Results for:
chemical Classification: imides

2-aminoguanidine

Compound Details

Synonymous names
aminoguanidine
Pimagedine
Hydrazinecarboximidamide
79-17-4
Guanyl hydrazine
2-aminoguanidine
Monoaminoguanidine
Imino semicarbazide
Aminate base
Pimagedine [INN]
GUANIDINE, AMINO-
Hydrazinecarboximidamide(9CI)
2-azanylguanidine
SCQ4EZQ113
CHEMBL225304
CHEBI:40618
Carbamimidic acid, hydrazide; Guanylhydrazine
GER-11
[3H]-Pimagedine
AGU
CCRIS 3511
EINECS 201-183-1
UNII-SCQ4EZQ113
amino guanidine
1-aminoguanidine
1-amino-guanidine
Aminoguanidine (AG)
Tocris-0787
Lopac-A-7009
Lopac-A-8835
AMINOGUANIDINE [MI]
PIMAGEDINE [MART.]
PIMAGEDINE [WHO-DD]
Lopac0_000050
Lopac0_000103
AMY873
GTPL5135
DTXSID5040964
BDBM86154
HY-B1041A
CAS_2146
NSC_2146
BDBM50207159
HSCI1_000380
STL190849
YM-585
AKOS009031153
CCG-204198
DB05383
MDL-201228
SDCCGSBI-0050039.P002
SDCCGSBI-0050091.P002
NCGC00015082-01
NCGC00015082-02
NCGC00015082-03
NCGC00015082-04
NCGC00015082-05
NCGC00015082-06
NCGC00015082-07
NCGC00015082-14
NCGC00015082-15
NCGC00024791-01
NCGC00024791-02
NCGC00024791-03
CS-0013747
NS00018672
AB00443011_04
Q409583
SR-01000075164-1
W-104265
BRD-K25114078-003-07-3
BRD-K25114078-003-08-1
Microorganism:

No

IUPAC name2-aminoguanidine
SMILESC(=NN)(N)N
InchiInChI=1S/CH6N4/c2-1(3)5-4/h4H2,(H4,2,3,5)
FormulaCH6N4
PubChem ID2146
Molweight74.09
LogP-1.5
Atoms5
Bonds0
H-bond Acceptor2
H-bond Donor3
Chemical Classificationnitrogen compounds imides hydrazines amines
CHEBI-ID40618

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


Pyrrolidine-2,5-dione

Compound Details

Synonymous names
SUCCINIMIDE
123-56-8
pyrrolidine-2,5-dione
2,5-Pyrrolidinedione
Butanimide
2,5-Dioxopyrrolidine
Succinic acid imide
2,5-Diketopyrrolidine
Succinic imide
Succinimide-sauba
3,4-Dihydropyrrole-2,5-dione
Dihydro-3-pyrroline-2,5-dione
3,4-Dihydropyrrolidine
NSC 11204
EINECS 204-635-6
BRN 0108440
SUCCIMIDE
CHEBI:9307
DTXSID8051629
AI3-08539
UNII-10X90O3503
MFCD00005495
NSC-11204
10X90O3503
DTXCID3030181
EC 204-635-6
5-21-09-00438 (Beilstein Handbook Reference)
Mercury, disuccinimido-
WLN: T5VMVTJ
2, mercury(2+) salt
Mercuric imidosuccinate
SUCCINIMIDE (MART.)
SUCCINIMIDE [MART.]
Succinimide, mercury(2+) salt
MERCURIC SUCCINIMIDE
584-43-0
NSC-38417
NSC-41221
succinimid
cis-succinimide
Succinimide pharbiol
2,5dioxopyrrolidine
Lubrizol 6406
pyrroldine-2,5-dione
succinimide(butanimide)
SUCCINIMIDE [MI]
Succinimide pharbiol (TN)
SUCCINIMIDE [WHO-DD]
BDBM7814
CHEMBL275661
NSC11204
NSC13114
NSC38417
NSC41221
NSC49152
Tox21_303851
NSC-13114
NSC-49152
STL163344
AKOS000118776
DB13376
MCULE-8278049979
NCGC00357119-01
BP-21153
CAS-123-56-8
NS00001653
Succinimide, Vetec(TM) reagent grade, 98%
EN300-17963
C07273
D08532
Q419430
Z57127349
F1908-0169
1BBF5533-77F1-4B20-96F3-0BB022C36CD3
InChI=1/C4H5NO2/c6-3-1-2-4(7)5-3/h1-2H2,(H,5,6,7
Microorganism:

