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2,3-DIMETHOXY-5-METHYL-6-[ALL TRANS]FARNESYLFARNESYL-1,4-BENZOQUINONE

CAS No.
1065-31-2
Chemical Name:
2,3-DIMETHOXY-5-METHYL-6-[ALL TRANS]FARNESYLFARNESYL-1,4-BENZOQUINONE
Synonyms
COENZYME Q6;ubiquinone 6;Ubiquinone Q6;UBIQUINONE-30;Isatin Impurity 5;coenzyme Q6 from saccharomyces*cerevisiae;2,3-dimethoxy-5-methyl-6-(farnesylfarnesyl)-1,4-benzoquinone;2,3-DIMETHOXY-5-METHYL-6-[ALL TRANS]FARNESYLFARNESYL-1,4-BENZOQUINONE;2,3-Dimethoxy-5-methyl-6-(farnesylfarnesyl)-1,4-benzoquinone, Ubiquinone-30;p-Benzoquinone, 2-(3,7,11,15,19,23-hexamethyl-2,6,10,14,18,22-tetracosahexaenyl)-5,6-dimethoxy-3-methyl-, (all-E)-
CBNumber:
CB5447936
Molecular Formula:
C39H58O4
Molecular Weight:
590.88
MDL Number:
MFCD00055698
MOL File:
1065-31-2.mol
Last updated:2023-07-06 08:28:06

2,3-DIMETHOXY-5-METHYL-6-[ALL TRANS]FARNESYLFARNESYL-1,4-BENZOQUINONE Properties

Boiling point 688.7±55.0 °C(Predicted)
Density 0.99±0.1 g/cm3(Predicted)
storage temp. -20°C
FDA UNII X9HU3BD5Q3

SAFETY

Risk and Safety Statements

WGK Germany  3

2,3-DIMETHOXY-5-METHYL-6-[ALL TRANS]FARNESYLFARNESYL-1,4-BENZOQUINONE Chemical Properties,Uses,Production

Uses

CoQ6 has been used:

  • as an internal standard for the liquid-chromatography mass-spectrometry for the quantification of CoQ6
  • to determine its effect on peroxisome proliferator-activated receptor (PPAR)
  • in reversed-phase high pressure liquid chromatography to quantify yeast quinones

Definition

ChEBI: A ubiquinone compound having a (2E,6E,10E,14E,18E)-3,7,11,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaen-1-yl substituent at position 2.

General Description

Coenzyme Q6 (CoQ6) is also known as ubiquinone-30 in Saccharomyces cerevisiae. It is a flavoprotein that utilizes flavin adenine dinucleotide (FAD) as a co-factor for the synthesis of coenzyme Q. It is composed of three conserved regions- a FAD/ nicotinamide adenine dinucleotide (NAD) + hydrogen (H) (NADH) binding motif, an adenine di phosphate (ADP) binding motif and a consensus sequence, that binds to the ribityl moiety of FAD.

Biochem/physiol Actions

Coenzyme Q6 (CoQ6) in the plasma membrane of Saccharomyces cerevisiae is involved in the ascorbate stabilization at the plasma membrane.

118579-97-8
1065-31-2
Synthesis of 2,3-DIMETHOXY-5-METHYL-6-[ALL TRANS]FARNESYLFARNESYL-1,4-BENZOQUINONE from Benzene, 1-[(2E,6E,10E,14E,18E)-3,7,11,15,19,23-hexamethyl-2,6,10,14,18,22-tetracosahexaenyl]-2,3,4,5-tetramethoxy-6-methyl- (9CI)

2,3-DIMETHOXY-5-METHYL-6-[ALL TRANS]FARNESYLFARNESYL-1,4-BENZOQUINONE Preparation Products And Raw materials

Raw materials

Preparation Products

2,3-DIMETHOXY-5-METHYL-6-[ALL TRANS]FARNESYLFARNESYL-1,4-BENZOQUINONE Suppliers

Global( 8)Suppliers
Supplier Tel Email Country ProdList Advantage
Sigma-Aldrich 021-61415566 800-8193336 orderCN@merckgroup.com China 51456 80
guoyungurui 18162595016; 18162595016 3287908757@qq.com China 10335 58
Hubei CuiRan Biotechnology Co., Ltd. 18162791556 3152548389@qq.com China 4351 58
SHANGHAI ZZBIO CO., LTD. 15102117276 19921389125 tech@zzbioco.com China 12065 58

1065-31-2(2,3-DIMETHOXY-5-METHYL-6-[ALL TRANS]FARNESYLFARNESYL-1,4-BENZOQUINONE)Related Search:

COENZYME Q6 2,3-DIMETHOXY-5-METHYL-6-[ALL TRANS]FARNESYLFARNESYL-1,4-BENZOQUINONE UBIQUINONE-30 coenzyme Q6 from saccharomyces*cerevisiae 2,3-dimethoxy-5-methyl-6-(farnesylfarnesyl)-1,4-benzoquinone ubiquinone 6 2,3-Dimethoxy-5-methyl-6-(farnesylfarnesyl)-1,4-benzoquinone, Ubiquinone-30 2-[(2E,6E,10E,14E,18E)-3,7,11,15,19,23-Hexamethyl-2,6,10,14,18,22-tetracosahexenyl]-3-methyl-5,6-dimethoxy-1,4-benzoquinone 2-[(2E,6E,10E,14E,18E)-3,7,11,15,19,23-Hexamethyl-2,6,10,14,18,22-tetracosahexenyl]-5,6-dimethoxy-3-methyl-2,5-cyclohexadiene-1,4-dione Ubiquinone Q6 2,5-Cyclohexadiene-1,4-dione, 2-(3,7,11,15,19,23-hexamethyl-2,6,10,14,18,22-tetracosahexaenyl)-5,6-dimethoxy-3-methyl-, (all-E)- p-Benzoquinone, 2-(3,7,11,15,19,23-hexamethyl-2,6,10,14,18,22-tetracosahexaenyl)-5,6-dimethoxy-3-methyl-, (all-E)- 2,5-Cyclohexadiene-1,4-dione, 2-[(2E,6E,10E,14E,18E)-3,7,11,15,19,23-hexamethyl-2,6,10,14,18,22-tetracosahexaen-1-yl]-5,6-dimethoxy-3-methyl- Isatin Impurity 5 1065-31-2 C39H58O4 Metabolic Pathways Metabolomics Cofactors and Substrates Electron Transport and Cellular Respiration BioChemical