Results for:
chemical Classification: lactones

2-butyl-2H-furan-5-one

Compound Details

Synonymous names
5-Butylfuran-2(5H)-one
30336-14-2
5-butyl-2(5H)-furanone
EINECS 250-133-5
(1)-5-Butylfuran-2(5H)-one
2-octen-4-olide
EINECS 274-596-8
SCHEMBL9993726
DTXSID30952684
70404-04-5
NS00050283
Microorganism:

No

IUPAC name2-butyl-2H-furan-5-one
SMILESCCCCC1C=CC(=O)O1
InchiInChI=1S/C8H12O2/c1-2-3-4-7-5-6-8(9)10-7/h5-7H,2-4H2,1H3
FormulaC8H12O2
PubChem ID121779
Molweight140.18
LogP2
Atoms10
Bonds3
H-bond Acceptor2
H-bond Donor0
Chemical Classificationlactones heterocyclic compounds

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAntrodia CamphorataNAChen et al. 2007
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAntrodia Camphoratano


5-[(Z)-oct-2-enyl]oxolan-2-one

Mass-Spectra

Compound Details

Synonymous names
18679-18-0
(Z)-4-Hydroxy-6-dodecenoic acid lactone
(Z)-Dihydro-5-(2-octenyl)furan-2(3H)-one
(Z)-6-Dodecen-4-olide
CIS-4-HYDROXYDODEC-6-ENOIC ACID LACTONE
FEMA No. 3780
gamma-Dodecen-6-lactone
cis-6-Dodecen-4-olide
5-[(Z)-oct-2-enyl]oxolan-2-one
2(3H)-Furanone, dihydro-5-(2-octenyl)-, (Z)-
(Z)-Dodec-6-en-4-olide
5-[(2Z)-oct-2-en-1-yl]oxolan-2-one
O8B631XC2S
4-Hydroxy-6-dodecenoic acid lactone, cis-
5-[(2Z)-2-Octenyl]dihydro-2(3H)-furanone
2(3H)-Furanone, dihydro-5-(2Z)-2-octen-1-yl-
(Z)-dairy lactone
2(3H)-Furanone, dihydro-5-(2Z)-2-octenyl-
6-Dodecen-4-olide, cis-
UNII-O8B631XC2S
(Z)-6-dodeceno-.gamma.-lactone
1,4-Dodec-6-enolactone, cis-
EINECS 242-497-9
cis-4-Hydroxy-6-dodecenoic acid lactone
Dihydro-5-(2-octenyl)-2(3H)-furanone, (Z)-
cis-1,4-Dodec-6-enolactone
SCHEMBL309361
.gamma.-6-(Z)-Dodecenolactone
.gamma.-Dodec-cis-6-enolactone
cis-.gamma.-Dodec-6-enolactone
(Z)-6-Dodecen-.gamma.-lactone
6-(Z)-Dodecen-.gamma.-lactone
CHEBI:172053
DTXSID601016535
(Z)-6-Dodecenyl-.gamma.-lactone
(+,-)-(Z)-6-Dodecen-4-olide
LMFA07040067
laquo gammaRaquo -6-(Z)-dodecenolactone
laquo gammaRaquo -dodec-cis-6-enolactone
(Z)-6-Dodecen-laquo gammaRaquo -lactone
6-(Z)-Dodecen-laquo gammaRaquo -lactone
cis-Laquo gammaRaquo -Dodec-6-enolactone
(6Z)-4-hydroxy-6-dodecenoic acid lactone
(Z)-6-dodeceno-laquo gammaRaquo -lactone
(Z)-6-dodecenyl-laquo gammaRaquo -lactone
NS00052592
(Z)-Dihydro-5-(2-octenyl)-2(3H)-furanone
Dihydro-5-(2-octenyl)-(Z)-2(3H)-Furanone
Dihydro-5-(2Z)-2-octen-1-yl-2(3H)-furanone
4-HYDROXY-6-DODECENOIC ACID LACTONE, (6Z)-
4-HYDROXY-6-DODECENOIC ACID, LACTONE [FHFI]
Q27285474
Microorganism:

Yes

IUPAC name5-[(Z)-oct-2-enyl]oxolan-2-one
SMILESCCCCCC=CCC1CCC(=O)O1
InchiInChI=1S/C12H20O2/c1-2-3-4-5-6-7-8-11-9-10-12(13)14-11/h6-7,11H,2-5,8-10H2,1H3/b7-6-
FormulaC12H20O2
PubChem ID5352428
Molweight196.29
LogP3.6
Atoms14
Bonds6
H-bond Acceptor2
H-bond Donor0
Chemical Classificationlactones esters heterocyclic compounds
CHEBI-ID172053
Supernatural-IDSN0304312-03

Species emitting the compound
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaLoktanella Sp.n/an/ano
ProkaryotaDinoroseobacter Sp.n/an/ano
ProkaryotaPlanococcus Citreusn/an/ano
ProkaryotaDinoroseobacter Shibaen/an/ano
EukaryotaZygosaccharomyces RouxiiYPD mediumGC-MSno