Yes

IUPAC namepyrrolidine-2,5-dione
SMILESC1CC(=O)NC1=O
InchiInChI=1S/C4H5NO2/c6-3-1-2-4(7)5-3/h1-2H2,(H,5,6,7)
FormulaC4H5NO2
PubChem ID11439
Molweight99.09
LogP-1
Atoms7
Bonds0
H-bond Acceptor2
H-bond Donor1
Chemical Classificationimides heterocyclic compounds nitrogen compounds
CHEBI-ID9307
Supernatural-IDSN0199596

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaCandida ParapsilosisNANAFitzgerald et al. 2022
Aspergillus NigerKate et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaCandida ParapsilosisYPDSPME/GC-MSno
Aspergillus Nigerinoculated potato samplesGC-MSno


Butanimidamide

Compound Details

Synonymous names
Butanimidamide
Butyramidine
107-90-4
Butyrimidamide
Butyric acid amidine
Butanoic acid amidine
NSC-56360
amidinopropane
Propane, 1-guanyl-
HSB7V5A6Z6
DTXSID60274604
NSC56360
AKOS000187373
MCULE-9230704591
AM802888
DB-002668
NS00010088
EN300-56500
A926953
Microorganism:

Yes

IUPAC namebutanimidamide
SMILESCCCC(=N)N
InchiInChI=1S/C4H10N2/c1-2-3-4(5)6/h2-3H2,1H3,(H3,5,6)
FormulaC4H10N2
PubChem ID18182
Molweight86.14
LogP0.1
Atoms6
Bonds2
H-bond Acceptor1
H-bond Donor2
Chemical Classificationamines imides 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-methylpyrrolidine-2,5-dione

Compound Details

Synonymous names
N-Methylsuccinimide
1121-07-9
1-methylpyrrolidine-2,5-dione
2,5-Pyrrolidinedione, 1-methyl-
Succinimide, N-methyl-
1-Methyl-2,5-pyrrolidinedione
N-METHYL SUCCINIMIDE
FT9GT286W2
1-Methyl-pyrrolidine-2,5-dione
NSC-11324
AI3-07107
1-Methyl-2,5-pyrrolidinedione; N-Methyl-2,5-pyrrolidinedione; NSC 11324
N-Methylsuccinimide, 99%
UNII-FT9GT286W2
SCHEMBL27941
AMY228
CHEMBL317929
DTXSID40149902
NSC11324
MFCD00005517
NSC 11324
STL444522
AKOS002845657
N-METHYL-2,5-PYRROLIDINEDIONE
DS-5966
AC-15701
DB-041043
CS-0151201
M2207
NS00123033
D70368
EN300-211529
A894650
J-002708
Q27462406
InChI=1/C5H7NO2/c1-6-4(7)2-3-5(6)8/h2-3H2,1H
Microorganism:

Yes

IUPAC name1-methylpyrrolidine-2,5-dione
SMILESCN1C(=O)CCC1=O
InchiInChI=1S/C5H7NO2/c1-6-4(7)2-3-5(6)8/h2-3H2,1H3
FormulaC5H7NO2
PubChem ID70717
Molweight113.11
LogP-0.9
Atoms8
Bonds0
H-bond Acceptor2
H-bond Donor0
Chemical Classificationnitrogen compounds imides heterocyclic compounds

