183990-46-7 Usage
Description
8-[(2-hydroxybenzoyl)amino]octanoic acid, also known as C8, is a chemical compound belonging to the class of benzoic acid derivatives. It is a derivative of amino acid and benzoic acid, featuring a molecular structure with a benzene ring and a hydroxyl group attached at the ortho position. 8-[(2-hydroxybenzoyl)amino]octanoic acid is recognized for its potential skin-lightening properties and is commonly used in skincare products and cosmetics.
Uses
Used in Skincare Products:
8-[(2-hydroxybenzoyl)amino]octanoic acid is used as a skin-lightening agent for its ability to inhibit melanin production in the skin, effectively treating hyperpigmentation and dark spots.
Used in Cosmetics:
In the cosmetics industry, 8-[(2-hydroxybenzoyl)amino]octanoic acid is utilized as an ingredient for its skin-lightening and beautifying effects, enhancing the appearance of the skin by reducing the visibility of pigmented areas.
Used in Antioxidant Formulations:
8-[(2-hydroxybenzoyl)amino]octanoic acid is used as an antioxidant in skincare formulations to protect the skin from oxidative stress and environmental damage, contributing to the maintenance of skin health and vitality.
Used in Anti-inflammatory Formulations:
In anti-inflammatory applications, 8-[(2-hydroxybenzoyl)amino]octanoic acid serves to reduce skin inflammation and irritation, making it suitable for sensitive skin types and conditions such as acne or rosacea.
Check Digit Verification of cas no
The CAS Registry Mumber 183990-46-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,9,9 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 183990-46:
(8*1)+(7*8)+(6*3)+(5*9)+(4*9)+(3*0)+(2*4)+(1*6)=177
177 % 10 = 7
So 183990-46-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H21NO4/c17-13-9-6-5-8-12(13)15(20)16-11-7-3-1-2-4-10-14(18)19/h5-6,8-9,17H,1-4,7,10-11H2,(H,16,20)(H,18,19)
183990-46-7Relevant articles and documents
Use of oligosalicylates in the preparation of phenolic amido acids
Gschneidner, David,Corvino, JoAnne,Freeman, John,O'Toole, Doris,Shields, Lynn,Wang, Eric
, p. 1567 - 1575 (2005)
A simplified methodology has been developed for preparing salicylamides from the corresponding acids via oligosalicylates which both protect the phenolic group and, at the same time, activate the carboxyl for coupling. Copyright Taylor & Francis, Inc.
Synthesis method of sodium N-(8-[2-hydroxybenzoyl]-amino)caprylate
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Paragraph 0027; 0030-0033; 0035-0038; 0040-0043, (2022/01/08)
The present invention discloses a method for synthesizing N- (8-[2-hydroxybenzoyl]- amino) sodium caprylate. First, methyl o-hydroxybenzoate was added to the reaction vessel, and then a solvent and 8-aminocaprylic acid were added to the reaction; after th
Method for preparing N-[8-(2-hydroxybenzoyl)amino]caprylic acid
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Paragraph 0042; 0058-0061; 0062; 0077-0078, (2021/07/01)
The invention provides a method for preparing N-[8-(2-hydroxybenzoyl)amino]caprylic acid. The method is characterized in that salicylamide is used as an initial raw material and subjected to four-step reactions including cyclization, two-step nucleophilic substitution, hydrolysis and decarboxylation to obtain the N-[8-(2-hydroxybenzoyl)amino]caprylic acid. The preparation method has the advantages of easily available raw materials, low production cost, less three-waste pollution, simple process route and easy industrial production, and solves the problems that existing preparation methods are complex, raw materials are not easily available, requirements on equipment are low, and impurities are easily generated.
