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18375-59-2

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18375-59-2 Usage

General Description

N-hexyl-D-gluconamide is a chemical compound that is derived from glucose and consists of a hexyl chain attached to a D-gluconic acid molecule. It is commonly used in personal care and cosmetic products as an emollient and conditioning agent due to its ability to moisturize and soften the skin and hair. N-hexyl-D-gluconamide is also utilized in pharmaceutical formulations as a solubilizer and permeation enhancer, helping to improve the absorption of drugs through biological membranes. Additionally, it has been studied for its potential as a drug delivery agent and has shown promise as a non-toxic, biodegradable alternative to traditional pharmaceutical excipients. Overall, N-hexyl-D-gluconamide has a diverse range of applications and is valued for its skin conditioning and drug delivery properties.

Check Digit Verification of cas no

The CAS Registry Mumber 18375-59-2 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, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18375-59:
(7*1)+(6*8)+(5*3)+(4*7)+(3*5)+(2*5)+(1*9)=132
132 % 10 = 2
So 18375-59-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H25NO6/c1-2-3-4-5-6-13-12(19)11(18)10(17)9(16)8(15)7-14/h8-11,14-18H,2-7H2,1H3,(H,13,19)/t8-,9-,10+,11-/m1/s1

18375-59-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-hexyl-D-gluconamide

1.2 Other means of identification

Product number -
Other names D-Gluconamido-n-hexan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:18375-59-2 SDS

18375-59-2Downstream Products

18375-59-2Relevant articles and documents

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

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