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N,N-Dichloro-N-methylamine, also known as Methylenimine Dichloride, is an organic compound with the chemical formula C2H5NCl2. It is a colorless, volatile liquid with a pungent odor. N,N-Dichloro-N-methylamine is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is also used as a reagent in organic synthesis and as a chlorinating agent. Due to its high reactivity and potential toxicity, it is essential to handle N,N-Dichloro-N-methylamine with caution and proper safety measures.

7651-91-4

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7651-91-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7651-91-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,5 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7651-91:
(6*7)+(5*6)+(4*5)+(3*1)+(2*9)+(1*1)=114
114 % 10 = 4
So 7651-91-4 is a valid CAS Registry Number.
InChI:InChI=1/CH3Cl2N/c1-4(2)3/h1H3

7651-91-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dichloromethanamine

1.2 Other means of identification

Product number -
Other names methanamine dichloride

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:7651-91-4 SDS

7651-91-4Relevant academic research and scientific papers

DISPROPORTIONATION KINETICS OF N-CHLOROMETHYLAMINE AND N-CHLOROETHYLAMINE

Antelo, J. M.,Arce, F.,Parajo, M.,Rodriguez, P.

, p. 1031 - 1036 (2007/10/02)

The kinetics of disproportionation of N-Cl-methylamine and N-Cl-ethylamine in water were studied at acid pH.Its disproportionation and protonation constants and the coefficients of absorption of N,N-dichloramines are calculated and the mechanism of its disproportionation is discussed.

ELECTROCHEMICAL CHLORINATION OF AMINES

Petrosyan, V. A.,Lyalin, B. V.,Smetanin, A. V.

, p. 542 - 546 (2007/10/02)

We have studied the laws governing the electrochemical chlorination of primary and secondary amines in aqueous solution on a ruthenium-titanium anode under conditions of diaphragm electrolysis.It was found that in order to ensure the most complete conversion of the amines into the corresponding chloramines it is necessary to add NaHCO3 to the electrolyte .Under the conditions of electrolysis primary amines are converted almost quantitatively into dichloramines.High yields of the N-chloro-derivatives of secondary amines can be obtained with high current densities and concentrations of NaCl.

Antibacterial agents

-

, (2008/06/13)

Novel naphthyridine-, quinoline- and benzoxazine-carboxylic acids as antibacterial agents are described as well as methods for their manufacture, formulation, and use in treating bacterial infections including the description of certain novel intermediates used in the manufacture of the antibacterial agents.

Vacuum Gas/Solid N-Chlorination: Preparative Scale Synthesis of Volatile N-Chloramines

Guillemin, J. C.,Denis, J. M.

, p. 1131 - 1133 (2007/10/02)

A simple method for the preparative scale synthesis of volatile chloramines free from impurities starting from the corresponding primary or secondary amine using N-chlorosuccinimide as chlorinating agent is described.

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