Results for:
chemical Classification: Epoxide

Compound Details

Synonymous names
Oxirane
ETHYLENE OXIDE
75-21-8
Epoxyethane
1,2-Epoxyethane
Oxacyclopropane
Dihydrooxirene
Oxidoethane
Oxyfume
Ethene oxide
Dimethylene oxide
Amprolene
Anprolene
Anproline
Aethylenoxid
1,2-Epoxyaethan
Merpol
Oxiran
Oxyfume 12
T-Gas
Oxirene, Dihydro-
Ethyleenoxide
Oxiraan
Ethox
Etylenu tlenek
FEMA No. 2433
oxyde d'ethylene
Rcra waste number U115
Caswell No. 443
Qazi-ketcham
ETO
NCI-C50088
Etilene (ossido di)
alpha,beta-Oxidoethane
CCRIS 297
Ethylene (oxyde d')
ENT-26263
ethyleneoxy
HSDB 170
UN 1040
CHEBI:27561
Oxiranyl radical
UNII-JJH7GNN18P
JJH7GNN18P
EINECS 200-849-9
EPA Pesticide Chemical Code 042301
E.O.
AI3-26263
CIBA-GEIGY 9138
DTXSID0020600
EC 200-849-9
epoxide or oxirane
Sterilizing gas ethylene oxide 100%
Oxirane; Ethylene oxide
Oxiraan [Dutch]
ETHYLENE OXIDE (IARC)
ETHYLENE OXIDE [IARC]
ETHYLENE OXIDE (MART.)
ETHYLENE OXIDE [MART.]
Aethylenoxid [German]
Ethyleenoxide [Dutch]
ethyleneoxide
ethylenoxide
Etylenu tlenek [Polish]
Oxide, Ethylene
1,2-Epoxyaethan [German]
1,2-Epoxy ethane
Ethylene (oxyde d') [French]
Ethylene Oxide 1000 microg/mL in Triacetin
Etilene (ossido di) [Italian]
UN1040
RCRA waste no. U115
monooxirane
Oxiranyl
ethylene-oxide
epoxy ethane
Caswell no 443
Fema no 2433
Epitope ID:116215
.alpha.,.beta.-Oxidoethane
ETHYLENE OXIDE [MI]
DTXCID60600
ETHYLENE OXIDE [FHFI]
ETHYLENE OXIDE [HSDB]
Ethylene oxide, >=99.5%
Ethylene oxide, >=99.9%
ALPHA, BETA-OXIDOETHANE
CHEMBL1743219
ETHYLENE OXIDE [WHO-DD]
DTXSID30185475
Ethylene oxide, purum, >=99.8%
c0527
MFCD00014482
AKOS009031564
USEPA/OPP Pesticide Code: 042301
E0647
E0689
E0690
E0692
E0693
InChI=1/C2H4O/c1-2-3-1/h1-2H
NS00005032
C06548
D03474
Q407473
Ethylene oxide 50000 microg/mL in Dichloromethane
Ethylene oxide 10000 microg/mL in Dimethylsulfoxide
E O
Ethylene oxide, or ethlene oxide with nitrogen up to a total pressure of 1Mpa (10 bar) at 50 degrees C
Ethylene oxide, or ethlene oxide with nitrogen up to a total pressure of 1Mpa (10 bar) at 50 degrees C [UN1040] [Poison gas]
Microorganism:

Yes

IUPAC nameoxirane
SMILESC1CO1
InchiInChI=1S/C2H4O/c1-2-3-1/h1-2H2
FormulaC2H4O
PubChem ID6354
Molweight44.05
LogP-0.1
Atoms3
Bonds0
H-bond Acceptor1
H-bond Donor0
Chemical Classificationcyclic ethers epoxides heterocyclic compounds ethers
CHEBI-ID27561
Supernatural-IDSN0140791

mVOC Specific Details

Boiling Point
DegreeReference
10.6 °C peer reviewed
Volatilization
The Henry's Law constant for ethylene oxide is 1.48X10-4 atm-cu m/mole(1). This Henry's Law constant indicates that ethylene oxide 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 6 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 4 days(SRC). Ethylene oxide is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 1.31X10+3 mm Hg(3). Although no data on the volatilization of ethylene oxide from soil could be found, a study of the dissipation of ethylene oxide from fumigated commodities gave half-life values of 4 hr to 17.5 days(4).
Literature: (1) Conway RA et al; Environ Sci Technol 17:107-112 (1983) (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 (1985) (4) Bogyo DA et al; Investigations of Selected Potential Environmental Contaminants: Epoxides. USEPA-560/11-80-005 p. 70-90 (1980)
Soil Adsorption
Koc of ethylene oxide was reported to be 2.20(1). According to a classification scheme(2), this estimated Koc value suggests that ethylene oxide is expected to have very high mobility in soil(SRC).
Literature: (1) Chu W, Chan KH; Sci Total Environ 248: 1-10 (2000) (2) Swann RL et al; Res Rev 85: 17-28 (1983)
Vapor Pressure
PressureReference
1,310 mm Hg at 25 deg C (extrapolated)Daubert, T.E., R.P. Danner. Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, D.C.: Taylor and Francis, 1989.
Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaBacillus Toyonensisisolate from Irish potato soilsHeenan-Daly et al. 2021
EukaryotaPleurotus Ostreatusnawidespread in many temperate and subtropical forests throughout the world, saprobeLo Cantore et al. 2015
MicrobacteriumBallot et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaBacillus ToyonensisTSB mediaSPME/GC-MSno
EukaryotaPleurotus OstreatusMEASPME-GCno
Microbacteriumtryptone soy (TS medium; Carl Roth, Karlsruhe, Germany)GC-QQQ-MSno


