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(2,2,6-trimethyl-4-piperidyl) benzoate

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Identification
Molecular formula
C15H21NO2
CAS number
94-09-7
IUPAC name
(2,2,6-trimethyl-4-piperidyl) benzoate
State
State

The compound is in a solid state at room temperature, appearing as a white crystalline substance.

Melting point (Celsius)
80.50
Melting point (Kelvin)
353.70
Boiling point (Celsius)
318.50
Boiling point (Kelvin)
591.70
General information
Molecular weight
263.35g/mol
Molar mass
263.3680g/mol
Density
1.0200g/cm3
Appearence

(2,2,6-Trimethyl-4-piperidyl) benzoate typically appears as a white or off-white crystalline solid. Its crystalline structure is fine and it may appear in powdered form.

Comment on solubility

Solubility of (2,2,6-trimethyl-4-piperidyl) benzoate

(2,2,6-trimethyl-4-piperidyl) benzoate, with the chemical formula C16H23NO2, is an interesting compound when it comes to its solubility properties.

Solubility Characteristics:

  • Polar vs. Nonpolar Solvents: This compound is expected to exhibit solubility in moderately polar solvents, thanks to the presence of the benzoate functional group, which can engage in hydrogen bonding.
  • Temperature Influence: As with many organic compounds, solubility may increase with elevating temperatures, allowing for a greater molecular movement and interactions.
  • pH Dependence: The solubility of (2,2,6-trimethyl-4-piperidyl) benzoate can also be influenced by the pH of the solution; in more acidic environments, the benzoate may ionize, potentially increasing solubility.

In summary, while definitive solubility data may vary, one could posit that the compound shows enhanced solubility in polar organic solvents, creating a balance that allows for effective dissolution under suitable conditions. The intricate structure of (2,2,6-trimethyl-4-piperidyl) benzoate enriches our understanding of solubility dynamics in organic chemistry.

Interesting facts

Interesting Facts About (2,2,6-trimethyl-4-piperidyl) benzoate

(2,2,6-trimethyl-4-piperidyl) benzoate is a fascinating compound with several intriguing aspects that draw the attention of both chemists and industry professionals alike. This compound is best known for its application as a photographic stabilizer and UV absorber, which makes it valuable in various fields.

Applications and Uses

  • Photographic Industry: Widely used as a stabilizer in photographic films, ensuring protection against oxidation and degradation due to light exposure.
  • Plastic Industry: Acts as a UV stabilizer in polymers, enhancing the durability and longevity of plastic products.
  • Personal Care Products: Employed in sunscreens and cosmetics to protect formulations from UV radiation.

Chemical Structure Insights

The structure of (2,2,6-trimethyl-4-piperidyl) benzoate contributes significantly to its properties. Here are some noteworthy features of its molecular make-up:

  • Functional Groups: The presence of the benzoate and piperidine functional groups allows for unique interactions with UV light.
  • Steric Effects: The bulky trimethyl groups enhance the compound's stability and reduce susceptibility to degradation.

Health and Safety Considerations

While (2,2,6-trimethyl-4-piperidyl) benzoate is effective in its applications, it’s essential to consider safety protocols:

  • Safety Data: Always refer to the Safety Data Sheets (SDS) for handling to minimize exposure risks.
  • Regulatory Status: Evaluated by various health and environmental regulatory agencies, ensuring it meets safety standards for consumer use.

In summary, (2,2,6-trimethyl-4-piperidyl) benzoate stands out as a versatile compound with significant roles across multiple industries. As research continues, more advanced applications and methods of utilization may emerge, reinforcing its importance in modern chemistry.

Synonyms
BETA-EUCAINE
Betacain
Eucain B
500-34-5
(2,2,6-TRIMETHYL-4-PIPERIDYL) BENZOATE
(2,2,6-trimethylpiperidin-4-yl) benzoate
Eucain
Oprea1_276630
Oprea1_675869
SCHEMBL420179
CHEMBL4800463
CHEBI:35068
DTXSID70862056
NSC49860
WLN: T6MTJ B1 B1 DOVR& F1
2,2,6-Trimethyl-4-piperidinyl benzoate #
4-Piperidinol,2,6-trimethyl-, benzoate (ester)
Q27116398
4-Piperidinol,2,6-trimethyl-, benzoate (ester), stereoisomer