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Vinyl isobutyrate

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Identification
Molecular formula
C6H10O2
CAS number
3306-88-5
IUPAC name
1-methylprop-1-enyl acetate
State
State

At room temperature, vinyl isobutyrate is in a liquid state.

Melting point (Celsius)
-107.00
Melting point (Kelvin)
166.15
Boiling point (Celsius)
96.00
Boiling point (Kelvin)
369.15
General information
Molecular weight
114.14g/mol
Molar mass
128.1710g/mol
Density
0.8770g/cm3
Appearence

Vinyl isobutyrate is a colorless liquid with a faint fruity odor. Its appearance is typically clear and free from any suspended particles.

Comment on solubility

Solubility of 1-methylprop-1-enyl acetate

1-methylprop-1-enyl acetate, with the chemical formula C5H8O2, exhibits notable solubility characteristics that are important for various applications. Here are some key points regarding its solubility:

  • Solubility in water: 1-methylprop-1-enyl acetate is expected to have limited solubility in water. Generally, compounds with non-polar hydrocarbon chains tend to be hydrophobic.
  • Solubility in organic solvents: This compound is more soluble in organic solvents such as ethanol and ether. The presence of the acetate group enhances compatibility with polar solvents, providing greater solubility compared to purely hydrocarbon substances.
  • Temperature effects: Like many organic esters, the solubility can increase with temperature. Higher temperatures can promote better solvation and dissolution in solvents.

In summary, while 1-methylprop-1-enyl acetate is not highly soluble in water, it demonstrates significant solubility in organic solvents. This characteristic makes it a valuable compound in both laboratory and industrial contexts, where appropriate solvent choice is crucial for efficient use.

Interesting facts

Interesting Facts About 1-Methylprop-1-enyl Acetate

1-Methylprop-1-enyl acetate, commonly known in the fragrance industry for its delightful aroma, has several fascinating characteristics that make it a compound of interest in both scientific and commercial contexts.

  • Natural Presence: This compound is found in various essential oils, contributing to the characteristic scents of certain fruits and flowers. Its fruity aroma often resembles that of ripe apples and other sweet fruits.
  • Synthesis: The synthesis of 1-methylprop-1-enyl acetate can be performed through esterification reactions, typically involving acetic acid and an appropriate alcohol, showcasing the versatility of organic reactions.
  • Applications: It is widely used in the perfume and cosmetics industry as a flavoring agent. Additionally, its pleasant smell makes it a popular choice for use in air fresheners and scented candles.
  • Reactivity: 1-Methylprop-1-enyl acetate can participate in various chemical reactions, including hydrolysis and polymerization, making it a valuable substrate for organic synthesis and research.
  • Safety Profile: While generally recognized as safe when used correctly, it's important to handle this compound with care, as with all chemical substances. Always consult safety data sheets when working in a laboratory setting.

This compound not only plays a significant role in enhancing fragrances but also serves as an excellent example of the intersection between chemistry and sensory experience. As a scent compound, it offers a glimpse into the intricate world of organic chemistry and its real-world applications.

Synonyms
2-Buten-2-ol, 2-acetate
2-ACETOXY-2-BUTENE
SCHEMBL530968
OOCFREXEVDCHGU-UHFFFAOYSA-N
DTXSID501313485
NS00044207