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Tolterodine

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Identification
Molecular formula
C22H31NO2
CAS number
124937-51-5
IUPAC name
(1-methyl-3-piperidyl)methyl N-(o-tolyl)carbamate
State
State

The compound is usually found in its salt form, appearing as a solid at room temperature. However, as a free base, it is typically a liquid.

Melting point (Celsius)
192.00
Melting point (Kelvin)
465.15
Boiling point (Celsius)
364.50
Boiling point (Kelvin)
637.65
General information
Molecular weight
325.44g/mol
Molar mass
325.4420g/mol
Density
1.1100g/cm3
Appearence

The compound is generally available as a colorless or slightly yellow liquid. It does not have a distinct appearance in solid form as it is typically formulated into a resin or tartrate salt for pharmaceutical applications.

Comment on solubility

Solubility of (1-methyl-3-piperidyl)methyl N-(o-tolyl)carbamate

(1-methyl-3-piperidyl)methyl N-(o-tolyl)carbamate is a compound that exhibits interesting solubility characteristics. Its solubility can be influenced by several factors such as temperature, solvent type, and molecular structure.

Key Points About Solubility:

  • Polar vs Nonpolar Solvents: This compound is likely to be more soluble in polar organic solvents due to the presence of the carbamate functional group which can engage in hydrogen bonding.
  • Temperature Dependency: As with many organic compounds, solubility typically increases with temperature. Therefore, higher temperatures can enhance the solubility of (1-methyl-3-piperidyl)methyl N-(o-tolyl)carbamate.
  • Molecular Interactions: The presence of a piperidine ring and a toluylic group may also affect its solubility profile through steric hindrance and electron-donating abilities.

Due to its unique structure, it is important to conduct empirical solubility tests for practical applications. Always consider the specific conditions and solvents when assessing the solubility of this compound.

Interesting facts

Interesting Facts about (1-methyl-3-piperidyl)methyl N-(o-tolyl)carbamate

(1-methyl-3-piperidyl)methyl N-(o-tolyl)carbamate is a fascinating compound that serves various purposes across multiple fields, particularly in medicinal chemistry. Here are some notable points about this compound:

  • Medicinal Applications: This compound showcases considerable potential as a pharmaceutical agent, often being studied for its efficacy in treating various ailments, including neurological disorders.
  • Mechanism of Action: Its action often involves modulation of neurotransmitter systems, contributing to its therapeutic effects. Such interactions are worth exploring for their implications in drug development.
  • Analogs and Derivatives: The unique structure of this carbamate allows for the synthesis of various analogs. These derivatives can be tailored to improve potency or reduce side effects, enhancing drug design processes.
  • Research Studies: Numerous studies have focused on understanding the pharmacodynamics and pharmacokinetics of this compound. Scientists analyze how it is metabolized in the body and its interaction with biological targets.
  • Environmental Impact: As with many synthetic compounds, understanding its environmental behavior is crucial. Researchers investigate its stability and degradation pathways to assess potential ecological risks.

In conclusion, (1-methyl-3-piperidyl)methyl N-(o-tolyl)carbamate is more than just a chemical formula; it represents a gateway to advancements in medicinal chemistry and a deeper understanding of how we can manipulate chemical structures for beneficial uses. Its complexity and potential make it a significant point of interest for both chemists and pharmacologists.

Synonyms
21184-56-5
o-Methylcarbanilic acid (1-methyl-3-piperidyl)methyl ester
CARBANILIC ACID, o-METHYL-, (1-METHYL-3-PIPERIDYL)METHYL ESTER
BRN 1474661
RefChem:1081117
DTXSID90943518
(1-Methylpiperidin-3-yl)methyl hydrogen (2-methylphenyl)carbonimidate