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B22852

Sigma-Aldrich

Benzylhydrazin -dihydrochlorid

97%

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About This Item

Lineare Formel:
C6H5CH2NHNH2 · 2HCl
CAS-Nummer:
20570-96-1
Molekulargewicht:
195.09
Beilstein:
3688990
EG-Nummer:
243-887-1
MDL-Nummer:
MFCD00012921
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24891643
NACRES:
NA.22

Qualitätsniveau

200

Assay

97%

Form

powder

mp (Schmelzpunkt)

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

InChIKey

MSJHOJKVMMEMNX-UHFFFAOYSA-N

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Verwandte Kategorien

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

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

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

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4-Methoxyphenylhydrazin -hydrochlorid 95%

Sigma-Aldrich

152137

4-Methoxyphenylhydrazin -hydrochlorid

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
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.
David B Langley et al.
Acta crystallographica. Section F, Structural biology and crystallization communications, 64(Pt 7), 577-583 (2008-07-09)
Complexes of Arthrobacter globiformis amine oxidase (AGAO) with the inhibitors benzylhydrazine and tranylcypromine (an antidepressant drug) have been refined at 1.86 and 1.65 A resolution, respectively. Both inhibitors form covalent adducts with the TPQ cofactor. A tyrosine residue, proposed to
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
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