3-methyl-2H-furan-5-one

Mass-Spectra

Compound Details

Synonymous names
4-Methyl-2(5H)-furanone
6124-79-4
4-Methylfuran-2(5H)-one
3-methyl-2H-furan-5-one
2(5H)-Furanone, 4-methyl-
4-Methyl-5H-furan-2-one
4-methyl-2,5-dihydrofuran-2-one
4-Hydroxy-3-methyl-2-butenoic Acid gamma-Lactone
3-methyl-2H-uran-5-one
4-Methyl-2(5H)-furanone #
DTXSID60210148
CHEBI:167068
MFCD00191546
ZB1098
AKOS015996769
SB61224
CS-0205200
M1079
EN300-99428
C16080
A868778
Microorganism:

No

IUPAC name3-methyl-2H-furan-5-one
SMILESCC1=CC(=O)OC1
InchiInChI=1S/C5H6O2/c1-4-2-5(6)7-3-4/h2H,3H2,1H3
FormulaC5H6O2
PubChem ID145832
Molweight98.1
LogP0.1
Atoms7
Bonds0
H-bond Acceptor2
H-bond Donor0
Chemical Classificationlactones esters heterocyclic compounds
CHEBI-ID167068
Supernatural-IDSN0484282

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaTuber BorchiiT. melanosporum, T. borchii were collected from northern Italy (Piedmont) and T. indicum from Yunnan and Sichuan Provinces (China). Splivallo et al. 2007b
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaTuber Borchiiyes


6-octyloxan-2-one

Compound Details

Synonymous names
7370-92-5
delta-Tridecanolactone
6-octyloxan-2-one
6-Octyltetrahydro-2H-pyran-2-one
delta-Tridecalactone
5-tridecanolide
2H-Pyran-2-one, tetrahydro-6-octyl-
.delta.-Tridecalactone
WP2V9305A9
Tetrahydro-6-octyl-2H-pyran-2-one
EINECS 230-927-8
TRIDECA-1,5-LACTONE
UNII-WP2V9305A9
DELTA-OCTYLVALEROLACTONE
SCHEMBL1132969
.DELTA.-TRIDECANOLACTONE
FEMA NO. 4685
DTXSID00864048
CHEBI:183496
delta-Tridecalactone, >=95%, FG
MFCD00083590
(R,S)-.DELTA.-TRIDECALACTONE
Tetrahydro-6-n-octyl-2H-pyran-2-one
BS-23514
.DELTA.-OCTYL-.DELTA.-VALEROLACTONE
NS00044259
T1349
6-Octyltetrahydro-2H-pyran-2-one, AldrichCPR
E78210
(+/-)-6-OCTYLTETRAHYDRO-2H-PYRAN-2-ONE
5-HYDROXYTRIDECANOIC ACID .DELTA.-LACTONE
TRIDECANOIC ACID, 5-HYDROXY-, .DELTA.-LACTONE
Microorganism:

Yes

IUPAC name6-octyloxan-2-one
SMILESCCCCCCCCC1CCCC(=O)O1
InchiInChI=1S/C13H24O2/c1-2-3-4-5-6-7-9-12-10-8-11-13(14)15-12/h12H,2-11H2,1H3
FormulaC13H24O2
PubChem ID110977
Molweight212.33
LogP4.2
Atoms15
Bonds7
H-bond Acceptor2
H-bond Donor0
Chemical Classificationlactones esters heterocyclic compounds
CHEBI-ID183496
Supernatural-IDSN0339815

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaZygosaccharomyces RouxiiNANAPei et al. 2022
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaZygosaccharomyces RouxiiYPD mediumGC-MSno


6-hexyloxan-2-one

Compound Details

Synonymous names
710-04-3
delta-Undecalactone
6-Hexyltetrahydro-2H-pyran-2-one
6-hexyloxan-2-one
2H-PYRAN-2-ONE, 6-HEXYLTETRAHYDRO-
5-Undecanolide
Undecanoic delta-lactone
Delta undecalactone
Undecanolide-1,5
5-Hydroxyundecanoic acid lactone
delta-Undecanolactone
FEMA No. 3294
.delta.-Hexylvalerolactone
.delta.-Undecalactone
MFCD00006650
2H-Pyran-2-one, tetrahydro-3-hexyl-
ERL32M2M38
DTXSID9047099
.delta.-Hexyl-.delta.-valerolactone
6-HEXYL-2H-TETRAHYDROPYRAN-2-ONE
Undecanoic acid, 5-hydroxy-, .delta.-lactone
Undecanoic |A-lactone
delta-Hexylvalerolactone
EINECS 211-915-1
5-Hexyl-5-hydroxypentanoic acid lactone
BRN 0122724
UNII-ERL32M2M38
AI3-36029
Undecanoic acid, 5-hydroxy-, delta-lactone
Undecan-5-olide
.delta.-Undecanolide
1,5-Undecanolactone
Undecanoic delta -lactone
5-17-09-00097 (Beilstein Handbook Reference)
.DELTA.-UNDECANOLACTONE
CHEMBL372447
SCHEMBL1132045
Undecanoic delta-lactone, 98%
DTXCID7027099
FEMA 3294
YZRXRLLRSPQHDK-UHFFFAOYSA-
DELTA-UNDECALACTONE [FCC]
delta-Undecalactone, >97%, FG
CHEBI:171846
(RS)-.DELTA.-UNDECALACTONE
Tox21_302328
.DELTA.-UNDECALACTONE [FHFI]
5-Hydroxyundecanoic Acid delta-Lactone
AKOS024386550
(+/-)-.DELTA.-UNDECALACTONE
5-Hydroxyundecanoic acid lactone, 8CI
CS-W016998
MCULE-7844383556
SB47812
NCGC00255642-01
AS-61729
CAS-710-04-3
SY051695
DB-055478
5-Hydroxy-n-undecanoic acid .delta.-lactone
H0344
NS00013315
HENDECANOIC ACID, 5-HYDROXY-, LACTONE
D70227
W-104538
Q27277328
InChI=1/C11H20O2/c1-2-3-4-5-7-10-8-6-9-11(12)13-10/h10H,2-9H2,1H3
Microorganism:

Yes

IUPAC name6-hexyloxan-2-one
SMILESCCCCCCC1CCCC(=O)O1
InchiInChI=1S/C11H20O2/c1-2-3-4-5-7-10-8-6-9-11(12)13-10/h10H,2-9H2,1H3
FormulaC11H20O2
PubChem ID61204
Molweight184.27
LogP3.1
Atoms13
Bonds5
H-bond Acceptor2
H-bond Donor0
Chemical Classificationlactones esters heterocyclic compounds
CHEBI-ID171846
Supernatural-IDSN0464587

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaBacillus SubtilisNANALee et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaBacillus SubtilisTryptone soy broth (TSB)HPLCno


6-propylpyran-2-one

Compound Details

Synonymous names
6-propyl-2h-pyran-2-one
6-propylpyran-2-one
2H-Pyran-2-one, 6-propyl-
5247-93-8
BCB02_000145
SCHEMBL981554
DTXSID50425002
CHEBI:216240
BCB03_000242
Microorganism:

No

IUPAC name6-propylpyran-2-one
SMILESCCCC1=CC=CC(=O)O1
InchiInChI=1S/C8H10O2/c1-2-4-7-5-3-6-8(9)10-7/h3,5-6H,2,4H2,1H3
FormulaC8H10O2
PubChem ID6610108
Molweight138.16
LogP1.9
Atoms10
Bonds2
H-bond Acceptor2
H-bond Donor0
Chemical Classificationlactones esters pyranones heterocyclic compounds
CHEBI-ID216240
Supernatural-IDSN0066986

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaTrichoderma Sp.NAWickel et al. 2013
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaTrichoderma Sp.no


4-hydroxy-6-pentyloxan-2-one

Compound Details

Synonymous names
Compound NP-011223
SCHEMBL9420002
(+)-3-hydroxydecano-5-lactone
WPOYJLMQCBFDQM-UHFFFAOYSA-N
AKOS040739176
MCULE-6406474540
4-hydroxy-6-pentyl-tetrahydropyran-2-one
4-Hydroxy-6-pentyltetrahydro-2H-pyran-2-one #
2H-Pyran-2-one, tetrahydro-4-hydroxy-6-pentyl-
Microorganism:

Yes

IUPAC name4-hydroxy-6-pentyloxan-2-one
SMILESCCCCCC1CC(CC(=O)O1)O
InchiInChI=1S/C10H18O3/c1-2-3-4-5-9-6-8(11)7-10(12)13-9/h8-9,11H,2-7H2,1H3
FormulaC10H18O3
PubChem ID538589
Molweight186.25
LogP2
Atoms13
Bonds4
H-bond Acceptor3
H-bond Donor1
Chemical Classificationalcohols lactones esters heterocyclic compounds
Supernatural-IDSN0416598

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaPichia FermentansNANAMozūraitis et al. 2022
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaPichia FermentansYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno


(5R)-5-[(E)-oct-1-enyl]oxolan-2-one

Compound Details

Synonymous names
(r,e)-dodec-5-en-4-olide
SCHEMBL5148278
CHEBI:210914
(5R)-5-[(E)-oct-1-enyl]oxolan-2-one
Microorganism:

Yes

IUPAC name(5R)-5-[(E)-oct-1-enyl]oxolan-2-one
SMILESCCCCCCC=CC1CCC(=O)O1
InchiInChI=1S/C12H20O2/c1-2-3-4-5-6-7-8-11-9-10-12(13)14-11/h7-8,11H,2-6,9-10H2,1H3/b8-7+/t11-/m0/s1
FormulaC12H20O2
PubChem ID87786981
Molweight196.29
LogP3.7
Atoms14
Bonds6
H-bond Acceptor2
H-bond Donor0
Chemical Classificationlactones heterocyclic compounds esters
CHEBI-ID210914
Supernatural-IDSN0003067-01

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaLoktanella Sp.n/aNASchulz and Dickschat 2007
ProkaryotaDinoroseobacter Sp.n/aNASchulz and Dickschat 2007
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaLoktanella Sp.n/an/ano
ProkaryotaDinoroseobacter Sp.n/an/ano


(5R)-5-[(Z)-oct-1-enyl]oxolan-2-one

Compound Details

Synonymous names
Dodec-5Z-en-4R-olide
5R-(Oct-1Z-enyl)-oxacyclopentan-2-one
5R-(oct-1Z-enyl)dihydrofuran-2(3H)-one
(R,Z)-5-dodecen-4-olide
SCHEMBL5148270
ADZMLQKJPQFTIS-TVRMLOFPSA-N
CHEBI:195913
LMFA07040029
(5R)-5-[(Z)-oct-1-enyl]oxolan-2-one
(r,z)-5-(-)-(oct-1-enyl)oxacyclopentan-2-one
Microorganism:

