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61186-96-7

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61186-96-7 Usage

Chemical compound

2,4-Hexadienedioic acid, monomethyl ester, (Z,Z)-

Usage

Preservative in food and drinks to prevent mold, yeast, and fungi growth

Stereochemistry

(Z,Z)designation indicates positions of double bonds in the molecule

Usage in cosmetics and personal care products

Monomethyl ester form as fragrance ingredient

Physical properties

Clear, colorless liquid with fruity odor

Stability

Relatively stable under normal conditions

Reactivity

Can react with strong oxidizing agents

Degradation

Prolonged exposure to air or light can cause degradation

Check Digit Verification of cas no

The CAS Registry Mumber 61186-96-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,1,8 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61186-96:
(7*6)+(6*1)+(5*1)+(4*8)+(3*6)+(2*9)+(1*6)=127
127 % 10 = 7
So 61186-96-7 is a valid CAS Registry Number.

61186-96-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2Z,4Z)-5-methoxycarbonyl-2,4-pentadieonic acid

1.2 Other means of identification

Product number -
Other names 2,4-HEXADIENEDIOICACID,1-METHYLESTER,(2Z,4Z)-

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:61186-96-7 SDS

61186-96-7Relevant articles and documents

Sustainable production of dimethyl adipate by non-heme iron(iii) catalysed oxidative cleavage of catechol

Jastrzebski, Robin,Van Den Berg, Emily J.,Weckhuysen, Bert M.,Bruijnincx, Pieter C. A.

, p. 2103 - 2109 (2015/04/14)

Adipic acid and its esters are important bulk chemicals whose principal use is in the production of the nylon-6,6 polymer. There is considerable interest in finding novel green routes from sustainable feedstocks towards these important intermediates. Herein, we describe the catalytic oxidative cleavage of catechol to muconic acids using a catalyst prepared in situ from iron(iii) nitrate, tris(2-pyridylmethyl)amine and ammonium acetate. An investigation of catalyst loading, temperature and oxygen pressure, allowed a turnover frequency of 120 h-1 to be obtained. The subsequent hydrogenation and transesterification of the obtained muconic acid products were shown to proceed well over commercially available supported catalysts. After vacuum distillation, dimethyl adipate could be isolated in 62% yield from catechol, thus demonstrating a green and sustainable route to this important bulk chemical.

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