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Merck
CN

114596

N,N-Diphenylhydrazine hydrochloride

97%

Synonym(s):

N,N-Diphenylhydrazine hydrochloride (asym.)

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About This Item

Linear Formula:
(C6H5)2NNH2 · HCl
CAS Number:
Molecular Weight:
220.70
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-481-0
Beilstein/REAXYS Number:
3569340
MDL number:
Assay:
97%
Form:
solid
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assay

97%

form

solid

SMILES string

Cl.NN(c1ccccc1)c2ccccc2

InChI

1S/C12H12N2.ClH/c13-14(11-7-3-1-4-8-11)12-9-5-2-6-10-12;/h1-10H,13H2;1H

InChI key

MIVUDWFNUOXEJM-UHFFFAOYSA-N

Application

N,N-Diphenylhydrazine hydrochloride is used in the synthesis of 2-Vinyloxyethyloxy-4-diethylaminophenyl-1-carbaldehyde N,N-diphenylhydrazone (hole-transporting hydrazine).

Other Notes

Small amounts of moisture cause melting point to vary greatly


signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges



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Reduction of N-nitrosodiphenylamine to the corresponding hydrazine by guinea pig liver preparations.
K Tatsumi et al.
Chemical & pharmaceutical bulletin, 30(10), 3842-3845 (1982-10-01)
New reactive hole-transporting hydrazone and its adducts with diol and dithiol.
Journal of Optoelectronics and Advanced Materials, 8(4), 1533-1533 (2006)
K Tatsumi et al.
Biochemical and biophysical research communications, 118(3), 958-963 (1984-02-14)
The present study provides the first evidence for in vitro metabolic conversion of a 1,1-disubstituted hydrazine to the corresponding nitrosamine. The study shows that superoxide radical which is generated by NADPH-cytochrome c reductase is involved in the oxidation of 1,1-diphenylhydrazine



Global Trade Item Number

SKUGTIN
114596-25G04061838702777