Yes

IUPAC name(5R)-5-[(Z)-oct-1-enyl]oxolan-2-one
SMILESCCCCCCC=CC1CCC(=O)O1
InchiInChI=1S/C12H20O2/c1-2-3-4-5-6-7-8-11-9-10-12(13)14-11/h7-8,11H,2-6,9-10H2,1H3/b8-7-/t11-/m0/s1
FormulaC12H20O2
PubChem ID56936043
Molweight196.29
LogP3.7
Atoms14
Bonds6
H-bond Acceptor2
H-bond Donor0
Chemical Classificationlactones heterocyclic compounds esters
CHEBI-ID195913
Supernatural-IDSN0003067-03

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaLoktanella Sp.Is the pheromone of some scarab beetles.NASchulz and Dickschat 2007
ProkaryotaDinoroseobacter Sp.Is the pheromone of some scarab beetles.NASchulz and Dickschat 2007
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaLoktanella Sp.n/an/ano
ProkaryotaDinoroseobacter Sp.n/an/ano


5-[(E)-oct-1-enyl]oxolan-2-one

Compound Details

Synonymous names
(e)-dodec-5-en-4-olide
SCHEMBL2597364
ADZMLQKJPQFTIS-BQYQJAHWSA-N
DTXSID501016287
862852-65-1
Microorganism:

Yes

IUPAC name5-[(E)-oct-1-enyl]oxolan-2-one
SMILESCCCCCCC=CC1CCC(=O)O1
InchiInChI=1S/C12H20O2/c1-2-3-4-5-6-7-8-11-9-10-12(13)14-11/h7-8,11H,2-6,9-10H2,1H3/b8-7+
FormulaC12H20O2
PubChem ID18466382
Molweight196.29
LogP3.7
Atoms14
Bonds6
H-bond Acceptor2
H-bond Donor0
Chemical Classificationlactones heterocyclic compounds esters
Supernatural-IDSN0003067-02

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaLoktanella Sp.n/aNADickschat et al. 2005_4
ProkaryotaDinoroseobacter Shibaen/aNADickschat et al. 2005_4
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaLoktanella Sp.n/an/ano
ProkaryotaDinoroseobacter Shibaen/an/ano


7,7-dimethyl-9-oxatricyclo[6.2.2.01,6]dodecan-10-one

Compound Details

Synonymous names
7,7-Dimethyl-9-oxatricyclo[6.2.2.0(1,6)]dodecan-10-one
KENHWGDYBGSSPY-UHFFFAOYSA-N
Microorganism:

Yes

IUPAC name7,7-dimethyl-9-oxatricyclo[6.2.2.01,6]dodecan-10-one
SMILESCC1(C2CCCCC23CCC1OC3=O)C
InchiInChI=1S/C13H20O2/c1-12(2)9-5-3-4-7-13(9)8-6-10(12)15-11(13)14/h9-10H,3-8H2,1-2H3
FormulaC13H20O2
PubChem ID577932
Molweight208.3
LogP3.4
Atoms15
Bonds0
H-bond Acceptor2
H-bond Donor0
Chemical Classificationlactones heterocyclic compounds esters

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaBacillus Tequilensisantifungal activity against the hyphae growth of Ceratocystis fimbriatarhizosphere soil of a sweet potato variety (Xushu-36) from Xuzhou Academy of Agricultural Sciences in China in 2016Xu et al. 2021
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaBacillus TequilensisLB mediaHS-SPME/GC-MSno


7a-methyl-3,3a,4,5,6,7-hexahydro-1-benzofuran-2-one

Compound Details

Synonymous names
YGHCAHWARGVWQD-UHFFFAOYSA-N
2(3H)-Benzofuranone, hexahydro-7a-methyl-
7a-Methylhexahydro-1-benzofuran-2(3H)-one #
Microorganism:

Yes

IUPAC name7a-methyl-3,3a,4,5,6,7-hexahydro-1-benzofuran-2-one
SMILESCC12CCCCC1CC(=O)O2
InchiInChI=1S/C9H14O2/c1-9-5-3-2-4-7(9)6-8(10)11-9/h7H,2-6H2,1H3
FormulaC9H14O2
PubChem ID574136
Molweight154.21
LogP1.7
Atoms11
Bonds0
H-bond Acceptor2
H-bond Donor0
Chemical Classificationlactones heterocyclic compounds esters

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


2,4-dimethyl-2H-furan-5-one

Compound Details

Synonymous names
5584-69-0
xi-3,5-Dimethyl-2(5H)-furanone
2,4-dimethyl-2H-furan-5-one
3,5-dimethyl-5H-furan-2-one
3,5-dimethylfuran-2(5H)-one
2-Furanone, 2,5-dihydro-3,5-dimethyl
NSC252859
SCHEMBL691387
3,5-dimethyl-3-oxol-2-one
CHEMBL253848
2,4-dimethyl-2H-uran-5-one
3,5-Dimethyl-2(5H)-furanone
DTXSID10312348
CHEBI:173378
SAXRUMLUKZBSTO-UHFFFAOYSA-N
3,5-Dimethyl-2(5H)-furanone #
3,5-dimethyl-2,5-dihydrofuran-2-one
NSC-252859
Microorganism:

Yes

IUPAC name2,4-dimethyl-2H-furan-5-one
SMILESCC1C=C(C(=O)O1)C
InchiInChI=1S/C6H8O2/c1-4-3-5(2)8-6(4)7/h3,5H,1-2H3
FormulaC6H8O2
PubChem ID318158
Molweight112.13
LogP1
Atoms8
Bonds0
H-bond Acceptor2
H-bond Donor0
Chemical Classificationlactones heterocyclic compounds esters
CHEBI-ID173378
Supernatural-IDSN0340528

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


5-dodecyloxolan-2-one

Compound Details

Synonymous names
730-46-1
2(3H)-Furanone, 5-dodecyldihydro-
5-dodecyloxolan-2-one
gamma-Palmitolactone
5-Dodecyldihydro-2(3H)-furanone
Hexadeca-1,4-lactone
5-Dodecyldihydrofuran-2(3H)-one
.gamma.-Palmitolactone
Hexadecanoic acid, 4-hydroxy-, .gamma.-lactone
g-Palmitolactone
4-hexadecanolide
NSC33746
NSC 33746
.gamma.-Hexadecalactone
starbld0023054
Palmito-.gamma.-lactone
2(3H)-Furanone, 5-dodecyldihydro- (9CI)
4-Dodecyl-g-butyrolactone
SCHEMBL1029290
laquo gammaRaquo -palmitolactone
laquo gammaRaquo -hexadecalactone
DTXSID30862390
Palmito-laquo gammaRaquo -lactone
CHEBI:170094
gamma-Hydroxypalmitic acid lactone
Hexadecanoic acid, .gamma.-lactone
5-Dodecyldihydro-2(3H)-furanone #
NSC-33746
NS00076566
Hexadecanoic acid, 4-hydroxy-, gamma-lactone
G66129
Hexadecanoic acid, 4-hydroxy-, gamma-lactone (8CI)
Q67879898
Hexadecanoic acid, 4-hydroxy-, laquo gammaRaquo -lactone
Microorganism:

Yes

IUPAC name5-dodecyloxolan-2-one
SMILESCCCCCCCCCCCCC1CCC(=O)O1
InchiInChI=1S/C16H30O2/c1-2-3-4-5-6-7-8-9-10-11-12-15-13-14-16(17)18-15/h15H,2-14H2,1H3
FormulaC16H30O2
PubChem ID97747
Molweight254.41
LogP6
Atoms18
Bonds11
H-bond Acceptor2
H-bond Donor0
Chemical Classificationlactones heterocyclic compounds esters
CHEBI-ID170094
Supernatural-IDSN0353271

mVOC Specific Details

Boiling Point
DegreeReference
348 median

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaEscherichia ColiNANADixon et al. 2022
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaEscherichia ColiLBTD/GC-MSno


4-methyl-2H-furan-5-one

Compound Details

Synonymous names
3-Methyl-2(5H)-furanone
22122-36-7
3-Methylfuran-2(5H)-one
4-methyl-2H-furan-5-one
2(5H)-Furanone, 3-methyl-
2-Methyl-2-butenolide
N9KXQ3851K
MFCD00191545
.alpha.-Methyl-.gamma.-crotonolactone
2(5H)-Furanone, methyl-
UNII-N9KXQ3851K
3-methyl-5H-furan-2-one
2-Methyl-2-buten-4-olide
FEMA NO. 4902
VGHBEMPMIVEGJP-UHFFFAOYSA-
DTXSID50176643
GEO-01823
AKOS015916280
SY051333
DB-008319
CS-0204540
M1078
T72100
3-Methyl-2(5H)-furanone, technical grade, 90%
4-Hydroxy-2-methyl-2-butenoic Acid gamma-Lactone
W-200229
Q27284743
InChI=1/C5H6O2/c1-4-2-3-7-5(4)6/h2H,3H2,1H3
Microorganism:

Yes

IUPAC name4-methyl-2H-furan-5-one
SMILESCC1=CCOC1=O
InchiInChI=1S/C5H6O2/c1-4-2-3-7-5(4)6/h2H,3H2,1H3
FormulaC5H6O2
PubChem ID30945
Molweight98.1
LogP0.6
Atoms7
Bonds0
H-bond Acceptor2
H-bond Donor0
Chemical Classificationlactones heterocyclic compounds esters
Supernatural-IDSN0389481

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaLentilactobacillus BuchneriNANASquara et al. 2022
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaLentilactobacillus Buchnerimaize silageHS-SPME coupled with GC-TOF MSno


4-ethyloxolan-2-one

Compound Details

Synonymous names
4-ethyloxolan-2-one
16496-51-8
4-ethyldihydrofuran-2(3H)-one
2(3H)-Furanone, 4-ethyldihydro-
Aethyl-butyrolacton
4-Ethylbutan-4-olide
Aethyl-butyrolacton [German]
BRN 0107277
Dihydro-4-ethyl-2(3H)-furanone
2(3H)-FURANONE, DIHYDRO-4-ETHYL-
Brivaracetam Impurity 28
5-17-09-00042 (Beilstein Handbook Reference)
SCHEMBL9616911
DTXSID90937018
MDQZVJSUBKPTHG-UHFFFAOYSA-N
BS-46704
F77504
Microorganism:

