| Weight | 219.284 g/mol |
|---|---|
| Formula | C13H17NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
Ritalinic acid (19395-41-6)
alpha-phenyl-2-piperidineacetic acid · ritalinic acid, (R*,R*)-(+-)-isomer
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- Sigma-Aldrich - Ritalinic acid130.00 - 288.50 USD
- Fisher Scientific - Search for Ritalinic acid
- TCI - Ritalinic acid81.00 - 276.00 USD
- [3H]Threo()Methylphenidate Binding to 3,4Dihydroxyphenylethylamine Uptake Sites in Corpus Striatum: Correlation with the Stimulant Properties of Ritalinic Acid Esters (Journal of Neurochemistry, 1985)
- Methylphenidate Hydrochloride Given With or Before Breakfast: II. Effects on Plasma Concentration of Methylphenidate and Ritalinic Acid (Pediatrics, 1983)
- High-throughput selected reaction monitoring liquid chromatographymass spectrometry determination of methylphenidate and its major metabolite, ritalinic acid, in rat plasma employing monolithic columns (Journal of Chromatography B, 2003)
- Analysis of methylphenidate and its metabolite ritalinic acid in monkey plasma by liquid chromatography/electrospray ionization mass spectrometry (Rapid Communications in Mass Spectrometry, 2000)
- Liquid chromatography-tandem mass spectrometry method for the simultaneous analysis of multiple hallucinogens, chlorpheniramine, ketamine, ritalinic acid, and metabolites, in urine. (Journal of Analytical Toxicology, 2007)
- Potential Trends in Attention Deficit Hyperactivity Disorder (ADHD) Drug Use on a College Campus: Wastewater Analysis of Amphetamine and Ritalinic Acid (Science of The Total Environment, 2013)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - alpha-phenyl-2-piperidineacetic acid
- ritalinic acid, (R*,R*)-(+-)-isomer
-
SMILESC1CCNC(C1)C(C2=CC=CC=C2)C(=O)O
-
InChIKeyINGSNVSERUZOAK-UHFFFAOYSA-N
- Pubchem - Ritalinic acid
- Wikipedia - ritalinic acid
Ritalinic acid is a substituted phenethylamine and an inactive major metabolite of the psychostimulant drugs methylphenidate and ethylphenidate. When administered orally, methylphenidate is extensively metabolized in the liver by hydrolysis of the ester group yielding ritalinic acid. The hydrolysis was found to be catalyzed by carboxylesterase 1 (CES1).
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Synthesis
benzene
+
Reactant
(Friedel-Crafts alkylation)
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Ritalinic acid
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