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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
Structure of ISOPROPYLPHENIDATE, THREO-

SMILES

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

InChI

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

HIDE SMILES / InChI

Molecular Formula C16H23NO2
Molecular Weight 261.3593
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 11:23:36 GMT 2023
Edited
by admin
on Sat Dec 16 11:23:36 GMT 2023
Record UNII
N93Y7VG3XF
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ISOPROPYLPHENIDATE, THREO-
Common Name English
ISOPROPYLPHENIDATE
Common Name English
2-PIPERIDINEACETIC ACID, .ALPHA.-PHENYL-, 1-METHYLETHYL ESTER
Systematic Name English
PROPAN-2-YL 2-PHENYL-2-(PIPERIDIN-2-YL)ACETATE
Systematic Name English
RITALINIC ACID ISOPROPYL ESTER
Common Name English
2-PIPERIDINEACETIC ACID, .ALPHA.-PHENYL-, ISOPROPYL ESTER
Common Name English
Classification Tree Code System Code
WIKIPEDIA Designer-drugs-Isopropylphenidate
Created by admin on Sat Dec 16 11:23:36 GMT 2023 , Edited by admin on Sat Dec 16 11:23:36 GMT 2023
Code System Code Type Description
CAS
99088-49-0
Created by admin on Sat Dec 16 11:23:36 GMT 2023 , Edited by admin on Sat Dec 16 11:23:36 GMT 2023
PRIMARY
FDA UNII
N93Y7VG3XF
Created by admin on Sat Dec 16 11:23:36 GMT 2023 , Edited by admin on Sat Dec 16 11:23:36 GMT 2023
PRIMARY
CAS
93148-46-0
Created by admin on Sat Dec 16 11:23:36 GMT 2023 , Edited by admin on Sat Dec 16 11:23:36 GMT 2023
NON-SPECIFIC STEREOCHEMISTRY
WIKIPEDIA
ISOPROPYLPHENIDATE
Created by admin on Sat Dec 16 11:23:36 GMT 2023 , Edited by admin on Sat Dec 16 11:23:36 GMT 2023
PRIMARY Isopropylphenidate (also known as IPH and IPPD) is a piperidine based stimulant drug, closely related to methylphenidate, but with the methyl ester replaced by an isopropyl ester. It has similar effects to methylphenidate but with a longer duration of action, and was banned in the UK as a Temporary Class Drug from April 2015 following its unapproved sale as a designer drug.
EPA CompTox
DTXSID001032294
Created by admin on Sat Dec 16 11:23:36 GMT 2023 , Edited by admin on Sat Dec 16 11:23:36 GMT 2023
PRIMARY
SMS_ID
300000037432
Created by admin on Sat Dec 16 11:23:36 GMT 2023 , Edited by admin on Sat Dec 16 11:23:36 GMT 2023
PRIMARY
PUBCHEM
124637657
Created by admin on Sat Dec 16 11:23:36 GMT 2023 , Edited by admin on Sat Dec 16 11:23:36 GMT 2023
PRIMARY
MANUFACTURER PRODUCT INFORMATION
ISOPROPYLPHENIDATE
Created by admin on Sat Dec 16 11:23:36 GMT 2023 , Edited by admin on Sat Dec 16 11:23:36 GMT 2023
PRIMARY
MANUFACTURER PRODUCT INFORMATION
IPH
Created by admin on Sat Dec 16 11:23:36 GMT 2023 , Edited by admin on Sat Dec 16 11:23:36 GMT 2023
PRIMARY Isopropylphenidate: an ester homolog of methylphenidate with sustained and selective dopaminergic activity and reduced drug interaction liability.Markowitz JS1, Zhu HJ, Patrick KS.J Child Adolesc Psychopharmacol. 2013 Dec;23(10):648-54. doi: 10.1089/cap.2013.0074. Epub 2013 Nov 21.
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY