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Butanoic acid, 2,2-dimethyl-, 1-methylethyl ester, also known as tert-butyl 2,2-dimethylpropanoate, is an organic compound with the chemical formula C8H16O2. It is a colorless liquid with a fruity odor and is derived from the esterification of 2,2-dimethylbutanoic acid and tert-butanol. This ester is commonly used as a flavoring agent in the food and beverage industry, particularly in the production of artificial fruit flavors. It is also employed as a solvent and a chemical intermediate in the synthesis of various organic compounds. Due to its relatively low toxicity, it is considered safe for use in these applications. However, like many organic compounds, it should be handled with care to avoid potential health and environmental risks.

5129-42-0

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5129-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5129-42-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,2 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5129-42:
(6*5)+(5*1)+(4*2)+(3*9)+(2*4)+(1*2)=80
80 % 10 = 0
So 5129-42-0 is a valid CAS Registry Number.

5129-42-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name isopropyl 2,2-dimethylbutanoate

1.2 Other means of identification

Product number -
Other names -

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:5129-42-0 SDS

5129-42-0Downstream Products

5129-42-0Relevant academic research and scientific papers

The first examples of selective carbonylation of n-butane and n-pentane

Akhrem, Irena,Orlinkov, Alexander,Afanas'eva, Lyudmila,Petrovskii, Pavel,Vitt, Sergei

, p. 5897 - 5900 (2007/10/03)

The polyhalomethane based superelectrophilic systems allowed us to accomplish the first efficient and selective carbonylation of n-butane and n- pentane with CO. Depending on the nature of the superelectrophilic system, Me3CCOOR or EtCH(Me)COOR (R = H, Alk) can be obtained at -20°C, 1 atm from n-butane and CO after water (α alcohol) treatment in = 90% yield based on the superelectrophilic system. Pentane reacts with CO in the presence d the CBr4 · 2AlBr3 superacid to give a single product, EtC(Me)2COOR, in almost quantitative yield.

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