5090-03-9

Basic information

• Product Name: 1-Decanaminium, N,N,N-triethyl-, bromide
• CAS NO: 5090-03-9
• Molecular Formula: C16H36N.Br
• Mol File: 5090-03-9.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1-Decanaminium, N,N,N-triethyl-, bromide(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Decanaminium, N,N,N-triethyl-, bromide(5090-03-9)
• EPA Substance Registry System: 1-Decanaminium, N,N,N-triethyl-, bromide(5090-03-9)

Safety Data

• Hazardous Substances Data: 5090-03-9(Hazardous Substances Data)

Usage

Common uses

Surfactant and antistatic agent in industrial and commercial applications

Type of compound

Quaternary ammonium compound

Structure

Positively charged nitrogen atom and three ethyl groups linked to a decyl chain

Applications

Hair care products, fabric softeners, disinfectants, and sanitizing agents

Properties

Effective emulsifying and cleansing agent, reduces friction and static buildup in fabrics and plastics

Precautions

Can cause irritation to skin, eyes, and respiratory system if not used properly

Upstream product

• 112-29-8 1-bromo dodecane 
• 121-44-8 triethylamine 

Relevant articles and documents

Antibacterial and?antifungal activity of?acyclic and?macrocyclic uracil derivatives with quaternized nitrogen atoms in?spacers

The reactions of 1,3-bis(α,ω-bromoalkyl)-6-methyluracils with 1,3-bis(α,ω-ethylaminoalkyl)-6-methyluracils or 1,3-bis(bromopentyl)thymine with butylamine afforded pyrimidinophanes containing one or two uracil units and nitrogen atoms in bridging polymethy

Improving Cellulose Dissolution in Ionic Liquids by Tuning the Size of the Ions: Impact of the Length of the Alkyl Chains in Tetraalkylammonium Carboxylate

Twenty ionic liquids based on tetraalkylammonium cations and carboxylate anions have been synthesized, characterized, and tested for cellulose dissolution. The amount of cellulose dissolved in these ionic liquids depends strongly on the size of the ions:

Process for preparing 2,2-azobis(2,4-dimethylpentanenitrile)

A process for the preparation of 2,2'-azobis (2,4-dimethylpentanenitrile) with improved filtering and drying characteristics, said process comprising reacting 2-amino-2,4-dimethylpentanenitrile with a metal hypochlorite in the presence of water, a mixture of quaternary ammonium surface active compounds and ionic bromide wherein the equivalent ratio of ionic bromide to surface active compound is 0.4:1-12.0:1 at a temperature of about -10° C. to about 30° C., and recovering 2,2'-azobis(2,4-dimethylpentanenitrile) from the reaction mixture.