Results for:
chemical Classification: hydrazines

N-(propan-2-ylideneamino)methanamine

Compound Details

Synonymous names
2-Propanone, methylhydrazone
N-(propan-2-ylideneamino)methanamine
Acetone methylhydrazone
5771-02-8
1-methyl-2-(propan-2-ylidene)hydrazine
Acetone N-methylhydrazone
METHYLHYDRAZONE ACETONE
DTXSID20206421
NSC64710
NSC 64710
NSC-64710
NSC166797
1-methyl-2-(2-propylidene)hydrazine
NSC 166797
NSC-166797
Microorganism:

Yes

IUPAC nameN-(propan-2-ylideneamino)methanamine
SMILESCC(=NNC)C
InchiInChI=1S/C4H10N2/c1-4(2)6-5-3/h5H,1-3H3
FormulaC4H10N2
PubChem ID79840
Molweight86.14
LogP0.5
Atoms6
Bonds1
H-bond Acceptor2
H-bond Donor1
Chemical Classificationhydrazines nitrogen compounds

mVOC Specific Details

Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAspergillus NigerNANACosta et al. 2016
EukaryotaCandida AlbicansNANACosta et al. 2016
EukaryotaPenicillium ChrysogenumNANACosta et al. 2016
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAspergillus NigerYeast Glucose ChloramphenicolSPME/GCxGC-MSno
EukaryotaCandida AlbicansYeast Glucose ChloramphenicolSPME/GCxGC-MSno
EukaryotaPenicillium ChrysogenumYeast Glucose ChloramphenicolSPME/GCxGC-MSno


Furan-2-carbohydrazide

Compound Details

Synonymous names
furan-2-carbohydrazide
3326-71-4
2-Furoic acid hydrazide
2-Furoic hydrazide
2-Furohydrazide
Furoylhydrazide
2-Furoylhydrazine
2-Furancarbohydrazide
2-Furoylhydrazide
2-Furancarboxylic acid, hydrazide
Furoic acid, hydrazide
2-Furylcarbonylhydrazide
2-furancarboxylic acid hydrazide
2-Furancarbohydrazonic acid
2-FUROIC ACID, HYDRAZIDE
Pyromucic acid hydrazide
2-Furancarbonyl hydrazide
2-Furylcarboxylic acid hydrazide
MFCD00003235
Furan-2-carboxylic acid hydrazide
NSC 11957
NSC 35574
WLN: T5OJ BVMZ
NSC11957
NSC35574
Furancarboxylic acid, hydrazide
2-Furoicacidhydrazide
EINECS 222-046-2
BRN 0114435
AI3-62534
2-furanhydrazide
2-Furoichydrazide
2-furanoic hydrazide
furan 2-carbohydrazide
2-Furoic hydrazide, 98%
5-18-06-00125 (Beilstein Handbook Reference)
SCHEMBL140989
CHEMBL340492
DTXSID10186900
HMS1775C18
CS-M1764
NSC-11957
NSC-35574
STK121925
AKOS000194881
AM10044
MCULE-6130017029
AS-57679
SY048471
DB-048376
DB-293084
F1015
NS00029450
2-Furoic hydrazide, purum, >=97.0% (NT)
EN300-17784
F10405
A821702
AN-068/40170015
J-019120
J-521392
Z57036326
F3145-4915
InChI=1/C5H6N2O2/c6-7-5(8)4-2-1-3-9-4/h1-3H,6H2,(H,7,8
Microorganism:

Yes

IUPAC namefuran-2-carbohydrazide
SMILESC1=COC(=C1)C(=O)NN
InchiInChI=1S/C5H6N2O2/c6-7-5(8)4-2-1-3-9-4/h1-3H,6H2,(H,7,8)
FormulaC5H6N2O2
PubChem ID18731
Molweight126.11
LogP-0.5
Atoms9
Bonds1
H-bond Acceptor3
H-bond Donor2
Chemical Classificationhydrazines ethers furan derivatives heterocyclic compounds nitrogen compounds
Supernatural-IDSN0348234

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaMetschnikowia HawaiiensisNANALjunggren et al. 2019
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaMetschnikowia Hawaiiensisliquid YPD mediumGC-MSno


4-methoxybenzohydrazide

Mass-Spectra

Compound Details

Synonymous names
4-Methoxybenzhydrazide
4-Methoxybenzohydrazide
3290-99-1
p-Anisic hydrazide
p-Anisoylhydrazine
4-Methoxybenzoic acid hydrazide
Anisic hydrazide
4-Methoxybenzoylhydrazine
Anisoylhydrazine
p-Anisic acid, hydrazide
Anisic acid hydrazide
(p-Methoxybenzoyl)hydrazine
Benzoic acid, 4-methoxy-, hydrazide
4-Methoxybenzene-1-carbohydrazide
p-Methoxybenzoic acid hydrazide
p-Methoxybenzoic hydrazide
(4-Methoxybenzoyl)hydrazide
p-Methoxy benzhydrazide
Hydrazine, 4-methoxybenzoyl-
4-Methoxybenzoyl hydrazide
p-Anisohydrazide
(4-Methoxybenzoyl)hydrazine
Benzoic acid, p-methoxy-, hydrazide
NSC 76223
p-methoxybenzhydrazide
4-methoxy benzhydrazide
p-Methoxybenzoyl hydrazide
CHEMBL1588015
MFCD00017073
NSC-76223
33BK77102I
p-Anisic acid hydrazide
p-methoxy benzohydrazide
EINECS 221-952-5
4-Methoxybenzoic hydrazide
anisohydrazide
BRN 0389017
UNII-33BK77102I
p-methoxybenzohydrazide
4MeOPhCON2
4-methoxy-benzohydrazide
P-ANISOYLHYDRAZIDE
4-Methoxybenzohydrazide #
WLN: ZMVR DO1
Oprea1_578754
Oprea1_834050
303084-44-8
4-10-00-00454 (Beilstein Handbook Reference)
MLS000833598
4-Methoxybenzhydrazide, 97%
SCHEMBL407188
METHOXYBENZHYDRAZIDE, 4-
4-methoxy-benzoic acid hydrazide
4-Methoxybenzoic acid, hydrazide
DTXSID60186556
HMS2804K19
NSC76223
STR02684
BBL005388
BDBM50340089
STK089128
AKOS000194883
MCULE-8901256628
NCGC00246653-01
SMR000457119
SY005826
DB-013162
AM20040183
CS-0116725
M1770
NS00029380
4-methoxybenzohydrazide;4-Methoxybenzhydrazide
EN300-18129
I11428
A821514
W-106806
Q27256258
Z57199662
F1335-0033
Microorganism:

