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Ethyl acetyl lactate, also known as 2-acetoxy-2-methylbutanoic acid, is a synthetic, volatile organic compound that is highly valued for its unique aroma and taste. It is primarily used in the flavor and fragrance industries and can be found in a variety of foods, beverages, perfumes, and cosmetics.

2985-28-6

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2985-28-6 Usage

Uses

Used in Flavor and Fragrance Industry:
Ethyl acetyl lactate is used as a flavoring agent for its sweet, fruity, and cream scent, enhancing the taste and aroma of processed fruits, alcoholic drinks, and dairy products.
Used in Perfumes and Cosmetics:
Ethyl acetyl lactate is used as a fragrance ingredient in perfumes and cosmetics, providing a pleasant and distinctive scent to these products.
Safety Consideration:
It is important to handle ethyl acetyl lactate with care, as it may pose potential health risks due to its chemical properties. Proper safety measures should be taken to minimize any adverse effects on human health.

Check Digit Verification of cas no

The CAS Registry Mumber 2985-28-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,8 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2985-28:
(6*2)+(5*9)+(4*8)+(3*5)+(2*2)+(1*8)=116
116 % 10 = 6
So 2985-28-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O4/c1-4-10-7(9)5(2)11-6(3)8/h5H,4H2,1-3H3

2985-28-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-acetyloxypropanoate

1.2 Other means of identification

Product number -
Other names 2-acetoxy-propionic acid ethyl ester

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:2985-28-6 SDS

2985-28-6Relevant academic research and scientific papers

SELECTIVE REDUCTION OF α-KETO ESTERS WITH ORGANOTIN HYDRIDES APPLICATION TO ASYMMETRIC SYNTHESES

Rahm, A.,Pereyre, M.

, p. 843 - 848 (2007/10/02)

Organotin hydrides selectively reduce the keto functional group in α-keto esters such as pyruvates or benzoylformates.Hydrostannation of (-)-menthyl benzoylformate with achiral reagents occurs with 5-20percent asymmetric induction while the reaction of (-)-2-butyldiphenyltin hydride with ethyl benzoylformate only proceeds with a very low optical yield.

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