No

IUPAC name4-ethyloxolan-2-one
SMILESCCC1CC(=O)OC1
InchiInChI=1S/C6H10O2/c1-2-5-3-6(7)8-4-5/h5H,2-4H2,1H3
FormulaC6H10O2
PubChem ID27893
Molweight114.14
LogP1
Atoms8
Bonds1
H-bond Acceptor2
H-bond Donor0
Chemical Classificationlactones heterocyclic compounds esters
CHEBI-ID201213
Supernatural-IDSN0222797

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaPenicillium Crustosumn/aNAFischer et al. 1999
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaPenicillium Crustosumyeast extract sucrose agarn/ano


6-butyloxan-2-one

Mass-Spectra

Compound Details

Synonymous names
DELTA-NONALACTONE
3301-94-8
2H-Pyran-2-one, 6-butyltetrahydro-
6-Butyltetrahydro-2H-pyran-2-one
6-butyloxan-2-one
5-Nonanolide
delta-Nonanolactone
5-Nonalactone
Hydroxynonanoic acid delta-lactone
5-Butyl-delta-valerolactone
Nonan-1,5-olide
.delta.-Nonalactone
delta-Butyl-delta-valerolactone
FEMA No. 3356
5-Hydroxynonanoic acid, lactone
delta-Hydroxypelargonic acid lactone
5-Hydroxynonanoic acid delta-lactone
.delta.-Butylvalerolactone
DMB99B4WCF
5-Butyl-5-hydroxypentanoic acid lactone
Nonanoic acid, 5-hydroxy-, delta-lactone
MFCD00036500
2H-Pyran-2-one, tetrahydro-6-butyl
UNII-DMB99B4WCF
beta -nonalactone
EINECS 221-974-5
.delta. Nonalactone
delta-Pelargonolactone
AI3-36027
5-Hydroxynonanoicacidlactone
laquo deltaRaquo -nonanolide
.DELTA.-NONANOLACTONE
SCHEMBL918003
5-Hydroxynonanoic acid lactone
DELTA-NONALACTONE [FCC]
FEMA 3356
DTXSID70863149
(RS)-.DELTA.-NONALACTONE
CHEBI:171747
(+/-)-DELTA-NONALACTONE
delta-Nonalactone, 98%, FCC, FG
6-Butyltetrahydro-2H-pyran-2-one #
AKOS015914962
CS-W018000
delta-Nonalactone, natural, 98%, FG
HY-W017284
MCULE-5855223168
SB46699
SB46732
6-Butyltetrahydro-2H-pyran-2-one, 9CI
AS-62019
SY050146
.DELTA.-BUTYL-.DELTA.-VALEROLACTONE
NONANOIC ACID, 5-HYDROXY-, LACTONE
N0424
NS00013033
5-HYDROXYNONANOIC ACID .DELTA.-LACTONE
D91705
delta-Nonalactone;5-n-Butyl-delta-valerolactone
HYDROXYNONANOIC ACID .DELTA.-LACTONE [FHFI]
J-018980
NONANOIC ACID, 5-HYDROXY-, .DELTA.-LACTONE
Q25323843
105140-26-9
Microorganism:

Yes

IUPAC name6-butyloxan-2-one
SMILESCCCCC1CCCC(=O)O1
InchiInChI=1S/C9H16O2/c1-2-3-5-8-6-4-7-9(10)11-8/h8H,2-7H2,1H3
FormulaC9H16O2
PubChem ID18698
Molweight156.22
LogP2.4
Atoms11
Bonds3
H-bond Acceptor2
H-bond Donor0
Chemical Classificationlactones heterocyclic compounds esters
CHEBI-ID171747
Supernatural-IDSN0297933

Species emitting the compound
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaDinoroseobacter Shibaen/an/ano
EukaryotaTrichoderma Atrovirideno
ProkaryotaCarnobacterium Divergensn/an/ano
ProkaryotaDinoroseobacter Sp.n/an/ano
ProkaryotaLentilactobacillus Buchnerimaize silageHS-SPME coupled with GC-TOF MSno
ProkaryotaLacticaseibacillus Paracaseimaize silageHS-SPME coupled with GC-TOF MSno
EukaryotaHanseniaspora Uvarumgrape juiceLC-15C HPLCno
EukaryotaSaccharomycopsis Crataegensisgrape juiceLC-15C HPLCno
EukaryotaMetschnikowia Pulcherrimagrape juiceLC-15C HPLCno
EukaryotaPichia Kluyverigrape juiceLC-15C HPLCno
EukaryotaRhodosporidiobolus Lusitaniaegrape juiceLC-15C HPLCno