Yes

IUPAC name4-methoxybenzohydrazide
SMILESCOC1=CC=C(C=C1)C(=O)NN
InchiInChI=1S/C8H10N2O2/c1-12-7-4-2-6(3-5-7)8(11)10-9/h2-5H,9H2,1H3,(H,10,11)
FormulaC8H10N2O2
PubChem ID76792
Molweight166.18
LogP0.2
Atoms12
Bonds2
H-bond Acceptor3
H-bond Donor2
Chemical Classificationhydrazines benzenoids ethers aromatic compounds nitrogen compounds
Supernatural-IDSN0323114

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaMycobacterium Bovisclinical isolate,abscess,bladder cancerMellors et al. 2017
ProkaryotaMycobacterium Intracellulareclinical isolate,sputum,AIDS patientMellors et al. 2017
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaMycobacterium Bovis7H9 broth, Tween 80, glycerolTenaxGC,Chromosorb,HS-SPME, GC-MSno
ProkaryotaMycobacterium Intracellulare7H9 broth, Tween 80, glycerolTenaxGC,Chromosorb,HS-SPME, GC-MSno


1-methyl-1-phenylhydrazine

Compound Details

Synonymous names
1-Methyl-1-phenylhydrazine
618-40-6
1-Methylphenylhydrazine
N-Methyl-N-phenylhydrazine
Hydrazine, 1-methyl-1-phenyl-
N-Phenyl-N-methylhydrazine
1-methyl-1-phenyl-hydrazine
.alpha.-Methyl-.alpha.-phenylhydrazine
YHB9CZB63U
N-methyl-N-phenyl-hydrazine
MFCD00007627
NSC-525518
Hydrazine, methylphenyl-
alpha-Methyl-alpha-phenylhydrazine
EINECS 210-547-9
UNII-YHB9CZB63U
NSC 525518
methylphenylhydrazine
NSC525518
methyl phenylhydrazine
n-methylphenylhydrazine
SCHEMBL788
1-methyl 1-phenylhydrazine
1-phenyl-1-methylhydrazine
1-methyl-1-phenyl hydrazine
.alpha.-Methylphenylhydrazine
DTXSID2060678
HMS1761M15
1-Methyl-1-phenylhydrazine, 97%
AMY22640
618-40-6 pound OIAe pound(c)
BBL100336
STL554118
AKOS001098542
FS-4236
MCULE-1026323460
s11053
J29.560D
SY049215
A8562
M0399
NS00034808
EN300-18464
J-505003
Q27294527
Z57985384
InChI=1/C7H10N2/c1-9(8)7-5-3-2-4-6-7/h2-6H,8H2,1H
Microorganism:

Yes

IUPAC name1-methyl-1-phenylhydrazine
SMILESCN(C1=CC=CC=C1)N
InchiInChI=1S/C7H10N2/c1-9(8)7-5-3-2-4-6-7/h2-6H,8H2,1H3
FormulaC7H10N2
PubChem ID36299
Molweight122.17
LogP1.6
Atoms9
Bonds1
H-bond Acceptor2
H-bond Donor1
Chemical Classificationamines hydrazines heterocyclic compounds nitrogen 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


3-aminobenzohydrazide

Compound Details

Synonymous names
3-Aminobenzhydrazide
14062-34-1
3-Aminobenzohydrazide
3-Aminobenzoyl hydrazine
Benzoic acid, 3-amino-, hydrazide
m-Aminobenzhydrazide
m-Amino benzhydrazide
m-Aminobenzoic acid hydrazide
3-aminobenzoic acid hydrazide
459AL52KFJ
NSC-28878
m-Aminobenzohydrazide
3-Amino-benzoic acid hydrazide
C7-H9-N3-O
EINECS 237-907-8
3-Aminobenzohydrazide #
UNII-459AL52KFJ
3-AMINOBENZOYLHYDRAZIDE
3-AMINOBENZOYLHYDRAZINE
SCHEMBL294944
3-Aminobenzoic acid, hydrazide
M-AMINOBENZOIC HYDRAZIDE
CHEMBL125641
DTXSID4074516
NSC28878
MFCD00017067
NSC 28878
AKOS008966956
MCULE-3299646715
AS-61578
DB-042526
CS-0206379
NS00024558
EN300-17375
E85335
Z56922179
Microorganism:

