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Dodecyl 3-methylbutanoate, also known as 3-methylbutanoic acid dodecyl ester, is an organic compound with the chemical formula C17H34O2. It is a colorless to pale yellow liquid with a mild, fruity odor. This ester is formed by the reaction of dodecanol (a 12-carbon alcohol) and 3-methylbutanoic acid (a 5-carbon carboxylic acid). It is commonly used in the fragrance industry as a fixative and in the production of various perfumes, due to its ability to blend well with other fragrance components and enhance their stability. Additionally, dodecyl 3-methylbutanoate is employed in the formulation of personal care products, such as soaps, lotions, and creams, where it serves as a skin conditioning agent and emollient.

6938-56-3

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6938-56-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6938-56-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,3 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6938-56:
(6*6)+(5*9)+(4*3)+(3*8)+(2*5)+(1*6)=133
133 % 10 = 3
So 6938-56-3 is a valid CAS Registry Number.

6938-56-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name dodecyl 3-methylbutanoate

1.2 Other means of identification

Product number -
Other names Dodecyl3-methylbutyrate

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:6938-56-3 SDS

6938-56-3Downstream Products

6938-56-3Relevant academic research and scientific papers

Broadly Applicable Ytterbium-Catalyzed Esterification, Hydrolysis, and Amidation of Imides

Guissart, Céline,Barros, Andre,Rosa Barata, Luis,Evano, Gwilherm

supporting information, p. 5098 - 5102 (2018/09/13)

An efficient, broadly applicable, operationally simple, and divergent process for the transformation of imides into a range of carboxylic acid derivatives under mild conditions is reported. By simply using catalytic amounts of ytterbium(III) triflate as a Lewis acid promoter in the presence of alcohols, water, amines, or N,O-dimethylhydroxylamine, a broad range of imides is smoothly and readily converted to the corresponding esters, carboxylic acids, amides, and Weinreb amides in good yields. This method notably enables an easy cleavage of oxazolidinone-based auxiliaries.

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