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Pyridinium, 4-formyl-3-hydroxy-5-(hydroxymethyl)-1,2-dimethyl-, chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13432-98-9

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13432-98-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13432-98-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,3 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13432-98:
(7*1)+(6*3)+(5*4)+(4*3)+(3*2)+(2*9)+(1*8)=89
89 % 10 = 9
So 13432-98-9 is a valid CAS Registry Number.

13432-98-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dimethyl-3-hydroxy-4-formyl-5-hydroxy-methylpyridinium chloride

1.2 Other means of identification

Product number -
Other names N-methylpyridoxal chloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13432-98-9 SDS

13432-98-9Downstream Products

13432-98-9Relevant academic research and scientific papers

Pyridoxal Methochloride Catalysis of the β-Elimination Reaction of Methyl 3-Chloroalaninate in Water

Kondo, Hiroki,Morita, Kanzi,Kitamikado, Tatsuya,Sunamoto, Junzo

, p. 1031 - 1034 (1984)

The β-elimination reaction of methyl 3-chloroalaninate has been investigated in the absence and presence of pyridoxal methochloride (2) or pyridoxal (3).Apparently, compound 2 was about twice as effective as 3 in the catalytic reaction that proceeds via a Schiff base of substrate and 2 or 3.The pH-rate profiles for the catalytic reaction with 2 and 3 were analyzed in terms of ionization of the various Schiff base species present in solution.It was found that the reactivity of the Schiff base decreases as the ionization of the molecule progresses.The reaction mechanism and its relevance to the catalysis of pyridoxal phosphate-dependent enzymes are discussed.

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