Yes

IUPAC name3-aminobenzohydrazide
SMILESC1=CC(=CC(=C1)N)C(=O)NN
InchiInChI=1S/C7H9N3O/c8-6-3-1-2-5(4-6)7(11)10-9/h1-4H,8-9H2,(H,10,11)
FormulaC7H9N3O
PubChem ID84178
Molweight151.17
LogP-0.9
Atoms11
Bonds1
H-bond Acceptor3
H-bond Donor3
Chemical Classificationbenzenoids aromatic compounds hydrazines nitrogen compounds amides amines
Supernatural-IDSN0173921

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


N-[(E)-(4-nitrophenyl)methylideneamino]benzamide

Compound Details

Synonymous names
N'-(4-Nitrobenzylidene)benzohydrazide
N'-[(E)-(4-Nitrophenyl)methylidene]benzohydrazide
PhCON2 4NO2PhCH
Benzoic acid, (4-nitrobenzylidene)hydrazide
N-[(E)-(4-nitrophenyl)methylideneamino]benzamide
MVQGNPRBTFWEMO-XNTDXEJSSA-N
BDBM192660
STK364451
AKOS000612303
MCULE-5950867660
Benzoic acid, (4-nitrophenyl)-methylenehydrozide
N-[(E)-(4-nitrophenyl)methyleneamino]benzamide
A819418
N’-(4-nitrophenylmethylene)benzohydrazide (1k)
N'-[(E)-(4-Nitrophenyl)methylidene]benzohydrazide #
Microorganism:

Yes

IUPAC nameN-[(E)-(4-nitrophenyl)methylideneamino]benzamide
SMILESC1=CC=C(C=C1)C(=O)NN=CC2=CC=C(C=C2)[N+](=O)[O-]
InchiInChI=1S/C14H11N3O3/c18-14(12-4-2-1-3-5-12)16-15-10-11-6-8-13(9-7-11)17(19)20/h1-10H,(H,16,18)/b15-10+
FormulaC14H11N3O3
PubChem ID6861632
Molweight269.25
LogP2.4
Atoms20
Bonds3
H-bond Acceptor4
H-bond Donor1
Chemical Classificationbenzenoids nitrogen compounds aromatic compounds amides hydrazines

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


Benzyl N-aminocarbamate

Compound Details

Synonymous names
Benzyl carbazate
5331-43-1
Benzyl hydrazinecarboxylate
Carbobenzoxyhydrazide
Hydrazinecarboxylic acid, phenylmethyl ester
Carbazic acid, benzyl ester
Benzyloxycarbonyl hydrazide
benzyl N-aminocarbamate
Benzylcarbazate
((Benzyloxy)carbonyl)hydrazine
Z-hydrazine
N-Cbz-hydrazine
Carbazic Acid Benzyl Ester
Hydrazinecarboxylic acid benzyl ester
carbobenzyloxyhydrazine
benzylhydrazinecarboxylate
(benzyloxy)carbohydrazide
(Benzyloxycarbonyl)hydrazine
H7GM2H55TC
DTXSID1047447
NSC-2287
MFCD00041890
[(Benzyloxy)carbonyl]hydrazine
NSC 2287
Z-NHNH2 (free base)
EINECS 226-230-3
UNII-H7GM2H55TC
Cbz-Hydrazine
Carbobenzoxyhydrazine
carbobenzoxy hydrazine
z-NHNH2
Benzyl carbazate, 97%
Benzyl hydrazinocarboxylate
Hydrazine, n-cbz protected
benzyl hydrazine carboxylate
Benzyl hydrazinecarboxylate #
SCHEMBL156297
Phenylmethyl hydrazinecarboxylate
CHEMBL3187376
DTXCID9027447
phenylmethyl hydrazine carboxylate
NSC2287
N-[(phenylmethoxy)carbonyl]hydrazine
Tox21_302719
hydrazine carboxylic acid benzyl ester
AKOS005206814
AM10713
CS-W016057
PS-5980
NCGC00256697-01
SY017007
CAS-5331-43-1
HYDRAZINCARBOXYLIC ACID BENZYL ESTER
DB-007279
NS00022310
EN300-91928
C93486
W-105753
Q27279734
InChI=1/C8H10N2O2/c9-10-8(11)12-6-7-4-2-1-3-5-7/h1-5H,6,9H2,(H,10,11
Microorganism:

Yes

IUPAC namebenzyl N-aminocarbamate
SMILESC1=CC=C(C=C1)COC(=O)NN
InchiInChI=1S/C8H10N2O2/c9-10-8(11)12-6-7-4-2-1-3-5-7/h1-5H,6,9H2,(H,10,11)
FormulaC8H10N2O2
PubChem ID79242
Molweight166.18
LogP0.9
Atoms12
Bonds3
H-bond Acceptor3
H-bond Donor2
Chemical Classificationhydrazines benzenoids aromatic compounds
Supernatural-IDSN0338135

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
Saccharomyces CerevisiaeJi et al. 2024
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
Saccharomyces CerevisiaeSauce Meat during StorageSPME–GC–MSno