2-(methoxymethyl)oxirane

Compound Details

Synonymous names
Glycidyl methyl ether
2-(Methoxymethyl)oxirane
930-37-0
Methyl glycidyl ether
Oxirane, (methoxymethyl)-
1,2-EPOXY-3-METHOXYPROPANE
Glycidol methyl ether
(Methoxymethyl)oxirane
Methylglycidyl ether
3-Methoxypropylene oxide
3-Methoxy-1,2-epoxypropane
Denacol EX-131
Propane, 1,2-epoxy-3-methoxy-
2,3-Epoxypropyl-methyl ether
NSC 86950
Oxirane, 2-(methoxymethyl)-
87MK2KA66T
MFCD00005140
NSC-86950
glycidylmethylether
28325-89-5
CCRIS 2630
HSDB 5444
EINECS 213-216-7
BRN 0102505
UNII-87MK2KA66T
AI3-52869
2-methoxymethyl-oxirane
EPIOL M
2-(Methoxymethyl)oxirane #
Propane,2-epoxy-3-methoxy-
DTXSID9025613
LKMJVFRMDSNFRT-UHFFFAOYSA-
NSC86950
(R)-(-)-2-(Methoxymethyl)oxirane
GEO-04527
STL287735
(+/-)-GLYCIDYL METHYL ETHER
AKOS000138368
AKOS016037121
SY053022
1,2-EPOXY-3-METHOXYPROPANE [HSDB]
DB-054672
DB-054673
AM20120337
G0203
NS00039519
EN300-73694
F11173
Methyl glycidyl ether 1,2-Epoxy-3-methoxypropane
Q27269834
InChI=1/C4H8O2/c1-5-2-4-3-6-4/h4H,2-3H2,1H3
(S)-(+)-2-(Methoxymethyl)oxirane;(S)-(+)-Methyl glycidyl ether
Microorganism:

Yes

IUPAC name2-(methoxymethyl)oxirane
SMILESCOCC1CO1
InchiInChI=1S/C4H8O2/c1-5-2-4-3-6-4/h4H,2-3H2,1H3
FormulaC4H8O2
PubChem ID13589
Molweight88.11
LogP-0.2
Atoms6
Bonds2
H-bond Acceptor2
H-bond Donor0
Chemical Classificationethers epoxides

mVOC Specific Details


Species emitting the compound
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
Bacillus Thuringiensisbacteriological agar (BA, 15 g/L), gelatin peptone (GP, 5 g/L), and meat extract (ME, 3 g/L)GC–MSno
Bacillus Toyonensisbacteriological agar (BA, 15 g/L), gelatin peptone (GP, 5 g/L), and meat extract (ME, 3 g/L)GC–MSno


2-decyloxirane

Compound Details

Synonymous names
1,2-EPOXYDODECANE
2855-19-8
2-Decyloxirane
1-Dodecene oxide
Oxirane, decyl-
Decyloxirane
Decyl oxirane
Dodecene epoxide
Dodecane, 1,2-epoxy-
Nedox 1200
Oxirane, 2-decyl-
1,2-Dodecane oxide
1,2-Dodecene oxide
1,2-Epoxy-n-dodecene
1,2-Epoxy-N-dodecane
1,2-Dodecylene Oxide
1,2-Epoxydodekan
alpha-Dodecene oxide
NSC 6785
CCRIS 2616
HSDB 5538
2-decyl-oxirane
EINECS 220-667-3
1-Dodecene Epoxide
BRN 0105569
DTXSID9025243
UNII-736974CF3U
AI3-14199
NSC-6785
2-N-DECYLOXIRANE
736974CF3U
(+/-)-DECYLOXIRANE
1,2-DODECENE EPOXIDE
DTXCID305243
EC 220-667-3
5-17-01-00166 (Beilstein Handbook Reference)
(+/-)-1,2-EPOXYDODECANE
MFCD00005150
Dodecane, epoxy-
1,2-Epoxydodekan [Czech]
2-Decyloxirane #
Dodecane,2-epoxy-
2-(decyl)-oxirane
VIKOLOX 12
(+-)-DECYLOXIRANE
1,2-Epoxydodecane, 90%
1,2-Epoxydodecane, 95%
SCHEMBL52008
WLN: T3OTJ B10
.ALPHA.-DODECENE OXIDE
CHEMBL3183029
NSC6785
(+-)-1,2-EPOXYDODECANE
Tox21_301660
BBL027500
OXIRANE, DECYL-, (+-)-
STL373430
AKOS015903513
MCULE-4819613479
NCGC00255147-01
BP-26278
SY049817
VS-08556
CAS-2855-19-8
DB-059944
CS-0152245
D1984
NS00002778
D89968
EN300-342618
J-640003
J-800003
W-109829
Q27266143
Z1255485282
Microorganism:

Yes

IUPAC name2-decyloxirane
SMILESCCCCCCCCCCC1CO1
InchiInChI=1S/C12H24O/c1-2-3-4-5-6-7-8-9-10-12-11-13-12/h12H,2-11H2,1H3
FormulaC12H24O
PubChem ID17858
Molweight184.32
LogP5.2
Atoms13
Bonds9
H-bond Acceptor1
H-bond Donor0
Chemical Classificationethers epoxides heterocyclic compounds

mVOC Specific Details

Boiling Point
DegreeReference
123.88888888888889 median, REST, convertet to C

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaPseudomonas Fluorescens0Medicago spp. plant rhizospheresHernández-León et al. 2015
ProkaryotaPseudomonas Sp.antifungal activity against Thielaviopsis ethacetica mycelial growthBrazilian Biorenewables National Laboratory – LNBR/CNPEM Microorganism Collection, Campinas, SP; isolatedfrom soil and roots of highly productive sugarcane-producing regions; BrazilFreitas et al. 2022
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaPseudomonas FluorescensNutrient AgarSPME-GC-MSno
ProkaryotaPseudomonas Sp.LB mediaHS-SPME/GC-MSno


