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Alpha-ribazole, also known as 4-amino-3-(2-amino-5-bromo-4-chlorophenyl)-1,2,4-triazole, is a synthetic chemical compound that has been used as a feed additive to promote growth in livestock, particularly in the poultry industry. It is a derivative of the triazole class of compounds, which are known for their broad-spectrum antifungal properties. Alpha-ribazole works by mimicking the action of the essential amino acid tryptophan, which is a precursor to niacin (vitamin B3) in the body. By enhancing the conversion of tryptophan to niacin, it helps to improve feed efficiency and overall health in animals. However, its use has been a subject of controversy due to concerns about potential health risks to humans and the environment, leading to its ban in some countries.

132-13-8

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132-13-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132-13-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,3 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 132-13:
(5*1)+(4*3)+(3*2)+(2*1)+(1*3)=28
28 % 10 = 8
So 132-13-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H18N2O4/c1-7-3-9-10(4-8(7)2)16(6-15-9)14-13(19)12(18)11(5-17)20-14/h3-4,6,11-14,17-19H,5H2,1-2H3/t11-,12-,13-,14+/m1/s1

132-13-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name α-ribazole

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:132-13-8 SDS

132-13-8Downstream Products

132-13-8Relevant academic research and scientific papers

Deprotection of α-imidazole/benzimidazole ribonucleosides by catalytic carbon tetrabromide initiated photolysis

Chandra, Tilak,Brown, Kenneth L.

, p. 8617 - 8619 (2007/10/03)

Several protected benzimidazole and imidazole α-ribonucleosides were deprotected in excellent yield at ambient temperature using CBr4 initiated photolysis in methanol at ambient temperature. No selectivity was observed and both trityl and isopr

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