벤젠-1,3-디술폰산

벤젠-1,3-디술폰산
벤젠-1,3-디술폰산 구조식 이미지
카스 번호:
98-48-6
한글명:
벤젠-1,3-디술폰산
동의어(한글):
벤젠-1,3-디술폰산
상품명:
benzene-1,3-disulphonic acid
동의어(영문):
Ai3-28531;Einecs 202-672-2;831-59-4 (2 Sodium);1,3-Benzenedisulfoni;BENZENEMETA-DISULFONATE;benzene 1,3-disulfonate;Piraxostat Impurity 11;BENZENE-3-DISULFONICACID;BENZENE-M-DISULFONIC ACID;1,3-BENZENEDISULPHONICACID
CBNumber:
CB2927550
분자식:
C6H6O6S2
포뮬러 무게:
238.24
MOL 파일:
98-48-6.mol

벤젠-1,3-디술폰산 속성

녹는점
136.0 °C
밀도
1.764±0.06 g/cm3(Predicted)
산도 계수 (pKa)
-1.43±0.30(Predicted)
EPA
m-Benzenedisulfonic acid (98-48-6)

안전

벤젠-1,3-디술폰산 C화학적 특성, 용도, 생산

정의

ChEBI: A member of the class of benzenesulfonic acids consisting of benzene carrying two sulfo groups at positions 1 and 3 respectively.

생산 방법

Benzene-1,3-disulphonic acid is formed as the main product in the sulfonation of benzene or benzenesulfonic acid with excess oleum at temperatures of 80 – 250 ℃. In proportion to the oleum concentration and reaction temperature 1 – 29% of diphenyl sulfone disulfonic acid is formed as an undesired byproduct.

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.]

벤젠-1,3-디술폰산 준비 용품 및 원자재

원자재

준비 용품


벤젠-1,3-디술폰산 공급 업체

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