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26394-68-3

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26394-68-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26394-68-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,3,9 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 26394-68:
(7*2)+(6*6)+(5*3)+(4*9)+(3*4)+(2*6)+(1*8)=133
133 % 10 = 3
So 26394-68-3 is a valid CAS Registry Number.

26394-68-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromoethyl-hexadecyl-dimethylazanium,bromide

1.2 Other means of identification

Product number -
Other names 1-Hexadecanaminium,N-(2-bromoethyl)-N,N-dimethyl-,bromide

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:26394-68-3 SDS

26394-68-3Downstream Products

26394-68-3Relevant articles and documents

Two-Phase Reaction of 1-Bromooctane with Sodium Acetate and Potassium Acetate Catalyzed by Diquaternary Ammonium Salts

Schiefer, H.,Beger, J.,Lorenz, U.

, p. 383 - 398 (2007/10/02)

New unsaturated diquaternary ammonium salts (diquats) were prepared in two ways from ditertiary amines 3 and 1-bromoalkanes or from 1,4-dibromobut-2t-ene and tertiary monoamines.A comparison of their catalytic ability with that of saturated diquats and with that of corresponding monoquats was made.The reaction of n-C8H17Br with NaOAc or KOAc in the two phase system liquid-liquid without an additional solvent is catalyzed more effectively by the unsaturated diquats than by the saturated diquats and the monoquats.Most of the used quats catalyze the ester formation from NaOAc more effectively in the system liquid-liquid, however, the ester formation from KOAc more effectively in the system solid-liquid; KOAc is generally superior to NaOAc in both systems.Consequently, in the phase-transfer catalyzed ester formation from alkali acetate and alkyl halides not only the structure of the quat but also the inorganic cation of the acetate have influence on the rate of conversion.

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