14999-75-8

Basic information

• Product Name: Ethanamine, N,N-diethyl-, perchlorate
• CAS NO: 14999-75-8
• Molecular Formula: C6H15N.ClHO4
• Molecular Weight: 201.65
• Mol File: 14999-75-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Ethanamine, N,N-diethyl-, perchlorate(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanamine, N,N-diethyl-, perchlorate(14999-75-8)
• EPA Substance Registry System: Ethanamine, N,N-diethyl-, perchlorate(14999-75-8)

Safety Data

• Hazardous Substances Data: 14999-75-8(Hazardous Substances Data)

Upstream product

• 1923-70-2 tetrabutylammonium perchlorate 
• 900-50-5 triethyl-amine; picrate 
• 554-68-7 triethylamine hydrochloride 
• 636-70-4 triethylamine hydrobromide 
• 4636-73-1 triethylammonium iodide 
• 110-89-4 piperidine 

Downstream Products

• 1923-70-2 tetrabutylammonium perchlorate 
• 4636-73-1 triethylammonium iodide 
• 900-50-5 triethyl-amine; picrate 
• 554-68-7 triethylamine hydrochloride 
• 636-70-4 triethylamine hydrobromide 

Relevant articles and documents

AMINOLYSIS OF VINYLAMMONIUM SALTS. EFFECTS OF STRUCTURE AND MEDIUM

The kinetics of the aminolysis of a series of vinylammonium salts ZCH=CHN+R3*X- were investigated in polar solvents and in water at 25 deg C.A quantitative assessment was made of the effect of the nature of the medium and the structure of activating group Z on the rate of the investigated processes.The aminolysis rate of the salts increases with increase in the donating characteristics of the solvent on account of the greater stabilization of the transition state compared with the initial state.Increase in the accepting characteristics of the medium leads to retardation of the process as a result of increase in the electrophilic solvation of the amine in the initial state.