CAS 928-95-0

trans-2-Hexen-1-ol

Description:

Trans-2-Hexen-1-ol is an organic compound characterized by its structure as an unsaturated alcohol. It features a six-carbon chain with a double bond between the second and third carbon atoms, and a hydroxyl (-OH) group attached to the first carbon. This configuration gives it the "trans" designation, indicating that the substituents around the double bond are on opposite sides, which influences its physical and chemical properties. Trans-2-Hexen-1-ol is typically a colorless liquid with a distinctive odor, often described as grassy or green, making it of interest in the flavor and fragrance industries. It is soluble in water and organic solvents, reflecting its alcohol nature. The compound can participate in various chemical reactions, including oxidation and esterification, and is used as an intermediate in the synthesis of other organic compounds. Additionally, it has applications in the production of pheromones and as a potential bioactive compound in agricultural settings. Safety data indicates that it should be handled with care, as with many organic solvents.

Formula: C₆H₁₂O

InChI: InChI=1S/C6H12O/c1-2-3-4-5-6-7/h4-5,7H,2-3,6H2,1H3/b5-4+

InChI key: InChIKey=ZCHHRLHTBGRGOT-SNAWJCMRSA-N

SMILES: C(\CCC)=C/CO

Synonyms:

• (2E)-2-Hexen-1-ol
• (E)-2-Hexen-1-ol
• (E)-2-Hexene-1-ol
• (E)-2-Hexenol
• (E)-Hex-2-en-1-ol
• 1-Hydroxy-2-trans-hexene
• 2-Hexen-1-ol, (E)-
• 2-Hexen-1-ol, trans-
• Hex-2-En-1-Ol, (E)-
• Hex-2-Enol, Trans-
• Trans-2-Hexen-1-Ol
• Trans-Hex-2-Ene-1-Ol
• n-Hex-trans-2-en-1-ol
• trans-2-Hexene-1-ol
• trans-2-Hexenol
• trans-4-Ethyl-2-buten-1-ol
• trans-Hex-2-en-1-ol
• BRN 1719709
• UNII-BVP79C4821
• AI3-34792
• trans-2-Hexenol (natural)
• 4-01-00-02138 (Beilstein Handbook Reference)
• 2-Hexen-1-ol, (2E)-
• (2E)-hex-2-en-1-ol
• Hex-2(E)-enol
• TRANS-2-HEXEN-1-YL ALCOHOL
• trans-2-hexen-1-o
• 2-hexen-1-0l
• TRANS-1-HYDROXY-2-HEXENE
• T2 HEXENOL
• (E)-hex-2-enol
• 2-HEXENOL
• HEXEN-1-OL,TRANS-2-
• 2-(E)-hexenol
• FEMA 2562

trans-2-Hexen-1-ol

CAS: 928-95-0

Formula: C₆H₁₂O

Purity: >95.0%(GC)

Color and Shape: Colorless to Almost colorless clear liquid

Molecular weight: 100.16

Ref: 3B-H0346

trans-2-Hexen-1-ol, 97%

CAS: 928-95-0

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₆H₁₂O

Purity: 97%

Color and Shape: Liquid, Clear colorless

Molecular weight: 100.16

Ref: 02-A13272

2-HEXEN-1-OL, (2E)-

CAS: 928-95-0

Formula: C₆H₁₂O

Purity: 98%

Color and Shape: Liquid

Molecular weight: 100.1589

Ref: IN-DA00GRKS

Trans-2-Hexen-1-ol

CAS: 928-95-0

Trans-2-Hexen-1-ol

Purity: 97%

Molecular weight: 100.16g/mol

Ref: 54-OR1015261

trans-2-Hexen-1-ol

CAS: 928-95-0

trans-2-Hexen-1-ol is an alcohol compound exhibiting antimicrobial activity against Fusarium verticillioides.

Formula: C₆H₁₂O

Purity: 99%

Color and Shape: Solid

Molecular weight: 100.16

Ref: TM-TN5162

trans-2-Hexen-1-ol

CAS: 928-95-0

Formula: C₆H₁₂O

Molecular weight: 100.16

Ref: 7W-GL8577

trans-2-Hexen-1-ol

CAS: 928-95-0

Formula: C₆H₁₂O

Purity: 98%

Color and Shape: No data available.

Molecular weight: 100.161

Ref: 10-F544691

trans-2-Hexenol

CAS: 928-95-0

Trans-2-Hexenol is a naturally occurring unsaturated alkyl ester that is found in various plants and fruits. It has been shown to have an inhibitory effect on the growth of receptor cells and can also be used as a preservative in cosmetics. Trans-2-Hexenol binds to p-hydroxybenzoic acid, which is a major metabolite of salicylic acid, and prevents it from binding to the surface methodology. This helps prevent the formation of an anion radical scavenging system, which would otherwise cause damage to cell membranes. Trans-2-Hexenol also binds with allyl carbonate and enzyme hydrolysis, inhibiting population growth. The trigeminal nerve senses trans-2-hexenol and activates the weevil’s fatty acid metabolism, leading to allylation reactions that release isovaleric acid.

Formula: C₆H₁₂O

Purity: Min. 95%

Molecular weight: 100.16 g/mol

Ref: 3D-FH01412