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Details

Stereochemistry ACHIRAL
Molecular Formula C12H12N2
Molecular Weight 184.2371
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,2-DIPHENYLHYDRAZINE

SMILES

N(NC1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=YBQZXXMEJHZYMB-UHFFFAOYSA-N
InChI=1S/C12H12N2/c1-3-7-11(8-4-1)13-14-12-9-5-2-6-10-12/h1-10,13-14H

HIDE SMILES / InChI

Molecular Formula C12H12N2
Molecular Weight 184.2371
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Bioassay of hydrazobenzene for possible carcinogenicity.
1978
Copper-dependent DNA damage induced by hydrazobenzene, an azobenzene metabolite.
2000 Jun
Considerations necessary in gathering occurrence data for selected unstable compounds in the USEPA Unregulated Contaminant Candidate List in USEPA Method 526.
2001 May 1
Hydrazobenzene.
2002
Identification of mammary carcinogens in rodent bioassays.
2002
Semiconductor-mediated photocatalysed degradation of two selected priority organic pollutants, benzidine and 1,2-diphenylhydrazine, in aqueous suspension.
2002 Oct
Mechanism of formation of hydrogen trioxide (HOOOH) in the ozonation of 1,2-diphenylhydrazine and 1,2-dimethylhydrazine: an experimental and theoretical investigation.
2003 Sep 24
Hydrazobenzene.
2004
Stepwise oxidation of anilines by cis-[RuIV(bpy)2(py)(O)]2+.
2004 Aug 23
Excited-state mixed valence in a diphenyl hydrazine cation: Spectroscopic consequences of coupling and transition dipole moment orientation.
2005 Feb 17
On-line membrane preconcentration for continuous monitoring of trace pharmaceuticals.
2005 Feb 7
Preparation and properties of a monomeric Mn(IV)-oxo complex.
2006 Jul 12
Reactivity of a sterically hindered Fe(II) thiolate dimer with amines and hydrazines.
2008 Dec 1
Tuning the electronic properties of cyclopentadienyl analogs with CB2N2 frameworks: 1,2-diphenyl-1,2-diaza-3,5-diborolyl ligands and their alkali metal salts.
2008 Jul 14
Catalytic reactivity of a zirconium(IV) redox-active ligand complex with 1,2-diphenylhydrazine.
2008 Mar 5
Characterisation of hydrazides and hydrazine derivatives as novel aspartic protease inhibitors.
2010 Oct
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:37:12 GMT 2023
Edited
by admin
on Fri Dec 15 17:37:12 GMT 2023
Record UNII
1G3CS09TUK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,2-DIPHENYLHYDRAZINE
Systematic Name English
NSC-3510
Code English
DIPHENYLHYDRAZINE, 1,2-
Systematic Name English
PHENYLBUTAZONE IMPURITY C [EP IMPURITY]
Common Name English
HYDRAZOBENZENE [HSDB]
Common Name English
Code System Code Type Description
NCI_THESAURUS
C44392
Created by admin on Fri Dec 15 17:37:12 GMT 2023 , Edited by admin on Fri Dec 15 17:37:12 GMT 2023
PRIMARY
CAS
122-66-7
Created by admin on Fri Dec 15 17:37:12 GMT 2023 , Edited by admin on Fri Dec 15 17:37:12 GMT 2023
PRIMARY
WIKIPEDIA
Hydrazobenzene
Created by admin on Fri Dec 15 17:37:12 GMT 2023 , Edited by admin on Fri Dec 15 17:37:12 GMT 2023
PRIMARY
FDA UNII
1G3CS09TUK
Created by admin on Fri Dec 15 17:37:12 GMT 2023 , Edited by admin on Fri Dec 15 17:37:12 GMT 2023
PRIMARY
EPA CompTox
DTXSID7020710
Created by admin on Fri Dec 15 17:37:12 GMT 2023 , Edited by admin on Fri Dec 15 17:37:12 GMT 2023
PRIMARY
HSDB
2882
Created by admin on Fri Dec 15 17:37:12 GMT 2023 , Edited by admin on Fri Dec 15 17:37:12 GMT 2023
PRIMARY
ECHA (EC/EINECS)
204-563-5
Created by admin on Fri Dec 15 17:37:12 GMT 2023 , Edited by admin on Fri Dec 15 17:37:12 GMT 2023
PRIMARY
NSC
3510
Created by admin on Fri Dec 15 17:37:12 GMT 2023 , Edited by admin on Fri Dec 15 17:37:12 GMT 2023
PRIMARY
PUBCHEM
31222
Created by admin on Fri Dec 15 17:37:12 GMT 2023 , Edited by admin on Fri Dec 15 17:37:12 GMT 2023
PRIMARY
MESH
C032041
Created by admin on Fri Dec 15 17:37:12 GMT 2023 , Edited by admin on Fri Dec 15 17:37:12 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
For the calculation of contents, multiply the peak areas by 0.55
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP