Marquis reagent


Marquis reagent is used as a simple spot-test to presumptively identify alkaloids as well as other compounds. It is composed of a mixture of formaldehyde and concentrated sulfuric acid, which is dripped onto the substance being tested. The United States Department of Justice method for producing the reagent is the addition of 100 mL of concentrated sulfuric acid to 5 mL of 40% formaldehyde. Different compounds produce different color reactions. Methanol may be added to slow down the reaction process to allow better observation of the colour change.

History

Marquis reagent was first discovered and tested in 1896 by pharmacologist Eduard Marquis, then a student of Rudolf Kobert at the University of Dorpat. The reagent was described by Marquis in his Master of Pharmacy dissertation in 1896 and subsequently named after him.
The reagent should be stored in the freezer for maximum shelf life.
It is the primary presumptive test used in Ecstasy reagent testing kits. It can also be used to test for such substances as opiates, and phenethylamines.
The test is performed by scraping off a small amount of the substance and adding a drop of the reagent. The results are analyzed by viewing the color of the resulting mixture, and by the time taken for the change in color to become apparent:

Results

Reagent test results develop very quickly and due to reactions with moisture and oxygen in air, any changes after the first 60 seconds should be discarded.
SubstanceColorTime Notes
MDMA or MDApurple to black0–5May have dark purple tint
Amphetamine, or methamphetamineorange to brown0–5May have a brown tint
2C-Byellow to green5–10Color may change from initial result
DXMgray to black15–30Initially no change; takes much longer to reach black than MDMA

SubstanceColor
βk-2C-BBright orange 30min
2C-BGreen-yellow 30min
2C-IGreen-yellow 30min
2,5-Dimethoxy-4-bromoamphetamine Olive green – yellow
2-FMARapidly fizzes and dissolves. Colourless/light yellow
25I-NBOMeOrange
25C-NBOMeClear, Transparent
25B-NBOMeDark green
4F-MPHTransparent, no reaction
5-EAPBPurple to black
5-MeO-MiPTClear/light brown
AspirinPink > deep red
AdrafinilDeep reddish orange – dark reddish brown
BenzphetamineDeep reddish brown
BenzylpiperazineClear
BuprenorphinePinkish violet
ButyloneYellow
ChlorpromazineDeep purplish red
CodeineVery dark purple
CaffeineTransparent, no change
CocaineTransparent, no change
d-AmphetamineStrong reddish orange – dark reddish brown
d-MethamphetamineDeep reddish orange – dark reddish brown
Diacetylmorphine Deep purplish red
Dimethoxy-4-amylamphetamine No color change
Dimethyltryptamine Orange
Diphenhydramine Yellow/orange > brown
Dimethoxymethamphetamine HCL Moderate olive
DoxepinBlackish red
DristanDark grayish red
ExedrineDark red
LSDClear, charring of paper may occur
MethoxetamineSlow pink
3,4-Methylenedioxyamphetamine Dark purple – black
Methylenedioxy-N-ethylamphetamine Dark purple – black
Methylenedioxymethamphetamine Dark purple – black
Methylenedioxypropylamphetamine Dark purple – black
Methylone Yellow
Methylenedioxypyrovalerone Yellow
Pethidine/MeperidineDeep brown
MescalineStrong orange
MethadoneLight yellowish pink
MethylphenidateModerate orange yellow
Methylene BlueDark green
ModafinilYellow/orange – brown
MorphineDeep purplish red
OpiumDark grayish reddish brown
OxycodonePale violet
PropoxypheneBlackish purple
SugarDark brown

Mechanism

The colour change from morphine is proposed to be a result of two molecules of morphine and two molecules of formaldehyde condensing to the dimeric product which is protonated to the oxocarbenium salt.