2-hexyloxirane

Compound Details

Synonymous names
1,2-EPOXYOCTANE
2984-50-1
2-Hexyloxirane
Hexyloxirane
1-Octene oxide
Oxirane, hexyl-
Octylene epoxide
1-Octene epoxide
Octane 1,2-oxide
Octene-1,2-oxide
1,2-Epoxy-n-octane
n-Octene-1,2-oxide
Octane, 1,2-epoxy-
Epoxyoctane
Oktylenoxid
1,2-Octylene oxide
1,2-Epoxyoktan
2-hexyl-oxirane
NSC 24246
.alpha.-Epoxyoctane
1,2-Epoxyoctane purum
alpha-Epoxyoctane
26637-94-5
Oktylenoxid [Czech]
1,2-Epoxyoktan [Czech]
Octane, epoxy-
CCRIS 3797
EINECS 221-047-5
BRN 0079912
octene oxide
n-Hexyloxirane
AI3-14197
1,2 epoxyoctane
Octane,2-epoxy-
1,2-epoxy octane
1,2-epoxy-octane
1,2-Epoxyoctane, 96%
WLN: T3OTJ B6
SCHEMBL39393
5-17-01-00138 (Beilstein Handbook Reference)
NJWSNNWLBMSXQR-UHFFFAOYSA-
DTXSID301031190
NSC24246
BBL027501
MFCD00005157
NSC-24246
STL373784
AKOS009158672
MCULE-5253323325
AS-48232
BP-26283
PD193090
CS-0152296
E0206
NS00048797
1,2-Epoxyoctane, purum, >=95.0% (GC)
EN300-157817
F20386
J-640005
J-640383
J-660062
J-800005
Z1020680070
InChI=1/C8H16O/c1-2-3-4-5-6-8-7-9-8/h8H,2-7H2,1H3
Microorganism:

Yes

IUPAC name2-hexyloxirane
SMILESCCCCCCC1CO1
InchiInChI=1S/C8H16O/c1-2-3-4-5-6-8-7-9-8/h8H,2-7H2,1H3
FormulaC8H16O
PubChem ID18126
Molweight128.21
LogP3
Atoms9
Bonds5
H-bond Acceptor1
H-bond Donor0
Chemical Classificationepoxides heterocyclic compounds ethers

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaStreptomyces ThermocarboxydusNANAPassari et al. 2019
ProkaryotaLactobacillus PlantarumNANAZhang et al. 2022
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaStreptomyces Thermocarboxydusactinomycetes isolation agar (AIA)GC-MSno
ProkaryotaLactobacillus Plantarumchickpea milkUHPLC/MSno


2,3-dimethyloxirane

Compound Details

Synonymous names
2,3-Epoxybutane
2,3-Dimethyloxirane
3266-23-7
2-Butene oxide
Oxirane, 2,3-dimethyl-
2,3-BUTYLENE OXIDE
Butane, 2,3-epoxy-
beta-Oxybutene
2-Butene expoxide
beta-Butylene oxide
2,3-Dimethyloxirane cis+trans
meso-2,3-Epoxybutane
(z)-2,3-epoxybutane
CCRIS 6033
2,3-Dimethyl-oxirane (Z)
EINECS 221-877-8
Pseudobutylene Oxide
Oxirane, 2,3-dimethyl-, (2R,3R)-rel-
(e)-2,3-epoxybutane
EC 221-877-8
Butane, 2,3-epoxy, trans-
DTXSID5025239
MFCD00137387
AKOS015899847
8-ACETAMIDONAPHTHALEN-2-YLACETATE
SY224137
B0720
NS00002698
EN300-96226
A821360
2,3-Dimethyloxirane, cis+trans, >=97.0% (GC)
J-018826
Q58824552
63864-69-7
Microorganism:

Yes

IUPAC name2,3-dimethyloxirane
SMILESCC1C(O1)C
InchiInChI=1S/C4H8O/c1-3-4(2)5-3/h3-4H,1-2H3
FormulaC4H8O
PubChem ID18632
Molweight72.11
LogP0.7
Atoms5
Bonds0
H-bond Acceptor1
H-bond Donor0
Chemical Classificationepoxides heterocyclic compounds ethers

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaSaccharomyces CerevisiaeNANAHarris et al. 2021
Meyerozyma GuilliermondiiXiong et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaSaccharomyces Cerevisiaemalt extract brothHS-SPME with GC-MSno
Meyerozyma GuilliermondiiYEPD, 10 g/L yeast extrac, 20 g/L peptone, 20 g dextroseGC-MS and GC-IMSno


1-(3-methyloxiran-2-yl)ethanone

Compound Details

Synonymous names
17257-79-3
1-(3-methyloxiran-2-yl)ethanone
3,4-epoxy-2-pentanone
2-Pentanone, 3,4-epoxy-
2beta-Acetyl-3alpha-methyloxirane
Ethanone, 1-(3-methyloxiranyl)-
1-(3-METHYLOXIRANYL)ETHANONE
SCHEMBL11881829
DTXSID60938173
IAHUKWSQLBRAIN-UHFFFAOYSA-N
1-(3-methyloxiran-2-yl)ethan-1-one
3,4-Anhydro-1,5-dideoxypent-2-ulose
3,4-Anhydro-1,5-dideoxypent-2-ulose #
Microorganism:

Yes

IUPAC name1-(3-methyloxiran-2-yl)ethanone
SMILESCC1C(O1)C(=O)C
InchiInChI=1S/C5H8O2/c1-3(6)5-4(2)7-5/h4-5H,1-2H3
FormulaC5H8O2
PubChem ID28429
Molweight100.12
LogP0.1
Atoms7
Bonds1
H-bond Acceptor2
H-bond Donor0
Chemical Classificationepoxides heterocyclic compounds ketones ethers

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaBacillus PumilusNAMülner et al. 2020
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaBacillus Pumilusnutrient agarHS-SPME/GC-MSno


