CAS 10276-85-4

Benzyl octanoate

Description:

Benzyl octanoate, with the CAS number 10276-85-4, is an ester formed from the reaction of benzyl alcohol and octanoic acid. It is typically a colorless to pale yellow liquid with a pleasant, fruity odor, making it useful in the fragrance and flavoring industries. The compound is characterized by its relatively low solubility in water, but it is soluble in organic solvents such as ethanol and ether. Benzyl octanoate has a moderate boiling point and a low vapor pressure, indicating that it is not highly volatile. Its chemical structure features a benzyl group attached to an octanoate moiety, which contributes to its properties. This compound is often used as a flavoring agent in food products and as a fragrance component in cosmetics and personal care items. Additionally, it may have applications in the production of various chemical intermediates. Safety data suggests that it should be handled with care, as with many organic compounds, to avoid potential irritation or adverse effects.

Formula: C₁₅H₂₂O₂

InChI: InChI=1S/C15H22O2/c1-2-3-4-5-9-12-15(16)17-13-14-10-7-6-8-11-14/h6-8,10-11H,2-5,9,12-13H2,1H3

InChI key: InChIKey=MWQWCHLIPMDVLS-UHFFFAOYSA-N

SMILES: C(OC(CCCCCCC)=O)C1=CC=CC=C1

Synonyms:

• Ai3-30977
• Benzyl caprylate
• Caprylic acid, benzyl ester
• NSC 23754
• Octanoic acid, benzyl ester
• Octanoic acid, phenylmethyl ester
• Phenylmethyl octanoate
• Benzyl octanoate

Benzyl Octanoate

CAS: 10276-85-4

Formula: C₁₅H₂₂O₂

Purity: >95.0%(GC)

Color and Shape: Colorless to Light yellow to Light orange clear liquid

Molecular weight: 234.34

Ref: 3B-B6116

Octanoic acid, phenylmethyl ester

CAS: 10276-85-4

Formula: C₁₅H₂₂O₂

Purity: 99%

Molecular weight: 234.3340

Ref: IN-DA0008B7

Benzyl Octanoate

CAS: 10276-85-4

Benzyl Octanoate

Purity: 99%

Molecular weight: 234.33g/mol

Ref: 54-OR1023561

Benzyl caprylate

CAS: 10276-85-4

Benzyl caprylate is a synthetic, activated compound that inhibits HDACs. It has shown anticancer activity in vitro and in vivo and has been used as a radiosensitizer for cancer treatment. Benzyl caprylate is a divalent hydrocarbon that reacts with other compounds to form esters. The hydroxy group on the benzyl group can be replaced by an acetoxy group or a carboxylic acid group, forming benzoates or benzoic acids respectively. These reactions are often catalyzed by enzymes such as alcohol dehydrogenase, fatty acid synthase, and acyl-CoA synthetases. Benzyl caprylate also has antibacterial properties against Gram-positive bacteria such as Staphylococcus aureus and Enterococcus faecalis due to its ability to inhibit protein synthesis. The acidic ph of benzyl caprylate makes it useful for pharmaceutical preparations containing acidic ingredients such as drugs, vitamins, or nutrients.

Formula: C₁₅H₂₂O₂

Purity: Min. 95%

Molecular weight: 234.33 g/mol

Ref: 3D-KAA27685