Determine the necessary mass, volume, or concentration for preparing a solution.
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≥98% 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 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Idebenone is a synthetic analog of coenzyme Q10 (CoQ10) and a brain stimulant.
An antioxidant and neuroprotective agent.
application:
Idebenone has been used:to treat mutant myocilin (mMYOC) cells for drug treatment assay,to validate C2C12 secondary cell screening assay
to treat obese mice, to test whether idebenone and CoQ10 bind directly to peroxisome proliferator-activated receptor (PPAR)LBDs, His-tagged PPARα, δ and γ LBDs
| ALogP | 4.3 |
|---|
| Pubchem Sid | 488179783 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488179783 |
| Sonrisas canónicas | CC1=C(C(=O)C(=C(C1=O)OC)OC)CCCCCCCCCCO |
| IUPAC Name | 2-(10-hydroxydecyl)-5,6-dimethoxy-3-methylcyclohexa-2,5-diene-1,4-dione |
| InChIKey | JGPMMRGNQUBGND-UHFFFAOYSA-N |
| INCHI | 1S/C19H30O5/c1-14-15(12-10-8-6-4-5-7-9-11-13-20)17(22)19(24-3)18(23-2)16(14)21/h20H,4-13H2,1-3H3 |
| Isómeros SMILES | CC1=C(C(=O)C(=C(C1=O)OC)OC)CCCCCCCCCCO |
| RTECS | GU5290000 |
| Peso molecular | 338.44 |
| Reaxy-Rn | 2001459 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2001459&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 |
| Clase | Prenol lipids |
| Subclass | Quinone and hydroquinone lipids |
| Intermediate Tree Nodes | Prenylquinones |
| Direct Parent | Ubiquinones |
| Alternative Parents | Fatty alcohols P-benzoquinones Vinylogous esters Primary alcohols Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | Ubiquinone skeleton - Fatty alcohol - P-benzoquinone - Quinone - Fatty acyl - Vinylogous ester - Cyclic ketone - Ketone - Alcohol - Hydrocarbon derivative - Primary alcohol - Organic oxide - Organooxygen compound - Organic oxygen compound - Carbonyl group - Aliphatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as ubiquinones. These are coenzyme Q derivatives containing a 5, 6-dimethoxy-3-methyl(1,4-benzoquinone) moiety to which an isoprenyl group is attached at ring position 2(or 6). |
| External Descriptors | primary alcohol - benzoquinones |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Jun 22, 2026 | I129330 | |
| Certificate of Analysis | Jan 09, 2025 | I129330 | |
| Certificate of Analysis | Jan 09, 2025 | I129330 | |
| Certificate of Analysis | Aug 02, 2024 | I129330 | |
| Certificate of Analysis | Aug 02, 2024 | I129330 | |
| Certificate of Analysis | Aug 02, 2024 | I129330 | |
| Certificate of Analysis | Aug 02, 2024 | I129330 | |
| Certificate of Analysis | Aug 02, 2024 | I129330 | |
| Certificate of Analysis | Aug 02, 2024 | I129330 | |
| Certificate of Analysis | Jun 27, 2024 | I129330 | |
| Certificate of Analysis | Sep 21, 2023 | I129330 | |
| Certificate of Analysis | Sep 21, 2023 | I129330 | |
| Certificate of Analysis | Sep 21, 2023 | I129330 | |
| Certificate of Analysis | Sep 21, 2023 | I129330 | |
| Certificate of Analysis | Sep 14, 2023 | I129330 | |
| Certificate of Analysis | Mar 10, 2023 | I129330 | |
| Certificate of Analysis | Oct 14, 2022 | I129330 |
| Solubilidad | Soluble in DMSO (>25 mg/ml), ethanol (>25 mg/ml), methanol, and chloroform. Insoluble in water. |
|---|---|
| Punto de fusión (°C) | 53℃ |
| Peso molecular | 338.400 g/mol |
| XLogP3 | 4.300 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 12 |
| Exact Mass | 338.209 Da |
| Monoisotopic Mass | 338.209 Da |
| Topological Polar Surface Area | 72.800 Ų |
| Heavy Atom Count | 24 |
| Formal Charge | 0 |
| Complexity | 502.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Zhiwen Li, Zhilin Zhou, Jianghua Wang, Tingxian Tao, Yingqiang Fu. (2023) Aggregation-induced emission enhancement N, S-CQDs for selective detection of CIP in the environment. NANOTECHNOLOGY, 34 (39): (395503). [PMID:37343538] [10.1088/1361-6528/ace05a] |
| 2. Xiao Tu, Jiaxin Hu, Jinghao Peng, Qihan Chen, Yangle Zhao, Zemao Gu. (2025) Discovery of thymoquinone analogues with high anthelmintic activity against monogenean infections in goldfish (Carassius auratus). VETERINARY PARASITOLOGY, [PMID:39837239] [10.1016/j.vetpar.2025.110401] |
| 3. Haiyan Zhu, Yijing Yang, Yenan Duan, Xin Zheng, Zixiong Lin, Jie Zhou. (2024) Nrf2/FSP1/CoQ10 axis-mediated ferroptosis is involved in sodium aescinate-induced nephrotoxicity. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, [PMID:39033970] [10.1016/j.abb.2024.110100] |
| 4. Lei Shu, Peili Luo, Chuanyu Ren, Ziwei Lai, Xuejuan Zhang, Chuanbin Wu, Xin Pan, Zhengwei Huang. (2025) Inhalable Fibroin Hybrid Liposomes for the Targeted Treatment of Lung Adenocarcinoma via Autophagy-Enhanced Ferroptosis. ACS Nano, [PMID:40878028] [10.1021/acsnano.5c09493] |