Coenzyme Q10


  • English nameCoenzyme Q10
  • CAS number992-78-9
  • Molecular formulaC59H90O4
  • Molecular weight863.3
  • content100%
  • appearanceoff-white powder
  • package0-1kg
  • ApplyHeart health,Fertility,Skin young.
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Description

Coenzyme Q10 exists in both ubiquinol and ubiquinone forms, but they have vastly different roles to play in the body. For instance, ubiquinol is an electron donor, while ubiquinone is an electron acceptor.

Ubiquinol (CoQH2)is a reduced form of coenzyme Q10 (CoQ10) that acts as an active antioxidant that prevents the initiation and propagation of lipid peroxidation in biological membranes and human low-density lipoprotein (LDL).

Ubiquinol is the active structure and present as the predominant form in human, e.g. 98% of the total amount of Coenzyme Q in serum exists as Ubiquinol.

 

Applications

1.used as a dietary supplement.

2. available as eye drops and other topical.

Advantage

24 months stability under room tempeature

6 months accerlated stability in finished formula of gummy, tablet, capsule,softgel

Patented Cocrystal Technology

Easy-to-absorb (8x more bioavailable)

 

Certificate

 

Manufacturer supply high quality Reduced Coenzyme Q10 992-78-9 with GMP standards

  • Molecular Formula:C59H92O4
  • Molecular Weight:865.377
  • 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 

992-78-9 Relevant articles

Method for synthesizing coenzyme Q10 from 5-demethoxy coenzyme Q10

-

Paragraph 0006; 0020; 0022; 0024; 0026; 0027; 0029; 0031, (2018/03/25)

The invention relates to a method for sy...

FORMULATIONS OF LIPOPHILIC BIOACTIVE MOLECULES

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Paragraph 0365; 0366; 0367, (2014/02/16)

This invention provides aqueous and non-...

COMPOSITION CONTAINING REDUCED COENZYME Q10, AND MANUFACTURING AND STABILISING METHODS THEREFOR

-

Paragraph 0156, (2013/06/26)

The present invention relates to a metho...

Dietary chlorophyll metabolites catalyze the photoreduction of plasma ubiquinone

Qu, Jinfeng,Ma, Li,Zhang, Junhua,Jockusch, Steffen,Washington, Ilyas

, p. 310 - 313 (2013/07/19)

Ubiquinol is a plasma antioxidant. The m...

992-78-9 Process route

ubidecarenone
303-98-0,55127-92-9

ubidecarenone

ascorbic acid
50-81-7,98966-42-8

ascorbic acid

ubiquinol
75426-26-5,992-78-9

ubiquinol

oxalic acid
144-62-7,97993-78-7

oxalic acid

Conditions
Conditions Yield
In ethanol; at 78 ℃; for 30h;
 
ubidecarenone
303-98-0,55127-92-9

ubidecarenone

ubiquinol
75426-26-5,992-78-9

ubiquinol

Conditions
Conditions Yield
With sodium thiosulfate; sodium chloride; In water; at 48 ℃; for 2h; pH=4 - 6;
99%
With sodium thiosulfate; sodium chloride; In n-heptane; water; at 25 ℃; for 2h; pH=4 - 6;
99%
With sodium hydroxide; ascorbic acid; In ethanol; at 50 ℃;
98%
With ascorbic acid; In ethanol; at 78 ℃; for 30h;
97%
With sodium hydrogencarbonate; ascorbic acid; In ethanol; at 78 ℃; for 30h;
97%
With ascorbic acid; In ethanol; at 78 ℃; for 30h; Product distribution / selectivity;
95%
With D-limonene; water; Ascorbyl palmitate; at 80 ℃; for 16h; Concentration; Reagent/catalyst; Time; Inert atmosphere;
95%
With sodium hydrogencarbonate; ascorbic acid; In acetone; at 50 ℃; for 45h;
93%
With sodium dithionite; In n-heptane; water; at 25 ℃; for 2h; pH=4 - 6;
92.8%
With acetic acid; zinc;
 
With sodium hydrogencarbonate; ascorbic acid; In ethanol; at 78 ℃; for 3h;
 
With sodium thiosulfate; In n-heptane; water; at 25 ℃; for 2h;
 
With sodium dithionite; In n-heptane; water; at 25 ℃; for 2h; pH=4 - 6; Conversion of starting material; Nitrogen atmosphere;
 
With sodium thiosulfate; In n-heptane; water; at 25 ℃; for 2h; pH=4 - 6;
 
With sodium hydrogencarbonate; ascorbic acid; In acetone; at 2 - 50 ℃; Conversion of starting material; Nitrogen atmosphere;
 
With sulfuric acid; zinc; In n-heptane; water; at 25 ℃; for 2h; pH=4 - 6; Conversion of starting material; Nitrogen atmosphere;
 
With sodium dithionite; oxygen; In hexane; water; at 25 ℃; for 2h; pH=4 - 6; Conversion of starting material;
 
With sodium dithionite; In water; ethyl acetate; at 25 ℃; for 2h; pH=4 - 6; Conversion of starting material; Nitrogen atmosphere;
 
With sodium dithionite; In n-heptane; water; at 25 ℃; for 2h; pH=4 - 6; Conversion of starting material; Nitrogen atmosphere;
 
With sodium dithionite; In water; toluene; at 25 ℃; for 2h; pH=4 - 6; Conversion of starting material; Nitrogen atmosphere;
 
