18375-65-0 Usage
General Description
N-hexadecyl-D-gluconamide is a chemical compound derived from glucose and a long-chain alkyl group. It is widely used in cosmetic and personal care products as an emollient and moisturizing agent due to its ability to improve the skin's moisture retention. The compound is also used as a surfactant and cleansing agent in various household and industrial products. N-hexadecyl-D-gluconamide is known for its mild and gentle nature, making it suitable for sensitive skin and is often used in products such as lotions, creams, shampoos, and body washes to provide a smooth and soft skin feel. Additionally, it has been found to have antimicrobial properties, making it valuable in skincare products that target acne and other skin issues.
Check Digit Verification of cas no
The CAS Registry Mumber 18375-65-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,7 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18375-65:
(7*1)+(6*8)+(5*3)+(4*7)+(3*5)+(2*6)+(1*5)=130
130 % 10 = 0
So 18375-65-0 is a valid CAS Registry Number.
InChI:InChI=1/C22H45NO6/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-23-22(29)21(28)20(27)19(26)18(25)17-24/h18-21,24-28H,2-17H2,1H3,(H,23,29)/t18-,19-,20+,21-/m1/s1
18375-65-0Relevant articles and documents
Pseudo-ceramide compound, method for preparing the same and cosmetic composition comprising the same
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Paragraph 0084-0089, (2018/05/24)
Disclosed is a pseudoceramide compound which is represented by chemical formula 1 by introducing alkylamine and an acyl group to D-gluconic acid. In the chemical formula 1, A is gluconic acid or an aqueous gluconic acid solution, R_1 refers to a straight or branched alkyl group with 10-22 carbon atoms, and R_2 refers to a straight or branched alkyl group with 11-21 carbon atoms or a straight or branched alkenyl group with 11-21 carbon atoms. According to the present invention, the pseudoceramide compound exhibits effects of improving skin moisturizing functions and compatibility.COPYRIGHT KIPO 2018
Direct amidation of aldoses and decarboxylative amidation of α-keto acids: An efficient conjugation method for unprotected carbohydrate molecules
Cho, Chia-Ching,Liu, Jia-Nan,Chien, Chung-Hsun,Shie, Jiun-Jie,Chen, Ying-Chu,Fang, Jim-Min
supporting information; experimental part, p. 1549 - 1556 (2009/07/24)
With use of iodine as an appropriate oxidant, unprotected and unmodified aldoses undergo oxidative amidation with a variety of functionalized amines, a-amino esters, and peptides, whereas KDO, sialic acid, and other a-keto acids proceed with oxidative dec
