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Glycidyl 2,2-dimethyloctanoate

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Identification
Molecular formula
C13H24O3
CAS number
72898-57-4
IUPAC name
oxiran-2-ylmethyl 2,2-dimethyloctanoate
State
State

At room temperature, Glycidyl 2,2-dimethyloctanoate exists as a liquid. It remains in liquid form in typical environmental conditions suitable for room temperature storage.

Melting point (Celsius)
-54.00
Melting point (Kelvin)
219.15
Boiling point (Celsius)
300.50
Boiling point (Kelvin)
573.65
General information
Molecular weight
228.33g/mol
Molar mass
228.3200g/mol
Density
0.9430g/cm3
Appearence

Glycidyl 2,2-dimethyloctanoate is typically a colorless liquid. It is commonly used in the formulation of epoxy resins where its appearance is not very distinct from other glycidyl esters.

Comment on solubility

Solubility of Oxiran-2-ylmethyl 2,2-dimethyloctanoate

Oxiran-2-ylmethyl 2,2-dimethyloctanoate exhibits unique solubility characteristics due to its chemical structure. The compound is primarily characterized by the presence of an epoxide ring and an ester functional group, influencing its interaction with various solvents.

Generally, the solubility of this compound can be summarized as follows:

  • Polar Solvents: Oxiran-2-ylmethyl 2,2-dimethyloctanoate shows moderate solubility in polar solvents such as water and methanol. The ability to form hydrogen bonds due to the polar nature of the ester group plays a crucial role in this solubility.
  • Non-Polar Solvents: It is more soluble in non-polar solvents like hexane or benzene because of its hydrocarbon tail, which tends to be hydrophobic.
  • Temperature Dependency: Like many organic compounds, its solubility may increase with an increase in temperature, allowing for a higher degree of dissolution in solvents.

In conclusion, the solubility profile of oxiran-2-ylmethyl 2,2-dimethyloctanoate is influenced by both its functional groups and the nature of the solvent. Understanding these properties is essential for applications in synthesis and formulation processes. To quote an old saying: "The solution to your problems often lies in the right solvent."

Interesting facts

Interesting Facts about Oxiran-2-ylmethyl 2,2-Dimethyloctanoate

Oxiran-2-ylmethyl 2,2-dimethyloctanoate is a fascinating compound that piques the interest of chemists and researchers due to its unique structure and potential applications. Here are some intriguing insights:

  • Functional Groups: This compound contains an oxirane (epoxide) functional group, which is characterized by its three-membered cyclic ether structure. Epoxides are known for their reactivity and are commonly used as intermediates in the synthesis of various chemicals.
  • Esters and Their Importance: As an ester, oxiran-2-ylmethyl 2,2-dimethyloctanoate is an important class of compounds in organic chemistry. Esters are often utilized in the production of fragrances, flavors, and as influential solvents.
  • Applications in Synthesis: The presence of both an epoxide and an ester functional group makes this compound a valuable building block in organic synthesis, allowing for versatile reactions such as ring-opening and esterification.
  • Potential Biological Activity: Compounds containing epoxide groups have been studied for their potential biological activities, including antimicrobial and anticancer properties, making research into oxiran-2-ylmethyl 2,2-dimethyloctanoate particularly intriguing.
  • Environmental Considerations: The synthetic pathways and degradation of such compounds are of interest to environmental chemists, given the burgeoning concerns over biodegradability and ecotoxicity.

In conclusion, oxiran-2-ylmethyl 2,2-dimethyloctanoate embodies the complexity and versatility that organic chemistry offers. Its unique structural features and potential applications continue to inspire further exploration and investigation in scientific research.

Synonyms
Glycidyl neodecanoate
Glydexx N 10
Neodecanoic acid, 2,3-epoxypropyl ester
1-Propanol, 2,3-epoxy-, neodecanoate
5V72X484L7
Neodecanoic acid, 2-oxiranylmethyl ester
RefChem:1085946
DTXSID8025705
26761-45-5
Neodecanoic acid, oxiranylmethyl ester
oxiran-2-ylmethyl 2,2-dimethyloctanoate
52636-92-7
DTXSID20275056
Cardura E 10
Cardura E 10P
Cardura E 10S
Epoxide 248
CCRIS 2627
Glycidyl ester of neodecanoic acid
EINECS 247-979-2
CARDURA E-10
SCHEMBL284419
Glycidyl 2,2-dimethyloctanoate
UNII-5V72X484L7
NS00073841
EC 247-979-2
Q27262920
neodecanoic acid, oxiranylmethyl ester;oxiran-2-ylmethyl 2,2-dimethyloctanoate;neodecanoic acid, oxiranylmethyl ester oxiran-2-ylmethyl 2,2-dimethyloctanoate