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Merck

B22852

Benzylhydrazine dihydrochloride

97%

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About This Item

Linear Formula:
C6H5CH2NHNH2 · 2HCl
CAS Number:
20570-96-1
Molecular Weight:
195.09
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24891643
EC Number:
243-887-1
Beilstein/REAXYS Number:
3688990
MDL number:
MFCD00012921

Key Documents

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Product Name

Benzylhydrazine dihydrochloride, 97%

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

SMILES string

Cl.Cl.NNCc1ccccc1

assay

97%

form

powder

mp

143-145 °C (dec.) (lit.)

Quality Level

200

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pictograms

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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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCD9382
MKBL3260V
MKBJ1003V
MKBF5325V
MKBD3576

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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.
L Morpurgo et al.
Biology of metals, 3(2), 114-117 (1990-01-01)
The role of copper in bovine serum amine oxidase was investigated by studying the effect of copper-binding inhibitors on the reactions of the pyrroloquinoline quinone carbonyl and on the reaction with oxygen. Hydrazines and hydrazides were used as carbonyl reagents
L Morpurgo et al.
The Biochemical journal, 260(1), 19-25 (1989-05-15)
Bovine serum amine oxidase is inhibited by benzylhydrazine (BHy), but recovers full activity after a few hours incubation [Hucko-Haas & Reed (1970) Biochem. Biophys. Res. Commun. 38, 396-400]. The first phase of the process, requiring about 15 min, was found
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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