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Decanedioic acid, ethyl methyl ester, also known as ethyl methyl sebacate, is a chemical compound with the molecular formula C14H26O4. It is an ester derived from the reaction of decanedioic acid (sebacic acid) and ethanol, with a methyl group attached to the ester. This organic compound is characterized by its colorless to pale yellow liquid appearance and a mild, fruity odor. Ethyl methyl sebacate is commonly used as a solvent, plasticizer, and in the production of various chemicals, including lubricants, resins, and synthetic fibers. It is also employed as a flavoring agent in the food and beverage industry, imparting a creamy, fruity taste to products. Due to its versatile applications, ethyl methyl sebacate plays a significant role in various industrial sectors.

692-88-6

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692-88-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 692-88-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 692-88:
(5*6)+(4*9)+(3*2)+(2*8)+(1*8)=96
96 % 10 = 6
So 692-88-6 is a valid CAS Registry Number.

692-88-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Decandisaeureethylmethylester

1.2 Other means of identification

Product number -
Other names Sebacinsaeure-ethylester-methylester

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:692-88-6 SDS

692-88-6Downstream Products

692-88-6Relevant academic research and scientific papers

Synthesis and Absolute Configuration of 2-Hydroxy-12-methyl Tridecanoic Acid

Balzer, Th.,Budzikiewicz, H.

, p. 1367 - 1368 (2007/10/02)

The synthesis of racemic 2-hydroxy-12-methyl tridecanoic acid is described.The absolute configuration of the two enantiomers has been determined by the method of Dale and Mosher. - Keywords: 2-Hydroxy-12-methyl Tridecanoic Acid, Absolute COnfiguration

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