Identification | Back Directory | [Name]
benzene-1,3-disulphonic acid | [CAS]
98-48-6 | [Synonyms]
Ai3-28531 Einecs 202-672-2 831-59-4 (2 Sodium) 1,3-Benzenedisulfoni benzene 1,3-disulfonate BENZENEMETA-DISULFONATE BENZENE-3-DISULFONICACID BENZENE-M-DISULFONIC ACID 1,3-Benzenedisulfonic acid 1,3-BENZENEDISULPHONICACID META-BENZENEDISULPHONICACID benzene-1,3-disulphonic acid Benzene-1,3-bis(sulfonic acid) | [EINECS(EC#)]
202-672-2 | [Molecular Formula]
C6H6O6S2 | [MOL File]
98-48-6.mol | [Molecular Weight]
238.24 |
Hazard Information | Back Directory | [Definition]
ChEBI: A member of the class of benzenesulfonic acids consisting of benzene carrying two sulfo groups at positions 1 and 3 respectively. | [Purification Methods]
Free it from H2SO4 by conversion to the calcium or barium salts (using Ca(OH)2 or Ba(OH)2, and filtering). The calcium salt is then converted to the potassium salt, using K2CO3. Both the potassium and the barium salts are recrystallised from H2O, and the acid is regenerated by passing through the H+ form of a strong cation exchange resin. The acid is recrystallised twice from conductivity water and dried over CaCl2 at 25o. [Atkinson et al. J Am Chem Soc 83 1570 1961.] It has also been crystallised from Et2O and dried in a vacuum oven. The S-benzylisothiuronium salt has m 214.3o (from EtOH/H2O). [Beilstein 11 IV 553.] It is best kept as the disodium salt [831-59-4] which decomposes on heating [Beilstein 11 H 199, 11 I 48, 11 II 213, 11 III 453.] |
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