3539-38-6 Usage
Description
2-hydroxypropyl myristate is a versatile chemical compound commonly used in the cosmetics and pharmaceutical industries as an emollient, emulsifier, and skin-conditioning agent. It is derived from myristic acid and isopropyl alcohol, and is known for its ability to soften and smooth the skin, making it a popular ingredient in lotions, creams, and other skincare products.
Used in Cosmetics Industry:
2-hydroxypropyl myristate is used as an emollient for its skin-softening and smoothing properties, making it a popular ingredient in lotions, creams, and other skincare products.
2-hydroxypropyl myristate is used as an emulsifier for its ability to create stable oil-in-water emulsions, which is essential in formulating various cosmetic products.
Used in Pharmaceutical Industry:
2-hydroxypropyl myristate is used as a solvent in pharmaceutical products due to its ability to dissolve and stabilize active ingredients.
2-hydroxypropyl myristate is used as a carrier for active ingredients in pharmaceutical products, enhancing their absorption and improving the overall efficacy of the formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 3539-38-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,3 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3539-38:
(6*3)+(5*5)+(4*3)+(3*9)+(2*3)+(1*8)=96
96 % 10 = 6
So 3539-38-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H34O3/c1-3-4-5-6-7-8-9-10-11-12-13-14-17(19)20-15-16(2)18/h16,18H,3-15H2,1-2H3
3539-38-6Relevant articles and documents
Effect of Alternation of Chloropropoxy and Propoxy Units and Impact of the Ethylol-Group Number on Properties of Surfactants
Ahmadova, Gulnara A.,Abilova, Aygul Z.,Rahimov, Ravan A.,Askerzade, Seadet M.,Asadov, Ziyafaddin H.,Zubkov, Fedor I.,Ahmadbayova, Saida F.
, p. 837 - 845 (2018)
Surfactants based on myristic acid, epichlorohydrin, and propylene oxide were obtained in two ways. First, the ester of myristic acid and epichlorohydrin was synthesised, and then with propylene oxide. Second, myristic acid was first reacted with propylene oxide, and then with epichlorohydrin. In both cases, the reactions were carried out at 150-160°C using triethylamine as a catalyst. The obtained chloropropoxy-propoxy and propoxy-chloropropoxy esters of myristic acid are non-ionic surfactants. These products were transformed into cationic surfactants by interaction with several ethanolamines. The specific electroconductance and surface activity of the obtained surfactants, characters that vary with the colloidal-chemical parameters of the surfactants, depended on such factors as the sequence of the epichlorohydrin and propylene oxide units inside the polar group of the obtained ionic surfactants, the presence of the methyl group linked to the N-atom, as well as the number of ethylol groups. It was revealed that the synthesised surfactants possess a property of localising thin (thickness 1 mm) petroleum films spread over different types of water.
