CAS 13019-22-2
:9-Decen-1-ol
Description:
9-Decen-1-ol is an unsaturated fatty alcohol characterized by a long carbon chain with a double bond located at the ninth carbon from the hydroxyl group. Its molecular formula is C10H20O, indicating it contains ten carbon atoms, twenty hydrogen atoms, and one oxygen atom. This compound is typically a colorless to pale yellow liquid with a characteristic fatty odor. It is soluble in organic solvents but has limited solubility in water due to its hydrophobic carbon chain. 9-Decen-1-ol is known for its applications in the fragrance and flavor industry, as well as in the production of surfactants and emulsifiers. Additionally, it can serve as a precursor in organic synthesis, particularly in the formation of other chemical compounds. The presence of the double bond contributes to its reactivity, allowing it to participate in various chemical reactions, including oxidation and polymerization. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.
Formula:C10H20O
InChI:InChI=1S/C10H20O/c1-2-3-4-5-6-7-8-9-10-11/h2,11H,1,3-10H2
InChI key:InChIKey=QGFSQVPRCWJZQK-UHFFFAOYSA-N
SMILES:C(CCCC=C)CCCCO
Synonyms:- 9-Decenol
- 9-Decenol-1
- Dec-9-En-1-Ol
- Decenoltech
- Decylenic alcohol
- NSC 103158
- Rosalva
- Trepanol
- ω-Decen-1-ol
- 9-Decen-1-ol
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Found 9 products.
9-Decen-1-ol
CAS:Formula:C10H20OPurity:>97.0%(GC)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:156.279-Decen-1-ol, 90+%
CAS:<p>It finds it uses in a wide range of fragrances, especially in fine fragrances and soaps, in floral, rose petal or herbal fragrances. 9-Decen-1-ol is used in the preparation of semifluorinated acids required for the synthesis of poly(styrene-b-semi fluorinated isoprene) block copolymers with -CF2H-te</p>Formula:C10H20OPurity:90+%Color and Shape:Clear colorless to pale yellow, LiquidMolecular weight:156.27Dec-9-en-1-ol
CAS:<p>Dec-9-en-1-ol (9-DECEN-1-OL) is an intermediate in synthetic rubber and is involved in the synthesis of polymers that can be used as energy sources.</p>Formula:C10H20OPurity:99.56%Color and Shape:SolidMolecular weight:156.279-Decen-1-ol
CAS:Controlled Product<p>Stability Light Sensitive<br>Applications 9-Decen-1-ol can be used to synthesize terminal olefins or generate epoxides.<br>References Blackwell, H. E., et al., J. Am. Chem. Soc. 122, 58 (2000); Coperet, C., et al.: Chem. Commun 16, 1565 (1997)<br></p>Formula:C10H20OColor and Shape:NeatMolecular weight:156.279-Decen-1-ol
CAS:<p>9-Decen-1-ol is an acyl chain that contains a hydroxyl group. It is a chemical precursor to the synthesis of long-chain fatty acids and other biologically important lipids. 9-Decen-1-ol is also used as a solid catalyst in organic synthesis reactions, such as the reaction mechanism for hydrochloric acid and fatty acids. The expression plasmid containing the gene for 9-decen-1-ol was introduced into Escherichia coli cells using cationic surfactant to create an E. coli strain that produces this chemical compound. This synthetic pathway has been shown to be stable in both water vapor and cell culture conditions. It also binds odorants, which may contribute its odorant binding properties. Intracellular calcium concentration increases when 9-decen-1-ol binds with G protein coupled receptors, leading to cellular activation of phospholipase A2 and increased free arachidonic acid release from membrane phosph</p>Formula:C10H20OPurity:Min. 95%Molecular weight:156.27 g/mol
