CAS 13038-21-6

8-Nonen-1-ol

Description:

8-Nonen-1-ol, with the CAS number 13038-21-6, is a long-chain unsaturated alcohol characterized by its linear structure featuring a nine-carbon chain and a double bond located between the eighth and ninth carbon atoms. This compound is classified as a fatty alcohol and is known for its hydrophobic properties, making it soluble in organic solvents but less so in water. The presence of the hydroxyl (-OH) group imparts some polar characteristics, allowing it to participate in hydrogen bonding. 8-Nonen-1-ol is typically a colorless to pale yellow liquid with a characteristic odor, and it is used in various applications, including as a flavoring agent, fragrance component, and in the synthesis of surfactants and other chemical intermediates. Its unsaturation can also make it reactive in certain chemical processes, such as polymerization or oxidation. Safety data indicates that, like many alcohols, it should be handled with care to avoid irritation or adverse effects upon exposure.

Formula: C₉H₁₈O

InChI: InChI=1/C9H18O/c1-2-3-4-5-6-7-8-9-10/h2,10H,1,3-9H2

SMILES: C=CCCCCCCCO

Synonyms:

• Non-8-En-1-Ol

8-Nonen-1-ol

CAS: 13038-21-6

Formula: C₉H₁₈O

Purity: >98.0%(GC)

Color and Shape: Colorless to Almost colorless clear liquid

Molecular weight: 142.24

Ref: 3B-N0650

8-Nonen-1-ol

CAS: 13038-21-6

Formula: C₉H₁₈O

Purity: 98%

Color and Shape: Liquid

Molecular weight: 142.2386

Ref: IN-DA000UCC

8-Nonen-1-ol

CAS: 13038-21-6

8-Nonen-1-ol

Purity: 98%

Molecular weight: 142.24g/mol

Ref: 54-OR1024638

8-Nonen-1-ol

CAS: 13038-21-6

Purity: 98%+(GC-MS);RG

Molecular weight: 142.2420044

Ref: 10-F626278

8-Nonen-1-ol

CAS: 13038-21-6

8-Nonen-1-ol is a thioether with a long carbon chain. It is an active natural product that has been found in the rhizome of the plant "Eucalyptus" and has been shown to be effective against pest insects. 8-Nonen-1-ol is used as a solvent and intermediate in organic synthesis. It is also used as a reagent for dehydration reactions, such as the conversion of alcohols to ethers, or the conversion of esters to acids. The compound can be synthesized by reacting boron trifluoride etherate with long-chain fatty alcohols at temperatures below 0°C. 8-Nonen-1-ol also forms monolayers on silica gel and other solid supports. Acid catalysis can be used to break down these layers, releasing the compounds from the surface.

Formula: C₉H₁₈O

Purity: Min. 95%

Molecular weight: 142.24 g/mol

Ref: 3D-NAA03821