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10309-79-2

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10309-79-2 Usage

Safety Profile

Poison by subcutaneous route. Questionable carcinogen with experimental carcinogenic, tumorigenic, and teratogenic data. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx.

Check Digit Verification of cas no

The CAS Registry Mumber 10309-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,0 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10309-79:
(7*1)+(6*0)+(5*3)+(4*0)+(3*9)+(2*7)+(1*9)=72
72 % 10 = 2
So 10309-79-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2/c1-9-10-7-8-5-3-2-4-6-8/h2-6,9-10H,7H2,1H3

10309-79-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-2-methylhydrazine

1.2 Other means of identification

Product number -
Other names 2-Benzyl-1-methylhydrazine

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:10309-79-2 SDS

10309-79-2Relevant articles and documents

Novel route to N-alkyl- and N,N′-dialkylhydrazines by high-pressure alkylation of azines

Agafonov,Dudin,Preobrazhenskii

, p. 714 - 716 (2004)

Reactions of alkyl halides with azines of p-nitrobenzaldehyde, benzaldehyde, and p-methoxybenzaldehyde at a high pressure (10 kbar) were studied. Hydrolysis of the reaction mixtures gives pure N-monoalkyl- or N,N′-dialkylhydrazines in high yields, depending on the structure of the starting azine and the solvent nature. It was found that non-symmetrical N,N′-dialkylhydrazines can be synthesized without isolating intermediate N-monoquaternary immonium salts. The effect of the phase transition of the solvent on the direction of the alkylation is discussed.

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