4-(2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl)but-3-en-2-one

Compound Details

Synonymous names
3-Buten-2-one, 4-(2,2,6-trimethyl-7-oxabicyclo[4.1.0]hept-1-yl)-
3-Buten-2-one, 4-(2,2,6-trimethyl-7-oxabicyclo(4.1.0)hept-1-yl)-
beta-ionone 5,6-epoxide
EINECS 245-542-0
5,6-beta-Ionone epoxide
DTXSID8051885
4-(1,2-Epoxy-2,6,6-trimethylcyclohexyl)-3-butenone-2
WLZ3135
ZTJZJYUGOJYHCU-UHFFFAOYSA-N
DB-282879
NS00013296
Q27159719
4-(2,6,6-trimethyl-1,2-epoxycyclohexyl)-3-buten-2-one
Microorganism:

Yes

IUPAC name4-(2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl)but-3-en-2-one
SMILESCC(=O)C=CC12C(CCCC1(O2)C)(C)C
InchiInChI=1S/C13H20O2/c1-10(14)6-9-13-11(2,3)7-5-8-12(13,4)15-13/h6,9H,5,7-8H2,1-4H3
FormulaC13H20O2
PubChem ID90899
Molweight208.3
LogP2
Atoms15
Bonds2
H-bond Acceptor2
H-bond Donor0
Chemical Classificationheterocyclic compounds epoxides ketones ethers terpenes
CHEBI-ID87546
Supernatural-IDSN0479774

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaCytophaga-Flavobacterium-Bacteroidesn/aNADickschat et al. 2005_3
ProkaryotaCalothrix Sp.n/aNASchulz and Dickschat 2007
ProkaryotaPlectonema Sp.n/aNASchulz and Dickschat 2007
ProkaryotaPhormidium Sp.n/aNASchulz and Dickschat 2007
ProkaryotaSpirulina Platensisn/aNASchulz and Dickschat 2007
ProkaryotaCytophaga-Flavobacteria-Bacteroides Groupn/aNASchulz and Dickschat 2007
ProkaryotaCyanobacteria Sp.n/aNAHoeckelmann et al. 2004
ProkaryotaCalothrix Parietinan/aNAHoeckelmann et al. 2004
ProkaryotaCalothrix Sp.n/aNAHoeckelmann et al. 2004
ProkaryotaPlectonema Notatumn/aNAHoeckelmann et al. 2004
ProkaryotaPlectonema Sp.n/aNAHoeckelmann et al. 2004
ProkaryotaTolypothrix Distortan/aNAHoeckelmann et al. 2004
ProkaryotaRivularia Sp.n/aNAHoeckelmann et al. 2004
ProkaryotaRivularia Sp./Calothrix Parietinan/aNAHoeckelmann et al. 2004
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaCytophaga-Flavobacterium-Bacteroidesn/an/ano
ProkaryotaCalothrix Sp.n/an/ano
ProkaryotaPlectonema Sp.n/an/ano
ProkaryotaPhormidium Sp.n/an/ano
ProkaryotaSpirulina Platensisn/an/ano
ProkaryotaCytophaga-Flavobacteria-Bacteroides Groupn/an/ano
ProkaryotaCyanobacteria Sp.n/an/ano
ProkaryotaCalothrix Parietinan/an/ano
ProkaryotaPlectonema Notatumn/an/ano
ProkaryotaTolypothrix Distortan/an/ano
ProkaryotaRivularia Sp.n/an/ano
ProkaryotaRivularia Sp./Calothrix Parietinan/an/ano


1-methyl-4-prop-1-en-2-yl-7-oxabicyclo[4.1.0]heptane

Mass-Spectra

Compound Details

Synonymous names
Limonene oxide
1195-92-2
Limonene epoxide
Limonene 1,2-epoxide
Limonene monoxide
1-methyl-4-(prop-1-en-2-yl)-7-oxabicyclo[4.1.0]heptane
Limonene 1,2-oxide
1,2-Epoxylimonene
1,2-Epoxy-p-menth-8-ene
7-Oxabicyclo[4.1.0]heptane, 1-methyl-4-(1-methylethenyl)-
p-Menth-8-ene, 1,2-epoxy-
4-Isopropenyl-1-methyl-7-oxabicyclo[4.1.0]heptane
1-methyl-4-prop-1-en-2-yl-7-oxabicyclo[4.1.0]heptane
CHEBI:16431
NSC12045
1-Methyl-4-(1-methylvinyl)-7-oxabicyclo(4.1.0)heptane
7-Oxabicyclo(4.1.0)heptane, 1-methyl-4-(1-methylethenyl)-
CCRIS 3763
EINECS 214-805-1
NSC 12045
AI3-24998
Limonene 1, 2-oxide
1-Methyl-4-(1-methylethenyl)-7-oxabicyclo(4.1.0)heptane
a limonene-1,2-epoxide
a 1,2-epoxymenth-8-ene
p-Menth-8-ene,2-epoxy-
SCHEMBL93297
3-isopropenyl-6-methyl-7-oxabicyclo[4.1.0]heptane
CHEMBL2268547
DTXSID50862594
13837-75-7
7-Oxabicyclo[4.1.0]heptane, 1-methyl-4-(1-methylethenyl)-, [1S-(1.alpha.,4.alpha.,6.alpha.)]-
BBL027497
MFCD00005127
MFCD00074770
NSC-12045
STK801933
AKOS006228851
MCULE-4064327350
SB44781
SY257451
VS-08553
DB-061578
CS-0442167
NS00041597
E83861
EN300-322402
(+)-LIMONENE OXIDE 97% MIXTURE OF CIS&
J-504945
Q27101901
Z1198147214
1-Methyl-4-(prop-1-en-2-yl)-7-oxa-bicyclo[4.1.0]Heptane
{7-Oxabicyclo[4.1.0]heptane,} 1-methyl-4-(1-methylethenyl)-
1-Methyl-4-(1-methylethenyl)-7-oxabicyclo[4.1.0]heptane, 9CI
4-isopropenyl-1-methyl-7-oxa-bicyclo[4.1.0]heptane, AldrichCPR
1-METHYL-4-(PROP-1-EN-2-YL)-7-OXABICYCLO[4.1.0]HEPTANE(TBC AS STABILIZER)
Microorganism:

