3,4-Methylenedioxyphentermine
(Redirected from Methylenedioxyphentermine)
A psychoactive drug of the phenethylamine and amphetamine classes
3,4-Methylenedioxyphentermine | |
---|---|
![]() | |
INN | |
Drug class | |
Routes of administration | Oral |
Pregnancy category | |
Bioavailability | |
Metabolism | |
Elimination half-life | |
Excretion | |
Legal status | Uncontrolled |
CAS Number | 32052-16-3 |
PubChem | 4436 |
DrugBank | |
ChemSpider | 4283 |
KEGG |
3,4-Methylenedioxyphentermine (MDPH) is a psychoactive drug of the phenethylamine and amphetamine chemical classes. It is structurally related to 3,4-methylenedioxyamphetamine (MDA) and 3,4-methylenedioxymethamphetamine (MDMA), which are well-known recreational drugs.
Chemical structure and properties[edit | edit source]
3,4-Methylenedioxyphentermine is a derivative of amphetamine with a methylenedioxy group attached to the phenyl ring. The chemical formula is C10H13NO2, and it has a molecular weight of 179.22 g/mol. The presence of the methylenedioxy group is thought to contribute to its psychoactive properties.
Pharmacology[edit | edit source]
MDPH acts as a central nervous system stimulant. It is believed to exert its effects by increasing the release of neurotransmitters such as dopamine, norepinephrine, and serotonin in the brain. This action is similar to that of other amphetamines and is responsible for its stimulant and empathogenic effects.
Effects[edit | edit source]
The effects of 3,4-methylenedioxyphentermine are not well-documented, but it is thought to produce effects similar to those of MDA and MDMA, including increased energy, euphoria, and enhanced sensory perception. However, due to limited research, the full range of effects and potential risks are not well understood.
Legal status[edit | edit source]
3,4-Methylenedioxyphentermine is not a controlled substance in most jurisdictions, but its structural similarity to other controlled substances may subject it to regulation under analogue laws.
Synthesis[edit | edit source]
The synthesis of MDPH involves the reaction of safrole with methylamine in the presence of a reducing agent. This process is similar to the synthesis of other methylenedioxy-substituted amphetamines.
Related compounds[edit | edit source]
- 3,4-Methylenedioxyamphetamine (MDA)
- 3,4-Methylenedioxymethamphetamine (MDMA)
- 3,4-Methylenedioxy-N-ethylamphetamine (MDEA)
See also[edit | edit source]
Related pages[edit | edit source]
3,4-Methylenedioxyphentermine[edit | edit source]
Search WikiMD
Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD
WikiMD's Wellness Encyclopedia |
Let Food Be Thy Medicine Medicine Thy Food - Hippocrates |
Translate this page: - East Asian
中文,
日本,
한국어,
South Asian
हिन्दी,
தமிழ்,
తెలుగు,
Urdu,
ಕನ್ನಡ,
Southeast Asian
Indonesian,
Vietnamese,
Thai,
မြန်မာဘာသာ,
বাংলা
European
español,
Deutsch,
français,
Greek,
português do Brasil,
polski,
română,
русский,
Nederlands,
norsk,
svenska,
suomi,
Italian
Middle Eastern & African
عربى,
Turkish,
Persian,
Hebrew,
Afrikaans,
isiZulu,
Kiswahili,
Other
Bulgarian,
Hungarian,
Czech,
Swedish,
മലയാളം,
मराठी,
ਪੰਜਾਬੀ,
ગુજરાતી,
Portuguese,
Ukrainian
Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.
Contributors: Prab R. Tumpati, MD