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Methyl 3-(acetyloxy)hexanoate is a chemical compound with the molecular formula C9H16O4. It is an ester, specifically a methyl ester of 3-(acetyloxy)hexanoic acid. This clear, colorless liquid possesses a pleasant odor and is relatively safe for use in approved applications.

21188-60-3

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21188-60-3 Usage

Uses

Used in Fragrance and Flavor Industry:
Methyl 3-(acetyloxy)hexanoate is used as a flavoring agent and fragrance ingredient for its ability to impart a fruity, floral, and sweet aroma to various products.
Used in Organic Synthesis:
Methyl 3-(acetyloxy)hexanoate is used as a solvent and a reagent in organic synthesis processes, contributing to the creation of a range of chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 21188-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,1,8 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21188-60:
(7*2)+(6*1)+(5*1)+(4*8)+(3*8)+(2*6)+(1*0)=93
93 % 10 = 3
So 21188-60-3 is a valid CAS Registry Number.

21188-60-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hexadecyl-2-methylpyridin-1-ium,bromide

1.2 Other means of identification

Product number -
Other names Pyridinium,1-hexadecyl-2-methyl-,bromide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:21188-60-3 SDS

21188-60-3Relevant academic research and scientific papers

Stereoselektive Synthese von Alkoholen, VII. Optisch aktive Homoallylalkohole durch Addition chiraler Boronsaeureester an Aldehyde

Hoffmann, Reinhard W.,Herold, Thomas

, p. 375 - 383 (2007/10/02)

Addition of the chiral boronates 1 and 4 to aldehydes led to homoallyl alcohols 2 and 5 of uniform absolute configuration.On addition to saturated aldehydes an asymmetric induction of around 70percent e. e. could be achieved.

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