Yes

IUPAC name1-methyl-4-prop-1-en-2-yl-7-oxabicyclo[4.1.0]heptane
SMILESCC(=C)C1CCC2(C(C1)O2)C
InchiInChI=1S/C10H16O/c1-7(2)8-4-5-10(3)9(6-8)11-10/h8-9H,1,4-6H2,2-3H3
FormulaC10H16O
PubChem ID91496
Molweight152.23
LogP2.5
Atoms11
Bonds1
H-bond Acceptor1
H-bond Donor0
Chemical Classificationethers heterocyclic compounds epoxides oxides terpenes
CHEBI-ID35672
Supernatural-IDSN0041737

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


2,7,7-trimethyl-3-oxatricyclo[4.1.1.02,4]octane

Mass-Spectra

Compound Details

Synonymous names
alpha-Pinene oxide
2,3-Epoxypinane
1686-14-2
alpha-Pinene epoxide
2-Pinene oxide
Pinane, 2,3-epoxy-
Pinene oxide
alpha-Pineneoxide
.alpha.-Pinene oxide
.alpha.-Pinene epoxide
3-Oxatricyclo[4.1.1.02,4]octane, 2,7,7-trimethyl-
2,7,7-Trimethyl-3-oxatricyclo[4.1.1.02,4]octane
Pinane, 2,3-epoxy-, (-)-
2,3-Epoxy-pinane
alpha-Pinene 2,3-oxide
CHEBI:29060
Pinane,3-epoxy-
NSC12148
3-Oxatricyclo[4.1.1.0(2,4)]octane, 2,7,7-trimethyl-
Pinane,3-epoxy-, (-)-
2,7,7-Trimethyl-3-oxatricyclo(4.1.1.02,4)octane
2,7,7-trimethyl-3-oxatricyclo[4.1.1.0(2,4)]octane
3-Oxatricyclo(4.1.1.02,4)octane, 2,7,7-trimethyl-
a-Pinene Oxide
CCRIS 3762
3-Oxatricyclo[4.1.1.02, 2,7,7-trimethyl-
NSC 5609
EINECS 216-869-6
NSC 12148
BRN 0080362
Alpha-pinane oxide
I+/--Pinene oxide
2,7,7-Trimethyl-3-oxatricyclo(4.1.1.0(sup 2,4))octane
?-PINENE OXIDE
3-Oxatricyclo(4.1.1.0(sup 2,4))octane, 2,7,7-trimethyl-
bmse000491
.alpha.-Pinene 2,3-oxide
SCHEMBL93429
5-17-01-00426 (Beilstein Handbook Reference)
218308_ALDRICH
CHEMBL274511
DTXSID5051781
NSC5609
NSC-5609
NSC-12148
NSC407160
AKOS015916312
HY-W130074
MCULE-1107037130
NSC-407160
AS-68305
CS-0188178
NS00123845
P1362
D97335
W-109695
Q27104051
2,7,7-Trimethyl-3-oxatricyclo[4.1.1.0~2,4~]octane
{3-Oxatricyclo[4.1.1.02,4]octane,} 2,7,7-trimethyl-
2,7,7-TRIMETHYL-3-OXATRICYCLO[4.1.1.0(2),?]OCTANE
Microorganism:

No

IUPAC name2,7,7-trimethyl-3-oxatricyclo[4.1.1.02,4]octane
SMILESCC1(C2CC1C3(C(C2)O3)C)C
InchiInChI=1S/C10H16O/c1-9(2)6-4-7(9)10(3)8(5-6)11-10/h6-8H,4-5H2,1-3H3
FormulaC10H16O
PubChem ID91508
Molweight152.23
LogP2.1
Atoms11
Bonds0
H-bond Acceptor1
H-bond Donor0
Chemical Classificationheterocyclic compounds epoxides oxides ethers terpenes
CHEBI-ID29060
Supernatural-IDSN0252360

mVOC Specific Details

Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaGanoderma Lucidumnasaprophytic on deciduous treesCampos Ziegenbein et al. 2006
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaGanoderma LucidumnaGC/MSno


2-pentyloxirane

Compound Details

Synonymous names
1,2-Epoxyheptane
5063-65-0
2-Pentyloxirane
Pentyloxirane
1-Heptene oxide
1,2-Heptylene Oxide
Oxirane, pentyl-
Heptene 1,2-oxide
Heptane, 1,2-epoxy-
Heptylene oxide
(R)-1,2-EPOXYHEPTANE
Heptane,2-epoxy-
2-Pentyloxirane #
NSC 24250
(+)-1,2-epoxyheptane
SCHEMBL50924
DTXSID30911736
NSC24250
MFCD00037521
NSC-24250
AKOS009157136
BS-22663
CS-0205209
E0312
T72538
EN300-1852162
InChI=1/C7H14O/c1-2-3-4-5-7-6-8-7/h7H,2-6H2,1H
Microorganism:

Yes

IUPAC name2-pentyloxirane
SMILESCCCCCC1CO1
InchiInChI=1S/C7H14O/c1-2-3-4-5-7-6-8-7/h7H,2-6H2,1H3
FormulaC7H14O
PubChem ID92215
Molweight114.19
LogP2.5
Atoms8
Bonds4
H-bond Acceptor1
H-bond Donor0
Chemical Classificationepoxides ethers heterocyclic compounds

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaLactobacillus PlantarumNANAZhang et al. 2022
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaLactobacillus Plantarumchickpea milkUHPLC/MSno


