Piperonyl methyl ketone

Structural formula
General
Surname	Piperonyl methyl ketone
other names	3,4-methylenedioxyphenylpropan-2-one; 1- (1,3-Benzodioxol-5-yl) propan-2-one; MDP2P;
Molecular formula	C 10 H 10 O 3
Brief description	colorless oil
External identifiers / databases
EC number	225-128-6
ECHA InfoCard	100.022.843
PubChem	78407
ChemSpider	70776
Wikidata	Q411580
properties
Molar mass	178.19 g mol −1
Physical state	liquid
boiling point	283-285 ° C
Refractive index	1.542
safety instructions
GHS labeling of hazardous substances Caution
H and P phrases	H: 315-319-335
	EUH: 071
	P: ?
	As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . Refractive index: Na-D line , 20 ° C

Piperonyl methyl ketone (MDP2P, also PMK) is the common name for 3,4-methylenedioxyphenylpropan-2-one , synonym 1- (1,3-benzodioxol-5-yl) propan-2-one , a substance that, like safrole, is used to produce MDMA (Ecstasy) can be used.

It falls under the Basic Substance Monitoring Act (GÜG), according to which transport quantities must be logged and the loss of the chemical must be reported.

Individual evidence

↑ Kevin D. Hesp, Rylan J. Lundgren, Mark Stradiotto: Palladium-Catalyzed Mono-α-arylation of Acetone with Aryl Halides and Tosylates . In: Journal of the American Chemical Society . tape 133 , no. 14 , April 13, 2011, ISSN 0002-7863 , p. 5194-5197 , doi : 10.1021 / ja200009c .
↑ Bhaskar H. Bhide, Kashmira K. Shah: Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry . tape 19 , no. 1 , 1980, p. 9-12 .
↑ Patent US3000903 : Phenylalkylhydrazines and use as psychotherapeutics. Published September 19, 1961 , Applicant: Lakeside Lab Inc, Inventor: John H. Biel. ‌
↑ Template: CL Inventory / not harmonized There is not yet a harmonized classification for this substance . A labeling of 1- (1,3-benzodioxol-5-yl) acetone in the Classification and Labeling Inventory of the European Chemicals Agency (ECHA), accessed on July 10, 2020, is reproduced from a self-classification by the distributor .

[DOI10.1021/ja200009c-1] Kevin D. Hesp, Rylan J. Lundgren, Mark Stradiotto: Palladium-Catalyzed Mono-α-arylation of Acetone with Aryl Halides and Tosylates . In: Journal of the American Chemical Society . tape 133 , no. 14 , April 13, 2011, ISSN 0002-7863 , p. 5194-5197 , doi : 10.1021 / ja200009c .

[2] Bhaskar H. Bhide, Kashmira K. Shah: Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry . tape 19 , no. 1 , 1980, p. 9-12 .

[3] Patent US3000903 : Phenylalkylhydrazines and use as psychotherapeutics. Published September 19, 1961 , Applicant: Lakeside Lab Inc, Inventor: John H. Biel. ‌

[4] Template: CL Inventory / not harmonized There is not yet a harmonized classification for this substance . A labeling of 1- (1,3-benzodioxol-5-yl) acetone in the Classification and Labeling Inventory of the European Chemicals Agency (ECHA), accessed on July 10, 2020, is reproduced from a self-classification by the distributor .