Farnesyl acetate
Farnesyl acetate (CAS: 29548-30-9), with the molecular formula C17H28O2 and a molecular weight of 264.40 g/mol, is an organic ester. It serves as a valuable building block in chemical synthesis and is categorized under carbonyl compounds and esters. This compound is primarily utilized in research and development settings for the creation of more complex organic molecules.

Chemical Synthesis
Farnesyl acetate is employed as a key intermediate and building block in organic synthesis. Its ester functionality and isoprenoid chain make it suitable for constructing complex molecules in various research and industrial applications.
Organic Building Blocks
As an organic building block, this compound can be utilized in the development of novel compounds within academic and industrial research laboratories. Its specific structure allows for diverse synthetic pathways.
Research and Development
This chemical is often used in R&D settings for exploratory chemistry and the synthesis of potential new materials or active pharmaceutical ingredients. It falls within the C12 to C63 category of organic compounds.
| Molecular weight | 264.40 |
|---|---|
| Empirical formula | C17H28O2 |
| Grade | technical |
| Density | 0.91 g/mL at 20 °C(lit.) |
| Refractive index | n20/D 1.477 |
| Protective equipment | Eyeshields, Gloves |
|---|---|
| Flash point | 95 °C / 203 °F |
| Water hazard class (WGK, DE) | 2 |
Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is Farnesyl acetate used for?
+
Farnesyl acetate is primarily used as a building block and intermediate in organic synthesis and research and development applications.
What are the CAS number and molecular formula for Farnesyl acetate?
+
The CAS number for Farnesyl acetate is 29548-30-9, and its molecular formula is C17H28O2.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies Farnesyl acetate in a technical grade. We do not represent this product as meeting USP, BP, EP, or any pharmacopoeial standards.
What are the safety precautions for handling Farnesyl acetate?
+
Handle Farnesyl acetate with appropriate personal protective equipment, including eyeshields and gloves. It is classified under WGK Germany 2. Avoid exposure and follow standard laboratory safety procedures.
Is Farnesyl acetate a controlled substance?
+
Based on the provided data, Farnesyl acetate (CAS: 29548-30-9) is not indicated as a controlled substance.
How is Farnesyl acetate shipped and exported?
+
Tech Serve Solutions is a global supplier and exporter of fine chemicals, including Farnesyl acetate, adhering to all international shipping and export regulations.
How can I request a quote or sample of Farnesyl acetate?
+
To request a quote or sample of Farnesyl acetate, please contact our sales team through the website or directly via email or phone.
▶ Related products

1-(2-Fluorobenzyl)piperazine
C11H15FN2
Chemical Synthesis
1-(2-Fluorophenyl)biguanide hydrochloride
Chemical Synthesis

1-(2-Fluorophenyl)cyclopropanecarboxylic acid
C10H9FO2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine
C10H13FN2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine monohydrochloride
C10H13FN2 · HCl
Chemical Synthesis
1-(2-Furoyl)-1H-benzotriazole
C11H7N3O2
Chemical Synthesis
1-(2-Furoyl)piperazine
C9H12N2O2
Chemical Synthesis
1-(2-Hydroxy-5-methylphenyl)-3-phenyl-1,3-propanedione
Chemical Synthesis
▶ Explore more

3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis

3-Methyl-1,5-pentanediol
Chemical Synthesis

3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis