114596
N,N-二苯肼盐酸盐
97%
别名:
N,N-二苯肼盐酸盐(不对称)
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关于此项目
线性分子式:
(C6H5)2NNH2 · HCl
化学文摘社编号:
分子量:
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
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
少量水分可引起熔点差别很大
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Formation of N-nitrosodiphenylamine from 1,1-diphenylhydrazine by rat liver microsomal preparations.
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)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 114596-25G | 04061838702777 |