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3-Butoxypropanoic acid methyl ester is an organic compound with the chemical formula C8H16O3. It is a colorless liquid with a fruity odor and is derived from the esterification of 3-butoxypropanoic acid and methanol. 3-Butoxypropanoic acid methyl ester is commonly used as a flavoring agent and fragrance component in various food, beverage, and cosmetic products due to its pleasant aroma. It is also known for its low toxicity and is considered safe for use in these applications. The ester is synthesized through a reaction between 3-butoxypropanoic acid and methanol in the presence of an acid catalyst, and it plays a significant role in enhancing the sensory experience of consumer products.

4126-55-0

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4126-55-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4126-55-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,2 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4126-55:
(6*4)+(5*1)+(4*2)+(3*6)+(2*5)+(1*5)=70
70 % 10 = 0
So 4126-55-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O3/c1-3-4-6-11-7-5-8(9)10-2/h3-7H2,1-2H3

4126-55-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-butoxypropanoate

1.2 Other means of identification

Product number -
Other names 3-Butoxy-propionsaeure-methylester

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:4126-55-0 SDS

4126-55-0Downstream Products

4126-55-0Relevant academic research and scientific papers

Catalytic Olefin hydroalkoxylation by nano particles of pollucite

Zamanian, Sara,Kharat, Ali Nemati

, p. 981 - 986 (2015/06/25)

The catalytic hydroalkoxylation of α,β-unsaturated esters, nitriles, and ethers with aliphatic and aromatic alcohols over pollucite using thermal and microwave-assisted methods was investigated. To study the effect of the alcohol structures on the mechanism of the hydroalkoxylation reaction, different alcohols, such as methanol to butanol, cyclohexanol, phenol, and 2-ethylhexanol were used. The activities of pollucite, in contrast to other basic solids, were scarcely affected by the presence of air and moisture. The correlation between alcohol acidity and reaction activity is discussed. The prepared pollucite was characterized by X-ray diffraction, volumetric nitrogen adsorption surface area analysis, and CO2 temperature-programmed desorption. Scanning electron microscopy analysis revealed that the size of the modified nano catalyst particles was under 40nm.

Omega-hydrofluoroalkyl ethers, precursor carboxylic acids and derivatives thereof, and their preparation and application

-

Page 14, (2010/01/31)

Normally liquid, omega-hydrofluoroalkyl ether compounds (and selected mixtures thereof) have a saturated perfluoroaliphatic chain of carbon atoms interrupted by one or more ether oxygen atoms. The compounds can be prepare, e.g. by decarboxylation of the corresponding fluoroalkyl ether carboxylic acids and are useful, e.g., in cleaning and drying applications.

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