PROPYLPHENIDATE, THREO-

Investigational

Details

Stereochemistry	RACEMIC
Molecular Formula	C16H23NO2
Molecular Weight	261.3593
Optical Activity	( + / - )
Defined Stereocenters	2 / 2
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

SMILES

[H][C@@]1(CCCCN1)[C@H](C(=O)OCCC)C2=CC=CC=C2

InChI

InChIKey=PRMWWEANNQSWAR-HUUCEWRRSA-N

InChI=1S/C16H23NO2/c1-2-12-19-16(18)15(13-8-4-3-5-9-13)14-10-6-7-11-17-14/h3-5,8-9,14-15,17H,2,6-7,10-12H2,1H3/t14-,15-/m1/s1

HIDE SMILES / InChI

Molecular Formula	C16H23NO2
Molecular Weight	261.3593
Charge	0
Count	MOL RATIO 1 MOL RATIO (average)

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	2 / 2
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical
Record UNII	0Q064445GT
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

PROPYLPHENIDATE, THREO-

Common Name

English

2-PIPERIDINEACETIC ACID, .ALPHA.-PHENYL-, PROPYL ESTER

Systematic Name

English

2-PIPERIDINEACETIC ACID, .ALPHA.-PHENYL-, PROPYL ESTER, (R*,R*)-(±)-

Common Name

English

PROPYLPHENIDATE

Common Name

English

PPH

Common Name

English

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Classification Tree

Code System

Code

Stimulants

WIKIPEDIA

Designer-drugs-Propylphenidate

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Code System

Code

Type

Description

WIKIPEDIA

PROPYLPHENIDATE

PRIMARY

Propylphenidate (also known as PPH) is a piperidine based stimulant drug, closely related to methylphenidate, but with the methyl ester replaced by an propyl ester. It was banned in the UK as a Temporary Class Drug from April 2015 following its unapproved sale as a designer drug. Propylphenidate can be synthesised from methylphenidate.

PUBCHEM

119025958

PRIMARY

FDA UNII

0Q064445GT

PRIMARY

WEB RESOURCE

PROPYL 2-PHENYL-2-(PIPERIDIN-2-YL)ACETATE

PRIMARY

MANUFACTURER PRODUCT INFORMATION

PROPYLPHENIDATE

PRIMARY

Propylphenidate (also known as PPH) is a piperidine based stimulant drug, closely related to methylphenidate, but with the methyl ester replaced by an propyl ester. It was banned in the UK as a Temporary Class Drug from April 2015 following its unapproved sale as a designer drug.[1] Propylphenidate can be synthesised from methylphenidate.[2] Legal status: Propylphenidate is illegal in Sweden as of 26. January 2016.[3] See also: ?3,4-Dichloromethylphenidate ?4-Fluoromethylphenidate ?4-Methylmethylphenidate?Dexmethylphenidate ?Ethylphenidate ?Isopropylphenidate ?HDEP-28 ?HDMP-28References 1. Methylphenidate-based NPS: A review of the evidence of use and harm. Advisory Council on the Misuse of Drugs, 31 March 2015 2. James Alain Bourland (1997). "The influence of ethanol on drug metabolism and disposition via carboxylesterase-mediated transesterification". 3. "31 nya ?mnen kan klassas som narkotika eller h?lsofarlig vara" (in Swedish). Folkh?lsomyndigheten. November 2015.

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