Results for:
chemical Classification: imidazoles

Imidazo[1,2-a]pyrimidine

Compound Details

Synonymous names
Imidazo[1,2-a]pyrimidine
274-95-3
MFCD06245377
1,3a,7-Triazaindene
1,8-Diazaindolizine
8-Azapyrimidazole
3,4-Diazaindolizine
Imidazo[1,2-a]-pyrimidine
SCHEMBL66214
imidazo[1,2-alpha]pyrimidine
CHEMBL206082
DTXSID80341928
Imidazo[1 pound not2-a]pyrimidine
STL302092
AKOS005071564
CS-W003279
Imidazo[1,2-a]pyrimidine, AldrichCPR
MCULE-3840032247
SY007505
DB-037997
AM20090342
I0798
EN300-67236
9X-0834
A819094
J-521506
Microorganism:

Yes

IUPAC nameimidazo[1,2-a]pyrimidine
SMILESC1=CN2C=CN=C2N=C1
InchiInChI=1S/C6H5N3/c1-2-7-6-8-3-5-9(6)4-1/h1-5H
FormulaC6H5N3
PubChem ID577018
Molweight119.12
LogP1.1
Atoms9
Bonds0
H-bond Acceptor2
H-bond Donor0
Chemical Classificationimidazoles heterocyclic compounds nitrogen compounds pyrimidines

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-methyl-1,4-dihydroimidazol-5-one

Compound Details

Synonymous names
4915-81-5
2-methyl-1,4-dihydroimidazol-5-one
NSC407932
DTXSID20324891
BMXVNDCWQYPPAB-UHFFFAOYSA-N
2-methyl-3,5-dihydroimidazol-4-one
4,5-Dihydro-2-methylimidazole-4-one
AKOS006353993
NSC-407932
2-methyl-4,5-dihydro(1h)imidazol-4-one
3,5-Dihydro-2-methyl-4H-imidazol-4-one
DB-151130
2-Methyl-1,5-dihydro-4H-imidazol-4-one #
Microorganism:

Yes

IUPAC name2-methyl-1,4-dihydroimidazol-5-one
SMILESCC1=NCC(=O)N1
InchiInChI=1S/C4H6N2O/c1-3-5-2-4(7)6-3/h2H2,1H3,(H,5,6,7)
FormulaC4H6N2O
PubChem ID348554
Molweight98.1
LogP-0.8
Atoms7
Bonds0
H-bond Acceptor2
H-bond Donor1
Chemical Classificationimidazoles heterocyclic compounds nitrogen 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


1,4-dimethylimidazole

Compound Details

Synonymous names
1,4-Dimethyl-1H-imidazole
1,4-Dimethylimidazole
6338-45-0
1H-Imidazole, 1,4-dimethyl-
5NF7MPO9DZ
MFCD02660800
NSC-40745
UNII-5NF7MPO9DZ
NSC40745
1,4-Dimethyl-1H-imidazole #
DTXSID20212784
NSC 40745
STL584300
AKOS005169259
MCULE-2469544518
AC-28884
AM804171
AS-57576
SY020437
DB-073317
CS-0047070
EN300-106922
A834353
Q27262595
Microorganism:

Yes

IUPAC name1,4-dimethylimidazole
SMILESCC1=CN(C=N1)C
InchiInChI=1S/C5H8N2/c1-5-3-7(2)4-6-5/h3-4H,1-2H3
FormulaC5H8N2
PubChem ID138733
Molweight96.13
LogP0.4
Atoms7
Bonds0
H-bond Acceptor1
H-bond Donor0
Chemical Classificationaromatic compounds imidazoles heterocyclic compounds nitrogen compounds
Supernatural-IDSN0028703

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-(1H-imidazol-5-yl)-2-oxoacetic Acid

Compound Details

Synonymous names
295345-28-7
1H-imidazol-4-yl(oxo)acetic acid
2-(1H-imidazol-4-yl)-2-oxoacetic acid
2-(1H-imidazol-5-yl)-2-oxoacetic acid
SCHEMBL9016391
RPVXUSIQSQEAFM-UHFFFAOYSA-N
DTXSID301302266
(1H-Imidazol-4-yl)oxoacetic acid
STK249712
AKOS005219629
I+/--Oxo-1H-imidazole-5-acetic acid
MCULE-8916685899
EN300-1818180
Microorganism:

