≥90%, a solution in heptane for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Protected from light,Store at -20°C Ships Ice chest + Ice pads 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.
Germacrene D is supplied as a solution in heptane. To change the solvent, simply evaporate the heptane under a gentle stream of nitrogen and immediately add the solvent of choice. Germacrene D is slightly soluble in chloroform and DMSO.
In Vitro
Germacrene D shows antibacterial and antifungal activities, the mechanism of antimicrobial action of it may be related to permeabilization of the cells and disruption of the membrane integrity. MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Form:Oil
IC50& Target:IC50: bacterial
| Sonrisas canónicas | CC1=CCCC(=C)C=CC(CC1)C(C)C |
|---|---|
| IUPAC Name | (1E,6E,8S)-1-methyl-5-methylidene-8-propan-2-ylcyclodeca-1,6-diene |
| InChIKey | GAIBLDCXCZKKJE-RXJOXMPGSA-N |
| INCHI | 1S/C15H24/c1-12(2)15-10-8-13(3)6-5-7-14(4)9-11-15/h7-8,10,12,15H,3,5-6,9,11H2,1-2,4H3/b10-8+,14-7+/t15-/m0/s1 |
| Isómeros SMILES | C/C/1=C\CCC(=C)/C=C/[C@@H](CC1)C(C)C |
| PubChem CID | 5317570 |
| Peso molecular | 204.35 |
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 |
| Clase | Prenol lipids |
| Subclass | Sesquiterpenoids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Germacrane sesquiterpenoids |
| Alternative Parents | Branched unsaturated hydrocarbons Cyclic olefins Unsaturated aliphatic hydrocarbons |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | Germacrane sesquiterpenoid - Branched unsaturated hydrocarbon - Cyclic olefin - Unsaturated aliphatic hydrocarbon - Unsaturated hydrocarbon - Olefin - Hydrocarbon - Aliphatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as germacrane sesquiterpenoids. These are sesquiterpenoids having the germacrane skeleton, with a structure characterized by a cyclodecane ring substituted with an isopropyl and two methyl groups. |
| External Descriptors | germacrene D |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 F2610399 | Certificate of Analysis | Jun 03, 2026 | G646231 |
| E2431198 | Certificate of Analysis | May 21, 2024 | G646231 |
| E2431226 | Certificate of Analysis | May 21, 2024 | G646231 |
| E2431199 | Certificate of Analysis | May 21, 2024 | G646231 |
| Sensibilidad | Light sensitive |
|---|---|
| Peso molecular | 204.350 g/mol |
| XLogP3 | 4.700 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 1 |
| Exact Mass | 204.188 Da |
| Monoisotopic Mass | 204.188 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 15 |
| Formal Charge | 0 |
| Complexity | 266.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| 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 |
