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Ubiquinol is the fully reduced, active antioxidant form of Coenzyme Q10 (CoQ10). It is a lipophilic endogenously synthesized benzoquinone found within the membranes of high-energy organelles. While standard CoQ10 supplements typically utilize the oxidized form (Ubiquinone), Ubiquinol possesses two additional hydrogen atoms. This renders it highly electron-rich and immediately bioavailable. Researchers investigate this lipid-soluble compound for its direct role as a mobile electron carrier within the mitochondrial respiratory chain, its potent suppression of cellular lipid peroxidation, and its ability to regenerate other essential endogenously active antioxidants.
For laboratory and in vitro evaluation, researchers often choose to buy CoQ10 (Ubiquinol) in high-purity chemical reference form. Because the reduced molecular structure is exceptionally sensitive to ambient air and light exposure. This emulsive solution must be stored carefully to prevent premature structural oxidation back into standard ubiquinone.
| Compound Name | CoQ10 Amino Acid Blend (Ubiquinol) |
|---|---|
| Quantity / Formats | 300MG/ML (20ML) |
| Synonyms / Alt Names | reduced coenzyme Q10; Ubiquinone hydroquinone; CoQH2 |
| CAS Number | 992-78-9 |
| Chemical Formula | C59H92O4 |
| Molecular Weight | 865.4 g/mol |
| IUPAC Name | 2-[(2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl]-5,6-dimethoxy-3-methylbenzene-1,4-diol |
| InChIKey | QNTNKSLOFHEFPK-UPTCCGCDSA-N |
| SMILES Code | CC1=C(C(=C(C(=C1O)OC)OC)O)C/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CCC=C(C)C |
The biochemical pathways and cellular targets of CoQ10 (Ubiquinol) include:
When evaluating research efficacy and published experimental literature for CoQ10 (Ubiquinol):
To evaluate absolute bioavailability, structural targeting parameters, and specific electron-shuttling potencies, researchers compare Ubiquinol against alternative ubiquinone configurations and engineered organelle-targeted derivatives:
| Compound | Primary Target | Structural Modifications | Biological Impact / Receptor Affinity |
|---|---|---|---|
| Ubiquinol | Mitochondrial Inner Membrane (Complex I-III Shuttle) & Lipid Bilayers | Fully reduced hydroquinone core structure containing two extra hydrogen atoms | Immediate, high bioavailability; acts as a direct antioxidant and electron carrier without requiring prior cellular reduction steps |
| Ubiquinone | Mitochondrial Inner Membrane Electron Transport Chain | Standard oxidized benzoquinone ring layout[cite: 1] | Requires energy-dependent enzymatic reduction by intracellular dehydrogenases to convert into active ubiquinol before providing significant antioxidant defense |
| MitoQ | Selective Mitochondrial Matrix Integration Only | Ubiquinone core covalently bound to a lipophilic triphenylphosphonium (TPP+) cation spacer | Accumulates rapidly inside the mitochondrial matrix driven by membrane potentials. Provides targeted protection against organelle free radicals; lacks general extra-mitochondrial membrane cycling |
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Certificates of analysis are provided for laboratory research reference. Expand a batch below to view the PDF. Only the newest three COAs for this product are listed here.
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