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Methylphenidate

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Identification
Molecular formula
C14H19NO2
CAS number
113-45-1
IUPAC name
(1-methyl-4-piperidyl) 2-hydroxy-5-methyl-2-phenyl-hex-3-ynoate
State
State

Methylphenidate is typically in a solid state at room temperature. It is available in various formulations, including tablets and capsules for medical applications.

Melting point (Celsius)
70.50
Melting point (Kelvin)
343.70
Boiling point (Celsius)
267.10
Boiling point (Kelvin)
540.30
General information
Molecular weight
233.31g/mol
Molar mass
233.3050g/mol
Density
1.2041g/cm3
Appearence

Methylphenidate is a white to off-white crystalline powder. It is odorless and has a bitter taste.

Comment on solubility

Solubility of (1-methyl-4-piperidyl) 2-hydroxy-5-methyl-2-phenyl-hex-3-ynoate

The solubility of the compound (1-methyl-4-piperidyl) 2-hydroxy-5-methyl-2-phenyl-hex-3-ynoate can be a complex topic due to its molecular structure and characteristics. Here are some important points to consider regarding its solubility:

  • Polarity: The presence of both hydrophilic (hydroxy) and hydrophobic (phenyl and alkyl groups) components in the molecule suggests that the compound may exhibit variable solubility in different solvents.
  • Solvent Interaction: It is likely to be soluble in organic solvents such as ethanol, acetone, or chloroform, while showing limited solubility in water due to its larger hydrophobic regions.
  • Temperature Dependency: The solubility may increase with temperature, making it more soluble in warmer solvents.
  • Complex Formation: Potential for forming hydrogen bonds may enhance solubility in certain polar solvents.

In summary, while the compound (1-methyl-4-piperidyl) 2-hydroxy-5-methyl-2-phenyl-hex-3-ynoate is expected to have a degree of solubility in organic solvents, its overall behavior will depend on a variety of factors such as temperature and the specific solvent used. Understanding these parameters is crucial for applications involving this compound.

Interesting facts

Interesting Facts About (1-methyl-4-piperidyl) 2-hydroxy-5-methyl-2-phenyl-hex-3-ynoate

(1-methyl-4-piperidyl) 2-hydroxy-5-methyl-2-phenyl-hex-3-ynoate is a fascinating compound that exhibits a variety of intriguing characteristics and applications. Here are some key points to consider:

  • Pharmaceutical relevance: This compound is often studied for its potential therapeutic effects, especially in the field of neuropharmacology. Its unique structure may interact with various receptors, offering insights into drug development.
  • Structural complexity: The compound contains a piperidine ring, which is significant in many biological systems. The presence of multiple functional groups, such as the hydroxy and ynoate moieties, adds to its chemical versatility.
  • Mechanism of action: Investigations into its mechanism of action suggest that it may modulate neurotransmitter systems, which could lead to potential applications in treating disorders like anxiety and depression.
  • Synthetic pathways: The synthesis of (1-methyl-4-piperidyl) 2-hydroxy-5-methyl-2-phenyl-hex-3-ynoate presents a challenge for chemists, making it a subject of interest for synthetic organic chemists exploring new methodologies.
  • Cited in research: Its importance is highlighted in various academic publications that explore its properties and potential uses, demonstrating its relevance in ongoing scientific investigations.

In summary, (1-methyl-4-piperidyl) 2-hydroxy-5-methyl-2-phenyl-hex-3-ynoate stands out not only due to its structural intricacies but also because of its promising applications in pharmaceuticals. Its study opens avenues to new treatments, making it a compound of interest for both scientific research and practical applications in medicine.

Synonyms
16862-13-8
N-Methyl-4-piperidylisopentynylphenylglycolate
Benzeneacetic acid, alpha-hydroxy-alpha-(3-methyl-1-butynyl)-, 1-methyl-4-piperidinyl ester
1-Methyl-4-piperidyl phenyl(3-methyl-1-butynyl)glycolate
(1-methylpiperidin-4-yl) 2-hydroxy-5-methyl-2-phenylhex-3-ynoate
BRN 1493814
alpha-(3-Methyl-1-butynyl)mandelic acid 1-methyl-4-piperidyl ester
DTXSID30937512
MANDELIC ACID, alpha-(3-METHYL-1-BUTYNYL)-, 1-METHYL-4-PIPERIDYL ESTER
N-methyl-4-piperidyl isopentynylphenylglycolate
1-METHYLPIPERIDIN-4-YL 2-HYDROXY-5-METHYL-2-PHENYLHEX-3-YNOATE