Ehrlich's reagent

Para-dimethylaminobenzaldehyde (DMBA): the active ingrediant in Ehrlich's reagent

Ehrlich's reagent, also known as the "DMAB test", is a chemical test to presumptively identify indoles. It is primarily used as a simple spot-test to identify possible psychoactive compounds such as tryptamines (i.e. DMT) and ergoloids (i.e. LSD). The reagent will also give a positive result for opium, despite the active alkaloids (opiates) not containing the indole moiety, because of the presence in opium of tryptophan.[1]

The reagent is prepared by dissolving 0.5[2]-2.0 g of p–dimethylaminobenzaldehyde (DMAB) in 50 mL of 95% ethanol and 50 mL of concentrated hydrochloric acid[3][4] and is best used when fresh.

Other alcohols such as 1-Propanol can also be used to prepare the ehrlich reagent.[5]

The ehrlich reagent is similar to a number of other indole tests:

See also

References

  1. 1.0 1.1 de Faubert Maunder, MJ. "Field and laboratory test for raw and prepared opium.". Bulletin on narcotics 27 (1): 71–6. PMID 1039285.
  2. Spratley, Trinette (2004). "Analytical Profiles for Five "Designer" Tryptamines" (PDF). Microgram Journal 3 (1-2): 55. Retrieved 2013-10-09.
  3. O’Neal, Carol L; Crouch, Dennis J; Fatah, Alim A (April 2000). "Validation of twelve chemical spot tests for the detection of drugs of abuse". Forensic Science International 109 (3): 189–201. doi:10.1016/S0379-0738(99)00235-2.
  4. "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.
  5. 02 July 2014. "Ehrlich's Reagent Safety Data Sheet". Labchem. Retrieved 11 January 2015.
  6. Ehmann, A. (1977). "The van URK-Salkowski reagent — a sensitive and specific chromogenic reagent for silica gel thin-layer chromatographic detection and identification of indole derivatives". Journal of Chromatography A 132 (2): 267–201. doi:10.1016/S0021-9673(00)89300-0.
  7. Maunder, M. J. de Faubert (August 1974). "A field test for hallucinogens: further improvements". Journal of Pharmacy and Pharmacology 26 (8): 637–638. doi:10.1111/j.2042-7158.1974.tb10677.x.

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