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1,3-Dioxolane-2-propanoic acid, 2-methyl-, 2-hydroxyethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62603-41-2

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62603-41-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62603-41-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,0 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62603-41:
(7*6)+(6*2)+(5*6)+(4*0)+(3*3)+(2*4)+(1*1)=102
102 % 10 = 2
So 62603-41-2 is a valid CAS Registry Number.

62603-41-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxyethyl 3-(2-methyl-1,3-dioxolan-2-yl)propanoate

1.2 Other means of identification

Product number -
Other names 1,3-Dioxolane-2-propanoic acid,2-methyl-,2-hydroxyethyl 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:62603-41-2 SDS

62603-41-2Relevant academic research and scientific papers

Heterogeneous catalysis for the ketalisation of ethyl levulinate with 1,2-dodecanediol: Opening the way to a new class of bio-degradable surfactants

Freitas, Flávio A.,Licursi, Domenico,Lachter, Elizabeth R.,Galletti, Anna Maria Raspolli,Antonetti, Claudia,Brito, Thamires C.,Nascimento, Regina Sandra V.

, p. 84 - 87 (2016)

The acid-catalysed ketalisation between ethyl levulinate and two different alkyl 1,2-diols (ethylene glycol and 1,2-dodecanediol) was investigated using different acid catalysts, e.g. p-toluensolfonic acid, Amberlyst 70, zeolite H-ZSM-5, and niobium phosphate. Good activity and recyclability were achieved in the reaction with ethylene glycol catalysed by niobium phosphate. Very promising results (both in diol conversion and in selectivity towards the desired ketal) were ascertained in the reaction with the longer-chain 1,2-dodecanediol catalysed by heterogeneous catalysts. The alkaline hydrolysis of the synthetised long-chain ketal ester allowed us to obtain a new green surfactant, with surface tension values falling in the range of the commercial anionic ones.

Acid Catalyzed Competitive Esterification and Ketalization of Levulinic Acid with 1,2 and 1,3-Diols: The Effect of Heterogeneous and Homogeneous Catalysts

Amarasekara, Ananda S.,Animashaun, Moriam A.

, p. 1819 - 1824 (2016/08/30)

Abstract: Condensation reactions of levulinic acid (LA) with 1,2-ethanediol (1,2-ED), 1,2-propanediol (1,2-PD), and 1,3-propanediol (1,3-PD) were studied using Amberlyst-15 as well as p-toluenesulfonic acid catalysts in benzene under Dean–Stark conditions. In Amberlyst-15 catalyzed reactions the products are ketals and ketal-esters, whereas p-toluenesulfonic acid catalyzed reactions produce esters and ketal-esters as products. In p-toluenesulfonic acid catalyzed reactions with 1,2-ED and 1,3-PD, LA monoester product is formed as the major product after 180?min in 75 and 97?% yields respectively. Unlike the previously reported acid catalyzed ketalization of ethyl levulinate with diols, combined ketalization–esterification of LA with diols is a complex process. Graphical Abstract: [Figure not available: see fulltext.]

POLYOL ETHERS AND PROCESS FOR MAKING THEM

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Paragraph 0094, (2011/05/14)

New polyol ether compounds and a process for their preparation. The process comprises reacting a polyol, a carbonyl compound, and hydrogen in the presence of hydrogenation catalyst, to provide the polyol ether. The molar ratio of polyol to carbonyl compound in the process is greater than 5:1.

POLYOL ETHERS AND PROCESS FOR MAKING THEM

-

Page/Page column 10, (2010/03/31)

New polyol ether compounds and a process for their preparation. The process comprises reacting a polyol, a carbonyl compound, and hydrogen in the presence of hydrogenation catalyst, to provide the polyol ether. The molar ratio of polyol to carbonyl compound in the process is greater than 5:1.

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