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Ubiquinol

Base Information
  • Chemical Name:Ubiquinol
  • CAS No.:992-78-9
  • Molecular Formula:C59H92O4
  • Molecular Weight:865.377
  • Hs Code.:2909500000
  • UNII:M9NL0C577Y
  • DSSTox Substance ID:DTXSID90912840
  • Nikkaji Number:J28.659A,J28.660E,J2.044.656K
  • Wikipedia:Ubiquinol
  • Metabolomics Workbench ID:42205
  • Mol file:992-78-9.mol
Ubiquinol

Synonyms:ubiquinol;ubiquinol 0;ubiquinol 1;ubiquinol 50;ubiquinol 6 (ubiquinol 30);ubiquinol 7;ubiquinol 9;ubiquinols;ubiquinone hydroquinone

Suppliers and Price of Ubiquinol
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • Ubiquinol
  • 1mg
  • $ 65.00
  • TRC
  • Ubiquinol
  • 250mg
  • $ 320.00
  • Medical Isotopes, Inc.
  • Ubiquinol
  • 1 mg
  • $ 390.00
  • Cayman Chemical
  • Ubiquinol ≥90%
  • 1mg
  • $ 178.00
  • Cayman Chemical
  • Ubiquinol ≥90%
  • 500μg
  • $ 99.00
  • Cayman Chemical
  • Ubiquinol ≥90%
  • 10mg
  • $ 1386.00
  • Cayman Chemical
  • Ubiquinol ≥90%
  • 5mg
  • $ 792.00
  • American Custom Chemicals Corporation
  • UBIQUINOL 95.00%
  • 1G
  • $ 525.00
  • AK Scientific
  • Ubiquinol(reducedCoenzymeQ10)
  • 25mg
  • $ 39.00
Total 91 raw suppliers
Chemical Property of Ubiquinol
Chemical Property:
  • Appearance/Colour:light yellow-orange solid 
  • Melting Point:48-49 °C 
  • Boiling Point:866.9±65.0 °C(Predicted) 
  • PKA:10.53±0.50(Predicted) 
  • PSA:58.92000 
  • Density:0.951±0.06 g/cm3(Predicted) 
  • LogP:18.47060 
  • Storage Temp.:Amber Vial, -20?C Freezer, Under Inert Atmosphere 
  • XLogP3:20.2
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:31
  • Exact Mass:864.69956141
  • Heavy Atom Count:63
  • Complexity:1600
Purity/Quality:

99% *data from raw suppliers

Ubiquinol *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=C(C(=C(C(=C1O)OC)OC)O)CC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)C
  • Isomeric SMILES: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
  • Recent ClinicalTrials:Coenzyme Q10 Phase III Trial in Gulf War Illness
  • Description Ubiquinol is a reduced form of coenzyme Q10 (CoQ10; ), which exists in three redox states: fully oxidized (CoQ10/ubiquinone), partially reduced (semiquinone/ubisemiquinone), and fully reduced (ubiquinol). CoQ10 acts as an electron shuttle in the electron transport chain via its reduction to ubiquinol between mitochondrial complexes I and II, also known as NADH dehydrogenase and succinate dehydrogenase, respectively, and mitochondrial complex III, also known as cytochrome bc1 complex. CoQ10 is also reduced to ubiquinol by ferroptosis suppressor protein 1 (FSP1) with NADPH as a cofactor, and ubiquinol traps lipid peroxyl radicals and inhibits lipid peroxidation helping to prevent ferroptosis.
  • Uses Reduced coenzyme Q for improving nervous system cell functions
Technology Process of Ubiquinol

There total 24 articles about Ubiquinol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With sodium thiosulfate; sodium chloride; In water; at 48 ℃; for 2h; pH=4 - 6;
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