55127-92-9

Basic information

• Product Name: vitamin Q
• Synonyms: vitamin Q
• CAS NO: 55127-92-9
• Molecular Formula: C59H90O4
• Molecular Weight: 863.3435
• Mol File: 55127-92-9.mol
• Article Data: 37

Chemical Properties

• Appearance: /
• CAS DataBase Reference: vitamin Q(CAS DataBase Reference)
• NIST Chemistry Reference: vitamin Q(55127-92-9)
• EPA Substance Registry System: vitamin Q(55127-92-9)

Safety Data

• Hazardous Substances Data: 55127-92-9(Hazardous Substances Data)

Usage

Description

Vitamin Q, also known as Coenzyme Q10 (CoQ10), is a naturally occurring compound found in every cell of the body and is essential for the production of energy. It acts as an antioxidant, protecting cells from damage caused by harmful molecules called free radicals. CoQ10 is also involved in the regulation of blood pressure, immune function, and muscle health. Additionally, it plays a crucial role in the production of ATP, the primary source of energy for cellular processes. While the body can produce CoQ10 on its own, levels decrease with age and certain health conditions, making supplementation beneficial for some individuals.

Uses

Used in Pharmaceutical Industry:
Vitamin Q is used as a dietary supplement for maintaining energy production, supporting heart health, and providing antioxidant protection against free radicals.
Used in Cosmetic Industry:
Vitamin Q is used as an ingredient in skincare products for its antioxidant properties, which help protect the skin from environmental damage and promote a youthful appearance.
Used in Food and Beverage Industry:
Vitamin Q is used as a fortifying agent in certain food and beverage products to enhance their nutritional value and support overall health and well-being.

Upstream product

• 947156-48-1 2-((2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-Decamethyl-tetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl)-5,6-dimethoxy-3-methyl-benzene-1,4-diol 
• 59242-49-8 1-((2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-Decamethyl-tetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl)-3,4-dimethoxy-2,5-bis-methoxymethoxy-6-methyl-benzene 
• 70854-63-6 1,4-bis(benzyloxy)-2-{(2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyl-5-[(4-methylphenyl)sulfonyl]tetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl}-5,6-dimethoxy-3-methylbenzene 
• 75-24-1 trimethylaluminum 
• 202843-56-9 2-chloromethyl-5,6-dimethoxy-3-methyl-[1,4]benzoquinone 
• 400010-22-2 (all-E)-2,6,10,14,18,22,26,30,34-nonamethyl-2,6,10,14,18,22,26,30,34-nonacontanonaen-38-yne 
• 400010-26-6 2-((2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-Decamethyl-tetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl)-5,6-dimethoxy-3-methyl-phenol 
• 605-94-7 2,3-Dimethoxy-5-methyl-1,4-benzoquinone 
• 68799-83-7 (all-E)-3,7,11,15,19,23,27,31,35,39-decamethyl-2,6,10,14,18,22,26,30,34,38-tetracontadecaenyl bromide 
• 82343-09-7 1-Benzyloxy-3-((2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyl-tetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl)-4,5,6-trimethoxy-2-methyl-benzene 
• 94828-17-8 (2'E,6'E,10'E,14'E,18'E,22'E,26'E,30'E,34'E,38'E)-1-(3',7',11',15',19',23',27',31',35',39'-decamethyltetraconta-2',6',10',14',18',22',26',30',34',38'-decaenyl)-6-methyl-2,3,4,5-tetramethoxybenzene 
• 64634-91-9 1-[(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-decaen-1-yl]-3,4-dimethoxy-2,5-bis(methoxymethoxy)-6-methylbenzene 
• 75426-26-5 ubiquinol 
• 96358-52-0 2,3-dimethoxy-5-methyl-6-(34',35'-dihydroxy-3',7',11',15',19',23',27',31',35'-nonamethylhexatriaconta-2'E,6'E,10'E,14'E,18'E,22'E,26'E,30'E-octaenyl)benzoquinone-1,4 

Downstream Products

• 1974-58-9 2-(3,7,11,15,19,23,27,31,35,39-decamethyl-tetracontyl)-5,6-dimethoxy-3-methyl-[1,4]benzoquinone 
• 28527-67-5 diethoxy-CoQ₁₀ 
• 28645-33-2 Hydronbichinon-bis-methylcarbamat 

Relevant articles and documents

Method for synthesizing coenzyme Q10 from 5-demethoxy coenzyme Q10

The invention relates to a method for synthesizing a coenzyme Q10 from a 5-demethoxy coenzyme Q10. The method comprises the following steps of: taking the 5-demethoxy coenzyme Q10 as a raw material, and carrying out a 1,4-addition reaction, a methoxylation reaction and an oxidation reaction to finally prepare the coenzyme Q10. According to the method, the 5-demethoxy coenzyme Q10 is used as a rawmaterial, the process route is short, the yield is high, the product purity is high, the content detected by adopting HPLC (High Performance Liquid Chromatography) of a pharmacopoeia analysis method is 98% or more, and the problem of a byproduct 5-demethoxy coenzyme Q10 generated in a production fermentation process of the coenzyme Q10 is solved, thereby changing wastes into valuables.

Novel Intermediates, Process for Their Preparation and Process for the Preparation of Coq10 Employing the Said Novel Intermediates

The present invention relates to an improved process for the preparation of Coenzyme Q. Coenzyme Q10 or CoQ10 has the chemical name 2-[(all-trans)-3,7,11,15,19,23,27,31,35,39-decamethyl-2,6,10,14,18,22,26,30,34,38-tetracontadecaenyl]-5,6-dimethoxy-3-methyl-1,4-benzoquinone and has the formula I. The invention also provides new intermediates useful for the preparation of CoQ10 and processes for their preparation.

NOVEL INTERMEDIATES, PROCESS FOR THEIR PREPARATION AND PROCESS FOR THE PREPARATION OF COQ10 EMPLOYING THE SAID NOVEL INTERMEDIATES

The present invention relates to an improved process for the preparation of Coenzyme Q. Coenzyme QlO or CoQlO has the chemical name 2- [(all -trans)- 3, 7,l l,15,19,23,27,31,35,39-decamethyl-2, 6, 10, 14, 18, 22, 26, 30, 34, 38 - tetracontadecaenyl]-5-6-dimethoxy -3- methyl -1,4-benzoquinone and has the formula 1. The invention also provides new intermediates useful for the preparation of CoQlO and processes for their preparation.