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CAS RN: 303-97-9 | Product Number: C3876
Coenzyme Q9
×
Purity: >98.0%(HPLC)
Synonyms:
- Ubiquinone-9
- CoQ9
- 2,3-Dimethoxy-5-methyl-6-((2E,6E,10E,14E,18E,22E,26E,30E)-3,7,11,15,19,23,27,31,35-nonamethylhexatriaconta-2,6,10,14,18,22,26,30,34-nonaen-1-yl)cyclohexa-2,5-diene-1,4-dione
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| 25MG |
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| Product Number | C3876 |
Purity / Analysis Method 
|
>98.0%(HPLC) |
| Molecular Formula / Molecular Weight | C__5__4H__8__2O__4 = 795.25 |
| Physical State (20 deg.C) | Solid |
| Storage Temperature
|
Frozen (<0°C) |
| Store Under Inert Gas | Store under inert gas |
| Condition to Avoid | Light Sensitive,Air Sensitive,Heat Sensitive |
| CAS RN | 303-97-9 |
| Reaxys Registry Number | 1900081 |
| MDL Number | MFCD00056635 |
Specifications
| Appearance | Light yellow to Yellow to Orange powder to crystal |
| Purity(HPLC) | min. 98.0 area% |
| Melting point | 41.0 to 45.0 °C |
| NMR | confirm to structure |
Properties (reference)
| Melting Point | 43 °C |
GHS
Related Laws:
| RTECS# | DK4786000 |
Transport Information:
| H.S.code* | 2914.69-000 |
Application
Mitochondria research
References
- Dysfunctional Coq9 protein causes predominant encephalomyopathy associated with CoQ deficiency
- The submitochondrial distribution of ubiquinone affects respiration in long-lived Mclk1+/- mice
- A Nonsense Mutation in COQ9 Causes Autosomal-Recessive Neonatal-Onset Primary Coenzyme Q10 Deficiency: A Potentially Treatable Form of Mitochondrial Disease
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