82684-41-1

Basic information

• Product Name: N-Hexadecylbenzamide
• Synonyms: N-Hexadecylbenzamide
• CAS NO: 82684-41-1
• Molecular Formula: C₂₃H₃₉NO
• Molecular Weight: 345.57
• Mol File: 82684-41-1.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: N-Hexadecylbenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-Hexadecylbenzamide(82684-41-1)
• EPA Substance Registry System: N-Hexadecylbenzamide(82684-41-1)

Safety Data

• Hazardous Substances Data: 82684-41-1(Hazardous Substances Data)

Usage

General Description

N-Hexadecylbenzamide is a chemical compound that belongs to the class of benzamides. It is composed of a hexadecyl chain attached to a benzene ring via an amide group. This chemical is commonly used as an emollient and conditioning agent in cosmetic and personal care products. It helps to soften and moisturize the skin, making it suitable for use in skincare products such as lotions, creams, and moisturizers. N-Hexadecylbenzamide also has surfactant properties, allowing it to reduce the surface tension of liquids and improve the spreading of products on the skin or hair. Additionally, it can act as a lubricant and thickening agent in various formulations. Overall, N-Hexadecylbenzamide serves as a multi-functional ingredient in cosmetic and personal care products, providing moisturization, emolliency, and surfactant properties.

Upstream product

• 143-27-1 hexadecylamine 
• 100-52-7 benzaldehyde 
• 98-88-4 benzoyl chloride 
• 55-21-0 benzamide 
• 65-85-0 benzoic acid 

Downstream Products

• 114084-54-7 N-benzyl-N-hexadecylamine 
• 1026674-14-5 2-{3-(benzyl-hexadecyl-amino)-1-[2-(benzyl-hexadecyl-amino)-ethyl]-propyl}-malonic acid diethyl ester 
• 1323910-16-2 benzyl 1,3-bis(benzyl(hexadecyl)amino)propan-2-yl 2-bromoethyl phosphate 
• 1323910-17-3 1,3-bis(benzyl(hexadecyl)amino)propan-2-yl 2-(trimethylammonio)ethyl phosphate 
• 1323910-14-0 1,3-bis(benzyl(hexadecyl)amino)propan-2-ol 

Relevant articles and documents

Development of new inhibitors for N-acylethanolamine-hydrolyzing acid amidase as promising tool against bladder cancer

The endocannabinoid system is a signaling system involved in a wide range of biological effects. Literature strongly suggests the endocannabinoid system role in the pathogenesis of cancer and that its pharmacological activation produces therapeutic benefi

Transamidation of carboxamides with amines over nanosized zeolite beta under solvent-free conditions

A highly efficient approach to transamidation of carboxamides with amines over nanosized zeolite beta under solvent-free conditions has been successfully demonstrated. Transamidation of a variety of amides with amines produced the respective N-alkyl amides in moderate to excellent yields.

Convenient synthesis of 6,6-bicyclic malonamides: A new class of conformationally preorganized ligands for f-block ion binding

A general synthetic approach was developed for the preparation of a series of 6,6-bicyclic malonamides, a class of ligands that provide a preorganized binding site for f-block ions (particularly trivalent lanthanides). The approach described is convenient to introduce a variety of functional groups at the amide nitrogens to tune the properties of the ligand without altering the preorganized binding. Each of the ten derivatives (that represent a range of functionality, including R = alkyl, hydroxy, phenyl, ester, perfluorocarbon) reported here derives from a single, readily prepared dialdehyde intermediate. This intermediate is converted to the final products via reductive amination with an appropriately functionalized benzylamine, followed by hydrogenolysis and lactam formation. Because derivatization occurs late in the synthesis, the approach is general, requiring only modification of the purification procedures for each new derivative. To aid in the purification of the bicyclic malonamides, we report a novel complexation-based purification method that takes advantage of the high affinity of the ligand for f-block metals.