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6942-58-1

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6942-58-1 Usage

General Description

2-hydroxyethyl isobutyrate, also known as HEIB, is a chemical compound that belongs to the family of alkyl carboxylic acids. It is a colorless liquid with a faint, sweet odor, and is soluble in water. HEIB is commonly used as a solvent in various industrial and commercial applications, including paint and coating formulations, as well as in the production of adhesives and sealants. It is also used as a flavoring agent in food products and as a fragrance ingredient in cosmetics and personal care products. HEIB is known for its low volatility and low toxicity, making it a safer alternative to other solvents in many applications.

Check Digit Verification of cas no

The CAS Registry Mumber 6942-58-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,4 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6942-58:
(6*6)+(5*9)+(4*4)+(3*2)+(2*5)+(1*8)=121
121 % 10 = 1
So 6942-58-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O3/c1-5(2)6(8)9-4-3-7/h5,7H,3-4H2,1-2H3

6942-58-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxyethyl 2-methylpropanoate

1.2 Other means of identification

Product number -
Other names ethylene glycol monoisobutyrate

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:6942-58-1 SDS

6942-58-1Downstream Products

6942-58-1Relevant articles and documents

Efficient Catalytic Oxidation of Cyclic Acetals with H2O2

Zlotsky, S. S.,Nazarov, M. N.,Kulak, L. G.,Rakhmankulov, D. L.

, p. 441 - 443 (1992)

-

Flavin-functionalized gold nanoparticles as an efficient catalyst for aerobic organic transformations

Imada, Yasushi,Osaki, Motonari,Noguchi, Mikiko,Maeda, Takatoshi,Fujiki, Misa,Kawamorita, Soichiro,Komiya, Naruyoshi,Naota, Takeshi

, p. 99 - 106 (2015/03/04)

Monolayer-protected gold clusters functionalized with synthetic flavins were synthesized and their catalytic activity in aerobic organic transformations investigated. Gold nanoparticles with 5-ethyl-3-(8-thiooctyl)lumiflavinium perchlorate acts as an efficient catalyst for the aerobic oxidation of organic sulfides to the corresponding sulfoxides upon treatment with hydrazine at room temperature and under atmospheric pressure in oxygen. With a catalytic amount of gold nanoparticles with 3-(8-thiooctyl)lumiflavin, diimide reduction of various olefins can be performed with hydrazine at room temperature under atmospheric pressure in air with greater yields of product alkanes than with non-supported 3-methyllumiflavin catalyst under the same conditions. Kinetic studies revealed that the mono-layer-protected gold cluster-catalyzed reactions proceeded faster than those with non-supported catalysts over the full substrate concentration range for the hydrogenation of olefins and at lower substrate concentrations for sulfoxidation. This positive effect was rationalized by assuming a Michaelis-Menten-type mechanism in which the specific inclusion of substrates into the enzyme-like reaction cavities was a key factor in the high efficiency of the supported flavin catalysts.

Organocatalytic chemoselective monoacylation of 1,n-linear diols

Yoshida, Keisuke,Furuta, Takumi,Kawabata, Takeo

supporting information; experimental part, p. 4888 - 4892 (2011/06/22)

Matters of length: Exclusive or predominant monoacylation of 1,n-linear diols took place in the presence of 1 when the chain length of linear diols was equal to or shorter than five carbon atoms. The chemoselectivity of acylation between 1,5-pentanediol (n=5) and 1,6-hexanediol (n=6) was 5.2, and that between 1,5-pentanediol and its monoacylate was 113. Copyright

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