≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C Ships Wet ice 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.
trans,trans-Farnesyl acetate is one of the most odor-active or key compounds of Hyuganatsu aroma in Hyuganatsu (Citrus tamurana Hort. ex Tanaka) peel oil. Asymmetric dihydroxylation of trans,trans-farnesyl acetate using the new Sharpless′ ligand has been studied.
| Canonical Smiles | CC(=CCCC(=CCCC(=CCOC(=O)C)C)C)C |
|---|---|
| IUPAC Name | [(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl] acetate |
| InChIKey | ZGIGZINMAOQWLX-NCZFFCEISA-N |
| INCHI | 1S/C17H28O2/c1-14(2)8-6-9-15(3)10-7-11-16(4)12-13-19-17(5)18/h8,10,12H,6-7,9,11,13H2,1-5H3/b15-10+,16-12+ |
| Isomeric SMILES | CC(=CCC/C(=C/CC/C(=C/COC(=O)C)/C)/C)C |
| WGK Germany | 3 |
| Molecular Weight | 264.4 |
| Reaxy-Rn | 1784823 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1784823&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 |
| Class | Prenol lipids |
| Subclass | Sesquiterpenoids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Sesquiterpenoids |
| Alternative Parents | Fatty alcohol esters Carboxylic acid esters Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Farsesane sesquiterpenoid - Sesquiterpenoid - Fatty alcohol ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. |
| External Descriptors | Wax monoesters |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 K2303145 | Certificate of Analysis | Oct 26, 2023 | T334917 |
| K2303146 | Certificate of Analysis | Oct 26, 2023 | T334917 |
| K2303147 | Certificate of Analysis | Oct 26, 2023 | T334917 |
| K2303148 | Certificate of Analysis | Oct 26, 2023 | T334917 |
| K2303149 | Certificate of Analysis | Oct 26, 2023 | T334917 |
| K2303192 | Certificate of Analysis | Oct 26, 2023 | T334917 |
| Refractive Index | n20/D 1.477 (lit.) |
|---|---|
| Flash Point(°F) | >235.4 °F |
| Flash Point(°C) | >113 °C |
| Boil Point(°C) | 115-125 °C/0.3 mmHg (lit.) |
| Molecular Weight | 264.400 g/mol |
| XLogP3 | 5.300 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 9 |
| Exact Mass | 264.209 Da |
| Monoisotopic Mass | 264.209 Da |
| Topological Polar Surface Area | 26.300 Ų |
| Heavy Atom Count | 19 |
| Formal Charge | 0 |
| Complexity | 355.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 2 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 2 |
| Covalently-Bonded Unit Count | 1 |
