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Methylenedioxyallylamphetamine

Field	Value
Verifiedfields	changed
Watchedfields	changed
verifiedrevid	425012554
drug_name	MDAL
image	MDAL.svg
image_class	skin-invert-image
width	250px
routes_of_administration	Oral
ATC_prefix	None
duration_of_action	Unknown
CAS_number_Ref
CAS_number	74698-45-6
PubChem	44719581
ChemSpiderID_Ref
ChemSpiderID	21106331
UNII_Ref
UNII	HYC85U2R8Z
synonyms	MDAL; 3,4-Methylenedioxy-N-allylamphetamine
IUPAC_name	N-[1-(2H-1,3-benzodioxol-5-yl)propan-2-yl]prop-2-en-1-amine
C	13	H=17	N=1	O=2
SMILES	C1=C2C(=CC=C1CC(C)NCC=C)OCO2
StdInChI_Ref
StdInChI	1S/C13H17NO2/c1-3-6-14-10(2)7-11-4-5-12-13(8-11)16-9-15-12/h3-5,8,10,14H,1,6-7,9H2,2H3
StdInChIKey_Ref
StdInChIKey	BMKCDDFQEGYEJC-UHFFFAOYSA-N

| Drugs.com =

| elimination_half-life =

Methylenedioxyallylamphetamine (MDAL or 3,4-methylenedioxy-N-allylamphetamine) is a lesser-known drug. It is also the N-allyl derivative of 3,4-methylenedioxyamphetamine (MDA). MDAL was first synthesized by Alexander Shulgin. In his book PiHKAL, the minimum dose is listed as 180 mg, and the duration unknown. MDAL produces few to no effects on its own, but may enhance the effects of psychedelic drugs like LSD. Very little data exists about the pharmacological properties, metabolism, and toxicity of MDAL.

Society and culture

Legal status

United Kingdom

This substance is a Class A drug in the Drugs controlled by the UK Misuse of Drugs Act.

References

[http://www.erowid.org/library/books_online/pihkal/pihkal101.shtml MDAL entry in ''PiHKAL'']
"UK Misuse of Drugs act 2001 Amendment summary". Isomer Design.

Wikipedia Source

This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.

allylamines methylenedioxyphenethylamines pihkal substituted-amphetamines

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