U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS
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Details

Stereochemistry ACHIRAL
Molecular Formula H4N2
Molecular Weight 32.0452
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Hydrazine

SMILES

NN

InChI

InChIKey=OAKJQQAXSVQMHS-UHFFFAOYSA-N
InChI=1S/H4N2/c1-2/h1-2H2

HIDE SMILES / InChI

Molecular Formula H4N2
Molecular Weight 32.0452
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Carbamoylating chemoresistance induced by cobalt pretreatment in C6 glioma cells: putative roles of hypoxia-inducible factor-1.
2004 Mar
Molecular mechanism of anaerobic ammonium oxidation.
2011 Oct 2
Small-molecule activators of AMP-activated protein kinase (AMPK), RSVA314 and RSVA405, inhibit adipogenesis.
2011 Sep-Oct
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:36:45 GMT 2025
Edited
by admin
on Mon Mar 31 18:36:45 GMT 2025
Record UNII
27RFH0GB4R
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Hydrazine
Systematic Name English
H 70 (FUEL)
Preferred Name English
Hydrazine [MI]
Common Name English
Hydrazine [WHO-DD]
Common Name English
Hydrazine [HSDB]
Common Name English
LEVOXINE
Brand Name English
Allopurinol Impurity F [EP IMPURITY]
Common Name English
NITROGEN HYDRIDE (N2H4)
Common Name English
Hydrazine [IARC]
Common Name English
Isoniazid Impurity E [EP IMPURITY]
Common Name English
Hydrazine anhydrous
Common Name English
OXYTREAT 35
Brand Name English
Classification Tree Code System Code
NCI_THESAURUS C1935
Created by admin on Mon Mar 31 18:36:45 GMT 2025 , Edited by admin on Mon Mar 31 18:36:45 GMT 2025
NCI_THESAURUS C667
Created by admin on Mon Mar 31 18:36:45 GMT 2025 , Edited by admin on Mon Mar 31 18:36:45 GMT 2025
Code System Code Type Description
WIKIPEDIA
HYDRAZINE
Created by admin on Mon Mar 31 18:36:45 GMT 2025 , Edited by admin on Mon Mar 31 18:36:45 GMT 2025
PRIMARY
FDA UNII
27RFH0GB4R
Created by admin on Mon Mar 31 18:36:45 GMT 2025 , Edited by admin on Mon Mar 31 18:36:45 GMT 2025
PRIMARY
HSDB
544
Created by admin on Mon Mar 31 18:36:45 GMT 2025 , Edited by admin on Mon Mar 31 18:36:45 GMT 2025
PRIMARY
EPA CompTox
DTXSID3020702
Created by admin on Mon Mar 31 18:36:45 GMT 2025 , Edited by admin on Mon Mar 31 18:36:45 GMT 2025
PRIMARY
MERCK INDEX
m6079
Created by admin on Mon Mar 31 18:36:45 GMT 2025 , Edited by admin on Mon Mar 31 18:36:45 GMT 2025
PRIMARY Merck Index
MESH
C029424
Created by admin on Mon Mar 31 18:36:45 GMT 2025 , Edited by admin on Mon Mar 31 18:36:45 GMT 2025
PRIMARY
CAS
302-01-2
Created by admin on Mon Mar 31 18:36:45 GMT 2025 , Edited by admin on Mon Mar 31 18:36:45 GMT 2025
PRIMARY
ECHA (EC/EINECS)
206-114-9
Created by admin on Mon Mar 31 18:36:45 GMT 2025 , Edited by admin on Mon Mar 31 18:36:45 GMT 2025
PRIMARY
CHEBI
15571
Created by admin on Mon Mar 31 18:36:45 GMT 2025 , Edited by admin on Mon Mar 31 18:36:45 GMT 2025
PRIMARY
PUBCHEM
9321
Created by admin on Mon Mar 31 18:36:45 GMT 2025 , Edited by admin on Mon Mar 31 18:36:45 GMT 2025
PRIMARY
EVMPD
SUB14130MIG
Created by admin on Mon Mar 31 18:36:45 GMT 2025 , Edited by admin on Mon Mar 31 18:36:45 GMT 2025
PRIMARY
SMS_ID
100000077596
Created by admin on Mon Mar 31 18:36:45 GMT 2025 , Edited by admin on Mon Mar 31 18:36:45 GMT 2025
PRIMARY
NCI_THESAURUS
C29097
Created by admin on Mon Mar 31 18:36:45 GMT 2025 , Edited by admin on Mon Mar 31 18:36:45 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
SOLVATE->ANHYDROUS
SALT/SOLVATE -> PARENT
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
PARENT -> IMPURITY
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
ACTIVE MOIETY