4-methyloxetan-2-one

Compound Details

Synonymous names
beta-Butyrolactone
3068-88-0
4-Methyloxetan-2-one
2-Oxetanone, 4-methyl-
(+/-)-b-Butyrolactone
4-METHYL-2-OXETANONE
.beta.-Butyrolactone
36536-46-6
Hydroxybutyric acid lactone
3-Hydroxybutyric acid lactone
DL-.beta.-Butyrolactone
(R)-4-Methyloxetan-2-one
8BB68V31MT
DTXSID1020223
CHEBI:82296
2-Oxetanone, 4-methyl-, (S)-
MFCD00005170
b-Butyrolactone
DTXCID50223
beta-Butyrolakton
beta-Butyrolakton [Czech]
CCRIS 111
CAS-3068-88-0
(4R)-4-methyloxetan-2-one
EINECS 221-330-3
EINECS 253-093-7
3-Hydroxybutanoic acid, beta-lactone
UNII-8BB68V31MT
(1)-4-Methyloxetan-2-one
beta -butyrolactone
.beta.-Butyrolakton
BETABUTYROLACTONE
beta-Methylpropiolactone
racemic beta-butyrolactone
beta-Butyrolactone, 98%
beta-Methyl-beta-propiolactone
CHEMBL1361205
RAC-.BETA.-BUTYROLACTONE
BETA-BUTYROLACTONE [IARC]
3-Hydroxybutyric acid beta-lactone
Tox21_201253
Tox21_302988
MFCD12827426
(+/-)-.BETA.-BUTYROLACTONE
AKOS015955924
3-Hydroxybutyric acid, .beta.-lactone
AT19323
beta-Butyrolactone, analytical standard
3-Hydroxybutanoic acid, .beta.-lactone
Butanoic acid, 3-hydroxy-, beta-lactone
NCGC00091733-01
NCGC00091733-02
NCGC00256595-01
NCGC00258805-01
SY051647
SY310635
(+/-)-.BETA.-METHYLPROPIOLACTONE
DB-243105
B0901
CS-0377913
NS00022032
NS00089056
C19201
EN300-6940117
J-018058
Q27155863
Microorganism:

Yes

IUPAC name4-methyloxetan-2-one
SMILESCC1CC(=O)O1
InchiInChI=1S/C4H6O2/c1-3-2-4(5)6-3/h3H,2H2,1H3
FormulaC4H6O2
PubChem ID18303
Molweight86.09
LogP0.3
Atoms6
Bonds0
H-bond Acceptor2
H-bond Donor0
Chemical Classificationlactones heterocyclic compounds esters
CHEBI-ID82296
Supernatural-IDSN0113875

mVOC Specific Details

Boiling Point
DegreeReference
71.11111111111111 median, REST, convertet to C
Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaLentilactobacillus BuchneriNANASquara et al. 2022
ProkaryotaLacticaseibacillus ParacaseiNANASquara et al. 2022
EukaryotaSaturnispora DiversaNANAZhao et al. 2022
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaLentilactobacillus Buchnerimaize silageHS-SPME coupled with GC-TOF MSno
ProkaryotaLacticaseibacillus Paracaseimaize silageHS-SPME coupled with GC-TOF MSno
EukaryotaSaturnispora Diversasynthetic grape juiceHS-SPMEno


6-heptyloxan-2-one

Mass-Spectra

Compound Details

Synonymous names
DELTA-DODECALACTONE
713-95-1
6-Heptyltetrahydro-2H-pyran-2-one
5-Dodecanolide
delta-Dodecanolactone
6-heptyloxan-2-one
Dodecan-5-olide
2H-Pyran-2-one, 6-heptyltetrahydro-
5-Dodecalactone
Dodecanolide-1,5
5-Hydroxydodecanoic acid lactone
xi-5-Dodecanolide
n-Heptyl-delta-valerolactone
.delta.-Dodecalactone
FEMA No. 2401
delta-Heptyl-delta-valerolactone
(+/-)-5-Dodecanolide
Dodecanoic acid, 5-hydroxy-, delta-lactone
33DIC582TL
6-Heptyl-tetrahydropyran-2-one
.delta.-Heptyl-.delta.-valerolactone
MFCD00006651
(+/-)-delta-Heptyl-delta-valerolactone
Dodecanoic acid, 5-hydroxy-, .delta.-lactone
delta-Dodecalactone (natural)
d-Dodecalactone
HSDB 292
EINECS 211-932-4
UNII-33DIC582TL
AI3-36030
delta-Laurolactone
DELTALACTONE
6-heptyl-2-oxanone
5-Hydroxydodecanoic acid delta-lactone
5-Dodecanolide, 99%
EC 211-932-4
SCHEMBL114922
n-Heptyl-.delta.-valerolactone
.DELTA.-DODECANE LACTONE
CHEMBL4636895
DTXSID9047596
6-heptyl-tetrahydro-pyran-2-one
QRPLZGZHJABGRS-UHFFFAOYSA-
DELTA-DODECALACTONE [FCC]
CHEBI:171817
5-Hydroxydodecanoic acid d-lactone
DELTA-DODECALACTONE [HSDB]
delta-Dodecalactone, >=97%, FG
.DELTA.-DODECALACTONE [MI]
(R,S)-.DELTA.-DODECALACTONE
BBL027600
LMFA07040040
STL373783
.DELTA.-DODECALACTONE [FHFI]
2H-Pyran-2-one, tetrahydro-6-heptyl
AKOS015915485
(+/-)-.DELTA.-DODECALACTONE
CS-W010531
MCULE-4837230476
SB47814
delta-Dodecalactone, analytical standard
DS-11405
SY015678
5-Hydroxydodecanoic acid, .delta.-lactone
6-(Hept-1-yl)tetrahydro-2H-pyran-2-one
(+/-)-6-Heptyltetrahydro-2H-pyran-2-one
DB-055522
AI 3-36030
D1414
NS00009933
D70226
A837171
W-109596
delta-Dodecalactone;6-Heptyltetrahydro-2H-pyran-2-one
Q27256257
3051-22-7
InChI=1/C12H22O2/c1-2-3-4-5-6-8-11-9-7-10-12(13)14-11/h11H,2-10H2,1H3
Microorganism:

