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Isovaleramide Epoxide

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Identification
Molecular formula
C9H17NO2
CAS number
101-88-7
IUPAC name
2-ethyl-3-propyl-oxirane-2-carboxamide
State
State

At room temperature, isovaleramide epoxide is in the liquid state.

Melting point (Celsius)
-85.00
Melting point (Kelvin)
188.15
Boiling point (Celsius)
150.00
Boiling point (Kelvin)
423.15
General information
Molecular weight
141.21g/mol
Molar mass
141.2090g/mol
Density
0.9154g/cm3
Appearence

Isovaleramide epoxide is a colorless liquid at room temperature. It is typically clear and may have a faint odor characteristic of epoxides.

Comment on solubility

Solubility of 2-ethyl-3-propyl-oxirane-2-carboxamide

The solubility of the compound 2-ethyl-3-propyl-oxirane-2-carboxamide can be influenced by several factors due to its unique molecular structure. Here are some key points to consider:

  • Polarity: The presence of the carboxamide functional group contributes to increased polarity, which typically enhances solubility in polar solvents such as water.
  • Hydrophobic Chains: The ethyl and propyl groups introduce hydrophobic characteristics, which may hinder solubility in polar media.
  • Solvent Compatibility: This compound may have better solubility in organic solvents like ethanol and acetone compared to water.
  • Temperature Effects: Increasing temperature often results in improved solubility for many organic compounds, potentially aiding the dissolution process.

In summary, while 2-ethyl-3-propyl-oxirane-2-carboxamide displays a complex interaction of hydrophilic and hydrophobic features, predicting its solubility requires careful consideration of the solvent environment and conditions. Therefore, it is advisable to conduct empirical solubility tests to ascertain practical solubility characteristics.

Interesting facts

Exploring 2-ethyl-3-propyl-oxirane-2-carboxamide

2-ethyl-3-propyl-oxirane-2-carboxamide, also known as a type of substituted oxirane, presents a fascinating profile in the realm of organic chemistry. This compound belongs to the family of epoxides, which are characterized by a three-membered cyclic ether. Here are some intriguing aspects of this compound:

  • Structural Diversity: The incorporation of both ethyl and propyl groups contributes to the structural diversity of this compound, offering unique reactivity patterns and physical properties.
  • Reactivity: As an oxirane, it is highly reactive, especially in nucleophilic substitution reactions. This makes it valuable in the synthesis of complex organic molecules.
  • Applications: Compounds like this one are often utilized in the production of polymers, serving as intermediates in the manufacture of numerous commercial products, such as adhesives and coatings.
  • Biological Importance: The carboxamide functional group can enhance the compound's biological activity, potentially leading to applications in pharmaceuticals and agrochemicals.
  • Environmental Impact: Understanding the behavior and stability of substituted oxiranes in the environment is crucial. Their potential for degradation can influence ecological assessments and regulatory measures.

As you delve deeper into the world of 2-ethyl-3-propyl-oxirane-2-carboxamide, you'll discover the critical balance between its reactivity and stability, exemplifying the beauty of organic synthesis and its applications in real-world scenarios. Remember, in the field of chemistry, every compound tells a story of its own!

Synonyms
Oxanamide
Oxanamida
Oxanamidum
126-93-2
2-ethyl-3-propyloxirane-2-carboxamide
Oxanamide [INN]
2,3-Epoxy-2-ethylhexanamide
050271194T
Quiactin
Oxanamidum [INN-Latin]
Oxanamida [INN-Spanish]
2-Ethyl-3-propylglycidamide
Glycidamide, 2-ethyl-3-propyl-
BRN 0119679
2-Ethyl-3-propyl-2,3-epoxypropionamide
HEXANAMIDE, 2,3-EPOXY-2-ETHYL-
OXANAMIDE [MI]
OXANAMIDE QUINACTIN
RefChem:1094000
SCHEMBL546912
CHEMBL2105297
DTXSID50925350
CHEBI:134786
WBLPIVIXQOFTPQ-UHFFFAOYSA-N
UNII-050271194T
AKOS006273432
2-Ethyl-3-propyloxirane-2-carboximidic acid
NS00126229
4-18-00-03857 (Beilstein Handbook Reference)
Q7115104