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17025-58-0

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17025-58-0 Usage

Physical state

Solid

Appearance

White crystalline powder

Uses

a. Production of hair dyes and pigments
b. Manufacturing of pharmaceuticals
c. Rubber chemicals
d. Dyes for textiles

Toxicity

Considered toxic

Carcinogenicity

Potential carcinogen

Health risks

Exposure should be minimized to prevent adverse health effects

Handling and storage

Handle and store with care to prevent accidents or environmental contamination

Check Digit Verification of cas no

The CAS Registry Mumber 17025-58-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,2 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17025-58:
(7*1)+(6*7)+(5*0)+(4*2)+(3*5)+(2*5)+(1*8)=90
90 % 10 = 0
So 17025-58-0 is a valid CAS Registry Number.

17025-58-0SDS

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 1,3-diaminobenzene monohydrochloride

1.2 Other means of identification

Product number -
Other names m-Phenylendiamin, Hydrochlorid

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:17025-58-0 SDS

17025-58-0Relevant articles and documents

Alternative method for the reduction of aromatic nitro to amine using TMDS-iron catalyst system

Pehlivan, Leyla,Métay, Estelle,Laval, Stéphane,Dayoub, Wissam,Demonchaux, Patrice,Mignani, Gérard,Lemaire, Marc

body text, p. 1971 - 1976 (2011/04/22)

The system 1,1,3,3-tetramethyldisiloxane (TMDS)/Fe(acac)3 is reported here as a new method to obtain amines from aromatic nitro compounds. Amines are synthetized in a straightforward step and are isolated as hydrochloride salts with good to excellent yields. This system has shown a good selectivity toward aryl-chloride, aryl-bromide, ester, carboxylic acid, and cyano groups. The reduction of alkylnitro compounds was unfortunately not possible using this method, only a mixture of mono and dialkylated amine was obtained.

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