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Peroxy-octanoic acid, 1,1-dimethylhexyl ester

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Identification
Molecular formula
C16H32O3
CAS number
26748-47-0
IUPAC name
octanoyl octaneperoxoate
State
State

This compound is typically found as a liquid at room temperature.

Melting point (Celsius)
-10.00
Melting point (Kelvin)
263.15
Boiling point (Celsius)
238.00
Boiling point (Kelvin)
511.15
General information
Molecular weight
288.51g/mol
Molar mass
230.3460g/mol
Density
0.8900g/cm3
Appearence

Peroxy-octanoic acid, 1,1-dimethylhexyl ester is a colorless liquid.

Comment on solubility

Solubility of Octanoyl Octaneperoxoate

Octanoyl octaneperoxoate, a unique compound, exhibits specific solubility characteristics that are of particular interest in various applications. Its solubility can be influenced by several factors:

  • Polarity: Being an organic compound, octanoyl octaneperoxoate tends to be more soluble in non-polar solvents. This is due to the long hydrocarbon chains present in its structure, which favor interactions with other non-polar molecules.
  • Solvent Compatibility: Common solvents that may dissolve octanoyl octaneperoxoate effectively include:
    • Hexane
    • Octane
    • Benzene
  • Temperature Effects: Generally, an increase in temperature can enhance the solubility of organic compounds as this promotes molecular movement, allowing more effective interactions between the solute and solvent molecules.

In summary, octanoyl octaneperoxoate is primarily soluble in non-polar organic solvents, making it essential to consider the solvation environment in experimental and practical applications. As always, careful handling and understanding of the conditions affecting solubility are key for optimal results.

Interesting facts

Interesting Facts about Octanoyl Octaneperoxoate

Octanoyl octaneperoxoate is a fascinating compound that plays a crucial role in the field of organic chemistry, particularly in the synthesis of various materials. Here are some intriguing facts about this unique compound:

  • Key Function: It is primarily used as an organic peroxide initiator, which means it can help in initiating polymerization reactions. This is invaluable in producing polymers, including plastics and resins.
  • Reactive Nature: Being a peroxide, octanoyl octaneperoxoate is known for its ability to release free radicals upon thermal decomposition. These free radicals can start chain reactions that lead to the formation of new compounds.
  • Synthetic Applications: This compound is often utilized in the manufacturing of various synthetic fibers and elastomers, enhancing their performance properties.
  • Safety Precautions: Due to its reactive nature, handling octanoyl octaneperoxoate requires caution. It should be stored in a cool, dry place and away from incompatible materials to prevent unwanted reactions.
  • Environmental Considerations: The use of peroxy compounds, including octanoyl octaneperoxoate, is a topic of interest in environmental chemistry. Researchers are continuously exploring ways to minimize their environmental impact.

In summary, octanoyl octaneperoxoate serves as an essential player in the synthesis and production of polymers, opening doors for advancements in material science while also presenting challenges in terms of safety and environmental stewardship.

Synonyms
Dioctanoyl peroxide
762-16-3
Octanoyl peroxide
Peroxide, bis(1-oxooctyl)
CAPRYLYL PEROXIDE
Caprolyl peroxide
Dicaprylyl peroxide
Capryl peroxide
H709TZ1FAF
PERKADOX SE
HSDB 2752
EINECS 212-094-2
CAPRYLYL PEROXIDE [HSDB]
DTXSID0061086
N-OCTANOYL PEROXIDE, (TECHNICALLY PURE)
N-OCTANOYL PEROXIDE, [TECHNICALLY PURE]
di-n-octanoyl peroxide
PEROYL O
PERKADOX SE 8
Peroxide, bis(1oxooctyl)
DTXCID7047855
212-094-2
octanoyl octaneperoxoate
UNII-H709TZ1FAF
SCHEMBL24125
AKOS028108376
NS00020542
A11799
A865536
Q27279717