6221-96-1 Usage
General Description
Hexadecyl propionate is a chemical compound used primarily as a fragrance ingredient in cosmetics and personal care products. It is an ester of hexadecyl alcohol and propionic acid, and it has a mild, sweet, and slightly floral scent. Hexadecyl propionate is often used to impart a pleasant aroma to products such as perfumes, lotions, and hair care products. It is considered safe for use in cosmetics, as it has low toxicity and is not known to cause skin irritation or other adverse effects when used in appropriate concentrations. Overall, hexadecyl propionate is a versatile and widely used ingredient that enhances the sensory experience of various personal care and cosmetic products.
Check Digit Verification of cas no
The CAS Registry Mumber 6221-96-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,2 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6221-96:
(6*6)+(5*2)+(4*2)+(3*1)+(2*9)+(1*6)=81
81 % 10 = 1
So 6221-96-1 is a valid CAS Registry Number.
InChI:InChI=1/C19H38O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-21-19(20)4-2/h3-18H2,1-2H3
6221-96-1Relevant articles and documents
Esters, retroesters, and a retroamide of palmitic acid: Pool for the first selective inhibitors of N-palmitoylethanolamine-selective acid amidase
Vandevoorde, Séverine,Tsuboi, Kazuhito,Ueda, Natsuo,Jonsson, Kent-Olov,Fowler, Christopher J.,Lambert, Didier M.
, p. 4373 - 4376 (2007/10/03)
Cyclohexyl hexadecanoate, hexadecyl propionate, and N-(3-hydroxypropionyl)pentadecanamide, respectively ester, retroester, and retroamide derivatives of N-palmitoylethanolamine, represent the first selective inhibitors of "N-palmitoylethanolamine hydrolase" described so far. These compounds are devoid of affinity for CB1 and CB 2 receptors and characterized by high percentages of inhibition of N-palmitoylethanolamine-selective acid amidase (84.0, 70.5, and 76.7% inhibition at 100 μM, respectively) with much lower inhibitory effect on either fatty acid amide hydrolase or the uptake of anandamide.
