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磺胺氯吡嗪

时间:2023-07-15  来源:化工号   作者:C10H9ClN4O2S
  • 磺胺氯吡嗪
  • 三字球虫粉
  • 磺胺氯吡嗪钠
  • 磺胺氯毗嗪钠
  • 磺胺氯吡嗪鈉
  • 磺胺氯吡嗪钠一水合物
  • 磺胺氯吡嗪(标准品)
  • 磺胺氯吡嗪溶液, 100PPM
  • N-(5-氯-3-吡嗪基)-4-氨基苯磺酰胺
  • 中文名 磺胺氯吡嗪
    英文名 Sulfaclozine
    别名 磺胺氯吡嗪
    三字球虫粉
    磺胺氯吡嗪钠
    磺胺氯毗嗪钠
    磺胺氯吡嗪鈉
    磺胺氯吡嗪钠一水合物
    磺胺氯吡嗪(标准品)
    磺胺氯吡嗪溶液, 100PPM
    N-(5-氯-3-吡嗪基)-4-氨基苯磺酰胺
    英文别名 SPZ
    Sulfaclozine
    Sulfaclozina
    sulfaclozine
    Sulfaclozinum
    UNII-69YP7Z48CW
    Sulfachlorpyrazin
    sulfachloropyrazine
    SULFACLOZINE SODIUM
    SULFACHLORPYRAZINE SODIUM
    SULFACHLOROPYRAZINE SODIUM
    Sulfachloropyrazine Sodium
    Sulfachloropyrazinum Natricum
    SULFACHLOROPYRAZINE SODIUM H2O
    Sulfachloropyrazine,sodium salt
    N1-(6-Chlor-2-pyrazinyl)sulfanilamid
    N(sup 1)-(6-Chloropyrazinyl)sulfanilamide
    N-(5-Chloro-3-Pyrazine)-4-Aminobenzenesulfonamino
    4-amino-N-(5-chloropyrazin-2-yl)benzenesulfonamide
    4-amino-N-(6-chloropyrazin-2-yl)benzenesulfonamide
    N-(5-CHLORO-3-PYRAZINE)-4-AMINOBENZENESULFONAININO SODIUM MONOHYDRATE
    CAS 102-65-8
    EINECS 203-044-0
    化学式 C10H9ClN4O2S
    分子量 284.72
    InChI InChI:1S/C10H9ClN4O2S/c11-9-5-13-6-10(14-9)15-18(16,17)8-3-1-7(12)2-4-8/h1-6H,12H2,(H,14,15)
    密度 1.588±0.06 g/cm3(Predicted)
    熔点 234.8-235.4 °C
    沸点 495.7±55.0 °C(Predicted)
    溶解度 DMSO (Slightly), Methanol (Slightly, Heated, Sonicated)
    酸度系数 4.83±0.10(Predicted)
    存储条件 2-8°C(protect from light)
    外观 Solid
    颜色 White to Off-White
    产品用途 禽畜消炎抗菌药,主要用于治疗鸡、兔、羊球虫病(盲肠球虫)鸡霍乱及伤寒等
    MDL号 MFCD00868569
    体外研究 The elimination of Sulfaclozine in the three systems: UV/TiO 2 , UV/K 2 S 2 O 8 , and UV/TiO 2 /K 2 S 2 O 8 . Sulfaclozine is weakly adsorbed on the surface of TiO 2 at pH 7 (< 5%) but efficiently eliminated with the following three systems: UV/TiO 2 , UV/K 2 S 2 O 8 , and UV/TiO 2 /K 2 S 2 O 8 in ultra pure water. Moreover, 12 of Sulfaclozine by-products are identified and reaction pathways show that, in addition of • OH and SO 4 •− radicals, the conduction-band electrons are responsible for the formation of some main by-products either directly or by the formation of superoxide radicals.
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