≥97%, stabilized with BHT,mixture of isomers for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
application：
Farnesalacetone is an intermediate in the synthesis of intermediates in the biosynthesis of carotenoids.
| Pubchem Sid | 488183459 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488183459 |
| Sorrisi canonici | CC(=CCCC(=CCCC(=CCCC(=O)C)C)C)C |
| IUPAC Name | 6,10,14-trimethylpentadeca-5,9,13-trien-2-one |
| InChIKey | LTUMRKDLVGQMJU-UHFFFAOYSA-N |
| INCHI | 1S/C18H30O/c1-15(2)9-6-10-16(3)11-7-12-17(4)13-8-14-18(5)19/h9,11,13H,6-8,10,12,14H2,1-5H3 |
| Isomeri SMILES | CC(=CCCC(=CCCC(=CCCC(=O)C)C)C)C |
| Peso molecolare | 262.43 |
| Beilstein | 1781239 |
| Reaxy-Rn | 1781239 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1781239&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Classe | Prenol lipids |
| Subclass | Diterpenoids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Acyclic diterpenoids |
| Alternative Parents | Ketones Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Acyclic diterpenoid - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as acyclic diterpenoids. These are diterpenoids (compounds made of four consecutive isoprene units) that do not contain a cycle. |
| External Descriptors | a terpenoid derivative |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
 C2212052 | Certificate of Analysis | Sep 09, 2025 | F136033 |
| K2109337 | Certificate of Analysis | May 09, 2025 | F136033 |
| D2318776 | Certificate of Analysis | Feb 06, 2025 | F136033 |
| D2318801 | Certificate of Analysis | Feb 06, 2025 | F136033 |
| D2318813 | Certificate of Analysis | Feb 06, 2025 | F136033 |
| F2610341 | Certificate of Analysis | Jul 06, 2024 | F136033 |
| I2207614 | Certificate of Analysis | Jun 17, 2024 | F136033 |
| I2207609 | Certificate of Analysis | Jun 17, 2024 | F136033 |
| C2212030 | Certificate of Analysis | Feb 23, 2022 | F136033 |
| Sensibilità | Light sensitive |
|---|---|
| Indice di rifrazione | 1.481 |
| Punto di infiammabilità (°F) | 230°F |
| Punto di infiammabilità (°C) | >110℃ |
| Peso molecolare | 262.400 g/mol |
| XLogP3 | 5.600 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 9 |
| Exact Mass | 262.23 Da |
| Monoisotopic Mass | 262.23 Da |
| Topological Polar Surface Area | 17.100 Ų |
| Heavy Atom Count | 19 |
| Formal Charge | 0 |
| Complexity | 352.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 2 |
| The total count of all stereochemical bonds | 2 |
| Covalently-Bonded Unit Count | 1 |
