Ubiquinol

Basic information

  • Product Name:Ubiquinol
  • CasNo.:992-78-9
  • MF:C59H92O4
  • MW:865.377

Physical and Chemical Properties

  • Purity:99%
  • Boiling Point:48-49 °C
  • Packing:light yellow-orange solid
  • Throughput:
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Product Details

CasNo: 992-78-9

MF: C59H92O4

Appearance: light yellow-orange solid

Cost-effective customized wholesale Ubiquinol 992-78-9

  • 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

-

, (2018/03/25)

The invention relates to a method for sy...

FORMULATIONS OF LIPOPHILIC BIOACTIVE MOLECULES

-

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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