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1-[(3-Methyl-1-piperidyl)methyl]benzotriazole

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Identification
Molecular formula
C13H17N3
CAS number
65291-80-7
IUPAC name
1-[(3-methyl-1-piperidyl)methyl]benzotriazole
State
State

At room temperature, this compound is typically a solid. It can dissolve in various organic solvents and may exhibit different states when dissolved depending on the solvent and conditions.

Melting point (Celsius)
108.50
Melting point (Kelvin)
381.65
Boiling point (Celsius)
452.45
Boiling point (Kelvin)
725.60
General information
Molecular weight
242.31g/mol
Molar mass
242.3050g/mol
Density
1.1800g/cm3
Appearence

1-[(3-Methyl-1-piperidyl)methyl]benzotriazole typically appears as a solid compound with a crystalline structure. The color may vary but it is often seen as a pale yellow to off-white solid. It may also be hygroscopic based on its chemical structure.

Comment on solubility

Solubility of 1-[(3-methyl-1-piperidyl)methyl]benzotriazole

1-[(3-methyl-1-piperidyl)methyl]benzotriazole, a compound with complex molecular structure, exhibits intriguing solubility characteristics. When exploring its solubility, consider the following insights:

  • Polarity: The presence of both the benzotriazole moiety and the piperidine derivative suggests a balance between hydrophilic and hydrophobic properties, impacting solubility in various solvents.
  • Solvent Interaction: This compound may show better solubility in organic solvents such as ethanol and dimethyl sulfoxide (DMSO), while having more limited solubility in protic solvents like water.
  • pH Dependence: Solubility might change with pH due to potential protonation of the piperidine nitrogen, which can enhance its solubility in acidic environments.
  • Temperature Influence: As with many organic compounds, an increase in temperature might improve solubility, making it essential to consider thermal conditions during experiments or applications.

Understanding these solubility aspects is crucial for applications in areas like pharmaceuticals, where the dissolution characteristics can dictate bioavailability and therapeutic effectiveness. Remember, "A compound's solubility profile is a window into its potential utility."

Interesting facts

Interesting Facts about 1-[(3-methyl-1-piperidyl)methyl]benzotriazole

1-[(3-methyl-1-piperidyl)methyl]benzotriazole is a fascinating compound that has captured the attention of chemists and material scientists alike. Here are some engaging points to consider:

  • Versatile Applications: This compound is renowned for its role as a UV stabilizer, which protects materials from the damaging effects of ultraviolet radiation. It is particularly useful in various industries, including plastics, coatings, and polymers.
  • Photostability: The benzotriazole moiety in the structure is known for its excellent ability to absorb UV light and dissipate it safely, thus preventing photo-induced degradation. This makes it a vital component in formulations designed for outdoor usage.
  • Biological Relevance: Beyond its industrial applications, research has indicated that benzotriazole derivatives possess biological activity. There is ongoing exploration into their potential as pharmaceuticals, particularly within the realm of anti-cancer therapies.
  • Synthesis and Chemistry: The synthesis of 1-[(3-methyl-1-piperidyl)methyl]benzotriazole involves intriguing reaction pathways that demonstrate the versatility of organic chemistry. The presence of the piperidine ring adds an interesting dimension to its reactivity.
  • Environmental Impact: As an emerging area of research, the environmental persistence of benzotriazole compounds has been under scrutiny. Scientists are actively investigating degradation pathways and possible ecological risks associated with their use.

In summary, 1-[(3-methyl-1-piperidyl)methyl]benzotriazole is not only significant from an industrial perspective but also holds great promise in the fields of chemistry and environmental science. As researchers continue to explore its properties, the compound could reveal new insights and applications that extend far beyond its current uses.

Synonyms
AKOS034336926
SR-01000056405
SR-01000056405-1
Z44100337