17616-24-9

Basic information

• Product Name: ETHYL-D5-AMINE
• Synonyms: ETHYL-D5-AMINE;ETHYLAMINE (D5);ETHYL-D5-AMINE (GAS) 99%;Ethan-d5-amine;ETHYLAMINE (D5, 98%)
• CAS NO: 17616-24-9
• Molecular Formula: C₂H₇N
• Molecular Weight: 50.11
• Product Categories: Alphabetical Listings;E-FStable Isotopes;Gases;Stable Isotopes
• Mol File: 17616-24-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 14.20 °C at 760 mmHg
• Appearance: /
• Density: 0.768 g/cm³
• Vapor Pressure: 1130mmHg at 25°C
• Refractive Index: 1.372
• CAS DataBase Reference: ETHYL-D5-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL-D5-AMINE(17616-24-9)
• EPA Substance Registry System: ETHYL-D5-AMINE(17616-24-9)

Safety Data

• Hazardous Substances Data: 17616-24-9(Hazardous Substances Data)

Usage

General Description

ETHYL-D5-AMINE is a deuterated compound, meaning it has hydrogen atoms replaced with deuterium atoms, specifically in the ethylamine molecule. Ethylamine is a colorless, flammable liquid with a strong ammonia-like odor, and the deuterated version is used in various research and laboratory applications. Deuterium is a stable isotope of hydrogen, and its incorporation into molecules like ethylamine can provide valuable insight into the behavior and interactions of these compounds in biological and chemical systems. ETHYL-D5-AMINE may be used as a precursor in the synthesis of pharmaceuticals, agrochemicals, and other advanced materials, and its deuterated nature makes it particularly useful in studies involving nuclear magnetic resonance (NMR) spectroscopy.

InChI:InChI=1/C2H7N/c1-2-3/h2-3H2,1H3/i1D3,2D2

Upstream product

• 2206-26-0 [D₃]acetonitrile 
• 121195-20-8 -ethyl phthalimide 

Relevant articles and documents

Synthesis of bisaramil labelled with carbon-14 and deuterium

[6,8-14C2]-Bisaramil: 3-methyl-7-ethyl-9α-(4-chlorobenzoyloxy)-3,7-diazabicyclo/3.3.1./nona ne-[6,8-14C2]monohydrochloride and [7-N-D5-ethyl]-Bisaramil: 3-methyl-7-[D5-ethyl]-9α-(4-chlorobe

The Collision-Induced Dissociations of Deprotonated Amines in the Gas Phase

The major collision-induced fragmentations of deprotonated primary and secondary amines are best rationalized as proceeding through the intermediacy of ion complexes.For example, the characteristic fragmentation of deprotonated ethylamine is MeCH2NH- -> -(CH2=NH)> -> CH2N- + CH4 Secondary alkylamines behave in a similar fashion.The occurrence of proton transfer as a prelude to fragmentation is rare: the only example observed in this study is the probable reaction PhNEt ->-> PhNHCHMe -> -> -> C7H6N- + CH4 which is preceded or accompanied by proton transfer between the methylene and phenyl substituents.Deprotonated aniline undergoes specific elimination of CNH from the 1-position to form the cyclopentadienyl anion.Finally, retro reactions are observed for the piperazine anion, e.g.HN(CH2CH2)2N- -> -CH2CH2N=CH2 + CH2NH