Skip to main content

(2-ethyl-3-propyl-oxiran-2-yl)methanol

ADVERTISEMENT
Identification
Molecular formula
C8H16O2
CAS number
13187-44-7
IUPAC name
(2-ethyl-3-propyl-oxiran-2-yl)methanol
State
State

This compound is typically a liquid at room temperature.

Melting point (Celsius)
-70.00
Melting point (Kelvin)
203.15
Boiling point (Celsius)
197.00
Boiling point (Kelvin)
470.15
General information
Molecular weight
130.19g/mol
Molar mass
130.1880g/mol
Density
1.0020g/cm3
Appearence

The compound (2-ethyl-3-propyl-oxiran-2-yl)methanol is a colorless liquid with a slight, sweet odor. It is clear and free from suspended particles.

Comment on solubility

Solubility of (2-ethyl-3-propyl-oxiran-2-yl)methanol

The solubility of a compound often plays a crucial role in its applications, and for (2-ethyl-3-propyl-oxiran-2-yl)methanol, several factors influence its behavior in various solvents.

  • Polar Solvents: Due to the alcohol functional group present in the compound, it is likely to exhibit solubility in polar solvents like water. Alcohol groups typically enhance solubility in polar media.
  • Non-Polar Solvents: Conversely, the hydrophobic ethyl and propyl substituents may limit solubility in non-polar solvents. Thus, while it could dissolve to some extent, the extent might not be significant.
  • Temperature Influence: Increased temperature generally improves solubility, especially in the case of organic compounds, so solubility might increase at higher temperatures.
  • pH Considerations: The pH of the solution can also affect solubility, particularly for alcohols; for instance, higher levels of acidity might lead to protonation reactions that could alter solubility characteristics.

In summary, while (2-ethyl-3-propyl-oxiran-2-yl)methanol is expected to be soluble in polar solvents, its solubility in non-polar solvents may be limited. Understanding these intricacies is vital for practical applications and further exploration.

Interesting facts

Interesting Facts about (2-ethyl-3-propyl-oxiran-2-yl)methanol

(2-ethyl-3-propyl-oxiran-2-yl)methanol, commonly referred to as an epoxide compound, holds a fascinating place in organic chemistry due to its unique structure and reactivity. This compound features an oxirane ring, a three-membered cyclic ether known for its strained bonds, which contribute to its high reactivity. Here are some intriguing aspects:

  • Reactive Nature: The presence of the epoxide ring makes (2-ethyl-3-propyl-oxiran-2-yl)methanol a versatile intermediate for various chemical reactions, including ring-opening reactions with nucleophiles. This makes it valuable in synthetic organic chemistry.
  • Applications in Synthesis: This compound acts as a key precursor in the formation of more complex molecules, including pharmaceuticals and agrochemicals. Its reactivity allows chemists to introduce functional groups efficiently.
  • Environmental Considerations: Epoxides, including (2-ethyl-3-propyl-oxiran-2-yl)methanol, can be subject to environmental scrutiny. Precaution is often taken regarding their stability and degradation pathways, as some epoxides are known to be toxic.
  • Biochemical Relevance: Compounds similar to this one can play a role in biological systems, serving as intermediates in the biosynthesis of natural products, influencing various metabolic pathways.

As highlighted in contemporary research, "the exploration of oxiranes continues to inspire novel approaches in chemical synthesis, allowing researchers to tap into the potential of these fascinating molecules."

In conclusion, (2-ethyl-3-propyl-oxiran-2-yl)methanol not only showcases the beauty of organic chemistry but also emphasizes the intricate relationship between structure and reactivity in chemical compounds.

Synonyms
78-72-8
(2-ethyl-3-propyloxiran-2-yl)methanol
2,3-Epoxy-2-ethyl hexanol
1-Hexanol, 2,3-epoxy-2-ethyl-
SCHEMBL8710726
2,3-epoxy-2-ethyl-1-hexanol
DTXSID50999258
VSHXAKJGKGGKKE-UHFFFAOYSA-N