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Eutylone is a potential designer drug with structural features shared by cathinones, amphetamines, and pyrovalerone. These compounds typically have stimulatory or entactogenic psychotropic effects. This product is intended for forensic purposes.
Formal Name 1-(1,3-benzodioxol-5-yl)-2-(ethylamino)-1-butanone, monohydrochloride
CAS Number 17764-18-0
Molecular Formula C13H17NO3 â€¢ HCl
Formula Weight 271.7
Formulation A crystalline solid
λmax 234, 281, 319 nm
Stability 2 years
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MDP is in the stimulant family and is a new research chemical with its chemical formula being C12H17NO2, an average mass of 492, a molecular mass of 207.13. The IUPAc name for MDP is (1-Benzo[1,3]dioxol-5-ylmethyl-propyl)-methyl-amine.
Research on MDP was published by ACD/Labs', US Environmental Protection Agency's EPISuite, and ChemAxon. In the reports by ACD/Labs the chemical has 15 hydrogen acceptors, 9 hydrogen donors, 12 freely rotating bonds, an index of refraction of 1.578, with a surface tension of 73.9±5.0 dyne/cm, a flash point of 572.9±34.3 °C and a boiling point of 1023.8±65.0 °C at 760 mmHg.
The research published by US Environmental Protection Agency's EPISuite showed the boiling point to be 902.59, a melting point of 349.84, and water solubility at 25 deg C (mg/L): 7.234e+004. Removal in wastewater treatment showed total removal at 1.85%, total biodegradation at .09% total sludge adsorption at 1.75%, and total to air at 0.00%.
ChemAxon published a topology analysis, which revealed an atom count of 66, bond count of 66, cyclomatic number of 1, chain atom count of 28, chain bond count of 28, asymmetric atom count of 8, and rotatable bond count of 12. Under geometry, the report revealed a dreiding energy equal to 87.71 kcal/mol with a volume equal to 433.23 Å3, a minimal projection area equal to 61.87 Å2 and maximum projection area equal to 129.34 Å2.
MDP is a research chemical and is intended for research purposes only in a controlled laboratory for scientific and forensic study and are NOT intended for human or animal consumption.
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