Trans-3-octene is an unsaturated hydrocarbon belonging to the alkene family, characterized by the presence of a double bond between the third and fourth carbon atoms in its linear chain. Its molecular formula is C8H16, indicating it has eight carbon atoms and sixteen hydrogen atoms. The "trans" configuration signifies that the substituents attached to the double bond are on opposite sides, which influences its physical properties and reactivity. Trans-3-octene is a colorless liquid at room temperature and has a distinctive odor. It is less dense than water and is insoluble in water but soluble in organic solvents. This compound is utilized in organic synthesis and can serve as an intermediate in the production of various chemicals. Additionally, its double bond makes it more reactive than saturated hydrocarbons, allowing it to participate in various addition reactions. Safety data indicates that it should be handled with care, as it may be flammable and irritate the skin and eyes.

trans-3-octene

14919-01-8: (3E)-3-Octene, (E)-3-Octene, 3-Octene, 3-Octene, (3E)-, 3-Octene, (E)-, NSC 95418, Oct-3-ene, γ-trans-Octene, trans-3-Octene

TRANS-3-OCTENE

Trans-3-Octene

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trans-3-Octene, 97%

3-Octene is an alkene with a hydroxy group and a hydrogen chloride. It is an organic acid with the chemical formula CH3CH=CH(OH)CH2Cl. 3-Octene is an isomer of octane, which has a methyl group instead of a hydroxy group. This compound can be synthesized from ethylbenzene by adding hydrogen chloride to the molecule. The reaction produces ethyl chloride and 3-octene. 3-Octene can also be produced by reacting benzaldehyde, acetone, and nitroethane in the presence of copper metal. 3-Octene has been studied for its synergistic effects on emissions with other compounds such as nitrogen atoms, chlorine, and copper complexes.

CAS 14919-01-8: trans-3-octene

TRANS-3-OCTENE

Ref: IN-DA003UXF

Trans-3-Octene

Ref: 10-F162402

trans-3-Octene, 97%

Ref: 02-043154

Trans-3-octene

Ref: 3D-FT178710

trans-3-Octene

Ref: 3B-O0134