160227-44-1 Usage
Description
(+/-)-3,4-METHYLENEDIOXYETHYLAMPHETAMINE-D6, also known as MDEA-D6, is a deuterated analogue of the psychoactive drug MDEA. It is a substituted amphetamine that acts as a serotonin-norepinephrine-dopamine releasing agent. MDEA-D6 is primarily used in scientific research as a stable isotope-labeled internal standard for the quantification of MDEA in biological samples. The incorporation of deuterium atoms in its structure enhances the accuracy and precision of analytical methods, making it a valuable tool for studying the pharmacokinetics and metabolism of MDEA.
Uses
Used in Scientific Research:
(+/-)-3,4-METHYLENEDIOXYETHYLAMPHETAMINE-D6 is used as a stable isotope-labeled internal standard for the quantification of MDEA in biological samples. Its application allows for improved accuracy and precision in analytical methods, which is crucial for studying the pharmacokinetics and metabolism of MDEA.
Used in Analytical Chemistry:
In the field of analytical chemistry, (+/-)-3,4-METHYLENEDIOXYETHYLAMPHETAMINE-D6 serves as a valuable tool for the development and validation of methods for the detection and quantification of MDEA. Its use as an internal standard helps to account for variations in sample preparation and instrumentation, ensuring more reliable and consistent results.
Used in Forensic Toxicology:
(+/-)-3,4-METHYLENEDIOXYETHYLAMPHETAMINE-D6 is utilized in forensic toxicology for the identification and quantification of MDEA in post-mortem toxicology cases or in cases of drug-facilitated crimes. Its stable isotope-labeled nature helps to differentiate MDEA from other substances and contributes to the reliability of the toxicological analysis.
Used in Drug Development:
In the pharmaceutical industry, (+/-)-3,4-METHYLENEDIOXYETHYLAMPHETAMINE-D6 can be employed in the development of new drugs targeting the serotonin, norepinephrine, and dopamine systems. Its use as a research tool can aid in understanding the mechanisms of action and potential therapeutic effects of MDEA and related compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 160227-44-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,2,2 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 160227-44:
(8*1)+(7*6)+(6*0)+(5*2)+(4*2)+(3*7)+(2*4)+(1*4)=101
101 % 10 = 1
So 160227-44-1 is a valid CAS Registry Number.