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34523-95-0

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34523-95-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34523-95-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,5,2 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 34523-95:
(7*3)+(6*4)+(5*5)+(4*2)+(3*3)+(2*9)+(1*5)=110
110 % 10 = 0
So 34523-95-0 is a valid CAS Registry Number.

34523-95-0SDS

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 dodecyl-[2-(ethylcarbamothioyloxy)ethyl]-dimethylazanium,bromide

1.2 Other means of identification

Product number -
Other names 2-Hydroxyethyldimethyldodecyl ammonium bromide,N-ethylthiocarbamate

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:34523-95-0 SDS

34523-95-0Downstream Products

34523-95-0Relevant articles and documents

Pharmaceutical composition containing novel quaternary ammonium compounds

-

, (2008/06/13)

Quaternary ammonium carbamate, thiocarbamate, dithiocarbamate and carbamide compounds. Typical examples are [C4 H9 NHCOO(CH2)2 N+(CH3)2 C12 H25 ]Br- [C4 H9 NHCSO(CH2)2 N+(CH3)2 C12 H25 ]Br- [CH3 NHCSS(CH2)2 N+(CH3)2 C12 H25 ]Br- [C2 H5 NHCONH(CH2)2 N+(CH3)2 C12 H25 ]Br- These compounds are effective against gram positive bacteria and fungi and reduce caries and inhibit formation of oral calculus. The thiocarbamates can be prepared by converting amino alcohols to sodium salts thereof with metallic sodium and reacting isothiocyanates with the sodium salts followed by quaternization. The carbamates can be prepared by reacting isocyanates with amino alcohols followed by quaternization. The dithiocarbamates can be prepared by reacting isothiocyanates with sodium salts of aminoalkanethiols followed by quaternization. The carbimides can be prepared by reacting isocyanates with alkanediamines followed by quaternization.

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