5466-51-3

Basic information

• Product Name: N-(carboxymethyl)-N,N-dimethylhexadecan-1-aminium
• CAS NO: 5466-51-3
• Molecular Formula: Br*C₂₀H₄₂NO₂
• Molecular Weight: 328.5524
• Mol File: 5466-51-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(carboxymethyl)-N,N-dimethylhexadecan-1-aminium(CAS DataBase Reference)
• NIST Chemistry Reference: N-(carboxymethyl)-N,N-dimethylhexadecan-1-aminium(5466-51-3)
• EPA Substance Registry System: N-(carboxymethyl)-N,N-dimethylhexadecan-1-aminium(5466-51-3)

Safety Data

• Hazardous Substances Data: 5466-51-3(Hazardous Substances Data)

Upstream product

• 112-69-6 N,N-dimethylhexadecylamine 
• 1068-52-6 sodium 2-bromoacetate 
• 96-32-2 bromoacetic acid methyl ester 
• 112-82-3 hexadecanyl bromide 

Downstream Products

• 693-33-4 (N-hexadecyl-N,N-dimethylammonio)acetate 

Relevant articles and documents

Coupling of epoxides and carbon dioxide catalyzed by Br?nsted acid ionic liquids

A series of Br?nsted acid ionic liquids (BAILs) containing a long chain Br?nsted acid site in the cationic part and a Lewis basic site in the anionic part were designed, synthesized, and used as catalyst for the coupling of epoxides and carbon dioxide to cyclic carbonates without a co-catalyst or co-solvent. The effects of catalyst structure and other parameters on the catalytic performance were investigated. The long chain 2-(N,N-dimethyldodecylammonium) acetic acid bromide ([(CH2COOH)DMDA]Br) showed high catalytic activity and good reusability. This protocol was expanded to various epoxides, which gave the corresponding cyclic carbonates in good yields. The acidity of the catalyst influenced its catalytic activity.

Smectic mesophases from Quaternary Amphiphilic Ammonium Salts Functionalized with Interacting Endgroups

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