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13-Ketobehenic acid methyl ester is a chemical compound derived from the behenic acid, a saturated fatty acid with an 18-carbon chain. It is characterized by the presence of a ketone group at the 13th carbon position and a methyl ester group at the carboxylic acid end. 13-Ketobehenic acid methyl ester is used in various applications, including the synthesis of surfactants, lubricants, and other industrial chemicals. Its chemical formula is C19H36O3, and it has a molecular weight of 312.49 g/mol. The compound is typically synthesized through the esterification of 13-ketobehenic acid with methanol, and it is known for its stability and resistance to oxidation.

2388-99-0

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2388-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2388-99-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2388-99:
(6*2)+(5*3)+(4*8)+(3*8)+(2*9)+(1*9)=110
110 % 10 = 0
So 2388-99-0 is a valid CAS Registry Number.

2388-99-0SDS

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 methyl 13-oxodocosanoate

1.2 Other means of identification

Product number -
Other names 13-oxo-docosanoic acid methyl ester

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:2388-99-0 SDS

2388-99-0Downstream Products

2388-99-0Relevant academic research and scientific papers

Synthesis of fatty ketoesters by tandem epoxidation-rearrangement with heterogeneous catalysis

Dorado, Vicente,Fraile, José M.,Gil, Lena,Herrerías, Clara I.,Mayoral, José A.

, p. 1789 - 1795 (2020/04/09)

Unsaturated fatty esters can be easily transformed into ketoesters through a two-step process. The highly efficient epoxidation is carried out with tert-butyl hydroperoxide (TBHP) in α,α,α-trifluorotoluene (TFT) using a Ti-silica heterogeneous catalyst. The formed epoxide is easily rearranged by a heterogeneous Br?nsted acid, with Nafion-silica SAC13 as the most efficient one. Both reactions can be combined in a tandem process, with separation of the Ti-silica catalyst by filtration from the reaction medium and addition of the second acid catalyst to perform the second reaction. Each catalyst is separated individually and can be reused, with or without re-activation, under the same conditions to maximize the productivity.

Highly efficient oxyfunctionalization of unsaturated fatty acid esters: An attractive route for the synthesis of polyamides from renewable resources

Winkler, Matthias,Meier, Michael A. R.

supporting information, p. 1784 - 1788 (2014/04/17)

An efficient and environmentally benign strategy for the oxyfunctionalization of fatty acid methyl esters (FAMEs) employing molecular oxygen as an oxidizing agent is described. Keto-fatty acid esters were directly synthesized by co-catalyst-free Wacker oxidations employing oxygen as a sole re-oxidant. Amine functionalization of the thus obtained keto-fatty acid esters was achieved by reductive amination. The prepared renewable AB-type monomers were studied in homopolymerizations as well as in copolymerization reactions with hexamethylendimethylamine and dimethyl adipate to modify the properties of conventional Nylon 6,6. The obtained (co)-polymers were characterized by SEC, NMR and DSC analysis as well as water uptake tests. the Partner Organisations 2014.

ELECTROGENERATED ACID AS A POWERFUL CATALYST FOR TRANSFORMATION OF EPOXIDES TO KETONES AND ACETONIDES

Uneyama, Kenji,Isimura, Akihiro,Fujii, Kazuyuki,Torii, Sigeru

, p. 2857 - 2860 (2007/10/02)

Electrochemical Transformation of epoxides 1 to ketones 2 and acetonides 3 were achieved by using an electrogenerated acid-catalyst.A combination of M(ClO4)n with polar aprotic solvents is useful for the electrochemical transformation.

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