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13497-63-7

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13497-63-7 Usage

Structure

Hexadecane chain with a chloromethoxy group attached at the first carbon

Molar mass

294.91 g/mol

Type of compound

Long-chain alkyl chloride

Uses

Building block for the synthesis of other organic compounds, particularly in the production of surfactants and emulsifiers

Applications

Industrial and consumer products (detergents, cosmetics, pharmaceuticals), chemical research and development (organic synthesis, medicinal chemistry)

Hazards

Hazardous if ingested, inhaled, or comes into contact with skin or eyes

Safety precautions

Handle with care and follow proper safety protocols

Check Digit Verification of cas no

The CAS Registry Mumber 13497-63-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,9 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13497-63:
(7*1)+(6*3)+(5*4)+(4*9)+(3*7)+(2*6)+(1*3)=117
117 % 10 = 7
So 13497-63-7 is a valid CAS Registry Number.

13497-63-7SDS

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 Chlormethylhexadecylether

1.2 Other means of identification

Product number -
Other names Hexadecylchlormethylether

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:13497-63-7 SDS

13497-63-7Relevant articles and documents

Synthesis and anti-microbial activities of choline-like quaternary ammonium chlorides

Pernak, Juliusz,Chwala, Przemyslaw

, p. 1035 - 1042 (2003)

New choline-like quaternary ammonium chlorides were obtained. The work-up procedure of synthesis was quick and efficient. The obtained chlorides showed anti-microbial activities. Quaternary ammonium chlorides derivatives of deanol esters exhibited strong

The action of new quartinary iminium compounds against bacteria and fungal strains. 22. Synthesis of 1-ethyloxymethyl-3-(n-alkoxymethyl) imidazolinium chlorides

Pernak,Skrzypczak,Michalak,Krysinski

, p. 654 - 655 (2007/10/02)

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