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3-Methylhept-1-ene

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Identification
Molecular formula
C8H16
CAS number
15990-43-9
IUPAC name
3-methylhept-1-ene
State
State

At room temperature, 3-Methylhept-1-ene exists as a liquid. It does not solidify easily and remains in the liquid state even at relatively low temperatures.

Melting point (Celsius)
-118.40
Melting point (Kelvin)
154.75
Boiling point (Celsius)
119.80
Boiling point (Kelvin)
392.95
General information
Molecular weight
112.21g/mol
Molar mass
112.2120g/mol
Density
0.7239g/cm3
Appearence

3-Methylhept-1-ene is a colorless liquid with a faint, gasoline-like odor. It is typically clear and free-flowing.

Comment on solubility

Solubility of 3-methylhept-1-ene

3-methylhept-1-ene, with the chemical formula C8H16, is a branched alkene that exhibits unique solubility characteristics. As a hydrocarbon, it is primarily nonpolar, which significantly influences its solubility behavior in various solvents.

  • Solubility in Water: Due to its nonpolar nature, 3-methylhept-1-ene is insoluble in water. Water is a polar solvent, and nonpolar compounds do not mix well with polar solvents, an observation encapsulated by the phrase "like dissolves like."
  • Solubility in Organic Solvents: Conversely, 3-methylhept-1-ene is soluble in a variety of organic solvents. This includes solvents such as:
    • Hexane
    • Ether
    • Acetone
    These solvents are nonpolar or weakly polar, allowing 3-methylhept-1-ene to mix readily with them.

In summary, the solubility of 3-methylhept-1-ene is defined by its nonpolar characteristics, making it incompatible with polar solvents like water, while being highly soluble in nonpolar organic solvents. Understanding these properties is crucial for applications in chemical synthesis and industrial processes.

Interesting facts

Interesting Facts About 3-Methylhept-1-ene

3-Methylhept-1-ene is an intriguing hydrocarbon that belongs to the family of alkenes, characterized by its double bond which plays a crucial role in its reactivity and applications. As a member of the heptene series, this compound is notable for its branched structure that contributes to its unique properties, making it a point of interest for chemists and industry practitioners alike.

Key Characteristics

  • Unsaturated Hydrocarbon: The presence of a double bond between carbon atoms allows for addition reactions, making 3-methylhept-1-ene versatile in organic synthesis.
  • Isomerism: This compound exists in various isomeric forms, highlighting the rich diversity of organic molecules and providing ample opportunities for research and application.
  • Industrial Significance: 3-Methylhept-1-ene is utilized as an intermediate in the production of various chemical compounds, serving as a building block for more complex molecules.

Applications and Uses

  • Synthesis: It is often used in the synthesis of alcohols, polymers, and other organic chemicals.
  • Research: Its double bond allows chemists to study reaction mechanisms and the behavior of alkenes in different conditions.

In the words of famous chemist Linus Pauling, "Chemistry is the science of matter, and life is a matter of chemistry." The study of compounds like 3-methylhept-1-ene certainly embodies this philosophy as they bridge the gap between simple molecular components and complex chemical behaviors.

As we continue to explore the world of organic chemistry, understanding the properties and applications of 3-methylhept-1-ene not only enhances our knowledge of hydrocarbons but also inspires innovations in materials science and synthetic chemistry.

Synonyms
3-METHYL-1-HEPTENE
3-Methylhept-1-ene
1-Heptene, 3-methyl-
EINECS 225-372-3
DTXSID50871101
3Methyl1heptene
DTXCID50818773
225-372-3
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4810-09-7
3-methyl-hept-1-ene
CHEBI:88860
LMFA11000592
AKOS006271536
NS00047207
Q27160866