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156153-06-9

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156153-06-9 Usage

General Description

POLYGLYCERYL-2 CAPRATE is a chemical compound derived from glycerin and capric acid. It is commonly used as an emulsifier and surfactant in various personal care products, such as shampoos, conditioners, and skin creams. As an emulsifier, POLYGLYCERYL-2 CAPRATE helps to blend and stabilize oil and water-based ingredients, creating a smooth and consistent texture in cosmetic products. Its surfactant properties enable it to reduce the surface tension of liquids, allowing for better dispersion and penetration of active ingredients in the skin. Moreover, it is often preferred in natural and organic formulations due to its mild nature and biodegradability.

Check Digit Verification of cas no

The CAS Registry Mumber 156153-06-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,1,5 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 156153-06:
(8*1)+(7*5)+(6*6)+(5*1)+(4*5)+(3*3)+(2*0)+(1*6)=119
119 % 10 = 9
So 156153-06-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H32O6/c1-2-3-4-5-6-7-8-9-16(20)22-13-15(19)12-21-11-14(18)10-17/h14-15,17-19H,2-13H2,1H3

156153-06-9SDS

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 3-(2,3-dihydroxypropoxy)-2-hydroxypropyl decanoate

1.2 Other means of identification

Product number -
Other names Polyglycerol-2-caprate

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:156153-06-9 SDS

156153-06-9Synthetic route

diglycerol
627-82-7

diglycerol

Methyl decanoate
110-42-9

Methyl decanoate

3-(2,3-dihydroxypropoxy)-2-hydroxypropyl decanoate
156153-06-9

3-(2,3-dihydroxypropoxy)-2-hydroxypropyl decanoate

Conditions
ConditionsYield
at 160℃; for 16h; Inert atmosphere;54%
diglycerol
627-82-7

diglycerol

3-(2,3-dihydroxypropoxy)-2-hydroxypropyl decanoate
156153-06-9

3-(2,3-dihydroxypropoxy)-2-hydroxypropyl decanoate

3-(3-(decyloxy)-2-hydroxypropoxy)propane-1,2-diol
88456-94-4

3-(3-(decyloxy)-2-hydroxypropoxy)propane-1,2-diol

Conditions
ConditionsYield
With 5%-palladium/activated carbon; hydrogen at 120℃; under 37503.8 Torr; for 16h; Autoclave;26%

156153-06-9Downstream Products

156153-06-9Relevant articles and documents

1-O-Alkyl (di)glycerol ethers synthesis from methyl esters and triglycerides by two pathways: Catalytic reductive alkylation and transesterification/reduction

Sutter, Marc,Dayoub, Wissam,Metay, Estelle,Raoul, Yann,Lemaire, Marc

supporting information, p. 786 - 797 (2013/04/24)

From available and bio-sourced methyl esters, monoglycerides or oleic sunflower refined oil, the corresponding 1-O-alkyl (di)glycerol ethers were obtained in both high yields and selectivity by two different pathways. With methyl esters, a reductive alkylation with (di)glycerol was realized under 50 bar hydrogen pressure in the presence of 1 mol% of Pd/C and an acid co-catalyst. A second two step procedure was evaluated from methyl esters or triolein and consisted of a first transesterification to the corresponding monoglyceride with a BaO/Al2O3 catalyst, then its reduction to the desired glycerol monoether with a recyclable heterogeneous catalytic system Pd/C and Amberlyst 35 under H2 pressure. In addition, a mechanism for the reaction was also proposed.

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