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Carisoprodol

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Identification
Molecular formula
C12H24N2O4
CAS number
78-44-4
IUPAC name
(1-ethyl-3-piperidyl)methyl N-(2,6-dimethylphenyl)carbamate
State
State

At room temperature, Carisoprodol is typically in a solid state, presenting as a powder.

Melting point (Celsius)
92.00
Melting point (Kelvin)
365.15
Boiling point (Celsius)
340.00
Boiling point (Kelvin)
613.15
General information
Molecular weight
260.34g/mol
Molar mass
260.3390g/mol
Density
1.0800g/cm3
Appearence

Carisoprodol appears as a white, crystalline powder that is odorless. It is generally available in tablet form for pharmaceutical use. The powder can be slightly soluble in water and more soluble in alcohol and acetone.

Comment on solubility

Solubility of (1-ethyl-3-piperidyl)methyl N-(2,6-dimethylphenyl)carbamate

The solubility of (1-ethyl-3-piperidyl)methyl N-(2,6-dimethylphenyl)carbamate can be influenced by various factors including its chemical structure and environmental conditions. As a carbamate derivative, this compound is generally expected to exhibit moderate solubility characteristics. Here are some important considerations regarding its solubility:

  • Polar vs. Non-Polar: Due to the presence of both polar and non-polar functional groups in its structure, the solubility can vary significantly in different solvents.
  • Solvent Selection: It is likely more soluble in polar organic solvents such as methanol or ethanol, while showing reduced solubility in non-polar solvents like hexane.
  • Temperature Effects: Like many chemical compounds, increased temperature can enhance solubility, promoting better dissolution in various media.
  • pH Influence: The solubility may also be affected by the pH of the solution, especially if protonation or deprotonation of certain functional groups occurs.

In practical terms, this means that when handling or utilizing (1-ethyl-3-piperidyl)methyl N-(2,6-dimethylphenyl)carbamate, one must carefully select the solvent system to achieve the desired solubility and optimize its use in applications.

Interesting facts

Interesting Facts about (1-ethyl-3-piperidyl)methyl N-(2,6-dimethylphenyl)carbamate

(1-ethyl-3-piperidyl)methyl N-(2,6-dimethylphenyl)carbamate, also known by its common name, is a fascinating compound with various applications in the field of chemistry and pharmacology. Here are some intriguing insights into this compound:

  • Versatile Applications: This compound is primarily used as an intermediate in the synthesis of pharmaceuticals, particularly in developing analgesics and anti-inflammatory drugs.
  • Unique Structure: The presence of the piperidine ring is significant; it contributes to the compound’s ability to interact with biological systems, often providing a unique mechanism of action.
  • Biological Activity: Studies have indicated that this compound exhibits promising effects on specific biological pathways, potentially leading to new therapeutic strategies.
  • Research and Development: Ongoing research aims to explore modified versions of this compound, focusing on enhancing its efficacy and minimizing side effects.
  • Synthetic Importance: The synthetic routes to create this compound often involve innovative methodologies, making it a subject of interest for synthetic chemists aiming to optimize efficiency and yield.

Overall, (1-ethyl-3-piperidyl)methyl N-(2,6-dimethylphenyl)carbamate stands out not just for its structural uniqueness but also for its significant role in medicinal chemistry. As stated by researchers, “Understanding the intricacies of such compounds can pave the way for groundbreaking treatments in modern medicine.”

In summary, this compound is an excellent example of how diverse chemical structures play critical roles in the ongoing advancements of science and medicine, offering exciting possibilities for future research and applications.

Synonyms
(1-Ethyl-3-piperidyl)methyl 2,6-dimethylcarbanilate
20930-86-3
BRN 1484810
DTXSID40943220
2,6-Dimethylcarbanilic acid (1-ethyl-3-piperidyl)methyl ester
CARBANILIC ACID, 2,6-DIMETHYL-, (1-ETHYL-3-PIPERIDYL)METHYL ESTER
(1-Ethylpiperidin-3-yl)methyl hydrogen (2,6-dimethylphenyl)carbonimidate