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1,8-Octanediol, acetate 4-methylbenzenesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

116206-55-4

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116206-55-4 Usage

Combination

Used in pharmaceutical and cosmetic industries

1,8-Octanediol

Clear, colorless liquid with a mild odor

1,8-Octanediol Use

Skin conditioning agent and preservative in personal care products

Antimicrobial Properties

Inhibits growth of bacteria and fungi

Acetate 4-methylbenzenesulfonate

Derivative of benzenesulfonic acid

Acetate 4-methylbenzenesulfonate Use

Stabilizer and solvent in pharmaceutical products

Additional Use

Reagent and intermediate in organic synthesis

Combination Purpose

Antimicrobial and preservative properties in skincare and pharmaceutical products

Check Digit Verification of cas no

The CAS Registry Mumber 116206-55-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,2,0 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 116206-55:
(8*1)+(7*1)+(6*6)+(5*2)+(4*0)+(3*6)+(2*5)+(1*5)=94
94 % 10 = 4
So 116206-55-4 is a valid CAS Registry Number.

116206-55-4SDS

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 acetic acid,4-methylbenzenesulfonic acid,octane-1,8-diol

1.2 Other means of identification

Product number -
Other names 1,8-Octanediol,acetate 4-methylbenzenesulfonate

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:116206-55-4 SDS

116206-55-4Relevant academic research and scientific papers

Synthesis of the chiral components of the sex pheromone of Adoxophyes leaf roller moths

Cheskis, B. A.,Moiseenkov, A. M.

, p. 89 - 91 (2007/10/02)

The optically pure (R) and (S) enantiomers of 10-methyldodecyl acetate were synthesized from (R)-5-acetoxy-4-methylpentanoic acid and (S)-2-methylbutanol, respectively, using the condensation of (R)- and (S)-2-methylbutylmagnesium bromides with 8-tosyloxyoctyl acetate in the presence of Li2CuCl4 in the key step.

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