MPH | |
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Salts [] | |
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Methylphenidate hydrochloride | |
Molecular structure via molpic | |
| |
Molecular formula | C14H19NO2 |
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Molecular mass | 233.31 g/mol |
Appearance | Crystals from ethanol (aqueous) |
Predicted LogP | 0.2 |
Melting point | 74-75 °C |
Boiling point | BP: 135 to 137 °C at 0.6 mm Hg |
Decomposition | When heated to decomposition it emits toxic fumes of nitroxides. |
Solubility | 1255mg/L |
Chirality | racemic |
Identifiers [] | |
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IUPAC name | methyl 2-phenyl-2-piperidin-2-ylacetate |
SMILES | COC(=O)C(C1CCCCN1)C2=CC=CC=C2 |
InChI | InChI=1S/C14H19NO2/c1-17-14(16)13(11-7-3-2-4-8-11)12-9-5-6-10-15-12/h2-4,7-8,12-13,15H,5-6,9-10H2,1H3 |
InChIKey | DUGOZIWVEXMGBE-UHFFFAOYSA-N |
Methylphenidate
Methylphenidate (also known as Methylphenidan, Phenidylate, Calocain, Plimasine, Methyl phenidylacetate, Concerta, Methylfenidan, Metilfenidato, Methylphenidatum or Methyl phenidate) is a stimulant substance of the phenidate class.
Chemistry
Methylphenidate is typically found in the form of its hydrochloride salt.
Stereochemistry
Methylphenidate is a racemic mixture of the optical stereoisomers:Stereoisomers [] | |
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Dexmethylphenidate | Levomethylphenidate |
See also
External links
- Methylphenidate (Wikipedia)
- Methylphenidate (Wikidata)
- Methylphenidate (DrugBank)
- Methylphenidate (PubChem)
- Methylphenidate (ChemSpider)
- Methylphenidate (ChEMBL)
- Methylphenidate (ChEBI)
- Methylphenidate (Common Chemistry)
- Methylphenidate (HMDB)
- Methylphenidate (KEGG)
- Methylphenidate (UNII)
- Methylphenidate (EPA DSSTox)