7418-61-3 Usage
Description
Trimethyl-(2-oxoethyl)ammonium is a quaternary ammonium ion that features nitrogen substituted by three methyl groups and a 2-oxoethyl group. It plays a significant role as an intermediate in the metabolism of amino acids such as glycine, serine, and threonine.
Uses
Used in Pharmaceutical Industry:
Trimethyl-(2-oxoethyl)ammonium is utilized as an intermediate in the synthesis of various pharmaceutical compounds. Its presence in the metabolism of essential amino acids makes it a crucial component in the development of drugs targeting specific metabolic pathways.
Used in Biochemical Research:
In the field of biochemical research, trimethyl-(2-oxoethyl)ammonium serves as a valuable tool for studying the metabolic processes of amino acids like glycine, serine, and threonine. This helps researchers better understand the underlying mechanisms of various biological functions and develop targeted therapies for related conditions.
Used in Diagnostic Applications:
Trimethyl-(2-oxoethyl)ammonium can be employed as a diagnostic marker in clinical settings. Its involvement in the metabolism of specific amino acids allows for the monitoring of metabolic activity and the assessment of an individual's health status.
Used in Nutritional Supplements:
Trimethyl-(2-oxoethyl)ammonium may also be used as an ingredient in nutritional supplements, particularly those designed to support amino acid metabolism and overall health. Its presence can contribute to the effectiveness of these supplements in promoting optimal metabolic function.
Check Digit Verification of cas no
The CAS Registry Mumber 7418-61-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,1 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7418-61:
(6*7)+(5*4)+(4*1)+(3*8)+(2*6)+(1*1)=103
103 % 10 = 3
So 7418-61-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H12NO/c1-6(2,3)4-5-7/h5H,4H2,1-3H3/q+1
7418-61-3Relevant articles and documents
Free-radical polymerization of itaconic acid in the presence of choline salts: Mechanism of persulfate decomposition
Bednarz, Szczepan,B?aszczyk, Alicja,B?azejewska, Diana,Bogda?, Dariusz
, p. 297 - 304 (2015/02/19)
Kinetics of decomposition of persulfate activated by choline in aqueous solution has been studied. Additionally, the products of choline degradation were analyzed by 1H NMR spectroscopy, and betaine aldehyde was identified as the main oxidation product. Thus, radical-chain redox mechanism is postulated to explain experimental results. The mechanism was successfully verified using kinetic modeling approach. Moreover, it was found that due to formation of complex of itaconic acid and choline chloride, the salt solubility of the acid in water was increased. Finally, free-radical polymerization of itaconic acid initiated by persulfate in aqueous solution of the choline salt yielded poly(itaconic acid) with higher molecular weight and increased polydispersity.