Skip to Content
Merck
All Photos(1)

Documents

859923

Sigma-Aldrich

3-Hydroxybenzylhydrazine dihydrochloride

97%

Synonym(s):

α-Hydrazino-m-cresol dihydrochloride, 3-(Hydrazinomethyl)phenol dihydrochloride, NSD-1015

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
HOC6H4CH2NHNH2 · 2HCl
CAS Number:
Molecular Weight:
211.09
Beilstein:
9282965
EC Number:
MDL number:
UNSPSC Code:
12352103

Assay

97%

mp

138-140 °C (lit.)

SMILES string

Cl[H].Cl[H].NNCc1cccc(O)c1

InChI

1S/C7H10N2O.2ClH/c8-9-5-6-2-1-3-7(10)4-6;;/h1-4,9-10H,5,8H2;2*1H

InChI key

ONOJPUDFIOEGCX-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Inhibitor of aromatic amino acid decarboxylase.

Biochem/physiol Actions

Inhibitor of L-aromatic amino acid decarboxylase; crosses blood brain barrier. Also inhibits GABA aminotransferase, as well as other pyridoxal-phosphate-requiring enzymes, by forming the 3-hydroxybenzylhydrazone of that cofactor.

replaced by

Product No.
Description
Pricing

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

L W Hunter et al.
Biochemical pharmacology, 45(6), 1363-1366 (1993-03-24)
The activity of the enzyme tyrosine hydroxylase (TH; EC 1.14.16.2) is commonly studied indirectly by quantifying the formation of the product, 3,4-dihydroxyphenylalanine (DOPA), after inhibition of aromatic L-amino acid decarboxylase (AAAD; EC 4.1.1.28), the enzyme which metabolizes DOPA. This study

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service