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Butanoic acid, 2-ethyl-2-methyl-, ethyl ester, also known as ethyl 2-ethyl-2-methylbutanoate, is a clear, colorless liquid with a fruity odor. It is a versatile organic compound that finds applications in various industries due to its unique properties.

19945-14-3

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19945-14-3 Usage

Uses

Used in Food and Beverage Industry:
Butanoic acid, 2-ethyl-2-methyl-, ethyl ester is used as a flavoring agent for providing a sweet, fruity flavor to products such as candies, baked goods, and beverages. Its fruity aroma enhances the taste and aroma of these food products, making them more appealing to consumers.
Used in Perfume and Fragrance Industry:
This ester is used in the production of perfumes and fragrances due to its pleasant fruity scent. It contributes to the creation of various fragrances used in personal care products, household items, and other scented products.
Used in Chemical and Pharmaceutical Manufacturing:
Butanoic acid, 2-ethyl-2-methyl-, ethyl ester is utilized in the manufacture of chemicals and pharmaceuticals. Its chemical properties make it a valuable intermediate in the synthesis of various compounds, contributing to the development of new products in these industries.
Used as a Solvent in Industrial Applications:
This ester also has some industrial applications as a solvent. Its ability to dissolve certain substances makes it useful in various processes, including cleaning and degreasing operations.
Used as a Reagent in Organic Synthesis:
Butanoic acid, 2-ethyl-2-methyl-, ethyl ester serves as a reagent in organic synthesis, facilitating various chemical reactions. Its reactivity allows chemists to synthesize new compounds and perform transformations that are essential in the development of new materials and products.
However, it is crucial to handle Butanoic acid, 2-ethyl-2-methyl-, ethyl ester with care, as it can be harmful if ingested, inhaled, or comes into contact with the skin. Proper safety measures should be taken to minimize the risk of exposure and ensure the safe use of this chemical in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 19945-14-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,4 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19945-14:
(7*1)+(6*9)+(5*9)+(4*4)+(3*5)+(2*1)+(1*4)=143
143 % 10 = 3
So 19945-14-3 is a valid CAS Registry Number.

19945-14-3SDS

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 ethyl 2-ethyl-2-methylbutanoate

1.2 Other means of identification

Product number -
Other names ethyl ester of 2-methyl-2-ethylbutyric acid

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:19945-14-3 SDS

19945-14-3Relevant academic research and scientific papers

SYNTHESIS OF ESTERS FROM 1-HEXANOL AND ETHYL FORMATE UNDER CONDITIONS OF SULFURIC ACID CATALYSIS

Ordyan, M. B.,Stepanyan, A. A.,Pirozhkov, S. D.,Manukyan, Sh. M.,Grigoryan, V. S.,Lapidus, A. L.

, p. 1429 - 1432 (2007/10/02)

The ethoxycarbonylation of 1-hexanol in one stage with concentrated sulfuric acid as catalyst and ethyl formate as acylating and esterifying agent was investigated.The products are mainly ethyl 2,2-dimethylpentanoate, 2-methyl-2-ethylbutyrate, and 2-ethylpentanoate and the corresponding acids.The content of the esters and acids with a quaternary carbon atom at position 2 in the reaction mixture increased with increase in the molar ratio of sulfuric acid to alcohol, with decrease in the molar ratio of ethyl formate to sulfuric acid, with increase in the rate of addition of the alcohol to the sulfuric acid, and with increase in the reaction temperature.

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