38170-37-5

Basic information

• Product Name: aminocholine
• Synonyms: aminocholine
• CAS NO: 38170-37-5
• Molecular Formula: C₅H₁₅N₂
• Molecular Weight: 0
• Mol File: 38170-37-5.mol
• Article Data: 2

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: g/cm³
• CAS DataBase Reference: aminocholine(CAS DataBase Reference)
• NIST Chemistry Reference: aminocholine(38170-37-5)
• EPA Substance Registry System: aminocholine(38170-37-5)

Safety Data

• Hazardous Substances Data: 38170-37-5(Hazardous Substances Data)

Usage

General Description

Aminocholine, also known as choline aminoethanol, is a chemical compound that belongs to the larger group of choline esters. It is a derivative of acetylcholine, a neurotransmitter that plays a crucial role in the functioning of the nervous system. Aminocholine is sometimes used in research as a precursor for the synthesis of acetylcholine in the brain. It may also have potential applications in the treatment of conditions related to neurotransmitter imbalances or deficiencies. Additionally, aminocholine has been studied for its potential use as a dietary supplement to support cognitive function and overall brain health. However, more research is needed to fully understand its potential benefits and risks.

InChI:InChI=1/C5H15N2O/c1-7(2,3)4-5(6)8/h5,8H,4,6H2,1-3H3/q+1

Upstream product

• 945713-45-1 2-((tert-butoxycarbonyl)amino)-N,N,N-trimethylethan-1-aminium 

Downstream Products

• 1311371-46-6 2-(3-(3-chloro-4-((5-(2-(4-chloro-3-methoxyphenyl)propan-2-yl)-1-(4-fluorophenyl)-1H-imidazol-2-ylthio)methyl)-5-fluorophenyl)ureido)-N,N,N-trimethylethanaminium 2,2,2-trifluoroacetate 
• 19829-29-9 4-pyridinethione 

Relevant articles and documents

Group of isotope labeling reagents for carboxyl labeling and synthetic method thereof

The invention provides a group of isotope labeling reagents for carboxyl labeling and a synthetic method thereof and belongs to the field of chemical synthesis. One end of an isotope labeling reagent is primary amine while the other end is trimethyl ammonium salt, and the primary amine and the trimethyl ammonium salt are connected through a plurality of carbon chains. The synthetic process comprises the following steps of: by taking N,N-dimethyl ethidene diamine and homologs thereof as a reaction raw material, protecting primary amino with di-tert-butyl dicarbonate ester ((BOC)2O); then performing a reaction with an iodomethane reagent containing isotopes D and 13C in an alkaline condition; and finally, removing the protecting group in an acidic condition to obtain a target product. A group of novel isotope labeling reagents capable of being used for efficiently labeling carboxyl are synthesized through nucleophilic substitution reaction, so that the reagents are low in price and simple to operate; and the analytical efficiency and accuracy can be remarkably improved after the isotope reagents obtained by the invention are used for labeling.