12H24
PubChem ID5364443
Molweight168.32
LogP5.8
Atoms12
Bonds8
H-bond Acceptor0
H-bond Donor0
Chemical Classificationalkenes unsaturated hydrocarbons

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaPsychrotrophic Bacterian/aBeef muscles (Longissiumus dorsi) from a slaughterhouseErcolini et al. 2009
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaPsychrotrophic Bacteriatryptic soy brothChemical analyses were performed after 0, 15, and 30 days of storage. A headspace (HS) solid-phase microextraction (SPME) analysis by GC/MS was carried out on 5 g of meat from the chopped samples.no