Ethyl N-aminocarbamate

Compound Details

Synonymous names
Ethyl carbazate
4114-31-2
Ethyl hydrazinecarboxylate
Hydrazinecarboxylic acid, ethyl ester
Carbethoxyhydrazine
Ethylcarbazate
Ethyl carbazinate
ethyl N-aminocarbamate
ethoxycarbohydrazide
Carboethoxyhydrazine
Monocarbethoxyhydrazine
N-(Carbethoxy)hydrazine
1-(Carbethoxy)hydrazine
(Ethoxycarbonyl)hydrazide
(Ethoxycarbonyl)hydrazine
Ethyl hydrazinocarboxylate
N-(Ethoxycarbonyl)hydrazine
1-(Ethoxycarbonyl)hydrazine
CARBAZIC ACID, ETHYL ESTER
1-Carbethoxy hydrazine
Ethoxycarbonyl hydrazide
Ethoxycarbonylhydrazine
NSC 2277
NSC 52663
ethylhydrazinecarboxylate
(Monocarbethoxy)hydrazine
MFCD00007595
Carbazic Acid Ethyl Ester
WLN: ZMVO2
EINECS 223-903-3
BRN 0878265
AI3-06208
ethyl hydrazinoformate
Ethoxy Formyl Hydrazine
Ethyl carbazate, 97%
ethylhydrazine carboxylate
ethyl hydrazine-carboxylate
hydrazinoformicacid ethylester
4-03-00-00174 (Beilstein Handbook Reference)
hydrazinoformic acid ethylester
SCHEMBL170635
hydrazinoformic acid ethyl ester
DTXSID1063308
VYSYZMNJHYOXGN-UHFFFAOYSA-
NSC2277
N-amino-carbamic acid ethyl ester
AMY23328
hydrazinecarboxylic acid ethyl ester
Hydrazinocarboxylic acid ethyl ester
NSC-2277
NSC52663
STR03390
BBL027647
NSC-52663
STL185589
AKOS000119588
CS-W008412
DB-049721
NS00021148
EN300-20511
D77690
A825450
W-106317
F0001-1162
Z104478458
InChI=1/C3H8N2O2/c1-2-7-3(6)5-4/h2,4H2,1H3,(H,5,6)
Microorganism:

No

IUPAC nameethyl N-aminocarbamate
SMILESCCOC(=O)NN
InchiInChI=1S/C3H8N2O2/c1-2-7-3(6)5-4/h2,4H2,1H3,(H,5,6)
FormulaC3H8N2O2
PubChem ID20064
Molweight104.11
LogP-0.4
Atoms7
Bonds2
H-bond Acceptor3
H-bond Donor2
Chemical Classificationnitrogen compounds hydrazines

mVOC Specific Details


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


Acetohydrazide

Compound Details

Synonymous names
Acethydrazide
Acetohydrazide
1068-57-1
Acetylhydrazine
Acetic hydrazide
Acetic acid hydrazide
Monoacetylhydrazine
Acetyl hydrazide
N-Acetylhydrazine
Monoacetyl hydrazine
Ethanehydrazonic acid
ACETIC ACID, HYDRAZIDE
Hydrazine, acetyl-
Acetyl hydrazine
acetohydrazine
ENT-61241
NSC 53155
Hydrazid kyseliny octove
NSC 2271
MFCD00007610
CHEBI:2422
SK0DPC9098
NSC-2271
NSC-53155
WLN: ZMV1
acethydrazine
CCRIS 4791
Hydrazid kyseliny octove [Czech]
EINECS 213-948-7
UNII-SK0DPC9098
AI3-61241
ethanoic hydrazide
AcN2 deriv
acetohydrazonic acid
acetic acid hydrazone
Acethydrazide, 90%
ethanoic acid hydrazide
methane, hydrazinocarbonyl-
CHEMBL3091859
DTXSID9020900
CHEBI:48978
OFLXLNCGODUUOT-UHFFFAOYSA-
NSC2271
Ald3-H_000034
CS-D1403
NSC53155
Ald3.1-H_000314
Ald3.1-H_000633
Ald3.1-H_000952
AB6005
BBL018600
STL194154
AKOS000104423
AB00888
GS-3116
BP-30010
Acetyl Hydrazine Contains~10% acetic acid
DB-029410
A0789
Acethydrazide (moist with methylene chloride)
AM20080014
NS00021483
EN300-18497
C07447
A801521
J-519529
Q4678005
Z58981787
InChI=1/C2H6N2O/c1-2(5)4-3/h3H2,1H3,(H,4,5)
Microorganism:

No

IUPAC nameacetohydrazide
SMILESCC(=O)NN
InchiInChI=1S/C2H6N2O/c1-2(5)4-3/h3H2,1H3,(H,4,5)
FormulaC2H6N2O
PubChem ID14039
Molweight74.08
LogP-1.6
Atoms5
Bonds0
H-bond Acceptor2
H-bond Donor2
Chemical Classificationnitrogen compounds hydrazines
CHEBI-ID2422
Supernatural-IDSN0264016

