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A2350612

Coenzyme Q10 , Analysis of standard products, ≥98% , 303-98-0

Synonym(s):
Coenzyme Q10;Q-10;Ubiquinone 50;Ubiquinone-10

CAS NO.:303-98-0

Empirical Formula: C59H90O4

Molecular Weight: 863.34

MDL number: MFCD00042919

EINECS: 206-147-9

Pack Size Price Stock Quantity
20MG RMB87.20 In Stock
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Update time: 2022-07-08

PRODUCT Properties

Melting point: 49-51 °C
Boiling point: 715.32°C (rough estimate)
Density  0.9145 (rough estimate)
refractive index  1.4760 (estimate)
storage temp.  -20°C
solubility  Soluble in chloroform.
form  Solid
color  Light Orange to Dark Orange
Sensitive  Light Sensitive
Merck  14,9843
BRN  1900141
Stability: Stable, but may be light or heat sensitive. Store in the dark at -20 C. Incompatible with strong oxidizing agents.
InChIKey ACTIUHUUMQJHFO-DQXDOXBUSA-N
LogP 19.119 (est)
CAS DataBase Reference 303-98-0(CAS DataBase Reference)
EPA Substance Registry System Ubidecarenone (303-98-0)

Description and Uses

Coenzyme Q10 (CoQ10) is a quinone that is found throughout the human body in cell membranes, primarily in mitochondrial membranes, with the highest levels in the heart, lungs, liver, kidneys, spleen, pancreas, and adrenal glands. It exists in three redox states: fully oxidized (CoQ10/ubiquinone), partially reduced (semiquinone or 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. Mutations in genes encoding enzymes involved in CoQ10 biosynthesis lead to primary CoQ10 deficiency, which is characterized by encephalopathy, cerebellar ataxia, infantile multisystemic form, nephropathy, and isolated myopathy. Secondary CoQ10 deficiency, induced by non-genetic impaired CoQ10 biosynthesis, insufficient CoQ10 intake, or excessive CoQ10 utilization, has been observed in a variety of conditions, including ataxia-oculomotor-apraxia 1 (AOA1), mitochondrial diseases, and hypercholesteremia with statin therapy. Formulations containing CoQ10 have been used in the treatment of CoQ10 deficiency.

Coenzyme Q10 (CoQ10) is a naturally occurring quinone found throughout the body in cell membranes, primarily in mitochondrial membranes, with highest concentrations in the heart, lungs, liver, kidneys, spleen, pancreas, and adrenal glands. It is a component of the electron transport chain and participates in aerobic cellular respiration, generating energy in the form of ATP. In its reduced form, CoQ10 acts as an antioxidant, preventing the formation of reactive oxygen species. CoQ10 deficiencies have been associated with heart failure, hypertension, parkinsonism, mitochondrial encephalomyopathies, and other chronic diseases.[Cayman Chemical]

Safety

Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  22-24/25-26
WGK Germany  3
RTECS  DK3900000
8-10
TSCA  Yes
HS Code  29146990
Toxicity LD50 intramuscular in mouse: > 500mg/kg

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