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B22852

Sigma-Aldrich

Benzylhydrazine dihydrochloride

97%

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About This Item

Fórmula lineal:
C6H5CH2NHNH2 · 2HCl
Número de CAS:
20570-96-1
Peso molecular:
195.09
Beilstein/REAXYS Number:
3688990
EC Number:
243-887-1
MDL number:
MFCD00012921
UNSPSC Code:
12352100
PubChem Substance ID:
24891643
NACRES:
NA.22

assay

97%

form

powder

mp

143-145 °C (dec.) (lit.)

SMILES string

Cl.Cl.NNCc1ccccc1

InChI

1S/C7H10N2.2ClH/c8-9-6-7-4-2-1-3-5-7;;/h1-5,9H,6,8H2;2*1H

InChI key

MSJHOJKVMMEMNX-UHFFFAOYSA-N

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Categorías relacionadas

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análisis (COA)

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Sigma-Aldrich

152137

4-Methoxyphenylhydrazine hydrochloride

F N Bolkenius et al.
Biochemical pharmacology, 53(11), 1695-1702 (1997-06-01)
Peptidylglycine alpha-hydroxylating monooxygenase (PHM; EC 1.14.17.3) catalyses the rate-limiting step in the post-translational activation of substance P, among other neuropeptides, from its glycine-extended precursor. Comparative kinetic studies were performed, using trans-styrylacetic acid or trans-styrylthioacetic acid as known mechanism-based inhibitors, of
Han-Zhong Zhang et al.
Bioorganic & medicinal chemistry, 12(13), 3649-3655 (2004-06-10)
A series of indole-2-carboxylic acid benzylidene-hydrazides has been identified as a new class of potent apoptosis inducers through a novel cell-based caspase HTS assay. The screening hit, 5-chloro-3-methyl-indole-2-carboxylic acid (4-nitrobenzylidene)-hydrazide (3a), was found to arrest T47D cells in G(2)/M and
A Bellelli et al.
European journal of biochemistry, 267(11), 3264-3269 (2000-05-29)
The presteady-state and steady-state kinetics of bovine serum amine oxidase (BSAO) were analyzed by stopped-flow transient spectroscopy. A simplified model of the catalytic cycle was found to describe the experimental data and the rate constants of the individual steps were
D J Merkler et al.
Archives of biochemistry and biophysics, 317(1), 93-102 (1995-02-20)
Peptidylglycine alpha-amidating enzyme catalyzes the two-step conversion of C-terminal glycine-extended peptides to C-terminal alpha-amidated peptides and glyoxylate in a reaction that requires O2, ascorbate and 2 mol of copper per mole of enzyme [Kulathila et al. (1994) Arch. Biochem. Biophys.
E G Lovering et al.
Journal of pharmaceutical sciences, 74(1), 105-107 (1985-01-01)
A GC procedure for the simultaneous determination of hydrazine and benzylhydrazine in isocarboxazid raw material and tablet formulations has been developed. The method is based on the reaction of benzoyltrifluoroacetone with hydrazine and benzylhydrazine to form the corresponding pyrazole derivatives.
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