544-86-5 Usage
General Description
Hentricontan-1-ol, also known as 1-hentricontanol, is a long-chain primary alcohol with the chemical formula C31H64O. It is a colorless, odorless, and tasteless compound that is commonly used in the production of surfactants, lubricants, and other industrial applications. Henricontan-1-ol is a fatty alcohol derived from natural sources such as coconut oil and isopropyl alcohol. It has emollient properties, making it a popular ingredient in skincare products for its moisturizing and softening effects on the skin. Additionally, it has also been studied for its potential antimicrobial properties and is used in a variety of pharmaceutical and cosmetic formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 544-86-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,4 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 544-86:
(5*5)+(4*4)+(3*4)+(2*8)+(1*6)=75
75 % 10 = 5
So 544-86-5 is a valid CAS Registry Number.
InChI:InChI=1/C31H64O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30-31-32/h32H,2-31H2,1H3
544-86-5Relevant articles and documents
Hentriacontanyl eicosanoate ester from Parthenium hysterophorus Linn. and its antimicrobial activity
Madan, Harsha,Sharma, Sharda
body text, p. 1033 - 1036 (2012/04/04)
Aerial parts of Parthenium hysterophorus Linn. on chemical investigation afforded a new aliphatic ester hentriacontanyl eicosanoate along with stigmasterol, parthenin, isoparthenin and coronopilin. The structures of isolated compounds were ascertained using various spectral (IR, 1H, 13C NMR, MS) techniques and hentriacontanyl eicosanoate has been evaluated for its antibacterial activity against Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa and antifungal activity against Aspergillus niger, Candida albicans and Fusarium oxysporum.
A New Synthesis of Long Chain Acid Esters and Carbinols
Rao, S. Jagadishwar,Bhalerao, U. T.,Tilak, B. D.
, p. 208 - 211 (2007/10/02)
A versatile synthesis of difficulty accessible long chain acid esters and carbinols is described.The synthesis involves acylations at 2- and 5-positions of thiophene.Thioketalation of the resulting ketoesters followed by Raney nickel desulfurization yield acid esters which on LAH reduction give the corresponding carbinols.
