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114596

Sigma-Aldrich

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:
530-47-2
Molecular Weight:
220.70
Beilstein/REAXYS Number:
3569340
EC Number:
208-481-0
MDL number:
MFCD00012950
UNSPSC Code:
12352100
PubChem Substance ID:
24847185
NACRES:
NA.22

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

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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_germany

WGK 3

ppe

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

Certificates of Analysis (COA)

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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
New reactive hole-transporting hydrazone and its adducts with diol and dithiol.
Journal of Optoelectronics and Advanced Materials, 8(4), 1533-1533 (2006)
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)
João M S Cardoso et al.
Journal of inorganic biochemistry, 166, 55-63 (2016-11-12)
Camphorsulphonylimine complexes [Ag(NO
Sara S M Fernandes et al.
ACS omega, 3(10), 12893-12904 (2018-11-10)
A series of push-pull heterocyclic N,N-diphenylhydrazones were prepared to study the effect of structural modifications (different π-spacers and electron-withdrawing groups) on the optical (linear and nonlinear) and electronic properties of the molecules. The photovoltaic response of dye-sensitized solar cells assembled
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