2,4-Hexadien-1-ol
$320.00
CAS No.: 111-28-4
Catalog No.: 195003
Purity: 95%
MF: C6H10O
MW: 98.145
Storage: 2-8 degree Celsius
SMILES: C(C=CC=CC)O
Catalog No.: 195003
Purity: 95%
MF: C6H10O
MW: 98.145
Storage: 2-8 degree Celsius
SMILES: C(C=CC=CC)O
2,4-Hexadien-1-ol; CAS No.: 111-28-4; 2,4-Hexadien-1-ol. PROPERTIES: 2,4-Hexadien-1-ol is a clear to pale yellow liquid with a slightly fruity odor. Its molecular formula is C6H10O, and it has a molecular weight of approximately 98.14 g/mol. The substance exhibits a boiling point around 140-142 C at 760 mmHg and a density of about 0.9 g/cm? at 20 C. It is moderately soluble in water and miscible with most organic solvents such as ethanol and diethyl ether. The compound is sensitive to air and light, which can lead to gradual polymerization and color darkening. For proper storage, 2,4-hexadien-1-ol should be kept in tightly sealed containers made of amber glass or other light-resistant materials, stored in a cool, dry place away from direct sunlight and heat sources. The temperature should be maintained below 10 C if possible. Handling precautions include using personal protective equipment such as chemical-resistant gloves, safety goggles, and lab coats due to its potential to cause skin and eye irritation. Inhalation of vapors should be avoided as it may irritate respiratory passages. In case of contact, immediate rinsing with water and seeking medical attention if necessary is advised. APPLICATIONS: 2,4-Hexadien-1-ol serves as a valuable intermediate in organic synthesis, particularly in the preparation of vitamins and fragrances. It is utilized in the synthesis of vitamin E derivatives due to its conjugated diene structure, which allows for selective chemical modifications (Journal of Organic Chemistry). In the fragrance industry, it functions as a precursor to various aroma compounds, contributing to floral and fruity notes in perfumery formulations (Perfume & Flavourist). Additionally, it finds application in the production of specialty chemicals and research reagents, where its reactive diene system enables participation in Diels-Alder reactions and other cycloaddition processes, facilitating the construction of complex organic frameworks (Tetrahedron Letters).
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