51930-97-3 Usage
Uses
Used in Pharmaceutical Industry:
rac 1,2-Bis-palmitol-3-chloropropanediol is used as an active pharmaceutical ingredient for the development of drugs targeting various health conditions. Its unique chemical structure allows for the creation of novel therapeutic agents with potential benefits in treating specific diseases.
Used in Cosmetics Industry:
In the cosmetics industry, rac 1,2-Bis-palmitol-3-chloropropanediol is used as an emollient, providing a smooth and soft texture to skincare products. Its ability to form stable emulsions makes it an ideal ingredient for creams, lotions, and other personal care formulations.
Used in Food Industry:
rac 1,2-Bis-palmitol-3-chloropropanediol is used as an additive in the food industry, particularly for its emulsifying properties. It helps to improve the texture, stability, and shelf life of various food products, such as baked goods, confectionery, and dairy products.
Used in Chemical Industry:
In the chemical industry, rac 1,2-Bis-palmitol-3-chloropropanediol is used as an intermediate in the synthesis of various compounds, including surfactants, lubricants, and other specialty chemicals. Its versatile chemical properties make it a valuable building block for creating new materials with specific applications.
Used in Research and Development:
rac 1,2-Bis-palmitol-3-chloropropanediol is also utilized in research and development for its potential applications in various fields. Scientists and researchers explore its properties and reactivity to develop new compounds and materials with improved performance and functionality.
Check Digit Verification of cas no
The CAS Registry Mumber 51930-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,9,3 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 51930-97:
(7*5)+(6*1)+(5*9)+(4*3)+(3*0)+(2*9)+(1*7)=123
123 % 10 = 3
So 51930-97-3 is a valid CAS Registry Number.
InChI:InChI=1/C35H67ClO4/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-34(37)39-32-33(31-36)40-35(38)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h33H,3-32H2,1-2H3
51930-97-3Relevant academic research and scientific papers
Bidirectional conversion between 3-monochloro-1,2-propanediol and glycidol in course of the procedure of DGF standard methods
Kaze, Naoki,Sato, Hirofumi,Yamamoto, Hiroshi,Watanabe, Yomi
experimental part, p. 1143 - 1151 (2011/11/12)
NMR observation revealed that bidirectional conversion occurred between 3-monochloropropane-1,2-diol (3-MCPD) and glycidol in the course of the analytical procedure of DFG standard method C-III 18 (09), option A; 3-MCPD was partly converted to glycidol at the transesterification step, and glycidol was converted partly to 3-MCPD at the derivatization step conducted at 80 °C under acidic condition in the presence of NaCl. Based on the proton numbers observed by 1H NMR, the degrees of the conversion were estimated to be 37 and >70%, respectively. In addition, epoxide ring-opening of glycidol and its esters was found to be ca. 90% by the acid treatment described in the method, option B. Thus, it was concluded that the standard method, option A, did not correctly give the combined amount of 3-MCPD esters and glycidyl esters in oils containing glycidyl esters, and the difference of the values obtained by options A and B did not correspond to the amount of glycidyl esters, either. In addition, derivatives of 3-MCPD with phenylboronic acid were not observed by NMR at the derivatization step, although they were detected by GC-MS in the organic phase at the following extraction step.
