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Balsalazide disodium salt dihydrate

CAS No. 150399-21-6

Balsalazide disodium salt dihydrate ( Balsalazide Disodium; balsalazide; BX 661A; Colazal; Colazide )

Catalog No. M18055 CAS No. 150399-21-6

Balsalazide is an anti-inflammatory compound used in the treatment of Inflammatory Bowel Disease.Balsalazide is a new 5-aminosalicylic acid (5-ASA) containing prodrug.

Purity : 98%

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
25MG 118 Get Quote
100MG 273 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
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Biological Information

  • Product Name
    Balsalazide disodium salt dihydrate
  • Note
    Research use only, not for human use.
  • Brief Description
    Balsalazide is an anti-inflammatory compound used in the treatment of Inflammatory Bowel Disease.Balsalazide is a new 5-aminosalicylic acid (5-ASA) containing prodrug.
  • Description
    Balsalazide Disodium is the disodium salt form of balsalazide, an aminosalicylate and oral prodrug that is enzymatically cleaved in the colon to produce the anti-inflammatory agent mesalazine. Mesalazine acts locally on the mucosa of the colon where it diminishes inflammation by blocking the production of arachidonic acid metabolites and other inflammatory agents. Balsalazide disodium is used to treat chronic inflammatory bowel disease.
  • Synonyms
    Balsalazide Disodium; balsalazide; BX 661A; Colazal; Colazide
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    STAT
  • Research Area
    Inflammation/Immunology
  • Indication
    ——

Chemical Information

  • CAS Number
    150399-21-6
  • Formula Weight
    437.31
  • Molecular Formula
    C17H17N3Na2O8
  • Purity
    98%
  • Solubility
    ——
  • SMILES
    [Na+].[Na+].O.O.O=C([O-])c1cc(ccc1O)/N=N/c2ccc(cc2)C(=O)NCCC([O-])=O
  • Chemical Name
    5-[4-(2-Carboxyethylcarbamoyl)phenylazo]salicylic Acid Disodium Salt Dihydrate

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Kruis W, et al. Gut, 2001. 49(6): p. 783-789.
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