mVOC Specific Details


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


Hydrazine

Compound Details

Synonymous names
HYDRAZINE
302-01-2
Diamine
Levoxine
Hydrazine base
Oxytreat 35
Diazane
Hydrazin
Hydrazyna
Hydrazine, anhydrous
Nitrogen hydride
Hydrazines
Hydrazine (anhydrous)
Hydrazyna [Polish]
RCRA waste number U133
Hydrazine anhydrous
CCRIS 335
Amerzine
HSDB 544
N2H4
H2NNH2
UNII-27RFH0GB4R
EINECS 206-114-9
27RFH0GB4R
CHEBI:15571
119775-10-9
DTXSID3020702
H 70 (FUEL)
NITROGEN HYDRIDE (N2H4)
HYDRAZINE (IARC)
HYDRAZINE [IARC]
HDZ
ISONIAZID IMPURITY E (EP IMPURITY)
ISONIAZID IMPURITY E [EP IMPURITY]
ALLOPURINOL IMPURITY F (EP IMPURITY)
ALLOPURINOL IMPURITY F [EP IMPURITY]
UN2029
UN3293
Hydrazine/Hydrazine sulfate
RCRA waste no. U133
Hydrazine Standard: N2H4 @ 100 mg/L in 1% Acetic Acid
Hydrazine Standard: N2H4 @ 1000 mg/L in 1% Acetic Acid
Diamidogen
Hidrazine
amino nitrogen
Zerox
Hydrazine fume
(anhydrous)
Catalyzed hydrazine
Scav-Ox II
HYDRAZINE (HYDRAZINE SULFATE)
Zerox (Salt/Mix)
Amerzine (Salt/Mix)
Diamine, hydrazine base
HYDRAZINE [MI]
HYDRAZINE [HSDB]
NH2NH2
Scav-Ox II (Salt/Mix)
HYDRAZINE [WHO-DD]
Hydrazine, anhydrous, 98%
Nitrogen hydride, (N2H4)
NH2-NH2
UN 2029 (Salt/Mix)
UN 2030 (Salt/Mix)
DTXCID30702
Hydrazine (hydrazine sulphate)
HYDRAZINE, (ANHYDROUS)
Catalyzed hydrazine (Salt/Mix)
CHEMBL1237174
HYDRAZINE AQUEOUS SOLUTION
DTXSID70159610
CREXVNNSNOKDHW-UHFFFAOYSA-N
MFCD00011417
STL281862
AKOS000269060
NCGC00188947-01
BP-13613
DB-007559
H0172
H0204
H0697
NS00014234
C05361
Q58447
J-017830
Q27110398
HZN
Microorganism:

No

IUPAC namehydrazine
SMILESNN
InchiInChI=1S/H4N2/c1-2/h1-2H2
FormulaH4N2
PubChem ID9321
Molweight32.046
LogP-1.5
Atoms2
Bonds0
H-bond Acceptor2
H-bond Donor2
Chemical Classificationnitrogen compounds hydrazines
CHEBI-ID15571
Supernatural-IDSN0260111

mVOC Specific Details

Boiling Point
DegreeReference
113.55 °C peer reviewed
Volatilization
A pKa of 7.96(1) indicates hydrazine will exist partially in the cation or anion form at pH values of 5 to 9 and, therefore, volatilization from water surfaces is not expected to be an important fate process(SRC). The Henry's Law constant for the neutral species of hydrazine is estimated as 6.07X10-7 atm-cu m/mole(SRC) derived from its vapor pressure, 14.4 mm Hg(2), and assigned value for water solubility of 1.0X10+6 mg/L (miscible)(3). This Henry's Law constant indicates that hydrazine is expected to be essentially nonvolatile from water and moist soil surfaces(4). With an air velocity at the liquid surface of 63.5 cm/sec, the volatilization of hydrazine from petri dishes containing 25%, 50% and 75% hydrazine-water mixtures was 0.5 g after 6.66 hr, about 1 g after 5 hr, and about 3 g after 5 hr, respectively(5). At each concentration, the rate of volatilization decreased with time(5). Hydrazine's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of hydrazine from dry soil surfaces may exist(SRC) based upon its vapor pressure(1).
Soil Adsorption
Using a structure estimation method based on molecular connectivity indices(1), the Koc of hydrazine can be estimated to be 13(SRC). According to a classification scheme(2), this estimated Koc value suggests that hydrazine is expected to have very high mobility in soil. The pKa of hydrazine is 7.92(3), indicating that this compound will exist partially in the cation form in the environment and cations generally adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts(4). The nature and extent of hydrazine adsorption by clays and soils is very dependent on suspension pH and on the types of surface functional groups present on the solid matrix. Under acidic conditions, pH 4.0, 99.9% of the hydrazine is present as the protonated species and should be able to readily replace Na+ from exchange sites(3). Under alkaline conditions, pH 8.0, approximately 50% of the hydrazine is protonated and 50% is in neutral form. The primary mechanism of hydrazine adsorption in a montmorillonite clay suspension was cation exchange, both at pH 4 and 8; adsorption of hydrazine was lower at the higher pH value(3). The main mechanism for hydrazine retention at pH 4 and at low hydrazine concentrations in the upper Arrendondo soil horizon (fine sand) was also cation exchange. At higher concentrations more than 60% of the hydrazine interacted with a different type of binding site, possibly with organic-surface functional groups such as carbonyl groups(3). Under alkaline conditions, using upper horizon Arrendondo soil, (at pH 8.0) hydrazine was adsorbed more readily than at pH 4(3).
Vapor Pressure
PressureReference
12.2

