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10146-04-0

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10146-04-0 Usage

Functional group

Azo dye (-N=N-)

Usage

Coloring agent in textiles, cosmetics, and food industries

Structure

Naphthalene ring with an attached amine group, diazo group, and a 4-methylphenyl group

Color

Vibrant red or orange

Application

Dyeing textiles and printing materials

Health and environmental concerns

Potential release of carcinogenic aromatic amines under certain conditions

Check Digit Verification of cas no

The CAS Registry Mumber 10146-04-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,4 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10146-04:
(7*1)+(6*0)+(5*1)+(4*4)+(3*6)+(2*0)+(1*4)=50
50 % 10 = 0
So 10146-04-0 is a valid CAS Registry Number.

10146-04-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(4-methylphenyl)diazenyl]naphthalen-2-amine

1.2 Other means of identification

Product number -
Other names 1-(4'-methylbenzeneazo)-2-amino-naphthalene

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:10146-04-0 SDS

10146-04-0Relevant articles and documents

A simple route to 2-aryl-substituted naphtho[2,1-e][1,2,4]triazinium and naphtho[2,1-e][1,2,3,4]tetrazinium salts from 1-arylazo-substituted 2-naphthylamines

Yu, Xiuling,Metz, Peter,Hartmann, Horst

, p. 431 - 435 (2018/06/18)

1-Arylazo-substituted 2-naphthylamines, which are easily obtainable by the coupling of arene diazonium salts with 2-aminonaphthalene-sulfonic acid, can be transformed by reaction with reactive carboxylic acid derivatives or nitrosation reagents into novel 2-aryl-substituted naphtho[2,1-e][1,2,4]triazinium and naphtho[2,1-e][1,2,3,4]tetrazinium salts, respectively.

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