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4534-49-0

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4534-49-0 Usage

Structure

A mixture of isomeric hydrocarbons with a benzene ring attached to a pentyloctyl group

Usage

High-boiling point solvent in industrial applications, such as paint and ink formulations

Use in synthesis

Used as a starting material in the synthesis of various organic compounds

Toxicity

Relatively low toxicity and not known to have significant adverse effects on human health or the environment when handled and used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 4534-49-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,3 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4534-49:
(6*4)+(5*5)+(4*3)+(3*4)+(2*4)+(1*9)=90
90 % 10 = 0
So 4534-49-0 is a valid CAS Registry Number.
InChI:InChI=1/C19H32/c1-3-5-7-8-11-15-18(14-10-6-4-2)19-16-12-9-13-17-19/h9,12-13,16-18H,3-8,10-11,14-15H2,1-2H3

4534-49-0SDS

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 tridecan-6-ylbenzene

1.2 Other means of identification

Product number -
Other names Tridecane,6-phenyl

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:4534-49-0 SDS

4534-49-0Upstream product

4534-49-0Downstream Products

4534-49-0Relevant articles and documents

Process for the production of phenylalkanes using a hydrocarbon fraction that is obtained from the Fischer-Tropsch process

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Page/Page column 4, (2008/06/13)

A process for the production of phenylalkanes comprising a reaction for alkylation of at least one aromatic compound by at least one hydrocarbon fraction that is directly obtained from the Fischer-Tropsch process comprising linear olefins that have 9 to 16 carbon atoms per molecule and oxygenated compounds is described. Said alkylation reaction is carried out in a catalytic reactor that contains at least one reaction zone that comprises at least one acidic solid catalyst, and said hydrocarbon fraction does not undergo any purification treatment prior to its introduction into said reaction zone.

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