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5-Ketolauric acid, also known as 5-oxolauric acid, is a chemical compound with the molecular formula C11H20O3. It is a derivative of lauric acid, a saturated fatty acid commonly found in coconut oil and palm oil. 5-Ketolauric acid is formed by the oxidation of lauric acid, specifically at the 5th carbon atom, resulting in the formation of a ketone group (C=O). 5-Ketolauric acid has various applications in the chemical industry, such as in the synthesis of surfactants, pharmaceuticals, and other organic compounds. It is also used as an intermediate in the production of certain fragrances and flavorings. Due to its unique chemical structure, 5-ketolauric acid exhibits different properties compared to its parent compound, lauric acid, making it a valuable component in various industrial processes.

3637-16-9

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3637-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3637-16-9 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 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3637-16:
(6*3)+(5*6)+(4*3)+(3*7)+(2*1)+(1*6)=89
89 % 10 = 9
So 3637-16-9 is a valid CAS Registry Number.

3637-16-9SDS

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 5-oxododecanoic acid

1.2 Other means of identification

Product number -
Other names 5-Keto-dodecansaeure-(1)

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:3637-16-9 SDS

3637-16-9Upstream product

3637-16-9Relevant academic research and scientific papers

Baeyer-villiger oxidation of cyclic ketones using aqueous hydrogen peroxide catalyzed by potassium salts of tungstophosphoric acid

Ma, Qingguo,Xing, Wanzhen,Xu, Junhui,Peng, Xinhua

, p. 941 - 943 (2014/06/23)

The salts of 12-tungstophosphoric acid catalysts are prepared with varying potassium content. The resulting catalysts are active for the Baeyer-Villiger oxidation of cyclic ketones with 30 wt% H2O2 and achieve good conversions and yields. KHPW is the preferred catalyst in the reaction because of its reusability and environmental benefits.

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