Eupatolide (CHEM114325)
| Record Information | |||||||||
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| Version | 1.0 | ||||||||
| Creation Date | 2026-04-06 01:36:58 UTC | ||||||||
| Update Date | 2026-05-21 00:49:31 UTC | ||||||||
| Accession Number | CHEM114325 | ||||||||
| Identification | |||||||||
| Common Name | Eupatolide | ||||||||
| Class | Small Molecule | ||||||||
| Description | Eupatolide is an organic compound with the chemical formula C15H20O3 and an average molecular weight of 248.32 g/mol. Eupatolide belongs to the terpene lactones, a subclass of prenol lipids within the organic compounds. This compound is found in or released from 13 recorded sources across multiple sectors. Within the healthcare, pharmaceuticals & veterinary products sector, it is associated with medical devices. In the energy, oil & gas and industrial manufacturing & chemical processing sectors, it is found in lubricants. Sources related to electrical & electronic equipment include batteries, capacitors, printed circuit boards, wires and cables, cell phones, and one additional source. It is also present in food packaging from the food, food processing & cookware sector, as well as synthetic textiles, carpets, and rugs from the textiles, leather & furnishings sector. One additional sector is also recorded. Recorded exposure routes for eupatolide include inhalation, oral, and touch. | ||||||||
| Contaminant Sources | Not Available | ||||||||
| Contaminant Type |
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| Chemical Structure |  | ||||||||
| Synonyms | Not Available | ||||||||
| Chemical Formula | C15H20O3 | ||||||||
| Average Molecular Mass | 248.322 g/mol | ||||||||
| Monoisotopic Mass | 248.141 g/mol | ||||||||
| CAS Registry Number | 6750-25-0 | ||||||||
| IUPAC Name | (3aR,4R,6E,10E,11aR)-4-Hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2(3H)-one | ||||||||
| Traditional Name | Not Available | ||||||||
| SMILES | CC1=C/CCC(C)=C[C@H]2OC(=O)C(=C)[C@@H]2[C@H](O)C1 | ||||||||
| InChI Identifier | InChI=1S/C15H20O3/c1-9-5-4-6-10(2)8-13-14(12(16)7-9)11(3)15(17)18-13/h5,8,12-14,16H,3-4,6-7H2,1-2H3/b9-5+,10-8+/t12-,13-,14-/m1/s1 | ||||||||
| InChI Key | PDEJECFRCJOMEN-OURLZOILSA-N | ||||||||
| Chemical Taxonomy | |||||||||
| Classification | Not classified | ||||||||
| Biological Properties | |||||||||
| Status | Detected and Not Quantified | ||||||||
| Origin | Not Available | ||||||||
| Cellular Locations | Not Available | ||||||||
| Biofluid Locations | Not Available | ||||||||
| Tissue Locations | Not Available | ||||||||
| Pathways | Not Available | ||||||||
| Applications | Not Available | ||||||||
| Biological Roles | Not Available | ||||||||
| Chemical Roles | Not Available | ||||||||
| Physical Properties | |||||||||
| State | Not Available | ||||||||
| Appearance | Not Available | ||||||||
| Experimental Properties |
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| Predicted Properties | Not Available | ||||||||
| Spectra | |||||||||
| Spectra |
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| Toxicity Profile | |||||||||
| Route of Exposure | Not Available | ||||||||
| Mechanism of Toxicity | Not Available | ||||||||
| Metabolism | Not Available | ||||||||
| Toxicity Values | Not Available | ||||||||
| Lethal Dose | Not Available | ||||||||
| Carcinogenicity (IARC Classification) | Not Available | ||||||||
| Uses/Sources | Not Available | ||||||||
| Minimum Risk Level | Not Available | ||||||||
| Health Effects | Not Available | ||||||||
| Symptoms | Not Available | ||||||||
| Treatment | Not Available | ||||||||
| Concentrations | |||||||||
| Not Available | |||||||||
| External Links | |||||||||
| Identifiers | Not Available | ||||||||
| References | |||||||||
| Synthesis Reference | Not Available | ||||||||
| MSDS | Not Available | ||||||||
| General References | Not Available | ||||||||
