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2095-01-4

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2095-01-4 Usage

Physical Appearance

Colorless to pale yellow liquid

Odor

Faint amine odor

Usage

Commonly used in the production of polymers, resins, and coatings

Typical Application

Curing agent in epoxy systems and polyurethane coatings, monomer in the production of polyurethane foams and rubbers, component in adhesives and sealants

Mechanical and Chemical Properties

Offers excellent mechanical and chemical resistance

Safety Measures

Toxic if ingested, inhaled, or comes into contact with skin. Proper safety measures, including the use of gloves and protective clothing, should be taken when handling this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 2095-01-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,9 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2095-01:
(6*2)+(5*0)+(4*9)+(3*5)+(2*0)+(1*1)=64
64 % 10 = 4
So 2095-01-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H18N2/c1-4-8-6-9(5-2)11(13)7(3)10(8)12/h6H,4-5,12-13H2,1-3H3

2095-01-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-diethyl-2-methylbenzene-1,3-diamine

1.2 Other means of identification

Product number -
Other names 4,6-diethyl-2-methyl-m-phenylenediamine

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:2095-01-4 SDS

2095-01-4Relevant articles and documents

Process for the isolation of alkylated aromatic amines

-

, (2008/06/13)

Alkylated aromatic amines can be isolated from crude catalyst-containing mixtures of these with olefins by a procedure in which in general equivalent amounts of an inorganic base and water are added to the alkylation mixture, the catalyst is hydrolysed, the water present in the reaction mixture after the hydrolysis is removed by distillation and the solid catalyst residue is separated off. The catalyst-free alkylation mixture which remains is then fed to customary further working up.

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