Yes

IUPAC name2-(1H-imidazol-5-yl)-2-oxoacetic acid
SMILESC1=C(NC=N1)C(=O)C(=O)O
InchiInChI=1S/C5H4N2O3/c8-4(5(9)10)3-1-6-2-7-3/h1-2H,(H,6,7)(H,9,10)
FormulaC5H4N2O3
PubChem ID1796254
Molweight140.1
LogP-0.2
Atoms10
Bonds2
H-bond Acceptor4
H-bond Donor2
Chemical Classificationacids imidazoles aromatic compounds organic acids heterocyclic compounds carboxylic acids ketones nitrogen compounds
Supernatural-IDSN0331993

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


(2S)-3-(1H-imidazol-5-yl)-2-(phenylmethoxycarbonylamino)propanoic Acid

Compound Details

Synonymous names
Z-His-OH
14997-58-1
N-Cbz-L-histidine
L-Histidine, N-[(phenylmethoxy)carbonyl]-
CBZ-histidine
Nalpha-Cbz-L-histidine
Nalpha-Carbobenzoxy-L-histidine
(2S)-3-(1H-imidazol-5-yl)-2-(phenylmethoxycarbonylamino)propanoic acid
MFCD00065960
N-[(Benzyloxy)carbonyl]-L-histidine
Histidine, N-[(phenylmethoxy)carbonyl]-
(2S)-2-{[(benzyloxy)carbonyl]amino}-3-(1H-imidazol-4-yl)propanoic acid
(s)-2-(((benzyloxy)carbonyl)amino)-3-(1h-imidazol-5-yl)propanoic acid
Cbz-L-histidine
Cbz-His
N-(alpha)-Carbobenzoxy-L-histidine
N-alpha-benzyloxycarbonyl-L-histidine
N|A-Cbz-L-histidine
benzyloxycarbonyl-L-histidine
N-CBZ-L-HISTIDINE-OH
Z-His-OH, 99%
SCHEMBL254638
SCHEMBL9230979
((Benzyloxy)carbonyl)-L-histidine
DTXSID501280353
Nalpha -benzyloxycarbonyl-histidine
AMY31373
(S)-2-(BENZYLOXYCARBONYLAMINO)-3-(1H-IMIDAZOL-4-YL)PROPANOIC ACID
AKOS015909985
AKOS015924085
CS-W013996
FD21657
HY-W013280
MCULE-4620948899
N-[(Phenylmethoxy)carbonyl]-L-histidine
AC-17159
AS-49151
DB-030164
B0265
NS00051681
EN300-121289
M03075
A808989
W-108080
Microorganism:

Yes

IUPAC name(2S)-3-(1H-imidazol-5-yl)-2-(phenylmethoxycarbonylamino)propanoic acid
SMILESC1=CC=C(C=C1)COC(=O)NC(CC2=CN=CN2)C(=O)O
InchiInChI=1S/C14H15N3O4/c18-13(19)12(6-11-7-15-9-16-11)17-14(20)21-8-10-4-2-1-3-5-10/h1-5,7,9,12H,6,8H2,(H,15,16)(H,17,20)(H,18,19)/t12-/m0/s1
FormulaC14H15N3O4
PubChem ID736313
Molweight289.29
LogP1.2
Atoms21
Bonds7
H-bond Acceptor5
H-bond Donor3
Chemical Classificationacids imidazoles benzenoids carbamates carboxylic acids heterocyclic compounds aromatic compounds nitrogen compounds organic acids

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-imidazol-1-ylethanone

Mass-Spectra

Compound Details

Synonymous names
1-Acetylimidazole
N-Acetylimidazole
2466-76-4
1-(1H-imidazol-1-yl)ethanone
1H-Imidazole, 1-acetyl-
Acetylimidazole
1-Acetyl-1H-imidazole
1-imidazol-1-ylethanone
IMIDAZOLE, 1-ACETYL-
1-(1H-imidazol-1-yl)ethan-1-one
Ethanone, 1-(1H-imidazol-1-yl)-
MFCD00005287
ZMP8X1Y11G
CHEBI:16984
3-acetylimidazole
CCRIS 6534
EINECS 219-577-7
UNII-ZMP8X1Y11G
BRN 0108425
N-acetyl imidazole
1- acetylimidazole
1-acetyl imidazole
1-Acetylimidazole, 98%
Imidazole N-1 deriv. 5
OZAGREL IMPURITY 1
1-Acetyl-1H-imidazole #
1-(methylcarbonyl)imidazole
SCHEMBL26238
5-23-04-00218 (Beilstein Handbook Reference)
MLS001074864
BDBM7944
CHEMBL1592087
DTXSID8062440
HMS2234I07
AKOS005208084
AC-7521
NCGC00246992-01
AS-11932
SMR000568396
SY049533
DB-031677
A0694
A5057
AM20090278
CS-0010103
NS00046189
C02560
EN300-748826
1-(1H-imidazol-1-yl)ethanone;N-Acetylimidazole
1-Acetylimidazole, Vetec(TM) reagent grade, 98%
1,1-[but-2-yne-1,4-diylbis(oxy)]bispropan-2-ol
Q-102345
Q27102162
Z1255402643
Microorganism:

No

IUPAC name1-imidazol-1-ylethanone
SMILESCC(=O)N1C=CN=C1
InchiInChI=1S/C5H6N2O/c1-5(8)7-3-2-6-4-7/h2-4H,1H3
FormulaC5H6N2O
PubChem ID17174
Molweight110.11
LogP-0.3
Atoms8
Bonds0
H-bond Acceptor2
H-bond Donor0
Chemical Classificationaromatic aldehydes imidazoles nitrogen compounds heterocyclic compounds aldehydes aromatic compounds
CHEBI-ID16984
Supernatural-IDSN0391079

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaPleurotus CystidiosusnanaUsami et al. 2014
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaPleurotus CystidiosusnaGC/MS, GC-O, AEDAno


1H-imidazole-2-carbaldehyde

Compound Details

Synonymous names
10111-08-7
1H-Imidazole-2-carbaldehyde
Imidazole-2-carboxaldehyde
2-Formylimidazole
1H-IMIDAZOLE-2-CARBOXALDEHYDE
2-Imidazolecarboxaldehyde
imidazole-2-aldehyde
MFCD00003544
Imidazole-2-carbaldehyde
1H-Imidazolecarboxaldehyde
2-Formyl-1H-imidazole
formylimidazole
Isovalericacid
imidazolealdehyde
2-formyl imidazole
2-formyl-imidazole
imidazole carbaldehyde
imidazolecarboxaldehyde
2-imidazolecarbaldehyde
2-imidazol-carbaldehyde
imidazol-2-carbaldehyde
2-imidazolcarboxaldehyde
imidazole-2-carboxaldeyde
2-imidazole carboxaldehyde
2-imidazole-carboxaldehyde
imidazole 2-carboxaldehyde
1H-2-imidazolecarbaldehyde
1H-imidazol-2-carbaldehyd
2-Formyl imidazole (Imidazole-2-carboxaldehyde)
1H-imidazole-2 carbaldehyde
1H-imidazole-2-carboaldehyde
YSWG441
1-H-imidazole-2-carbaldehyde
1H-Imidazole-2-carbaldehyde #
2-Imidazolecarboxaldehyde, 97%
DTXSID70143736
BCP27080
STR04050
BBL104408
STK503765
AKOS004910734
AC-6503
CS-W007321
HY-W007321
MCULE-7353417190
PB47438
PS-9350
BP-12787
SY014217
DB-005097
AM20070660
I0809
NS00023025
EN300-52542
A16251
W-200646
F8880-2426
Microorganism:

Yes

IUPAC name1H-imidazole-2-carbaldehyde
SMILESC1=CN=C(N1)C=O
InchiInChI=1S/C4H4N2O/c7-3-4-5-1-2-6-4/h1-3H,(H,5,6)
FormulaC4H4N2O
PubChem ID24955
Molweight96.09
LogP-0.1
Atoms7
Bonds1
H-bond Acceptor2
H-bond Donor1
Chemical Classificationaromatic aldehydes aromatic compounds imidazoles heterocyclic compounds aldehydes nitrogen 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


