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Essentials

CoQ10 Amino Acid Blend (Ubiquinol)

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What is CoQ10 (Ubiquinol)?

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.

Chemical and Molecular Data

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

What are the Mechanisms of Action?

The biochemical pathways and cellular targets of CoQ10 (Ubiquinol) include:

  • Mitochondrial Electron Transport: Research demonstrates that CoQ10 (Ubiquinol) acts as a continuous, mobile lipophilic electron shuttle within the inner mitochondrial membrane. It accepts pairs of electrons from Complex I (NADH dehydrogenase) and Complex II (succinate dehydrogenase) and transfers them directly to Complex III (cytochrome bc1 complex), a core kinetic step required to generate the proton gradient that powers ATP synthesis.
  • Lipid Membrane Peroxidation Prevention: In addition to bioenergetic transport, Ubiquinol functions as a direct, highly reactive radical scavenger within cellular lipid bilayers. It intercepts lipophilic peroxyl radicals before they can attack structural membrane phospholipids, protecting cellular and mitochondrial borders from oxidative stress damage.
  • Antioxidant Recycling Networks: Studies indicate that Ubiquinol interacts synergistically with other network antioxidants. By donating its extra electrons, it actively reduces oxidized vitamin E (alpha-tocopheroxyl radical) and vitamin C back into their functional, fully active states, preserving global cellular redox balances.

What are the Clinical & Preclinical Trials on Ubiquinol?

When evaluating research efficacy and published experimental literature for CoQ10 (Ubiquinol):

  • Bioavailability and Absorption Dynamics: Comparative preclinical pharmacokinetic evaluations demonstrated that Ubiquinol exhibits significantly superior absorption profiles compared to standard ubiquinone formulations. In vitro intestinal models show up to a four-fold to six-fold increase in structural accumulation metrics due to its hydroquinone structure bypassing early metabolic reduction requirements.
  • Myocardial Bioenergetics Under Strain: Preclinical models tracking induced hypoxic cardiomyopathy confirm that consistent administration of reduced Ubiquinol efficiently preserves mitochondrial cristae structures.  This maintains high ATP expression rates and limiting baseline tissue remodeling during heavy oxidative duress.
  • Environmental Oxidation Stability Assays: Analytical chemistry reviews focusing on formulation stability show that unshielded Ubiquinol is highly sensitive to rapid auto-oxidation when exposed to air.  This requires an oxygen-free or airtight packaging environments to keep the raw material in its active reduced layout.

How does CoQ10 (Ubiquinol) compare to other compounds?

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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Disclaimer: All compounds and research materials provided by Essential Aminos are strictly for laboratory and research professional use only. They are not approved for human or animal use nor consumption by the Food and Drug Administration (FDA). These products should not be used for any form of in vivo experimentation or for any other non-laboratory purpose. Any violation or indication of human or animal use will result in immediate removal from being able to purchase products in the future. By purchasing these products, you acknowledge that they will be used exclusively within a controlled and qualified research environment.

Certificate of Analysis

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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