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Methyl methacrylate

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Identification
Molecular formula
C5H8O2
CAS number
80-62-6
IUPAC name
methyl 2-methylbut-2-enoate
State
State

At room temperature, methyl methacrylate is in the liquid state.

Melting point (Celsius)
-48.20
Melting point (Kelvin)
224.95
Boiling point (Celsius)
101.00
Boiling point (Kelvin)
374.15
General information
Molecular weight
100.12g/mol
Molar mass
100.1160g/mol
Density
0.9170g/cm3
Appearence

Methyl methacrylate is a clear, colorless liquid with a distinctive fruity odor.

Comment on solubility

Solubility of Methyl 2-methylbut-2-enoate

Methyl 2-methylbut-2-enoate, with a chemical formula of C6H10O2, exhibits notable solubility characteristics that are important for various applications. Here are some key points regarding its solubility:

  • Solvent Interaction: This compound is generally soluble in organic solvents such as ethanol and ether, due to its relatively non-polar nature.
  • Water Solubility: Methyl 2-methylbut-2-enoate has limited solubility in water. This is attributed to its hydrophobic carbon chain, which is less favorable for interaction with polar water molecules.
  • Temperature Effects: Like many organic compounds, solubility can be influenced by temperature. Increased temperature typically enhances the solubility of organic compounds in organic solvents.

In summary, while methyl 2-methylbut-2-enoate is soluble in non-polar organic solvents, its solubility in water is quite limited. This solubility behavior is crucial for its potential uses in chemical synthesis and formulations.

Interesting facts

Interesting Facts about Methyl 2-Methylbut-2-enoate

Methyl 2-methylbut-2-enoate, often referred to in the lab by its more manageable name, is an intriguing compound in the world of organic chemistry. Here are some captivating insights:

  • Functional Group: This compound contains an ester functional group, which is pivotal in the formation of many natural products as well as synthetic materials.
  • Reactivity: Methyl 2-methylbut-2-enoate can participate in various chemical reactions, including nucleophilic addition and transesterification, making it a valuable intermediate in organic synthesis.
  • Scented Chemistry: Compounds like methyl 2-methylbut-2-enoate often have fruity aromas, contributing to their use in the fragrance and flavor industry. They can mimic the scent of various fruits, which makes them popular in formulations.
  • Biochemical Significance: Ester derivatives are often involved in biological systems, where they may play roles in metabolism and the formation of biomolecules.
  • Applications: This compound finds its utility not only in the laboratory but also in industries that require high-performance materials, such as polymers and coatings.
  • Research Potential: Due to its structural characteristics, methyl 2-methylbut-2-enoate is often studied for its properties in reaction mechanisms, providing insights into reaction pathways that are crucial for the advancement of chemical knowledge.

As a chemistry aficionado, studying compounds like methyl 2-methylbut-2-enoate can unveil the creativity and complexity inherent in the molecular world. This compound exemplifies how organic chemistry can interconnect with various fields, from industrial applications to nature's own designs.

Synonyms
methyl 2-methylbut-2-enoate
methyl (2Z)-2-methylbut-2-enoate
2-Butenoic acid, 2-methyl-, methyl ester, (2Z)-
DTXSID20863917
2-Methyl-2-butenoic acid methyl ester
DB-053406
DB-182395
NS00088633