1H-imidazol-5-ylmethanol

Compound Details

Synonymous names
822-55-9
IMIDAZOLE-4-METHANOL
(1H-Imidazol-4-yl)methanol
4-(Hydroxymethyl)imidazole
1H-Imidazole-4-methanol
1H-imidazol-5-ylmethanol
1H-Imidazol-4-ylmethanol
(3H-Imidazol-4-yl)-methanol
1H-Imidazole-5-methanol
(1H-imidazol-4-yl)-methanol
4-imidazolemethanol
4(5)-(Hydroxymethyl)imidazole
4(5)-Hydroxymethylimidazole
4-HYDROXYMETHYLIMIDAZOLE
(1H-imidazol-5-yl)methanol
CHEBI:28182
QD0132T507
1H-Imidazol-4-ylmethanol; 4-(Hydroxymethyl)imidazole; 4-Imidazolylmethanol; 4-Methylol-1H-imidazole
NSC-39016
4-hydroxymethyl imidazole hydrochloride
UNII-QD0132T507
MZ0
4-imidazole methanol
5-hydroxymethylimidazole
4-hydroxymethyl imidazole
4-Methylol-1H-imidazole
Lopac-H-1877
5-(hydroxymethyl)imidazole
4-IMIDAZOLYLMETHANOL
C05562
1H-imidazol-4-yl-methanol
Lopac0_000603
1H-Imidazol-4-ylmethanol #
(1H-Imidazol-4-yl)methanol,
4-(hydroxymethyl)-1H-imidazole
CHEMBL1397797
DTXSID40231619
IMIDAZOLE-4(OR 5)-METHANOL
MFCD00266718
AKOS005258761
AKOS015951052
4(5)-(Hydroxymethyl)imidazole, 97%
CCG-204692
MCULE-7372960664
PB24669
SDCCGSBI-0050585.P002
NCGC00015502-01
NCGC00015502-02
NCGC00015502-03
NCGC00015502-04
NCGC00015502-05
NCGC00093363-02
AC-23132
AM804377
AS-58725
PD034373
DB-032007
AM20090479
CS-0008531
EN300-50616
W10530
AB-131/25126047
Q-101887
Q-103115
Q27103551
Z234898057
Microorganism:

Yes

IUPAC name1H-imidazol-5-ylmethanol
SMILESC1=C(NC=N1)CO
InchiInChI=1S/C4H6N2O/c7-2-4-1-5-3-6-4/h1,3,7H,2H2,(H,5,6)
FormulaC4H6N2O
PubChem ID1745
Molweight98.1
LogP-0.8
Atoms7
Bonds1
H-bond Acceptor2
H-bond Donor2
Chemical Classificationaromatic compounds imidazoles heterocyclic compounds alcohols nitrogen compounds
CHEBI-ID28182

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


2-(4-fluoroimidazol-4-yl)ethanamine

Compound Details

Synonymous names
SCHEMBL3293231
Microorganism:

Yes

IUPAC name2-(4-fluoroimidazol-4-yl)ethanamine
SMILESC1=NC=NC1(CCN)F
InchiInChI=1S/C5H8FN3/c6-5(1-2-7)3-8-4-9-5/h3-4H,1-2,7H2
FormulaC5H8FN3
PubChem ID68584299
Molweight129.14
LogP-0.8
Atoms9
Bonds2
H-bond Acceptor3
H-bond Donor1
Chemical Classificationamines aromatic compounds halogenated compounds heterocyclic compounds imidazoles nitrogen compounds
Supernatural-IDSN0397394

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaMoraxella Catarrhalishumans, respiratory infectionsAbd El Qader et al. 2015
ProkaryotaLegionella Pneumophilahumans, respiratory infectionsAbd El Qader et al. 2015
ProkaryotaHaemophilus Influenzaecould serve as potential biomarkers to distinguish between viruses and bacteriaNAAbd El Qader et al. 2015
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaMoraxella Catarrhalisblood culture mediumSPME-GC-MSno
ProkaryotaLegionella Pneumophilablood culture mediumSPME-GC-MSno
ProkaryotaHaemophilus Influenzaeblood cultureSPME/GC-MS no


(2S,3R)-2-ethyl-3-(hydroxymethyl)-4-(3-methylimidazol-4-yl)butanoic Acid

Compound Details

Synonymous names
Pilocarpic acid
28406-15-7
978XN1E1ZN
(2S,3R)-2-ethyl-3-(hydroxymethyl)-4-(3-methylimidazol-4-yl)butanoic acid
UNII-978XN1E1ZN
Pilocarpinsaure
(2R,3R)-2-ethyl-3-(hydroxymethyl)-4-(3-methyl-4-imidazolyl)butanoic acid
1,2-SECOPILOCARPIN-2-OIC ACID
PILOCARPINE NITRATE IMPURITY B [EP IMPURITY]
Q27271985
PILOCARPINE HYDROCHLORIDE IMPURITY B [EP IMPURITY]
PILOCARPINE HYDROCHLORIDE IMPURITY PILOCARPIC ACID [USP IMPURITY]
(2S,3R)-2-ETHYL-3-(HYDROXYMETHYL)-4-(1-METHYL-1H-IMIDAZOL-5-YL)BUTANOIC ACID
(2S,3R)-2-Ethyl-4-hydroxy-3-((1-methyl-1H-imidazol-5-yl)methyl)butanoic acid
1H-Imidazole-5-butanoic acid, alpha-ethyl-beta-(hydroxymethyl)-1-methyl-, (alphaS,betaR)-
1H-Imidazole-5-butanoic acid, alpha-ethyl-beta-(hydroxymethyl)-1-methyl-, (S-(R*,S*))-
1H-IMIDAZOLE-5-BUTANOIC ACID, .ALPHA.-ETHYL-.BETA.-(HYDROXYMETHYL)-1-METHYL-, (.ALPHA.S,.BETA.R)-
1H-IMIDAZOLE-5-BUTANOIC ACID, .ALPHA.-ETHYL-.BETA.-(HYDROXYMETHYL)-1-METHYL-, (S-(R*,S*))-
Microorganism:

