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2-ETHYLHEXANOIC ANHYDRIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36765-89-6

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36765-89-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36765-89-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,6 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 36765-89:
(7*3)+(6*6)+(5*7)+(4*6)+(3*5)+(2*8)+(1*9)=156
156 % 10 = 6
So 36765-89-6 is a valid CAS Registry Number.
InChI:InChI=1/C16H30O3/c1-5-9-11-13(7-3)15(17)19-16(18)14(8-4)12-10-6-2/h13-14H,5-12H2,1-4H3

36765-89-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethylhexanoyl 2-ethylhexanoate

1.2 Other means of identification

Product number -
Other names Hexanoic acid,2-ethyl-,anhydride

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:36765-89-6 SDS

36765-89-6Downstream Products

36765-89-6Relevant academic research and scientific papers

USE OF ACID ANHYDRIDE ACCELERANTS FOR THE PRODUCTION OF HIGH PURITY POLYOL ESTERS

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Paragraph 0046; 0047, (2018/07/31)

A method of producing high purity polyol esters comprises reacting a polyol with an excess amount of a linear or branched aliphatic monocarboxylic C3-20 acid to esterify less than the total amount of the polyol present to form an intermediate reaction composition having a hydroxyl value of from 7 to about 50 mg KOH/g. An anhydride of the corresponding linear or branched aliphatic monocarboxylic C3-20 acid is added to the intermediate reaction composition in an amount of from 1 to about 2.5 equivalents of available OH in the intermediate composition to form a reaction mixture. The reaction mixture is heated for 5-30 minutes or until all of the corresponding anhydride has reacted to form a reaction product. The reaction product is then de-acidified. No metal or acid catalyst or bleaching agents are present in any of the above reaction steps at a concentration above about 15 ppm.

Formaldehyde fifth heavenly stem four mellow Shan Suo double-quarter of the six-ester

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Paragraph 0135-0137, (2017/03/21)

wherein the carboxylic acids comprise C9 branched aliphatic monocarboxylic acid, and any one of carboxylic acids selected from C4 to C8 aliphatic monocarboxylic acids. The hexaester is used as one component of a refrigerant oil composition, and gives excellent characteristics, such as oxidation stability, lubricity, and low temperature properties, to a refrigerant oil composition.

HEXAESTER OF MONO-FORMAL BIS PENTAERYTHRITOL

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Paragraph 0105, (2016/11/14)

To provide hexaester of bispentaerythritol monoformal, which is a mixed ester of bispentaerythritol monoformal represented by the following formula (I), and carboxylic acids: wherein the carboxylic acids comprise C9 branched aliphatic monocarboxylic acid, and any one of carboxylic acids selected from C4 to C8 aliphatic monocarboxylic acids. The hexaester is used as one component of a refrigerant oil composition, and gives excellent characteristics, such as oxidation stability, lubricity, and low temperature properties, to a refrigerant oil composition.

HEXAESTER OF MONO-FORMAL BIS PENTAERYTHRITOL

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Page/Page column 0093, (2015/11/18)

Provided is hexaester of bispentaerythritol monoformal, which comprises the bispentaerythritol monoformal represented by the following formula (I), and any one of carboxylic acids selected from C8 and C9 branched aliphatic monocarboxylic acids: The hexaester has well-balanced excellent characteristics, such as low temperature properties and oxidation stability, and is used for industrial lubricating oil, such as a refrigerant oil composition.

Ti-Crossed-Claisen condensation between carboxylic esters and acid chlorides or acids: A highly selective and general method for the preparation of various β-keto esters

Misaki, Tomonori,Nagase, Ryohei,Matsumoto, Kunshi,Tanabe, Yoo

, p. 2854 - 2855 (2007/10/03)

Ti-crossed-Claisen condensation between a 1:1 mixture of carboxylic esters and acid chlorides promoted by TiCl4-Bu3N-N-methylimidazole proceeded successfully to give various β-keto esters in good yields with excellent selectivities (19 examples, ~48-95% yield; cross/self-selectivity = ~96/4-99/1). The present method was extended to the condensation between a 1:1 mixture of carboxylic acids and carboxylic esters (six examples, ~70-92% yield; cross/self-selectivity = ~91/9-99/1). To demonstrate the utility of the present two Ti-crossed-Claisen condensations, we performed a couple of efficient short-step syntheses of two natural, representative, and useful perfumes, cis-jasmone and (R)-muscone. Copyright

Conversion of carboxylic acids to acyl chlorides with a hexaalkylguanidinium chloride catalyst

Gros, P.,Perchec, P. Le,Gauthier, P.,Senet, J. P.

, p. 554 - 561 (2007/10/02)

Hexaalkylguanidinium chloride displays different behavior toward carboxylic acids depending on the acid strength.Its high catalytic activity for the condensation of carboxylic acids with phosgene or thionyl chloride using molecular and grafted catalyst forms is described.Keywords - hexaalkylguanidinium chloride / catalyst / carboxylic acids / chlorination / phosgenation / mechanism

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