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Decanoic acid, 10-hydroxy-, ethyl ester, also known as 10-Hydroxydecanoic acid ethyl ester or Capric acid, 10-hydroxy-, ethyl ester, is a chemical compound with the molecular formula C12H24O3. It is an ester derived from decanoic acid, a saturated fatty acid with ten carbon atoms, and ethanol. Decanoic acid, 10-hydroxy-, ethyl ester is characterized by the presence of a hydroxyl group (-OH) at the 10th carbon position of the decanoic acid chain. It is a colorless liquid with a mild, fruity odor and is soluble in organic solvents. Decanoic acid, 10-hydroxy-, ethyl ester is used in the fragrance industry as a scent component, particularly in the creation of fruity and floral notes. It is also found in various natural sources, such as fruits and essential oils, and can be used in the synthesis of other chemicals and compounds.

3639-35-8

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3639-35-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3639-35-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,3 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3639-35:
(6*3)+(5*6)+(4*3)+(3*9)+(2*3)+(1*5)=98
98 % 10 = 8
So 3639-35-8 is a valid CAS Registry Number.

3639-35-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-hydroxydecanoic acid ethyl ester

1.2 Other means of identification

Product number -
Other names -

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3639-35-8 SDS

3639-35-8Upstream product

3639-35-8Relevant academic research and scientific papers

The Thioesterase of the Erythromycin-producing Polyketide Synthase: Mechanistic Studies in vitro to Investigate its Mode of Action and Substrate Specificity

Aggarwal, Ranjana,Caffrey, Patrick,Leadlay, Peter F.,Smith, Cameron J.,Staunton, James

, p. 1519 - 1520 (1995)

In vitro studies of the mode of action of the thioesterase of the erythromycin-producing PKS have shown that it cleaves ester groups by forming acyl enzyme intermediates, and that it has a broad substrate specificity.

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