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Methyl 4-methylhexanoate, also known as 4-methylhexyl methyl ester, is an organic compound with the chemical formula C8H16O2. It is a colorless liquid with a fruity, apple-like odor and is commonly used as a flavoring agent in the food and beverage industry. This ester is formed by the reaction of 4-methylhexanoic acid and methanol, and it is characterized by its fruity aroma, which makes it a popular choice for imparting a pleasant taste to various products. Methyl 4-methylhexanoate is also used in the fragrance industry to create natural and synthetic scents. It is generally recognized as safe (GRAS) by the U.S. Food and Drug Administration for use in food, and its properties make it a versatile component in the creation of both food flavors and fragrances.

2177-82-4

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2177-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2177-82-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,7 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2177-82:
(6*2)+(5*1)+(4*7)+(3*7)+(2*8)+(1*2)=84
84 % 10 = 4
So 2177-82-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O2/c1-4-7(2)5-6-8(9)10-3/h7H,4-6H2,1-3H3

2177-82-4SDS

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 METHYL 4-METHYLHEXANOATE

1.2 Other means of identification

Product number -
Other names rac.-4-Methylhexansaeuremethylester

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 -
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More Details:2177-82-4 SDS

2177-82-4Downstream Products

2177-82-4Relevant academic research and scientific papers

Highly selective formation of linear esters from terminal and internal alkenes catalysed by palladium complexes of bis-(di-tert-butylphosphinomethyl) benzene

Rodriguez, Cristina Jimenez,Foster, Douglas F.,Eastham, Graham R.,Cole-Hamilton, David J.

, p. 1720 - 1721 (2007/10/03)

The methoxycarbonylation of terminal or internal alkenes catalysed by palladium complexes of bis-(di-tert-butylphosphinomethyl)benzene under mild conditions leads to linear esters in 99% selectivity via a hydride mechanism.

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