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7685-30-5

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7685-30-5 Usage

Type of compound

Quaternary ammonium compound

Structure

Contains a positively charged nitrogen atom with four alkyl or aryl groups attached

Common use 1

Phase-transfer catalyst in organic synthesis and polymerization reactions

Common use 2

Emulsifying agent due to strong surfactant properties

Application 1

Formulation of cleaning and disinfecting products

Application 2

Pharmaceutical formulations

Application 3

Agricultural products

Industrial and commercial applications

Versatile properties and functions

Check Digit Verification of cas no

The CAS Registry Mumber 7685-30-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,8 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7685-30:
(6*7)+(5*6)+(4*8)+(3*5)+(2*3)+(1*0)=125
125 % 10 = 5
So 7685-30-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H18N.HI/c1-5-6-7-8(2,3)4;/h5-7H2,1-4H3;1H/q+1;/p-1

7685-30-5SDS

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 N,N,N-trimethyl-1-Butanaminium

1.2 Other means of identification

Product number -
Other names -

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:7685-30-5 SDS

7685-30-5Relevant articles and documents

ALKYLATING PROPERTIES OF DIALKYL PHOSPHITES

Gancarz, Roman

, p. 193 - 200 (2007/10/02)

When the mixture of amines and dialkyl phosphites is used in the reaction, as for example in the Kabachnik-Fields reaction, all possible N-alkylated products are formed.N-ethylation by diethyl phosphite is much slower than N-methylation by dimethyl phosphite and the latter can be easily formed via transesterification when the methanol is present in the mixture.Key words: Amine alkylation, dialkyl phosphites, Kabachnik-Fields synthesis.

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