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


2-cyanoacetohydrazide

Compound Details

Synonymous names
Cyanoacetohydrazide
2-Cyanoacetohydrazide
140-87-4
Cyacetacide
Cyacetazide
Cyanoacetic acid hydrazide
Cyanoacethydrazide
Cyacetacid
Cyacetazid
Mackreazid
Neohydrazid
Armazal
Cianazil
Cyanazide
Cyanizide
Cyazide
Dictycide
Dictyzide
Hidacian
Hidaciann
Leandin
Reazide
Tsiazid
Cyazid
Helmox
Reacid
Reazid
Cyanoethydrazide
Cyanacethydrazide
Cyanacetohydrazide
Cyanacetylhydrazide
Cyanoacetylhydrazide
Malonitrile hydrazide
ACETIC ACID, CYANO-, HYDRAZIDE
(Cyanoacetyl)hydrazine
Usaf kf-18
Malononitrile hydrazide
Cyanoacetyl hydrazide
Kyanacethydrazid
Cyanacetic acid hydrazide
AB-42
Cyanoacetic hydrazide
Cyanoacetylhydrazine
NSC-24261
Cyanacetic acid, hydrazide
.alpha.-Cyanoacetohydrazide
DTXSID9046572
40H59YCS67
NCGC00166240-01
Cyanacethydrazine
Cyacetacide [INN]
Cyazide (VAN)
DTXCID7026572
Ciacetacida
Cyacetacidum
Kyanacethydrazid [Czech]
USAF kf-28
Cyacetacidum [INN-Latin]
methane, C-cyano-C-hydrazinocarbonyl-
Ciacetacida [INN-Spanish]
CAS-140-87-4
HSDB 2701
Cyacetacide [INN:BAN]
EINECS 205-437-2
NSC 24261
BRN 1751498
UNII-40H59YCS67
AI3-23466
2-Cyanoacethydrazide
2-Cyanoacetylhydrazide
CYACETACIDE [MI]
cyanoacetic acid hydrazone
acetohydrazide, 2-cyano-
WLN: ZMV1CN
Cyanoacetohydrazide, 98%
CYACETACIDE [HSDB]
Cyanoacetic acid, hydrazide
CYACETACIDE [MART.]
4-02-00-01895 (Beilstein Handbook Reference)
(.alpha.-Cyanoacetyl)hydrazine
CHEMBL2106008
Alpha-cyanoacetic acid, hydrazide
AMY5330
Acetic acid, 2-cyano-, hydrazide
HY-B0994
NSC24261
Tox21_112366
BBL010619
MFCD00007611
STK298870
AKOS000119759
Tox21_112366_1
CCG-213834
CS-4488
NCGC00166240-02
DB-042536
NS00024567
EN300-19656
AB00442940_02
12B-129
AC-907/25014397
SR-01000944252
J-007426
J-520129
SR-01000944252-1
BRD-K39371216-001-01-3
Q27258330
F2111-0015
Z104474618
InChI=1/C3H5N3O/c4-2-1-3(7)6-5/h1,5H2,(H,6,7
Microorganism:

Yes

IUPAC name2-cyanoacetohydrazide
SMILESC(C#N)C(=O)NN
InchiInChI=1S/C3H5N3O/c4-2-1-3(7)6-5/h1,5H2,(H,6,7)
FormulaC3H5N3O
PubChem ID8820
Molweight99.09
LogP-1.3
Atoms7
Bonds1
H-bond Acceptor3
H-bond Donor2
Chemical Classificationnitrogen compounds nitriles hydrazines

mVOC Specific Details


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


Methylhydrazine

Compound Details

Synonymous names
METHYLHYDRAZINE
60-34-4
Hydrazine, methyl-
Methyl Hydrazine
Monomethylhydrazine
Methyl-hydrazine
1-Methylhydrazine
Metylohydrazyna
RCRA waste number P068
N-methylhydrazine
2-methylhydrazine
CH3NHNH2
MMH
UWA30B5Z1J
CHEMBL160520
DTXSID4020874
Monomethyl Hydrazine
Methylhydrazine (mono)
Metylohydrazyna [Polish]
20244-39-7
CCRIS 394
HSDB 1172
EINECS 200-471-4
UN1244
RCRA waste no. P068
UNII-UWA30B5Z1J
BRN 0635645
methyldiazane
methl hydrazine
AI3-52240
N-methyhydrazine
N-methyl hydrazine
N-methyl-hydrazine
2-methyl hydrazine
MeNHNH2
Methylhydrazine, 98%
H2NNHCH3
EC 200-471-4
METHYLHYDRAZINE [MI]
METHYLHYDRAZINE [HSDB]
BCP07836
BBL011339
BDBM50049259
STL146429
AKOS005720746
Methylhydrazine [UN1244] [Poison]
UN 1244
BP-11387
BP-30186
Methylhydrazine, purum, >=98.0% (GC)
M0558
NS00002460
InChI=1/CH6N2/c1-3-2/h3H,2H2,1H
A832701
Q417347
HDN
Microorganism:

Yes

IUPAC namemethylhydrazine
SMILESCNN
InchiInChI=1S/CH6N2/c1-3-2/h3H,2H2,1H3
FormulaCH6N2
PubChem ID6061
Molweight46.072
LogP-0.9
Atoms3
Bonds0
H-bond Acceptor2
H-bond Donor2
Chemical Classificationnitrogen compounds hydrazines

mVOC Specific Details

Boiling Point
DegreeReference
87.5 °C peer reviewed
Volatilization
1,2-Dimethylhydrazine is a weak base with a pKa of 7.87(1). This value indicates that methylhydrazine will partially exist as a cation in water and moist soil surfaces and cations do not volatilize. The Henry's Law constant for the free base of methylhydrazine is estimated as 3X10-6 atm-cu m/mole(SRC) from its vapor pressure, 50 mm Hg(2), and water solubility, 1X10+6 mg/L(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)(4) is estimated as 5 days (SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(4) is estimated as 62 days(SRC). Methylhydrazine's Henry's Law constant indicates that the free base may volatilize from moist soil surfaces(SRC). The potential for volatilization of methylhydrazine from dry soil surfaces may exist(SRC) based on its vapor pressure(2).
Soil Adsorption
Using a structure estimation method based on molecular connectivity indices(1), the Koc for methylhydrazine can be estimated to be 18(SRC). According to a classification scheme(2), this estimated Koc value suggests that methylhydrazine is expected to have very high mobility in soil. The pKa of methylhydrazine is 7.87(3). This pKa value indicates that this compound will partially exist as a cation in moist soils and cations generally adsorb more strongly to organic carbon and clay than the corresponding free base(4).
Vapor Pressure
PressureReference
43.8