mVOC Specific Details

Vapor Pressure
PressureReference
1.92e-4
Massbank-Links

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


1-hydroxypyrrolidine-2,5-dione

Compound Details

Synonymous names
N-Hydroxysuccinimide
6066-82-6
1-hydroxypyrrolidine-2,5-dione
HOSu
1-Hydroxysuccinimide
1-Hydroxy-2,5-pyrrolidinedione
Hydroxysuccinimide
2,5-Pyrrolidinedione, 1-hydroxy-
Succinimide, N-hydroxy-
N-hydroxy succinimide
N-hydroxysuccinimide (HOSu)
MFCD00005516
NHS
MJE3791M4T
NSC-74335
N-hydroxysuccinimid
CCRIS 2604
N-hydroxy-succinimide
EINECS 228-001-3
NSC 74335
UNII-MJE3791M4T
N-hydroxysucinimide
N-hyroxysuccinimide
N-Hydroxysuccinimde
N-Hydroxylsuccinimide
n-hydroxysuccin imide
1-Hydroxy-2,5-pyrrolidinedione; NHS
HOSu.
N-hydroxyl succinimide
2, 1-hydroxy-
N-hy dr oxy succinimide
n-hydroxysuccinimide (nhs)
SCHEMBL1123
Sigma 130672
N-hydroxysuccinic acid imide
N-Hydroxysuccinimide, 98%
NCIOpen2_000470
HYDROXYSUCCINIMIDE, N-
hydroxy-pyrrolidine-2,5-dione
CHEMBL403753
n-hydroxypyrrolidine-2,5-dione
DTXSID7064102
1-hydroxy-pyrrolidine-2,5-dione
N-HYDROXYSUCCINIMIDE [MI]
HY-Y0623
NSC74335
STR01867
STL183832
AKOS000121489
AB00437
AM83849
CS-W008598
N-HYDROXY-2,5-DIOXOPYRROLIDINE
PS-4557
AC-10509
AC-15786
BP-13159
SY001334
DB-298765
A8451
B0249
H0623
NS00022482
EN300-17439
N-Hydroxysuccinimide, purum, >=97.0% (T)
Q408833
Q-201468
Z56933833
F0001-1588
1-hydroxypyrrolidine-2,5-dione;N-Hydroxysuccinimide (HOSu)
InChI=1/C4H5NO3/c6-3-1-2-4(7)5(3)8/h8H,1-2H
Microorganism:

No

IUPAC name1-hydroxypyrrolidine-2,5-dione
SMILESC1CC(=O)N(C1=O)O
InchiInChI=1S/C4H5NO3/c6-3-1-2-4(7)5(3)8/h8H,1-2H2
FormulaC4H5NO3
PubChem ID80170
Molweight115.09
LogP-1.4
Atoms8
Bonds0
H-bond Acceptor3
H-bond Donor1
Chemical Classificationnitrogen compounds imides heterocyclic compounds
Supernatural-IDSN0252733

mVOC Specific Details


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


(2,5-dioxopyrrolidin-1-yl) Benzoate

Compound Details

Synonymous names
23405-15-4
BZ-OSU
N-(Benzoyloxy)succinimide
2,5-dioxopyrrolidin-1-yl benzoate
2,5-Pyrrolidinedione, 1-(benzoyloxy)-
(2,5-dioxopyrrolidin-1-yl) benzoate
Benzoic acid N-hydroxysuccinimide ester
n-succinimidyl benzoate
1-(benzoyloxy)-2,5-pyrrolidinedione
MFCD00078953
Benzoyloxysuccinimide
Benzoic Acid N-Succinimidyl Ester
Benzoyoxysuccinimide
SUCCINIMIDO BENZOATE
TimTec1_001999
n-hydroxysuccinimidyl benzoate
SCHEMBL133554
DTXSID00352011
N-(Benzoyloxy)succinimide, 96%
2,5-dioxopyrrolidin-1-ylbenzoate
HMS1539K19
o-benzoyl-n,n-succinylhydroxylamine
STK367712
AKOS001613433
CS-W009517
AS-11125
PD019251
SY019097
B4785
1-[(phenylcarbonyl)oxy]pyrrolidine-2,5-dione
benzoic Acid 2,5-Dioxo-pyrrolidin-1-yl Ester
C93448
benzoic acid (2,5-dioxo-pyrrolidin-1-yl) ester
A878253
AE-848/32609005
EN300-11685050
SR-01000404468
J-015099
J-519751
SR-01000404468-1
Microorganism:

Yes

IUPAC name(2,5-dioxopyrrolidin-1-yl) benzoate
SMILESC1CC(=O)N(C1=O)OC(=O)C2=CC=CC=C2
InchiInChI=1S/C11H9NO4/c13-9-6-7-10(14)12(9)16-11(15)8-4-2-1-3-5-8/h1-5H,6-7H2
FormulaC11H9NO4
PubChem ID716426
Molweight219.19
LogP0.9
Atoms16
Bonds3
H-bond Acceptor4
H-bond Donor0
Chemical Classificationaromatic compounds benzenoids imides nitrogen compounds

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
Kluyveromyces MarxianusJi et al. 2024
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
Kluyveromyces MarxianusSauce Meat during StorageSPME–GC–MSno