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6319-85-3

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6319-85-3 Usage

General Description

2-methyl-1,3,5-tri(propan-2-yl)benzene, also known as mesitylene, is a colorless liquid with a sweet aromatic odor. It is mainly used as a solvent in paints, varnishes, and adhesives. It is also used in the production of dyes, plastics, and pharmaceuticals. Mesitylene is considered to be a hazardous chemical, as exposure to it can cause irritation to the skin, eyes, and respiratory system. It is also flammable and should be handled with care. Additionally, mesitylene has been classified as a possible carcinogen and poses environmental hazards if improperly disposed of.

Check Digit Verification of cas no

The CAS Registry Mumber 6319-85-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6319-85:
(6*6)+(5*3)+(4*1)+(3*9)+(2*8)+(1*5)=103
103 % 10 = 3
So 6319-85-3 is a valid CAS Registry Number.

6319-85-3SDS

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 2-methyl-1,3,5-tri(propan-2-yl)benzene

1.2 Other means of identification

Product number -
Other names 2,4,6-Triisopropyltoluol

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:6319-85-3 SDS

6319-85-3Relevant articles and documents

Negishi-type coupling of bromoarenes with dimethylzinc

Herbert, John M.

, p. 817 - 819 (2007/10/03)

Treatment of bromoarenes with dimethylzinc in the presence of a palladium catalyst provides a high-yielding route to methylarenes. The process accommodates a wide range of aromatic substituents and, in the majority of cases, is free of side reactions.

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