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3-Methoxyisobutyric acid methyl ester, also known as MIBA, is a colorless liquid chemical compound with the formula C6H12O3. It possesses a fruity odor and is commonly utilized as a flavoring agent in the food and beverage industry, as well as a fragrance ingredient in cosmetics and personal care products. MIBA has also been identified as a potential biomarker for certain metabolic disorders and is being studied for its potential role in energy metabolism and lipid homeostasis. It is considered to be of low toxicity, with no known adverse effects on human health at typical exposure levels.

3852-11-7

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3852-11-7 Usage

Uses

Used in Food and Beverage Industry:
3-Methoxyisobutyric acid methyl ester is used as a flavoring agent for imparting a fruity aroma and taste to various food and beverage products, enhancing their overall sensory appeal.
Used in Cosmetics and Personal Care Products:
In the cosmetics and personal care industry, 3-Methoxyisobutyric acid methyl ester is used as a fragrance ingredient to provide a pleasant scent to products such as perfumes, lotions, and shampoos.
Used in Medical Research:
3-Methoxyisobutyric acid methyl ester is used as a potential biomarker in medical research for certain metabolic disorders, aiding in the identification and monitoring of these conditions.
Used in Metabolic and Lipid Homeostasis Studies:
MIBA is utilized in scientific research to study its potential role in energy metabolism and lipid homeostasis, which could contribute to the development of treatments for related health issues.

Check Digit Verification of cas no

The CAS Registry Mumber 3852-11-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,5 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3852-11:
(6*3)+(5*8)+(4*5)+(3*2)+(2*1)+(1*1)=87
87 % 10 = 7
So 3852-11-7 is a valid CAS Registry Number.

3852-11-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 3-Methoxyisobutyrate

1.2 Other means of identification

Product number -
Other names Methyl 3-Methoxy-2-methylpropionate

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:3852-11-7 SDS

3852-11-7Relevant academic research and scientific papers

MANUFACTURING METHOD OF β-SUBSTITUTED PROPIONIC ACID AMIDE AND N-SUBSTITUTED (METH)ACRYLAMIDE

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Paragraph 0046; 0048; 0050, (2018/07/03)

PROBLEM TO BE SOLVED: To provide a method for industrially manufacturing β-alkoxy propionic acid amide, β-amino propionic acid amide and N-substituted (meth)acryl amide using (meth)acrylic acid ester as starting material at high yield and high purity. SOLUTION: There is provided a method for obtaining N-substituted (meth)acryl amide represented by target compound formula (7) by conducting an amidation reaction with amine using β-substituted propionic acid ester represented by the formula (1) of a product of a Michael addition reaction of (meth)acrylic acid ester and alcohol or amine in presence of a metal complex as a catalyst to obtain β-substituted propionic acid amide represented by the formula (3) and conducting a thermal decomposition reaction of β-substituted propionic acid amide in presence of the metal complex as the catalyst to eliminate alcohol or amine. A-CH2-C(R1)H-C(=O)-OR2 (1), A-CH2-C(R1)H-C(=O)-N(R3)R4 (3), CH2=C(R1)-C(=O)-N(R3)R4 (7) SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT

METHOD FOR PRODUCING UNSATURATED ACID AND/OR UNSATURATED ACID ESTER

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Paragraph 0081-0082, (2015/07/02)

The present invention relates to a method for producing an unsaturated acid and/or an unsaturated acid ester, containing a process A of reacting a compound (1) represented by the following formula (1) at a temperature of 0° C. to 350° C. in the presence of a Br?nsted acid catalyst and/or a Lewis acid catalyst, to prepare a compound (2) represented by the following formula (2); in which each of R1, R2 and R4 independently represents a hydrogen atom, a deuterium atom or an alkyl group; each of R3 and R5 independently represents a hydrogen atom or a deuterium atom; R6 represents a hydrogen atom, a deuterium atom, or an alkyl group or an aryl group; and X represents a chlorine atom, a fluorine atom, a bromine atom, or an iodine atom.

QUATERNARY SALTS OF N,N-DIMETHYLAMINOETHYL ESTERS OF PIVALIC AND 2-METHYL-3-METHOXYPROPIONIC ACID AND THEIR HYDROLYSIS

Sevcik, Stanislav,Pradny, Martin

, p. 206 - 214 (2007/10/02)

The synthesis and kinetics of quaternization of model compounds of poly(N,N-dimethylaminoethyl methacrylate) in water-alcoholic solutions brought about by methyl iodide and the alkaline hydrolysis of products in water have been investigated.N,N-Dimethylaminoethyl pivalate was selected as a model of the structural unit of the reported polymer; N,N-dimethylaminoethyl-2-methyl-3-methoxypropionate was the model of the terminal unit of the anionically prepared polymer.

Method for the oxycarbonylation of ethylene and propylene

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, (2008/06/13)

A process for the catalytic oxycarbonylation of ethylene and propylene by reaction with carbon monoxide and oxygen in a methanolic or ethanolic reaction medium employing a catalyst which contains a compound of vanadium, chromium, iron, cobalt, nickel or copper and chloride, bromide, or iodide ions.

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