2,5-Dimethoxybenzo-1,4-quinone manufacturers
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| | 2,5-Dimethoxybenzo-1,4-quinone Basic information |
| Product Name: | 2,5-Dimethoxybenzo-1,4-quinone | | Synonyms: | 2,5-dimethoxy-4-benzoquinone;2,5-DIMETHOXY-1,4-BENZOQUINONE;2,5-DIMETHOXY-P-QUINONE;2,5-DIMETHOXY-PARA-BENZOQUINONE;2,5-Dimethoxybenzo-1,4-quinone;2,5-Dimethoxy-2,5-cyclohexadiene-1,4-dione;2,5-Dimethoxy-p-benzoquinone;2,5-DMBQ | | CAS: | 3117-03-1 | | MF: | C8H8O4 | | MW: | 168.15 | | EINECS: | | | Product Categories: | Anthraquinones, Hydroquinones and Quinones;Benzoquinones;Benzoquinones, etc. (Charge Transfer Complexes);Charge Transfer Complexes for Organic Metals;Functional Materials | | Mol File: | 3117-03-1.mol |  |
| | 2,5-Dimethoxybenzo-1,4-quinone Chemical Properties |
| Melting point | >200 °C (decomp) | | Boiling point | 311.1±42.0 °C(Predicted) | | density | 1.24±0.1 g/cm3(Predicted) | | storage temp. | -20°C Freezer | | solubility | Chloroform (Slightly, Heated), Methanol (Slightly, Heated) | | form | Solid | | color | Pale Yellow to Yellow |
| Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | HS Code | 2914500090 |
| | 2,5-Dimethoxybenzo-1,4-quinone Usage And Synthesis |
| Uses | 2,5-DMBQ (2,5-Dimethoxybenzoquinone) serves as an extracellular reductant. 2,5-DMBQ is involved in a crucial redox cycle, namely the extracellular hydroquinone-quinone redox cycle. In this cycle, 2,5-DMBQ is capable of reducing extracellular Fe3 and generating H2O2. 2,5-DMBQ plays a pivotal role in the biodegradation mechanism of brown rot fungal, assisting the fungi in decomposing and utilizing organic matter[1][2]. | | Definition | ChEBI: Thermophillin is a member of benzoquinones and a member of p-quinones. | | Synthesis Reference(s) | Journal of the American Chemical Society, 117, p. 8879, 1995 DOI: 10.1021/ja00139a033 | | References | [1] Varela E, et al. Effect of pH and oxalate on hydroquinone-derived hydroxyl radical formation during brown rot wood degradation. Appl Environ Microbiol. 2003;69(10):6025-6031. DOI:10.1128/AEM.69.10.6025-6031.2003 [2] Jensen KA Jr, et al. Pathways for extracellular Fenton chemistry in the brown rot basidiomycete Gloeophyllum trabeum. Appl Environ Microbiol. 2001 Jun;67(6):2705-11. DOI:10.1128/AEM.67.6.2705-2711.2001 |
| | 2,5-Dimethoxybenzo-1,4-quinone Preparation Products And Raw materials |
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