183990-46-7

Basic information

• Product Name: 8-[(2-hydroxybenzoyl)amino]octanoic acid
• Synonyms: 8-[(2-hydroxybenzoyl)amino]octanoic acid;salcaprozic acid;8-(2-hydroxybenzamido)octanoic acid(WX191662)
• CAS NO: 183990-46-7
• Molecular Formula: C₁₅H₂₁NO₄
• Molecular Weight: 279.33
• EINECS: 604-604-1
• Mol File: 183990-46-7.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 521.7°C at 760 mmHg
• Flash Point: 269.3°C
• Appearance: /
• Density: 1.171g/cm³
• Vapor Pressure: 1.03E-11mmHg at 25°C
• Refractive Index: 1.548
• CAS DataBase Reference: 8-[(2-hydroxybenzoyl)amino]octanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 8-[(2-hydroxybenzoyl)amino]octanoic acid(183990-46-7)
• EPA Substance Registry System: 8-[(2-hydroxybenzoyl)amino]octanoic acid(183990-46-7)

Safety Data

• Hazardous Substances Data: 183990-46-7(Hazardous Substances Data)

Usage

General Description

8-[(2-hydroxybenzoyl)amino]octanoic acid is a chemical compound that belongs to the class of compounds known as benzoic acid and derivatives. It is a derivative of amino acid and benzoic acid, and its molecular structure consists of a benzene ring with a hydroxyl group attached at the ortho position. 8-[(2-hydroxybenzoyl)amino]octanoic acid is also known as C8, an ingredient commonly used in skincare products and cosmetics due to its potential skin-lightening properties. Studies have shown that it can inhibit the production of melanin in the skin, making it an effective ingredient for treating hyperpigmentation and dark spots. Additionally, it has been reported to have antioxidant and anti-inflammatory properties, making it a versatile ingredient for various skincare formulations.

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)

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Relevant articles and documents

Use of oligosalicylates in the preparation of phenolic amido acids

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.

Preparation method of N-(8-[2-hydroxybenzoyl]-amino) sodium caprylate and intermediate thereof

The invention discloses a preparation method of N-(8-[2-hydroxybenzoyl]-amino) sodium caprylate and an intermediate thereof, and the preparation method of the intermediate comprises the following steps: reacting salicylamide with a protecting group reagen

Synthesis method of sodium N-(8-[2-hydroxybenzoyl]-amino)caprylate

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