156153-06-9 Usage
Uses
Used in Personal Care Industry:
POLYGLYCERYL-2 CAPRATE is used as an emulsifier for blending and stabilizing oil and water-based ingredients in products like shampoos, conditioners, and skin creams. This ensures a smooth and consistent texture, enhancing the product's performance and user experience.
POLYGLYCERYL-2 CAPRATE is also used as a surfactant to reduce the surface tension of liquids, allowing for better dispersion and penetration of active ingredients in the skin. This improves the efficacy of personal care products and contributes to their overall effectiveness.
Furthermore, POLYGLYCERYL-2 CAPRATE is utilized in natural and organic formulations as a preferred ingredient due to its mild nature and biodegradability, catering to the growing demand for eco-friendly and sustainable personal care products.
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
156153-06-9Relevant academic research and scientific papers
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.
