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| | 2,5-dihydroxybenzenesulphonic acid Basic information |
| Product Name: | 2,5-dihydroxybenzenesulphonic acid | | Synonyms: | 2,5-dihydroxybenzenesulphonic acid;EINECS 201-833-4;Dobesilate;Hydroquinonesulfonic Acid (Dobesilic Acid);Benzenesulfonic acid, 2,5-dihydroxy-;Dobesilic Acid;Calcium Dobesilate Impurity 22 | | CAS: | 88-46-0 | | MF: | C6H6O5S | | MW: | 190.17 | | EINECS: | 201-833-4 | | Product Categories: | | | Mol File: | 88-46-0.mol |  |
| | 2,5-dihydroxybenzenesulphonic acid Chemical Properties |
| density | 1.743±0.06 g/cm3(Predicted) | | pka | -0.51±0.30(Predicted) |
| | 2,5-dihydroxybenzenesulphonic acid Usage And Synthesis |
| Originator | Dicynone,Delalande,France,1965 | | Uses | Isopropyl Quinonesulfonate is a derivative of Sodium quinonesulfonate(51579-78-3), and an impurity of Calcium Dobesilate (C145100). | | Definition | ChEBI: A dihydroxybenzenesulfonic acid that is hydroquinone in which one of the phenyl hydrogens is substituted by a sulfonic acid group. | | Manufacturing Process | 163 grams of pure diethylamine bisulfite are added to an ethyl alcohol
solution of 108 grams of 1,4-benzoquinone at a temperature not above 5°C
and under continuous stirring. After reaction, the alcohol is removed by
distilling under vacuum. The product is recrystallized from ethyl alcohol at
80°C. Yield: 198 grams of diethylammonium cyclohexadienol 4-one-1-
sulfonate-4. MP 125°C. | | Therapeutic Function | Hemostatic |
| | 2,5-dihydroxybenzenesulphonic acid Preparation Products And Raw materials |
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