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6-methylhept-1-ene

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Identification
Molecular formula
C8H16
CAS number
7632-19-9
IUPAC name
6-methylhept-1-ene
State
State

At room temperature, 6-methylhept-1-ene is in a liquid state. It is a relatively volatile hydrocarbon.

Melting point (Celsius)
-119.00
Melting point (Kelvin)
154.15
Boiling point (Celsius)
119.30
Boiling point (Kelvin)
392.45
General information
Molecular weight
112.21g/mol
Molar mass
112.2140g/mol
Density
0.7218g/cm3
Appearence

6-Methylhept-1-ene is a colorless liquid. It typically has a mild, recognizable hydrocarbon smell.

Comment on solubility

Solubility of 6-methylhept-1-ene

6-methylhept-1-ene, with the chemical formula C8H16, is an organic compound characterized by the presence of a double bond in its structure. As an alkene, its solubility properties are influenced by several factors:

  • Polarity: 6-methylhept-1-ene is a non-polar molecule due to its hydrocarbon structure, which limits its ability to interact with polar solvents.
  • Hydrophobic nature: Being a hydrocarbon, it is more soluble in non-polar solvents such as hexane or benzene, while exhibiting low solubility in polar solvents like water.
  • Temperature effects: Increased temperature can improve the solubility of organic compounds due to higher kinetic energy, which can facilitate the mixing of 6-methylhept-1-ene with other organic solvents.

In summary, it can be stated that "like dissolves like." Therefore, 6-methylhept-1-ene will generally be more soluble in non-polar solvents than in polar ones, making it suitable for use in various organic solvent applications.

Interesting facts

Interesting Facts About 6-Methylhept-1-ene

6-Methylhept-1-ene is a fascinating organic compound that falls under the category of alkenes, which are characterized by at least one carbon-carbon double bond. As a member of the heptene family, it plays a variety of roles in both synthetic and natural processes. Here are some intriguing aspects of this compound:

  • Structure and Isomerism: The structure of 6-methylhept-1-ene includes a branched chain that provides flexibility in terms of reactivity. With its double bond located at the first carbon, it demonstrates geometric (cis/trans) isomerism, which can significantly influence its chemical behavior.
  • Reactivity: This compound is known for its participation in various chemical reactions, including electrophilic addition, which can lead to the formation of alcohols, halides, and other derivatives. Its double bond makes it a versatile intermediate in organic synthesis.
  • Commercial Applications: 6-Methylhept-1-ene is not just a theoretical interest; it finds application in the production of specialty chemicals and polymers. For instance, it can be a precursor for more complex molecules used in manufacturing plastics and synthetic fibers.
  • Natural Occurrence: Interestingly, alkenes like 6-methylhept-1-ene can be found in various natural products, including some essential oils and pheromones, which serve unique biological purposes.
  • Research Potential: There is ongoing research into the applications of alkenes in medicinal chemistry. Compounds like 6-methylhept-1-ene can be studied for their potential therapeutic effects and as a part of drug formulation processes.

In summary, 6-methylhept-1-ene is more than just a simple hydrocarbon; it's a compound rich with chemical potential and applications. As chemists continue to explore its properties, we can look forward to discovering even more about its utility and role in various fields of science.

Synonyms
6-METHYL-1-HEPTENE
Isooctene
6-methylhept-1-ene
1-Heptene, 6-methyl-
11071-47-9
5026-76-6
Isooctenes
iso-octene
AI3-37712
EINECS 234-294-9
UN1216
EC 234-294-9
DTXSID30891923
AKOS006275654
LS-13499
DB-051747
Isooctenes [UN1216] [Flammable liquid]
NS00001781
EN300-7208907