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


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


Tetrazolo[1,5-b]pyridazin-6-ylhydrazine

Compound Details

Synonymous names
STK094160
6-hydrazinyltetrazolo[1,5-b]pyridazine
52476-90-1
ChemDiv1_019833
Oprea1_201101
HMS643F11
6-Hydrazinotetrazolo(b)pyridazine
DTXSID30336400
ROUOGJAMSNIJAU-UHFFFAOYSA-N
AKOS003672429
6-hydrazinotetrazolo-[1,5-b]-pyridazine
6-Hydrazinotetraazolo[1,5-b]pyridazine #
Microorganism:

No

IUPAC nametetrazolo[1,5-b]pyridazin-6-ylhydrazine
SMILESC1=CC2=NN=NN2N=C1NN
InchiInChI=1S/C4H5N7/c5-6-3-1-2-4-7-9-10-11(4)8-3/h1-2H,5H2,(H,6,8)
FormulaC4H5N7
PubChem ID533518
Molweight151.13
LogP-0.6
Atoms11
Bonds1
H-bond Acceptor6
H-bond Donor2
Chemical Classificationaromatic compounds heterocyclic compounds hydrazines nitrogen compounds pyridazines

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-methylprop-1-enylhydrazine

Compound Details

Synonymous names
Isocrotylhydrazine
Hydrazine, (2-methyl-1-propenyl)-
QGIHARDIZKOSBE-UHFFFAOYSA-N
1-(2-Methyl-1-propenyl)hydrazine #
Microorganism:

No

IUPAC name2-methylprop-1-enylhydrazine
SMILESCC(=CNN)C
InchiInChI=1S/C4H10N2/c1-4(2)3-6-5/h3,6H,5H2,1-2H3
FormulaC4H10N2
PubChem ID534012
Molweight86.14
LogP0.9
Atoms6
Bonds1
H-bond Acceptor2
H-bond Donor2
Chemical Classificationhydrazines 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


Methyl 2-[2-(4-methoxycarbonyl-5-phenyl-1,3-thiazol-2-yl)hydrazinyl]-5-phenyl-1,3-thiazole-4-carboxylate

Compound Details

Synonymous names
SR-01000523626
ZQAYTOBRMWVOFO-UHFFFAOYSA-N
STK759863
AKOS001748285
SR-01000523626-2
1,2-Bis(4-methoxycarbonyl-5-phenyl-2-thiazolyl)hydrazine
dimethyl 2,2'-hydrazine-1,2-diylbis(5-phenyl-1,3-thiazole-4-carboxylate)
METHYL 2-{2-[4-(METHOXYCARBONYL)-5-PHENYL-1,3-THIAZOL-2-YL]HYDRAZIN-1-YL}-5-PHENYL-1,3-THIAZOLE-4-CARBOXYLATE
Microorganism:

No

IUPAC namemethyl 2-[2-(4-methoxycarbonyl-5-phenyl-1,3-thiazol-2-yl)hydrazinyl]-5-phenyl-1,3-thiazole-4-carboxylate
SMILESCOC(=O)C1=C(SC(=N1)NNC2=NC(=C(S2)C3=CC=CC=C3)C(=O)OC)C4=CC=CC=C4
InchiInChI=1S/C22H18N4O4S2/c1-29-19(27)15-17(13-9-5-3-6-10-13)31-21(23-15)25-26-22-24-16(20(28)30-2)18(32-22)14-11-7-4-8-12-14/h3-12H,1-2H3,(H,23,25)(H,24,26)
FormulaC22H18N4O4S2
PubChem ID578118
Molweight466.5
LogP6.2
Atoms32
Bonds9
H-bond Acceptor10
H-bond Donor2
Chemical Classificationaromatic compounds benzenoids ethers hydrazines nitrogen compounds sulfur compounds

mVOC Specific Details


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


1-amino-3-prop-2-enylthiourea

Compound Details

Synonymous names
4-Allylthiosemicarbazide
3766-55-0
4-Allyl-3-thiosemicarbazide
N-Allylhydrazinecarbothioamide
Allylthiosemicarbazide
Hydrazinecarbothioamide, N-2-propenyl-
1-amino-3-prop-2-enylthiourea
N-Allylthiosemicarbazide
SEMICARBAZIDE, 4-ALLYL-3-THIO-
NSC 75830
1-amino-3-(prop-2-en-1-yl)thiourea
NSC-75830
Allythiosemicarbazide
EINECS 223-186-7
BRN 1751645
C4H9N3S
ALLYL THIOSEMICARBAZIDE
NSC75830
FMA2DV4FPT
4-allyl-thiosemicarbazide
WLN: ZMYUS&M2U1
Hydrazinecarbothioamide, N-2-propenyl- (9CI)
SCHEMBL456759
N-Allylhydrazinecarbothioamide #
DTXSID80191081
ALBB-025600
4-(2-propenyl)-3-thiosemicarbazide
MFCD00007619
STK397858
AKOS000268202
AT24991
N-2-Propen-1-ylhydrazinecarbothioamide
SB86165
Hydrazinecarbothioamide, N-2-propen-1-yl-
N-(prop-2-en-1-yl)hydrazinecarbothioamide
DB-049161
CS-0206267
NS00030238
EN300-17012
Z56858230
F6660-0044
Microorganism:

