Simon's reagent
In today's world, Simon's reagent is a topic that has caught the attention of many people. With the advancement of technology and globalization, Simon's reagent has become a relevant topic for various areas of society. From its impact on health to its influence on the economy, Simon's reagent has generated much debate and generated a wide range of opinions. In this article, we will explore different perspectives on Simon's reagent and discuss its importance in the current context. From its historical origin to its possible future implications, Simon's reagent is a topic that leaves no one indifferent.
Simon's reagent is used as a simple spot-test to presumptively identify alkaloids as well as other compounds. It reacts with secondary amines like MDMA and methamphetamine to give a blue solution.
Uses
The primary use of this reagent is for detecting secondary amines, such as MDMA and methamphetamine, and is typically used after the mecke or marquis reagents to differentiate between the two mentioned and amphetamine or MDA.[1]
Chemistry
The reagent is typically provided in two parts:[2][1][3]
- A mixture of 2% sodium nitroprusside and 2% acetaldehyde in water (solution A)[4]
- A solution of 2% sodium carbonate in water (solution B)[4]
Separate storage of the aldehyde and base are necessary to prevent aldol polymerisation of the aldehyde.
When exposed to an amine, reaction with acetaldehyde produces the enamine, which subsequently reacts with sodium nitroprusside to the imine. Finally, the iminium salt is hydrolysed to the bright blue[1] Simon-Awe complex.[3][5]
Acetaldehyde can be replaced with acetone, in which case the reagent detects primary amines instead, giving a purple coloured product.[3]
Testing Method
A drop from each solution (A and B) is dripped onto the substance being tested, causing the two solutions to mix together.
See also
- Drug checking
- Dille–Koppanyi reagent
- Folin's reagent
- Froehde reagent
- Liebermann reagent
- Mandelin reagent
- Marquis reagent
- Mecke reagent
- Zwikker reagent
References
- ^ a b c "Simon's Reagent Testing Kit (Yellow & Green Labels)". Dancesafe. Archived from the original on 2014-02-15. Retrieved 2012-01-30.
- ^ Thompson, Robert; Thompson, Barbara Fritchman (2012-08-14). Illustrated Guide to Home Forensic Science Experiments: All Lab, No Lecture. "O'Reilly Media, Inc.". p. 255. ISBN 978-1-4493-3451-2.
- ^ a b c "Chemistry and Reaction Mechanisms of Rapid Tests for Drugs of Abuse and Precursors Chemicals" (PDF). UNODC. Retrieved 2012-01-30.
- ^ a b "Color Test Reagents/Kits for Preliminary Identification of Drugs of Abuse" (PDF). Law Enforcement and Corrections Standards and Testing Program. July 2000. Retrieved 2011-07-24.
- ^ Leeuwenkamp, O. R.; van Bennekom, W. P.; van der Mark, E. J.; Bult, A. (1984). "Nitroprusside, antihypertensive drug and analytical reagent". Pharmaceutisch Weekblad. 6 (4): 129–140. doi:10.1007/BF01954040. ISSN 0031-6911. PMID 6384923. S2CID 21283981.