Anodyne

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IPH
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
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261.36 g/mol [1]
1 [1]
Structural Identifiers
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C16H23NO2 [1]
propan-2-yl 2-phenyl-2-piperidin-2-ylacetate [1]
CC(C)OC(=O)C(C1CCCCN1)C2=CC=CC=C2 [1]
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 [1]
InChIKeyAZVPADMEIMLODT-UHFFFAOYSA-N [1]
Dosing[]
Insufflated
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Light≤ 50.9 mg(2x - 66.7%)
Common50.9 mg
Strong50 - 60 mg
Heavy60 - 66 mg
Extreme66 mg +(1x - 33.3%)
Statistically derived dosages via DBI-IGS
We do not take any responsibility for medical complications or loss of life sustained by following these dosages blindly.

Isopropylphenidate

Isopropylphenidate is a stimulant substance of the phenidate class.

Chemistry

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Isopropylphenidate is a racemic mixture of the

Stereoisomers
(6S,7S)-IsopropylphenidateGenerated by the Chemistry Development Kit (http://github.com/cdk)
(6R,7S)-IsopropylphenidateGenerated by the Chemistry Development Kit (http://github.com/cdk)
(6S,7R)-IsopropylphenidateGenerated by the Chemistry Development Kit (http://github.com/cdk)
(6R,7R)-IsopropylphenidateGenerated by the Chemistry Development Kit (http://github.com/cdk)

Subjective effects []

Anodyne Usernotes
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magnus / Isopropylphenidate[hydrochloride] via Oral and Insufflated

Legal status []

  • Canada: Isopropylphenidate is a Schedule III substance.
  • United Kingdom: Isopropylphenidate is a Class B substance.

See also []

  • Substituted phenidates
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 68314762, Isopropylphenidate. Accessed October 14, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/68314762