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Tetradecanoic acid, 12-oxo-, also known as 12-oxotetradecanoic acid or 12-ketotetradecanoic acid, is a chemical compound with the molecular formula C14H26O3. It is a derivative of tetradecanoic acid, a saturated fatty acid with 14 carbon atoms, where the 12th carbon atom has been oxidized to form a ketone group (C=O). This modification results in a more reactive and less stable molecule compared to its parent acid. 12-Oxotetradecanoic acid is an important intermediate in the biosynthesis of certain prostaglandins, which are hormone-like substances that play a crucial role in various physiological processes, including inflammation, pain, and blood clotting. The compound is also used in the synthesis of other bioactive molecules and as a research tool in the study of fatty acid metabolism and related pathways.

2177-96-0

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2177-96-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2177-96-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,7 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2177-96:
(6*2)+(5*1)+(4*7)+(3*7)+(2*9)+(1*6)=90
90 % 10 = 0
So 2177-96-0 is a valid CAS Registry Number.

2177-96-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 12-oxo-tetradecanoic acid

1.2 Other means of identification

Product number -
Other names 12-Ketotetradecansaeure

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:2177-96-0 SDS

2177-96-0Downstream Products

2177-96-0Relevant academic research and scientific papers

OZONOLYSIS OF ALKENES AND REACTIONS OF POLYFUNCTIONAL COMPOUNDS. XVIII. INVESTIGATION OF A NEW OZONOLYTIC SYNTHESIS OF CARBOXYLIC ACIDS

Odinokov, V. N.,Botsman, L. P.,Ishmuratov, G. Yu.,Tolstikov, G. A.

, p. 453 - 463 (2007/10/02)

By identification of the 18O isotope label in the oligomeric peroxide obtained by ozonization of a cyclic olefin in the presence of heavy oxygen and also in the product from catalytic isomerization of this peroxide ( the α,ο-dicarboxylic acids or its dimethyl ester ) it was shown that oxygen enters the ozonolysis product when the reaction is carried out in ether solvents.It is suggested that the increased content of active oxygen in the ozonolysis peroxy product is due to oxidation of the ether solvent to form α-hydroperoxide and addition of the latter to the oligomeric zwitterion, solvated by the polar solvents.It was established that the catalytic and thermal isomerization of the oligomeric peroxides and ozonides of cyclic olefins to the α,ο-dicarboxylic acids and ο-formyl carboxylic acids occurs through the oligomeric α-hydroxy peresters and α-hydroxy esters respectively.

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