Yes

IUPAC name(2S,3R)-2-ethyl-3-(hydroxymethyl)-4-(3-methylimidazol-4-yl)butanoic acid
SMILESCCC(C(CC1=CN=CN1C)CO)C(=O)O
InchiInChI=1S/C11H18N2O3/c1-3-10(11(15)16)8(6-14)4-9-5-12-7-13(9)2/h5,7-8,10,14H,3-4,6H2,1-2H3,(H,15,16)/t8-,10-/m0/s1
FormulaC11H18N2O3
PubChem ID182186
Molweight226.27
LogP0
Atoms16
Bonds6
H-bond Acceptor4
H-bond Donor2
Chemical Classificationalcohols heterocyclic compounds organic acids nitrogen compounds aromatic compounds carboxylic acids imidazoles

mVOC Specific Details


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


1-ethylimidazole

Mass-Spectra

Compound Details

Synonymous names
1-Ethylimidazole
1-Ethyl-1H-imidazole
7098-07-9
N-Ethylimidazole
Imidazole, 1-ethyl-
1H-Imidazole, 1-ethyl-
1-Ethylimidazole, >98%
T49PA5I372
MFCD00055389
1-ethyl imidazole
1-Ethyl-1H-imidazole #
CHEMBL13911
UNII-T49PA5I372
DTXSID10221209
EINECS 230-403-9
STL583912
AKOS000274662
AC-7525
CS-W011340
MCULE-1925854308
PS-9345
PD163435
DB-055475
E0132
NS00001048
EN300-53759
D70860
EC 230-403-9
W-104539
1-Ethylimidazole, produced by BASF, >=95.0% (HPLC)
Z286789018
InChI=1/C5H8N2/c1-2-7-4-3-6-5-7/h3-5H,2H2,1H
Microorganism:

Yes

IUPAC name1-ethylimidazole
SMILESCCN1C=CN=C1
InchiInChI=1S/C5H8N2/c1-2-7-4-3-6-5-7/h3-5H,2H2,1H3
FormulaC5H8N2
PubChem ID81540
Molweight96.13
LogP0.3
Atoms7
Bonds1
H-bond Acceptor1
H-bond Donor0
Chemical Classificationaromatic compounds aromatic aldehydes nitrogen compounds heterocyclic compounds aldehydes imidazoles

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaBacillus Pumilusn/aNAWei-wei et al. 2008
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaBacillus Pumilusn/an/ano


(E)-3-(2-amino-1H-imidazol-5-yl)prop-2-enoic Acid

Compound Details

Synonymous names
Imidazole, 2-amino-5-[(2-carboxy)vinyl]-
MTYDACZSYUGMLT-OWOJBTEDSA-N
(2E)-3-(2-Amino-1H-imidazol-5-yl)-2-propenoic acid #
Microorganism:

Yes

IUPAC name(E)-3-(2-amino-1H-imidazol-5-yl)prop-2-enoic acid
SMILESC1=C(NC(=N1)N)C=CC(=O)O
InchiInChI=1S/C6H7N3O2/c7-6-8-3-4(9-6)1-2-5(10)11/h1-3H,(H,10,11)(H3,7,8,9)/b2-1+
FormulaC6H7N3O2
PubChem ID5364104
Molweight153.14
LogP-0.3
Atoms11
Bonds2
H-bond Acceptor4
H-bond Donor3
Chemical Classificationamines aromatic compounds carboxylic acids heterocyclic compounds imidazoles nitrogen compounds organic acids

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
MicrobacteriumBallot et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
Microbacteriumtryptone soy (TS medium; Carl Roth, Karlsruhe, Germany)GC-QQQ-MSno