With sodium dithionite; In hexane; water; at 25 ℃; for 2h; pH=4 - 6; Conversion of starting material; Nitrogen atmosphere;
 
With sodium dithionite; In hexane; water; at 25 ℃; for 2h; pH=4 - 6; Conversion of starting material; Nitrogen atmosphere;
 
With sodium dithionite; In chloroform; water; at 25 ℃; for 2h; pH=4 - 6; Conversion of starting material; Nitrogen atmosphere;
 
With sodium dithionite; In tert-butyl methyl ether; water; at 25 ℃; for 2h; pH=4 - 6; Conversion of starting material; Nitrogen atmosphere;
 
With ascorbic acid; In ethanol; water; at 2 - 78 ℃; Conversion of starting material; Nitrogen atmosphere;
 
With ascorbic acid; In ethanol; at 50 ℃; for 24h; Conversion of starting material;
 
With ascorbic acid; In ethanol; at 2 - 78 ℃; Conversion of starting material; Nitrogen atmosphere;
 
ubidecarenone; With sodium hydrogencarbonate; ascorbic acid; In acetonitrile; at 55 ℃; for 40h; Nitrogen atmosphere;
In n-heptane; water; acetonitrile; at 25 ℃; Conversion of starting material; Nitrogen atmosphere;
 
ubidecarenone; With sulfuric acid; zinc; In n-heptane; water; at 25 ℃; for 6h; Nitrogen atmosphere;
With hydrogenchloride; In n-heptane; water; Conversion of starting material; Nitrogen atmosphere;
 
ubidecarenone; With sodium dithionite; In water; ethyl acetate; at 25 ℃; for 2h; pH=4 - 6; Nitrogen atmosphere;
In ethanol; water; ethyl acetate; at 2 ℃; Conversion of starting material; Nitrogen atmosphere;
 
ubidecarenone; With sodium dithionite; In water; ethyl acetate; at 25 ℃; for 2h; pH=4 - 6; Nitrogen atmosphere;
In ethanol; water; ethyl acetate; at 2 - 48 ℃; Conversion of starting material; Nitrogen atmosphere;
 
ubidecarenone; With sodium dithionite; In hexane; water; at 25 ℃; for 2h; pH=4 - 6; Nitrogen atmosphere;
In methanol; hexane; at 2 ℃; Conversion of starting material; Nitrogen atmosphere;
 
ubidecarenone; With sodium dithionite; In hexane; water; at 25 ℃; for 2h; pH=4 - 6; Nitrogen atmosphere;
In ethanol; at 2 - 50 ℃; Conversion of starting material; Nitrogen atmosphere;
 
ubidecarenone; With sodium dithionite; In water; at 50 ℃; for 2h; pH=4 - 6; Nitrogen atmosphere;
In ethanol; at 2 - 50 ℃; Conversion of starting material; Nitrogen atmosphere;
 
ubidecarenone; With sodium dithionite; In water; at 2 - 50 ℃; pH=4 - 6; Nitrogen atmosphere;
at 2 ℃; Conversion of starting material;
 
ubidecarenone; With sulfuric acid; zinc; In n-heptane; water; at 25 ℃; for 6h; Nitrogen atmosphere;
With hydrogenchloride; In n-heptane; water; Nitrogen atmosphere;
In ethanol; at 2 - 50 ℃; Conversion of starting material; Nitrogen atmosphere;
 
With sodium dithionite; In n-heptane; water; at 25 ℃; for 2h; pH=4 - 6; Product distribution / selectivity;
 
With ascorbic acid; In ethanol; at 78 ℃; for 30h;
 
With sodium dithionite; In n-heptane; water; at 25 ℃; for 2h; pH=4 - 6;
 
With ascorbic acid; In ethanol; at 78 ℃; for 30h;
 
With acetic acid; zinc; at 65 - 70 ℃; for 1h; Heating / reflux;
 
With ascorbic acid; In ethanol; at 78 ℃; for 30h; Product distribution / selectivity;
 
With sodium thiosulfate; In n-heptane; water; at 25 ℃; for 2h; pH=4 - 6; Product distribution / selectivity;
 
With sodium dithionite; In water; for 2h; Purification / work up;
 
With dihydrolipoic acid; at 4 - 50 ℃; for 30 - 1680h; pH=3.8 - 3.9; Product distribution / selectivity;
 
With sodium tetrahydroborate; In tetrahydrofuran; at 30 ℃; for 1h; Product distribution / selectivity;
 
With ascorbic acid; In ethanol; water; at 78 ℃; pH=3.6; Product distribution / selectivity;
 
With sodium dithionite; In hexane; Inert atmosphere;
 
With zinc pheophorbide a; ascorbic acid; Reagent/catalyst; Catalytic behavior; Irradiation; Inert atmosphere;
 
With Vitamin C; In water; at 90 - 95 ℃; for 1h; Solvent; Reagent/catalyst; Large scale;
 
With D-ascorbic acid; In ethanol; at 78 ℃; for 30h;
 
With sodium thiosulfate; In hexane; at 20 ℃; for 2h;
 
With sodium dithionite; In n-heptane; water; at 25 ℃; for 2h; pH=4 - 6;
 
With ascorbic acid; In ethanol; at 78 ℃; for 30h;
 
With ascorbic acid; In ethanol; at 78 ℃; for 30h;
 

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