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Carisoprodol

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Identification
Molecular formula
C12H18N2O4
CAS number
78-44-4
IUPAC name
(1-methyl-2-phenyl-ethyl) carbamate
State
State

At room temperature, Carisoprodol is typically found as a solid. It is available in the form of tablets for oral administration.

Melting point (Celsius)
92.00
Melting point (Kelvin)
365.15
Boiling point (Celsius)
310.00
Boiling point (Kelvin)
583.15
General information
Molecular weight
260.34g/mol
Molar mass
260.3360g/mol
Density
1.1655g/cm3
Appearence

Carisoprodol is typically a white or off-white crystalline powder. It may also come in tablet form for medicinal use. The compound is usually odorless, and when in pure form, it is slightly crystalline in texture.

Comment on solubility

Solubility of (1-methyl-2-phenyl-ethyl) carbamate

The solubility of (1-methyl-2-phenyl-ethyl) carbamate in various solvents is an interesting aspect worth exploring. Understanding solubility can provide insights into its applications and behavior in different environments.

  • Polar solvents: This compound exhibits moderate solubility in polar solvents such as water due to the presence of the carbamate functional group, which can engage in hydrogen bonding.
  • Non-polar solvents: Conversely, (1-methyl-2-phenyl-ethyl) carbamate tends to show higher solubility in non-polar organic solvents. This characteristic can be attributed to its hydrophobic aromatic and alkyl substituents.
  • Log P value: The lipophilicity of this compound, as indicated by its log P value, suggests that it is more soluble in organic solvents compared to aqueous solutions, making it useful in formulations where such properties are desired.

In summary, when considering the solubility of (1-methyl-2-phenyl-ethyl) carbamate, one must keep in mind that its solubility varies significantly between polar and non-polar solvents. This variance is crucial for its synthesis and application in both laboratory and industrial settings.

Interesting facts

Interesting Facts about (1-methyl-2-phenyl-ethyl) carbamate

Carbamates are a fascinating class of chemical compounds, and (1-methyl-2-phenyl-ethyl) carbamate is no exception. This compound is of particular interest due to its diverse applications and unique properties.

Applications

  • Agricultural Relevance: Like many carbamates, this compound can play a role in agriculture, often serving as a pesticide or herbicide, contributing to effective crop protection.
  • Pharmaceutical Uses: Its structure may lend itself to the development of pharmaceuticals, with potential benefits for therapeutic applications targeting specific biological pathways.
  • Research Interest: As a subject of study, (1-methyl-2-phenyl-ethyl) carbamate can help scientists understand reaction mechanisms and develop new synthetic methods in organic chemistry.

Chemical Behavior

The presence of both the methyl and phenyl groups in the compound's structure introduces interesting steric and electronic effects, affecting its reactivity and stability. These structural features can lead to:

  • The ability to form hydrogen bonds, which can enhance solubility in various solvents.
  • Interaction with biological macromolecules, making it a candidate for further pharmacological exploration.

Safety Measures

As with many chemical compounds, responsible handling is crucial. It is important for chemists and researchers to observe safety protocols while working with (1-methyl-2-phenyl-ethyl) carbamate, particularly considering:

  • Potential toxicity associated with carbamates, necessitating proper personal protective equipment (PPE).
  • The importance of adequate ventilation and controlled laboratory environments when conducting experiments.

In summary, (1-methyl-2-phenyl-ethyl) carbamate serves as a prominent example of how organic compounds can be both practically useful and scientifically intriguing. Continuous research into this compound may unveil new applications and deepen our understanding of chemical interactions.

Synonyms
Betaquil
Sa 217
CARBAMIC ACID, alpha-METHYLPHENETHYL ESTER
709-90-0
NSC 44683
BRN 1871591
1-phenylpropan-2-yl carbamate
Carbamic acid, .alpha.-methylphenethyl ester
WLN: ZVOY1&1R
SCHEMBL1811694
DTXSID901031936
NSC44683
NSC-44683