| CAS: | 605-94-7 |
| MF: | C9H10O4 |
| MW: | 182.17 |
| EINECS: | 210-100-8 |
| Product Categories: | Miscellaneous Biochemicals;Anthraquinones, Hydroquinones and Quinones;(intermediate of coenzyme Q10);Benzoquinones;Benzoquinones, etc. (Charge Transfer Complexes);Biochemistry;Charge Transfer Complexes for Organic Metals;Functional Materials;Vitamin Related Compounds;Vitamins |
| Mol File: | 605-94-7.mol |
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| 2,3-Dimethoxy-5-methyl-p-benzoquinone Chemical Properties |
| Melting point | 58-60 °C(lit.) |
| Boiling point | 331.4±42.0 °C(Predicted) |
| density | 1.19±0.1 g/cm3(Predicted) |
| storage temp. | 2-8°C |
| Water Solubility | almost transparency in hot Water |
| solubility | DMF: 100 mg/ml; DMSO: 100 mg/ml; Ethanol: 5 mg/ml; PBS (pH 7.2): 0.2 mg/ml |
| form | Crystalline Powder or Needles |
| color | Red to orange |
| Sensitive | Light Sensitive |
| BRN | 1640422 |
| Stability: | Stable. Combustible. Incompatible with strong oxidizing agents, reducing agents. |
| CAS DataBase Reference | 605-94-7(CAS DataBase Reference) |
| NIST Chemistry Reference | 2,5-Cyclohexadiene-1,4-dione, 2,3-dimethoxy-5-methyl-(605-94-7) |
| 2,3-Dimethoxy-5-methyl-p-benzoquinone Usage And Synthesis |
| Chemical Properties | red or orange crystals or fibres |
| Uses | 2,3-Dimethoxy-5-methyl-p-benzoquinone (Ubidecarenone EP Impurity A) |
| Definition | ChEBI: A derivative of benzoquinone carrying a 5-methyl substituent; and methoxy substituents at positions 2 and 3. The core structure of the ubiquinone group of compounds. |
| Synthesis Reference(s) | Chemical and Pharmaceutical Bulletin, 16, p. 2343, 1968 DOI: 10.1248/cpb.16.2343
The Journal of Organic Chemistry, 53, p. 5453, 1988 DOI: 10.1021/jo00258a010 |
| General Description | 2,3-Dimethoxy-5-methyl-p-benzoquinone (Coenzyme Q0 or DMM) is present in all the cells including neural cells. |
| Biochem/physiol Actions | 2,3-Dimethoxy-5-methyl-p-benzoquinone (Coenzyme Q0) interacts with tau protein and aids in the formation of filamentous structure. |
| Purification Methods | It crystallises in red needles from pet ether (b 40-60o) and sublimes at high vacuum at a bath temperature of 46-48o [Ashley et al. J Chem Soc 441 1938, UV in EtOH: Vischer J Chem Soc 815 1953, UV in cyclohexane: Morton et al. Helv Chim Acta 41 2343 1858, Aghoramurthy et al. Chem Ind (London) 1327 1954]. [Beilstein 8 IV 2721.] |
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Packing &shipping&Payment
Packing:25kg/drum
Shipping:by sea or by air
Payment:T/T,western union,moneygram
Packaging Details drum
Port:Tianjin
Lead Time :
| Quantity(Kilograms) | 1 - 10000 | >10000 |
| Est. Time(days) | 5 | To be negotiated |
Company information
Hebei Mojin Biotechnology Co., Ltd, Our company is a professional in 4'-Methylacetophenone,Levamisole hydrochloride ,N-Methylformamide and other chemical reagents research and development production enterprises. Our business covers more than 30 countries, most of the big customers come from Europe, America and other countries in the world, we can guarantee the quality and price. In recent decades, with the efforts of all employees, we have established many cooperative companies in shandong, henan, guangdong and other places. Our corporate purpose is based on the market, enhance the strength, take the road of scientific and environmental sustainable development, relying on the country. Technology r & d center, increase the investment in r & d, based on the domestic market, expand the international market, manufacturing quality products, sincere service to the society, into a modern, ecological, scientific and technological enterprise world.
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