Anodyne

4-MMPH
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
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247.33 g/mol [1]
0.6 [1]
Structural Identifiers
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C15H21NO2 [1]
methyl (2R)-2-(4-methylphenyl)-2-[(2S)-piperidin-2-yl]acetate [1]
CC1=CC=C(C=C1)[C@H]([C@@H]2CCCCN2)C(=O)OC [1]
InChI=1S/C15H21NO2/c1-11-6-8-12(9-7-11)14(15(17)18-2)13-5-3-4-10-16-13/h6-9,13-14,16H,3-5,10H2,1-2H3/t13-,14+/m0/s1 [1]
InChIKeyWJZNCJIOIACDBR-UONOGXRCSA-N [1]

4-Methylmethylphenidate

4-Methylmethylphenidate (also known as Threo-4-methylmethylphenidate, 4-Mmph, 4-Me-tmp, 2-Piperidineacetic acid, α-(4-methylphenyl)-, methyl ester, (αR,2S)-rel-, 4MeTMP, RefChem:1100096, Pdsp1_000877, Pdsp2_000863 or 2-Piperidineacetic acid, α-(4-methylphenyl)-, methyl ester, (αr,2s)-rel-) is a stimulant substance of the phenidate class.

Chemistry

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4-Methylmethylphenidate is a absolute mixture

Subjective effects []

Anodyne Usernotes
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magnus / 4-Methylmethylphenidate[hydrochloride] via Oral and Insufflatedeffects close to methylphenidat with lower potency and less clean, underwhelming

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 23815457, 4-Methylmethylphenidate. Accessed September 1, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/23815457

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 4-Methylmethylphenidate. UNII: 1Y11XUO4EY. Global Substance Registration System. Accessed September 1, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/1Y11XUO4EY