5,8,8-trimethyl-3-oxatricyclo[5.1.0.02,4]octane

Compound Details

Synonymous names
27867-36-3
PNJ58HM5VB
5,8,8-Trimethyl-3-oxatricyclo(5.1.0.02,4)octane
3-Oxatricyclo(5.1.0.02,4)octane, 5,8,8-trimethyl-
3-Oxatricyclo[5.1.0.02,4]octane, 5,8,8-trimethyl-
5,8,8-Trimethyl-3-oxatricyclo[5.1.0.0~2,4~]octane
5,8,8-TRIMETHYL-3-OXATRICYCLO[5.1.0.02,4]OCTANE
EINECS 248-701-2
car-4-ene oxide
UNII-PNJ58HM5VB
Carane, 4,5-epoxy-, trans
SCHEMBL10627107
DTXSID00950551
NS00049748
Microorganism:

Yes

IUPAC name5,8,8-trimethyl-3-oxatricyclo[5.1.0.02,4]octane
SMILESCC1CC2C(C2(C)C)C3C1O3
InchiInChI=1S/C10H16O/c1-5-4-6-7(10(6,2)3)9-8(5)11-9/h5-9H,4H2,1-3H3
FormulaC10H16O
PubChem ID119627
Molweight152.23
LogP2.4
Atoms11
Bonds0
H-bond Acceptor1
H-bond Donor0
Chemical Classificationepoxides ethers heterocyclic compounds

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


1-methyl-7-oxabicyclo[4.1.0]heptane

Compound Details

Synonymous names
1,2-Epoxy-1-methylcyclohexane
1713-33-3
1-Methyl-7-oxabicyclo[4.1.0]heptane
1-Methyl-1,2-epoxycyclohexane
1-Methylcyclohexene oxide
1,2-epoxy-1-methyl-cyclohexane
1-Methylepoxycyclohexane
1-Methylcyclohexene epoxide
7-Oxabicyclo[4.1.0]heptane, 1-methyl-
1-Methylcyclohexene 1,2-oxide
1-Methyl-1,2-cyclohexene oxide
MFCD11846121
7-Oxabicyclo[4.1.0]heptane, methyl-
NSC-12597
SCHEMBL1262673
DTXSID20873233
NSC12597
1-methyl-7-oxabicyclo[4.1.0]heptan
AKOS024015279
PB48889
BS-52385
SY054336
1-Methyl-7-oxabicyclo[4.1.0]heptane #
DB-238286
CS-0152704
M1983
EN300-86196
T71914
J-640018
J-800019
Z1255380027
Microorganism:

Yes

IUPAC name1-methyl-7-oxabicyclo[4.1.0]heptane
SMILESCC12CCCCC1O2
InchiInChI=1S/C7H12O/c1-7-5-3-2-4-6(7)8-7/h6H,2-5H2,1H3
FormulaC7H12O
PubChem ID224243
Molweight112.17
LogP1.4
Atoms8
Bonds0
H-bond Acceptor1
H-bond Donor0
Chemical Classificationepoxides ethers heterocyclic compounds

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


1-methyl-4-(2-methyloxiran-2-yl)-7-oxabicyclo[4.1.0]heptane

Compound Details

Synonymous names
Limonene dioxide
96-08-2
Limonene diepoxide
Dipentene dioxide
1-Methyl-4-(2-methyloxiran-2-yl)-7-oxabicyclo[4.1.0]heptane
Dipentene oxide
Dipentene diepoxide
Unox 269
Unox epoxide 269
Epoxide 269
Unoxat epoxide 269
1,2,8,9-Diepoxylimonene
p-Menthane, 1,2:8,9-diepoxy-
diepoxylimonene
Menthane, 1,2:8,9-diepoxy-
.alpha.-Limonene diepoxide
1,2:8,9-DIEPOXY-P-MENTHANE
1-METHYL-4-(2-METHYLOXIRANYL)-7-OXABICYCLO[4.1.0]HEPTANE
NSC 30545
M6TUW5WEJ9
MLS002639331
1-Methyl-4-(2-methyloxiranyl)-7-oxabicyclo(4.1.0)heptane
7-Oxabicyclo[4.1.0]heptane, 1-methyl-4-(2-methyloxiranyl)-
NSC-30545
NSC-54753
1,9-Diepoxylimonene
7-Oxabicyclo(4.1.0)heptane, 1-methyl-4-(2-methyloxiranyl)-
1,9-Diepoxy-p-menthane
4-(1,2-Epoxy-1-methylethyl)-1-methyl-7-oxabicyclo(4.1.0)heptane
7-Oxabicyclo(4.1.0)heptane, 4-(1,2-epoxy-1-methylethyl)-1-methyl-
Menthane,2:8,9-diepoxy-
p-Menthane,2:8,9-diepoxy-
7-Oxabicyclo(4.1.0)heptane, 1-methyl-4-(2-methyl-2-oxiranyl)-
WLN: T36 BOTJ A1 E- BT3OTJ B1
UNII-M6TUW5WEJ9
7-Oxabicyclo[4.1.0]heptane,2-epoxy-1-methylethyl)-1-methyl-
4-(1,2-Epoxy-1-methylethyl)-1-methyl-7-oxabicyclo[4.1.0]heptane
HSDB 5298
6-methyl-3-(2-methyloxiran-2-yl)-7-oxabicyclo[4.1.0]heptane
EINECS 202-475-1
BRN 0107989
AI3-26044
1,2:8,9-Diepoxylimonene
5-19-01-00324 (Beilstein Handbook Reference)
SCHEMBL215026
( not+/-)-Limonene diepoxide
1,2,8,9-diepoxy-p-menthane
CHEMBL1880461
NSC30545
NSC54753
AKOS006272591
LIMONENE 1,2:8,9-DIEPOXIDE
MCULE-8018911665
NCI60_002581
SMR001548776
DB-301487
1,2:8,9-DIEPOXY-P-MENTHANE [HSDB]
Q27283565
1,2-EPOXY-4-(2-METHYLOXIRANYL)-1-METHYLCYCLOHEXANE
1,2-EPOXY-1-METHYL-4-(1-METHYLEPOXYETHYL)CYCLOHEXANE
1-Methyl-4-(2-methyl-2-oxiranyl)-7-oxabicyclo[4.1.0]heptane #
Microorganism:

Yes

IUPAC name1-methyl-4-(2-methyloxiran-2-yl)-7-oxabicyclo[4.1.0]heptane
SMILESCC12CCC(CC1O2)C3(CO3)C
InchiInChI=1S/C10H16O2/c1-9-4-3-7(5-8(9)12-9)10(2)6-11-10/h7-8H,3-6H2,1-2H3
FormulaC10H16O2
PubChem ID232703
Molweight168.23
LogP1.1
Atoms12
Bonds1
H-bond Acceptor2
H-bond Donor0
Chemical Classificationepoxides ethers heterocyclic compounds
Supernatural-IDSN0320750

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
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
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaPseudomonas Sp.LB mediaHS-SPME/GC-MSno


7-(furan-3-yl)-1,8,12,16,16-pentamethyl-3,6-dioxapentacyclo[9.8.0.02,4.02,8.012,17]nonadecane-5,15,19-trione

Compound Details

Synonymous names
KETODIHYDROGENDUNIN
10584-64-2
NSC309911
7-(furan-3-yl)-1,8,12,16,16-pentamethyl-3,6-dioxapentacyclo[9.8.0.02,4.02,8.012,17]nonadecane-5,15,19-trione
Ekeberin C1
DTXSID70316988
HUKMOJLAHVSCJE-UHFFFAOYSA-N
NSC-309911
16,17-Seco-24-nor-5.alpha.,13.alpha.,14.beta.,17.alpha.-chola-20,22-dien-16-oic acid, 14,15.beta.:21,23-diepoxy-17-hydroxy-4,4,8-trimethyl-3,7-dioxo-, .delta.-l
D-Homo-24-nor-17-oxachola-20,22-diene-3,7,16-trione, 14,15:21,23-diepoxy-4,4,8-trimethyl-, (5.alpha.,13.alpha.,14.beta.,15.beta.,17a.alpha.)-
1-(3-Furyl)-4b,7,7,10a,12a-pentamethyldecahydronaphtho[2,1-f]oxireno[2,3-d]isochromene-3,5,8(3ah,4bh,6H)-trione #
16,13.alpha.,14.beta.,17.alpha.-chola-20,22-dien-16-oic acid, 14,15.beta.:21,23-diepoxy-17-hydroxy-4,4,8-trimethyl-3,7-dioxo-, .delta.-lactone
D-Homo-24-nor-17-oxachola-20,7,16-trione, 14,15:21,23-diepoxy-4,4,8-trimethyl-, (5.alpha.,13.alpha.,14.beta.,15.beta.,17a.alpha.)-
Oxireno[c]phenanthro[1,2-d]pyran-3,5,8(3aH,4bH,6H)-one, 1-(3-furanyl)decahydro-4b,7,7,10a,12a-pentamethyl-, (1S,3aS,4aR,4bR,6aR,10aS,10bR,12aS)-
Microorganism:

Yes

IUPAC name7-(furan-3-yl)-1,8,12,16,16-pentamethyl-3,6-dioxapentacyclo[9.8.0.02,4.02,8.012,17]nonadecane-5,15,19-trione
SMILESCC1(C2CC(=O)C3(C(C2(CCC1=O)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C
InchiInChI=1S/C26H32O6/c1-22(2)16-12-18(28)25(5)15(23(16,3)9-7-17(22)27)6-10-24(4)19(14-8-11-30-13-14)31-21(29)20-26(24,25)32-20/h8,11,13,15-16,19-20H,6-7,9-10,12H2,
FormulaC26H32O6
PubChem ID328941
Molweight440.5
LogP3.1
Atoms32
Bonds1
H-bond Acceptor6
H-bond Donor0
Chemical Classificationaromatic compounds epoxides esters ethers furan derivatives heterocyclic compounds ketones terpenes
Supernatural-IDSN0135731

mVOC Specific Details


Species emitting the compound
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
Aspergillus Flavusinoculated potato samplesGC-MSno
Aspergillus Nigerinoculated potato samplesGC-MSno
Pectobacterium Carotovoruminoculated potato samplesGC-MSno


2,7,7,10-tetramethyl-3-oxatetracyclo[7.3.0.02,4.06,8]dodecane

Compound Details

Synonymous names
Isoaromadendrene epoxide
GLKQAHXBJLGAFT-UHFFFAOYSA-N
1,3b,6,6-Tetramethyldecahydro-1H-cyclopropa[7,8]azuleno[4,5-b]oxirene
Q67879937
1,3b,6,6-Tetramethyldecahydro-1H-cyclopropa[7,8]azuleno[4,5-b]oxirene #
Microorganism:

No

IUPAC name2,7,7,10-tetramethyl-3-oxatetracyclo[7.3.0.02,4.06,8]dodecane
SMILESCC1CCC2C1C3C(C3(C)C)CC4C2(O4)C
InchiInChI=1S/C15H24O/c1-8-5-6-9-12(8)13-10(14(13,2)3)7-11-15(9,4)16-11/h8-13H,5-7H2,1-4H3
FormulaC15H24O
PubChem ID534398
Molweight220.35
LogP3.8
Atoms16
Bonds0
H-bond Acceptor1
H-bond Donor0
Chemical Classificationepoxides ethers terpenes
Supernatural-IDSN0108848

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAspergillus FumigatusNANAHeddergott et al. 2014
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAspergillus FumigatusBrian FE supp.SPME/GC-MSno