No

IUPAC name1-amino-3-prop-2-enylthiourea
SMILESC=CCNC(=S)NN
InchiInChI=1S/C4H9N3S/c1-2-3-6-4(8)7-5/h2H,1,3,5H2,(H2,6,7,8)
FormulaC4H9N3S
PubChem ID1551250
Molweight131.2
LogP-0.1
Atoms8
Bonds2
H-bond Acceptor2
H-bond Donor3
Chemical Classificationhydrazines nitrogen compounds sulfur compounds thiocarbamides

mVOC Specific Details


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


1-amino-3-octadecylthiourea

Compound Details

Synonymous names
6973-26-8
1-amino-3-octadecylthiourea
NSC44421
SCHEMBL11784133
N-octadecylhydrazinecarbothioamide
DTXSID60398652
HJDFNODKUDTBIV-UHFFFAOYSA-N
hydrazinecarbothioamide, N-octadecyl-
NSC-44421
Microorganism:

No

IUPAC name1-amino-3-octadecylthiourea
SMILESCCCCCCCCCCCCCCCCCCNC(=S)NN
InchiInChI=1S/C19H41N3S/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-21-19(23)22-20/h2-18,20H2,1H3,(H2,21,22,23)
FormulaC19H41N3S
PubChem ID4032100
Molweight343.6
LogP8.1
Atoms23
Bonds17
H-bond Acceptor2
H-bond Donor3
Chemical Classificationhydrazines nitrogen compounds sulfur compounds thiocarbamides

mVOC Specific Details


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


Ethyl (2Z)-2-chloro-2-(phenylhydrazinylidene)acetate

Compound Details

Synonymous names
28663-68-5
2-chloro-2-(phenylhydrazono)acetic acid ethyl ester
9000-40-2
ethyl (2Z)-2-chloro-2-(phenylhydrazinylidene)acetate
2-Chloro-2-(phenylhydrazono)acetic acid ethyl ether
1105636-26-7
Ethyl (Z)-2-chloro-2-(2-phenylhydrazono)acetate
Acetic acid, 2-chloro-2-(2-phenylhydrazinylidene)-, ethyl ester
Ethyl 2-chloro-2-(phenylhydrazono)acetate
STK367396
875800-25-2
Ethyl 2-chloro-2-(2-phenylhydrazono)acetate
Acetic acid, phenylhydrazonochloro-, ethyl ester
2-Chloro-2-(phenylhydrazono)acetic acid ethylether
SCHEMBL13901608
NSC333417
AKOS005443798
FS-4712
NSC-333417
ethyl 2-chloro-2-phenylhydrazonoacetate
BP-12175
CS-0009313
Ethyl (2Z)-chloro(phenylhydrazono)ethanoate #
EN300-7413225
A819526
ethyl (2Z)-chloro(2-phenylhydrazinylidene)ethanoate
2-chloro-2-(phenyl-hydrazono)-acetic acid ethyl ester
ethyl (2Z)-2-chloranyl-2-(phenylhydrazinylidene)ethanoate
ethyl (2Z)-2-chloro-2-(2-phenylhydrazin-1-ylidene)acetate
Ethyl (Z)-2-chloro-2-(2-phenylhydrazin-1-ylidene)acetate
(2Z)-2-chloro-2-(phenylhydrazinylidene)acetic acid ethyl ester
Microorganism:

Yes

IUPAC nameethyl (2Z)-2-chloro-2-(phenylhydrazinylidene)acetate
SMILESCCOC(=O)C(=NNC1=CC=CC=C1)Cl
InchiInChI=1S/C10H11ClN2O2/c1-2-15-10(14)9(11)13-12-8-6-4-3-5-7-8/h3-7,12H,2H2,1H3/b13-9-
FormulaC10H11ClN2O2
PubChem ID5708313
Molweight226.66
LogP4.1
Atoms15
Bonds5
H-bond Acceptor4
H-bond Donor1
Chemical Classificationaromatic compounds benzenoids chlorides esters halogenated compounds hydrazines nitrogen compounds

mVOC Specific Details


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


(4,6-dimethoxypyrimidin-2-yl)hydrazine

Compound Details

Synonymous names
13223-30-8
2-hydrazinyl-4,6-dimethoxypyrimidine
(4,6-DIMETHOXYPYRIMIDIN-2-YL)HYDRAZINE
(4,6-Dimethoxy-pyrimidin-2-yl)-hydrazine
SCHEMBL1006385
DTXSID50560806
4,6-dimethoxy-2-hydrazino-pyrimidine
AKOS006331599
pyrimidine, 2-hydrazinyl-4,6-dimethoxy-
DB-127772
F8885-0900
Microorganism:

No

IUPAC name(4,6-dimethoxypyrimidin-2-yl)hydrazine
SMILESCOC1=CC(=NC(=N1)NN)OC
InchiInChI=1S/C6H10N4O2/c1-11-4-3-5(12-2)9-6(8-4)10-7/h3H,7H2,1-2H3,(H,8,9,10)
FormulaC6H10N4O2
PubChem ID14479074
Molweight170.17
LogP0.4
Atoms12
Bonds3
H-bond Acceptor6
H-bond Donor2
Chemical Classificationaromatic compounds ethers heterocyclic compounds hydrazines nitrogen compounds pyrimidines

mVOC Specific Details


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