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Carisoprodol

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Identification
Molecular formula
C12H24N2O4S
CAS number
78-44-4
IUPAC name
ethyl N-[2-(4-hydroxy-4-phenyl-1-piperidyl)-1-methyl-ethyl]-N-phenyl-carbamate;sulfamic acid
State
State

At room temperature, carisoprodol is typically found in a solid state. It is commonly dispensed in tablet form for use in medical treatments. The tablets are designed to be easily ingested in solid form.

Melting point (Celsius)
94.00
Melting point (Kelvin)
367.20
Boiling point (Celsius)
465.40
Boiling point (Kelvin)
738.60
General information
Molecular weight
260.34g/mol
Molar mass
260.3360g/mol
Density
1.0845g/cm3
Appearence

Carisoprodol typically appears as a white to off-white crystalline powder. It is tasteless and odorless, making it rather innocuous in a solid form. It is often pressed into tablets for medical use.

Comment on solubility

Solubility of Ethyl N-[2-(4-hydroxy-4-phenyl-1-piperidyl)-1-methyl-ethyl]-N-phenyl-carbamate Sulfamic Acid (C12H24N2O4S)

The solubility characteristics of this complex chemical compound present an interesting landscape. Here are some key points regarding its solubility:

  • Polar vs. Nonpolar Behavior: The presence of multiple functional groups such as carbamate and sulfamic acid suggests potential polar characteristics, which may enhance its solubility in polar solvents like water.
  • Hydrogen Bonding: The hydroxy group in the structure could facilitate hydrogen bonding with polar solvents, potentially increasing solubility.
  • Temperature Influence: As with many organic compounds, solubility can be temperature-dependent, with increased solubility likely at elevated temperatures.
  • Potential Challenges: Considering the complex structural features, the solubility might be limited in nonpolar solvents, as steric hindrance and intermolecular forces play a significant role.

In summary, while ethyl N-[2-(4-hydroxy-4-phenyl-1-piperidyl)-1-methyl-ethyl]-N-phenyl-carbamate sulfamic acid exhibits potential for good solubility in polar environments due to its functional group interactions, it may face significant solubility challenges in nonpolar mediums. Understanding these solubility properties is crucial for applications involving this compound.

Interesting facts

Interesting Facts about Ethyl N-[2-(4-Hydroxy-4-Phenyl-1-Piperidyl)-1-Methyl-Ethyl]-N-Phenyl-Carbamate;

With a Touch of Sulfamic Acid

Ethyl N-[2-(4-hydroxy-4-phenyl-1-piperidyl)-1-methyl-ethyl]-N-phenyl-carbamate combined with sulfamic acid creates a fascinating intersection of medicinal chemistry and synthetic methodologies. Here are some compelling insights about this remarkable compound:

  • Pharmaceutical Relevance: This compound is a part of a broader class known as piperidine derivatives, which have gained attention due to their significance in drug design and development.
  • Mechanism of Action: Compounds like this one can act on various neurochemical pathways, potentially impacting neurotransmitters in the central nervous system and making it a candidate for treatments in various neurological disorders.
  • Sulfamic Acid Synergy: The incorporation of sulfamic acid, which is known for its versatility in organic synthesis, introduces *sulfonamide functionality*, enhancing the compound's reactivity and biological profile.
  • Versatile Applications: Beyond medicinal use, such compounds are also investigated for their roles in agricultural chemistry, particularly as protectants in plant growth systems.
  • Cyclic Structures: The piperidine ring in its structure plays a crucial role in determining both the physiochemical properties and the biological activity of the compound, showing how minor changes can result in drastic variations in effect.

As a chemistry student or a scientist, understanding the properties and interactions of such compounds opens up a wealth of opportunities in both research and industrial applications. The exploration of piperidine derivatives reinforces the mantra that *the synthesis of diverse structures can lead to discoveries that transform lives*.

In conclusion, the study of ethyl N-[2-(4-hydroxy-4-phenyl-1-piperidyl)-1-methyl-ethyl]-N-phenyl-carbamate with sulfamic acid stands as a testament to the innovation within the field of chemistry, where each compound is a key to unlocking new therapeutic avenues.

Synonyms
57-49-8
Carbanilic acid, N-(2-(4-hydroxy-4-phenylpiperidino)-1-methyl)ethyl-, ethyl ester, sulfamate
DTXSID10972486
WTBBQSREXFAQOR-UHFFFAOYSA-N
Sulfamic acid--ethyl [1-(4-hydroxy-4-phenylpiperidin-1-yl)propan-2-yl]phenylcarbamate (1/1)