96236-05-4 Usage
Uses
Used in Research Applications:
5-Methoxytryptamine-alpha,alpha,beta,beta-d4 is used as a research compound for studying the properties and mechanisms of action of tryptamines and their analogs. Its isotopically labeled nature allows for enhanced tracking and detection in experiments, facilitating a deeper understanding of its interactions with biological systems and potential applications in various fields.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-Methoxytryptamine-alpha,alpha,beta,beta-d4 serves as a valuable tool for the development of new drugs and therapies. Its unique properties can be harnessed to investigate the effects of tryptamines on the central nervous system, potentially leading to the discovery of novel treatments for neurological and psychiatric disorders.
Used in Forensic Science:
5-Methoxytryptamine-alpha,alpha,beta,beta-d4 is also utilized in forensic science for the identification and analysis of tryptamine-based substances. Its isotopically labeled form provides a reliable means of distinguishing between naturally occurring compounds and synthetic analogs, aiding in the investigation of drug-related crimes and the development of forensic methodologies.
Used in Environmental Studies:
In environmental studies, 5-Methoxytryptamine-alpha,alpha,beta,beta-d4 can be employed to examine the presence and distribution of tryptamines in various ecosystems. This information can contribute to a better understanding of the ecological roles of these compounds and their potential impact on the environment and human health.
Check Digit Verification of cas no
The CAS Registry Mumber 96236-05-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,2,3 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 96236-05:
(7*9)+(6*6)+(5*2)+(4*3)+(3*6)+(2*0)+(1*5)=144
144 % 10 = 4
So 96236-05-4 is a valid CAS Registry Number.
96236-05-4Relevant academic research and scientific papers
Electron Impact and Chemical Ionization Fragmentation of 5-Methoxytryptamine and Some 6-Methoxy-β-carbolines
Gynther, Jukka,Peura, Pekka,Salmi, Seija
, p. 849 - 860 (2007/10/02)
Electron impact (EI) and chemical ionization (CI) mass spectra of 5-methoxytryptamine (5-MT) and seven 6-methoxy-β-carbolines have been recorded and interpreted.Proposed fragmentation pathways are depicted on the basis of spectra of deuterium labelled analogs of 5-MT, 6-methoxy-1,2,3,4-tetrahydro-β-carboline (6-MeO-THBC) and 6-Methoxy-1-methyl-1,2,3,4-tetrahydro-β-carboline (6-MeO-1-Me-THBC).In the EI mass spectrum of 5-MT, the base peak m/z 160 is formed by the expulsion of CH4N.The positive ion so formed is suggested to have a quinolinium structure.In chemical ionization with CH4 as the reaction gas, the most abundant ion is produced by cleavage of NH3.The ion m/z 173 yields the base peak in the EI mass spectrum of 6-MeO-THBC.This ion is formed by a retro Diels-Alder reaction, an important fragmentation pathway of 6-MeO-1-Me-THBC, too. 6-MeO-harmalan easily loses one hydrogen atom in EI fragmentation followed by methyl loss from the methoxy group, this latter process yielding the base peak, m/z 197 in the EI mass spectrum of 6-MeO-harman.M+1 is the base peak in the CI mass spectra of all 6-MeO-β-carbolines.
Mass spectra of some specifically deuterated tryptamines.
Shaw,Wright,Milne
, p. 348 - 353 (2007/10/04)
The mass spectra of the four tryptamine derivatives, N-acetyl-5-methoxytryptamine (melatonin), N-acetyl-5-hydroxytryptamine (N-acetyl-serotonin), N,N-dimethyl-5-hydroxtryptamine (bufotenine) and N,N-dimethyl-5-methoxytryptamine (O-methylbufotenine), with specifically labeled [D4] aminoethyl sidechains have been measured. Comparison of these spectra with those of the unlabeled compounds enable the major fragmentations of the compounds to be defined.