Yes

IUPAC name6-heptyloxan-2-one
SMILESCCCCCCCC1CCCC(=O)O1
InchiInChI=1S/C12H22O2/c1-2-3-4-5-6-8-11-9-7-10-12(13)14-11/h11H,2-10H2,1H3
FormulaC12H22O2
PubChem ID12844
Molweight198.3
LogP3.6
Atoms14
Bonds6
H-bond Acceptor2
H-bond Donor0
Chemical Classificationlactones heterocyclic compounds esters
CHEBI-ID171817
Supernatural-IDSN0313340

mVOC Specific Details

Solubility
INSOL IN WATER
Literature: Fenaroli's Handbook of Flavor Ingredients. Volume 2. Edited, translated, and revised by T.E. Furia and N. Bellanca. 2nd ed. Cleveland: The Chemical Rubber Co., 1975., p. 155
Literature: #SOL IN ETHANOL; POORLY SOL IN PROPYLENE GLYCOL
Literature: Fenaroli's Handbook of Flavor Ingredients. Volume 2. Edited, translated, and revised by T.E. Furia and N. Bellanca. 2nd ed. Cleveland: The Chemical Rubber Co., 1975., p. 155
MS-Links
Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaZygosaccharomyces RouxiiNANAPei et al. 2022
ProkaryotaBacillus SubtilisNANALee et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaZygosaccharomyces RouxiiYPD mediumGC-MSno
ProkaryotaBacillus SubtilisTryptone soy broth (TSB)HPLCno


Oxan-2-one

Compound Details

Synonymous names
delta-Valerolactone
542-28-9
TETRAHYDRO-2H-PYRAN-2-ONE
5-Valerolactone
oxan-2-one
2H-Pyran-2-one, tetrahydro-
tetrahydropyran-2-one
Valerolactone
Tetrahydro-2-pyranone
.delta.-Valerolactone
26354-94-9
.delta.-Valeryllactone
tetrahydro-pyran-2-one
1-Oxacyclohexan-2-one
NSC 6247
CHEMBL452383
DTXSID6044438
CHEBI:16545
NSC-6247
MFCD00006645
14V1X9149L
Penta-1,5-lactone
delta-Valeryllactone
d-valerolactone
Cyclopentanolide
o-Valerolactone
o-Valeryllactone
5-pentanolide
UNII-14V1X9149L
Pentan-5-olide
Delta valerolactone
2-oxotetrahydropyran
Delta-Valerolactotie
EINECS 208-807-1
delta -Valerolactone
.delta.-Pentalactone
tetrahydro-4H-pyranone
AI3-25024
Pentanoic acid, 5-hydroxy-, delta-lactone
Valeric acid, delta-hydroxy-, delta-lactone
WLN: T6OVTJ
Tetrahydro-2H-2-pyranone
EC 208-807-1
SCHEMBL37722
Valeric acid, .delta.-lactone
DTXCID4024438
Pentanoic acid, .delta.-lactone
NSC6247
DELTA-VALEROLACTONE [INCI]
NSC65442
STR08736
delta-Valerolactone, technical grade
Tox21_302166
BDBM50360797
NSC 65442
NSC-65442
s3099
AKOS009158729
CS-W013713
HY-W012997
MCULE-4682307363
5-Hydroxypentanoic acid .delta.-lactone
NCGC00255756-01
CAS-542-28-9
Delta-valerolactone (may contain polymer)
SY018264
DB-050659
NS00005148
V0039
EN300-43042
Pentanoic acid, 5-hydroxy-, .delta.-lactone
tetrahydro-2H-pyran-2-one,2-Perhydropyranone
C02240
(Difluoro-trimethylsilanyl-methyl)-phosphonicacid
Q903610
Valeric acid, .delta.-hydroxy-, .delta.-lactone
W-105654
InChI=1/C5H8O2/c6-5-3-1-2-4-7-5/h1-4H
Z432085120
Microorganism:

Yes

IUPAC nameoxan-2-one
SMILESC1CCOC(=O)C1
InchiInChI=1S/C5H8O2/c6-5-3-1-2-4-7-5/h1-4H2
FormulaC5H8O2
PubChem ID10953
Molweight100.12
LogP-0.3
Atoms7
Bonds0
H-bond Acceptor2
H-bond Donor0
Chemical Classificationlactones heterocyclic compounds esters
CHEBI-ID16545
Supernatural-IDSN0279228

mVOC Specific Details

Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaEscherichia ColiNANADixon et al. 2022
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaEscherichia ColiLBTD/GC-MSno