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97-64-3

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97-64-3 Usage

General Description

DL-Ethyl lactate is a chemical compound that is a mixture of both D-Ethyl lactate and L-Ethyl lactate. It is a clear, colorless liquid that is commonly used as a solvent in various applications such as inks, coatings, adhesives, and cleaning products. It is also used as a flavoring agent and fragrance ingredient in the food and cosmetic industries. DL-Ethyl lactate is known for its low toxicity, biodegradability, and low volatility, making it a preferred choice in environmentally friendly and sustainable products. It is considered safe for use in food and cosmetic products when used in accordance with regulations and guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 97-64-3 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 97-64:
(4*9)+(3*7)+(2*6)+(1*4)=73
73 % 10 = 3
So 97-64-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H10O3/c1-3-8-5(7)4(2)6/h4,6H,3H2,1-2H3/t4-/m1/s1

97-64-3 Well-known Company Product Price

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  • Sigma-Aldrich

  • (08996)  Ethyllactate  analytical standard

  • 97-64-3

  • 08996-1ML

  • 458.64CNY

  • Detail

97-64-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl lactate

1.2 Other means of identification

Product number -
Other names Acytol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Solvents
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:97-64-3 SDS

97-64-3Relevant articles and documents

Ni-Catalyzed C(sp3)–O Arylation of α-Hydroxy Esters

Monteith, John J.,Rousseaux, Sophie A. L.

supporting information, p. 9485 - 9489 (2021/12/09)

A Negishi cross-coupling of α-hydroxy ester derivatives and arylzinc reagents has been developed. This reaction tolerates both primary and secondary C(sp3)–O alcohol precursors and achieves efficient cross-coupling under Ni catalysis without the need for added external metal reductant, photocatalyst, or additives. The arylation of readily accessible C(sp3)–O electrophiles in this operationally simple, rapid, and mild reaction provides a complementary way of accessing desirable α-aryl ester products.

Asymmetric Synthesis of N-Substituted α-Amino Esters from α-Ketoesters via Imine Reductase-Catalyzed Reductive Amination

Yao, Peiyuan,Marshall, James R.,Xu, Zefei,Lim, Jesmine,Charnock, Simon J.,Zhu, Dunming,Turner, Nicholas J.

supporting information, p. 8717 - 8721 (2021/03/16)

N-Substituted α-amino esters are widely used as chiral intermediates in a range of pharmaceuticals. Here we report the enantioselective biocatalyic synthesis of N-substituted α-amino esters through the direct reductive coupling of α-ketoesters and amines employing sequence diverse metagenomic imine reductases (IREDs). Both enantiomers of N-substituted α-amino esters were obtained with high conversion and excellent enantioselectivity under mild reaction conditions. In addition >20 different preparative scale transformations were performed highlighting the scalability of this system.

Process method for producing ethyl lactate by using reactive distillation dividing wall tower technology

-

Paragraph 0039; 0040; 0046-0049, (2020/02/14)

The invention provides a process method for producing ethyl lactate by using a reactive distillation dividing wall tower technology. According to the process, the production of ethyl lactate is completed in a reactive distillation dividing wall tower, an esterification reaction of lactic acid and ethanol is completed in a middle section feeding side reaction section of the reactive distillation dividing wall tower to generate ethyl lactate and water, and the separation of ethanol and esterification product water is completed through a middle section extraction side rectification section, meanwhile, ethyl lactate purification is realized in a middle section feeding side stripping section and a middle section extracting side stripping section, and finally a food-grade ethyl lactate product is obtained at the bottom of the tower. Compared with the prior art, the process has the advantages of high ethyl lactate product yield, high equipment integration, short process flow, low one-time investment, low operation cost and the like.

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