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Clenbuterol

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Identification
Molecular formula
C12H18ClN
CAS number
21898-19-1
IUPAC name
N-[(4-chlorophenyl)methyl]-1,7,7-trimethyl-norbornan-2-amine
State
State

At room temperature, Clenbuterol is generally a solid when in its pure form. It can also be found in various formulations, including tablets and liquids, depending on its intended use.

Melting point (Celsius)
174.50
Melting point (Kelvin)
447.60
Boiling point (Celsius)
354.70
Boiling point (Kelvin)
627.90
General information
Molecular weight
277.19g/mol
Molar mass
277.1930g/mol
Density
1.0655g/cm3
Appearence

Clenbuterol typically appears as a white or off-white crystalline powder. It is often found in the form of tablets or as part of a liquid formulation when used in medicinal contexts.

Comment on solubility

Solubility of N-[(4-chlorophenyl)methyl]-1,7,7-trimethyl-norbornan-2-amine

The solubility of N-[(4-chlorophenyl)methyl]-1,7,7-trimethyl-norbornan-2-amine can be quite interesting due to its unique structure.

  • Polarity: The molecule contains both hydrophobic (the norbornane ring) and hydrophilic (the amine functional group) parts. This dual nature often influences its interaction with solvents.
  • Solvent Compatibility: Generally, such compounds show better solubility in organic solvents like ethanol, acetonitrile, or chloroform, while their solubility in water is often limited.
  • Temperature Effects: Temperature can play a significant role in the solubility of this compound; typically, increasing the temperature may enhance solubility in organic solvents.
  • pH Influence: As an amine, the solubility may also be affected by the pH of the solution, as protonation can increase solubility in aqueous environments.

In summary, solubility varies significantly based on the solvent used and external conditions such as temperature and pH. Understanding these factors can be crucial for applications in organic chemistry and pharmaceuticals.

Interesting facts

Interesting Facts about N-[(4-chlorophenyl)methyl]-1,7,7-trimethyl-norbornan-2-amine

N-[(4-chlorophenyl)methyl]-1,7,7-trimethyl-norbornan-2-amine is a fascinating compound due to its unique structural and functional characteristics. Here are some engaging insights into this intriguing molecule:

  • Global Health Implications: This compound can be related to the field of pharmaceuticals. Many compounds with similar structures serve as drug candidates, specifically in treating conditions related to the central nervous system and other therapeutic areas.
  • Synthetic Versatility: The synthetic routes to obtain such compounds often involve multi-step reactions, where intermediates can lead to a variety of chemical derivatives. This increases the scope for developing new materials and understanding chemical behavior.
  • Chirality: The presence of stereogenic centers in the molecular structure makes this compound chiral. This chiral nature can have significant implications in biological activity, where different enantiomers may elicit varying physiological responses. As the renowned chemist Linus Pauling once said, “The properties of a substance depend on the arrangement of the atoms in the molecules of that substance.”
  • Environmentally Relevant: Compounds with chlorinated aromatic rings are frequently studied for their environmental impact, particularly in the context of accumulation in biological systems. Understanding such compounds helps in assessing and mitigating potential risks related to pollution.
  • Potential in Material Science: Beyond pharmacological applications, compounds like N-[(4-chlorophenyl)methyl]-1,7,7-trimethyl-norbornan-2-amine may also find utility in the development of novel materials, such as polymers or ligands in catalytic processes, due to the stability and reactivity of their structural components.

In summary, N-[(4-chlorophenyl)methyl]-1,7,7-trimethyl-norbornan-2-amine is not just a chemical entity but a gateway into vast applications in medicine, environmental science, and materials chemistry. Its study epitomizes the continual connection between structure and function in the chemical sciences.

Synonyms
AKOS008990508