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Glycerol triisovalerate, also known as triisovalin, is a colorless, odorless liquid with a sweet taste, derived from glycerol and isovaleric acid. It is commonly used as a flavoring agent in food and beverages, and also serves as a plasticizer in the manufacturing of plastics and a solvent for various applications. With low toxicity and considered safe for use in food and other consumer products, glycerol triisovalerate is stable under normal conditions and has a high boiling point, making it suitable for a wide range of industrial and commercial uses.

620-63-3

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620-63-3 Usage

Uses

Used in Food and Beverage Industry:
Glycerol triisovalerate is used as a flavoring agent for its sweet taste, enhancing the taste and aroma of various food and beverage products.
Used in Plastics Manufacturing:
Glycerol triisovalerate is used as a plasticizer to increase the flexibility and workability of plastics during the manufacturing process.
Used in Solvent Applications:
Glycerol triisovalerate is used as a solvent for a variety of applications, including industrial processes and commercial products, due to its ability to dissolve a wide range of substances.

Check Digit Verification of cas no

The CAS Registry Mumber 620-63-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 620-63:
(5*6)+(4*2)+(3*0)+(2*6)+(1*3)=53
53 % 10 = 3
So 620-63-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H32O6/c1-12(2)7-16(19)22-10-15(24-18(21)9-14(5)6)11-23-17(20)8-13(3)4/h12-15H,7-11H2,1-6H3

620-63-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-bis(3-methylbutanoyloxy)propyl 3-methylbutanoate

1.2 Other means of identification

Product number -
Other names 1,2,3-Propanetriyl 3-methylbutanoate

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:620-63-3 SDS

620-63-3Relevant academic research and scientific papers

Hydroalkoxycarbonylation of isobutylene with polyhydric alcohols in the presence of catalytic systems based on palladium compounds and tertiary phosphines

Suerbaev,Chepaikin,Appazov,Dzhiembaev

experimental part, p. 189 - 193 (2012/09/08)

The reaction of isobutylene hydroalkoxycarbonylation at low carbon monoxide pressures (≤2.0 MPa) with ethylene glycol and glycerol in the presence of catalytic systems based on Pd and mono- and bidentate organic phosphines has been studied. The effect of different conditions of the reaction in the presence of the Pd(Acac)2-PPh3-TsOH catalyst system on the ratio of the products, mono- and diglycolides (mono-, di-and triglycerides) of isovaleric acid has been investigated. The relative catalytic activity of a number of binary and ternary systems based on synthesized Pd(Acac)2, Pd(PPh3)4, and PdCl2(PPH3) 2 complexes has been determined. Pleiades Publishing, Ltd., 2012.

Catalytic hydroxycarbonylation of isobutylene with carbon monoxide and polyhydric alcohols in the presence of the Pd(acac)2-PPh 3-TsOH system

Suerbaev,Chepajkin,Dzhiembaev,Appazov,Abyzbekova

, p. 345 - 347 (2008/04/03)

The reaction of isobutylene hydroalcoxycarbonylation with CO and polyhydric alcohols (ethylene glycol, glycerol) in the presence of the catalytic system Pd(aacac)2-PPh3-TsOH has been investigated. It was found that carbonylation of isobutylene with CO in the presence of ethylene glycol yields a mixture of mono-and diglycol esters of isovaleric acid, irrespective of the initial reactant ratio. During the hydroalcoxycarbonylation of isobutylene with glycerol, either mono- and di- or mono-, di-, and triglycerides of isovaleric acid are formed depending on the reactant ratio.

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