3,4-Methylenedioxyphenethylamine
Chemical compound
Chemical Compound | |
---|---|
Identifiers | |
CAS Number | |
PubChem CID | |
ChemSpider ID | |
UNII | |
ChEBI | |
ChEMBL | |
Properties | |
Chemical Formula | |
Molar Mass | |
Appearance | |
Density | |
Melting Point | |
Boiling Point | |
Hazards | |
GHS Pictograms | [[File:|50px]] |
GHS Signal Word | |
GHS Hazard Statements | |
NFPA 704 | [[File:|50px]] |
References | |
3,4-Methylenedioxyphenethylamine (MDPEA) is a chemical compound belonging to the class of phenethylamines. It is structurally related to other compounds such as 3,4-methylenedioxyamphetamine (MDA) and 3,4-methylenedioxymethamphetamine (MDMA), but it is not known to have psychoactive effects.
Chemical structure and properties[edit | edit source]
3,4-Methylenedioxyphenethylamine is characterized by the presence of a methylenedioxy group attached to the phenyl ring of the phenethylamine structure. This group consists of two oxygen atoms connected by a methylene bridge, forming a 1,3-dioxole ring. The chemical formula for MDPEA is C9H11NO2.
Synthesis[edit | edit source]
The synthesis of 3,4-methylenedioxyphenethylamine can be achieved through several methods, often involving the use of safrole or isosafrole as starting materials. These compounds undergo oxidation to form the corresponding aldehyde, which is then subjected to reductive amination to yield MDPEA.
Pharmacology[edit | edit source]
Unlike its more famous analogs, MDPEA does not appear to have significant psychoactive properties. It is not known to act as a serotonin or dopamine releaser, nor does it have significant affinity for the serotonin receptors that are typically involved in the action of psychoactive phenethylamines.
Potential uses[edit | edit source]
While 3,4-methylenedioxyphenethylamine itself is not used in medicine or research, its structure serves as a basis for the synthesis of other compounds that may have pharmacological activity. Researchers may study MDPEA as a reference compound to understand the structure-activity relationships of related psychoactive substances.
Safety and legality[edit | edit source]
MDPEA is not a controlled substance in most jurisdictions, but its structural similarity to controlled substances like MDMA may subject it to certain regulatory scrutiny. It is important to note that the legal status of chemical compounds can vary widely between countries and regions.
Related pages[edit | edit source]
Gallery[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