3,7,7,10-tetramethyl-2-oxatetracyclo[7.3.0.01,3.06,8]dodecane

Mass-Spectra

Compound Details

Synonymous names
Ledene oxide-(I)
OZNHATCGPKOFBH-UHFFFAOYSA-N
1,4a,7,7-Tetramethyldecahydrocyclopropa[7,8]azuleno[3a,4-b]oxirene
1,4a,7,7-Tetramethyldecahydrocyclopropa[7,8]azuleno[3a,4-b]oxirene #
Microorganism:

No

IUPAC name3,7,7,10-tetramethyl-2-oxatetracyclo[7.3.0.01,3.06,8]dodecane
SMILESCC1CCC23C1C4C(C4(C)C)CCC2(O3)C
InchiInChI=1S/C15H24O/c1-9-5-8-15-11(9)12-10(13(12,2)3)6-7-14(15,4)16-15/h9-12H,5-8H2,1-4H3
FormulaC15H24O
PubChem ID534497
Molweight220.35
LogP3.5
Atoms16
Bonds0
H-bond Acceptor1
H-bond Donor0
Chemical Classificationepoxides ethers terpenes
Supernatural-IDSN0279342

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAspergillus FumigatusNANAHeddergott et al. 2014
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAspergillus FumigatusBrian FE supp.SPME/GC-MSno


3-methyl-7-oxabicyclo[4.1.0]heptane

Compound Details

Synonymous names
36099-51-1
4-METHYL-1,2-CYCLOHEXENE OXIDE
3-Methyl-7-oxabicyclo[4.1.0]heptane
MFCD09742280
4-METHYL-1,2-CYCLOHEXENEOXIDE
7-Oxabicyclo[4.1.0]heptane, 3-methyl-
4-Methyl-1,2-cyclohexene oxide, cis + trans
SCHEMBL716267
ULPDSNLBZMHGPI-UHFFFAOYSA-N
DTXSID501346737
AKOS000149212
AKOS017343173
AS-81457
3-Methyl-7-oxabicyclo[4.1.0]heptane #
4-Methyl-1,2-cyclohexene oxide,(cis+trans)
CS-0451652
Microorganism:

Yes

IUPAC name3-methyl-7-oxabicyclo[4.1.0]heptane
SMILESCC1CCC2C(C1)O2
InchiInChI=1S/C7H12O/c1-5-2-3-6-7(4-5)8-6/h5-7H,2-4H2,1H3
FormulaC7H12O
PubChem ID535184
Molweight112.17
LogP1.6
Atoms8
Bonds0
H-bond Acceptor1
H-bond Donor0
Chemical Classificationepoxides ethers heterocyclic compounds

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


(5-acetamido-7-oxabicyclo[4.1.0]heptan-2-yl) Acetate

Compound Details

Synonymous names
DBNRPIBPYDPKSJ-UHFFFAOYSA-N
5-(Acetylamino)-7-oxabicyclo[4.1.0]hept-2-yl acetate #
Cyclohexane, 1R-acetamido-2,3-cis-epoxy-4-trans-acetoxy-
Microorganism:

No

IUPAC name(5-acetamido-7-oxabicyclo[4.1.0]heptan-2-yl) acetate
SMILESCC(=O)NC1CCC(C2C1O2)OC(=O)C
InchiInChI=1S/C10H15NO4/c1-5(12)11-7-3-4-8(14-6(2)13)10-9(7)15-10/h7-10H,3-4H2,1-2H3,(H,11,12)
FormulaC10H15NO4
PubChem ID537213
Molweight213.23
LogP-0.2
Atoms15
Bonds3
H-bond Acceptor4
H-bond Donor1
Chemical Classificationamides epoxides esters heterocyclic compounds nitrogen compounds

mVOC Specific Details


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


2-nonyloxirane

Compound Details

Synonymous names
2-Nonyloxirane
1,2-Epoxyundecane
17322-97-3
1-undecene oxide
2-nonyl-oxirane
2-Nonyloxirane #
SCHEMBL50887
DTXSID90336986
AKOS015905873
Microorganism:

Yes

IUPAC name2-nonyloxirane
SMILESCCCCCCCCCC1CO1
InchiInChI=1S/C11H22O/c1-2-3-4-5-6-7-8-9-11-10-12-11/h11H,2-10H2,1H3
FormulaC11H22O
PubChem ID537737
Molweight170.29
LogP4.6
Atoms12
Bonds8
H-bond Acceptor1
H-bond Donor0
Chemical Classificationepoxides heterocyclic compounds oxides ethers

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaPseudomonas Veroniinarhizosphere of field-grown potato plantsHunziker et al. 2015
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaPseudomonas VeroniiLB mediumGC/MSyes


2-[12-(oxiran-2-yl)dodecyl]oxirane

Compound Details

Synonymous names
1,2-15,16-Diepoxyhexadecane
800375-27-3
1,12-Di(oxiran-2-yl)dodecane
2-[12-(oxiran-2-yl)dodecyl]oxirane
SCHEMBL20702046
KHOGZDMZNQXOFX-UHFFFAOYSA-N
DTXSID001015991
2-[12-(2-Oxiranyl)dodecyl]oxirane #
Microorganism:

Yes

IUPAC name2-[12-(oxiran-2-yl)dodecyl]oxirane
SMILESC1C(O1)CCCCCCCCCCCCC2CO2
InchiInChI=1S/C16H30O2/c1(3-5-7-9-11-15-13-17-15)2-4-6-8-10-12-16-14-18-16/h15-16H,1-14H2
FormulaC16H30O2
PubChem ID543423
Molweight254.41
LogP5.4
Atoms18
Bonds13
H-bond Acceptor2
H-bond Donor0
Chemical Classificationethers epoxides heterocyclic compounds

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
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
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaPseudomonas Sp.DYGS mediaHS-SPME/GC-MSno