Meglumine

CAS No. 6284-40-8

Meglumine ( 1-Deoxy-1-(methylamino)-D-glucitol; Iosulamide; N-Methyl-D-glucamine )

Catalog No. M15376 CAS No. 6284-40-8

Meglumine is an amino sugar derived from sorbitol.

Purity : >98%(HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
500MG 45 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Meglumine
  • Note
    Research use only, not for human use.
  • Brief Description
    Meglumine is an amino sugar derived from sorbitol.
  • Description
    Meglumine is an amino sugar derived from sorbitol. It is often used as an excipient in pharmaceuticals and in conjunction with iodinated compounds in contrast media such as diatrizoate meglumine and iodipamide meglumine.
  • Synonyms
    1-Deoxy-1-(methylamino)-D-glucitol; Iosulamide; N-Methyl-D-glucamine
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    Other Indications
  • Indication
    ——

Chemical Information

  • CAS Number
    6284-40-8
  • Formula Weight
    195.21
  • Molecular Formula
    C7H17NO5
  • Purity
    >98%(HPLC)
  • Solubility
    Water: 39 mg/mL (199.78 mM); DMSO: 39 mg/mL (199.78 mM)
  • SMILES
    O[C@H]([C@H]([C@@H]([C@@H](CO)O)O)O)CNC
  • Chemical Name
    (2R,3R,4R,5S)-6-(methylamino)hexane-1,2,3,4,5-pentaol

Shipping & Storage Information

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

Reference

1.Navaei A, et al. Drug Dev Ind Pharm. 2014 Jun;40(6):701-10.
molnova catalog
related products
  • Albiglutide TFA (782...

    Albiglutide TFA, a glucagon-like peptide (GLP)-1 mimetic, is a long acting GLP-1 receptor agonist for the treatment of type 2 diabetes mellitus (T2DM).

  • ELA-32 (human)

    Potent, high affinity apelin receptor agonist (IC50 = 0.27 nM; Kd = 0.51 nM). Exhibits no binding GPR15 and GPR25. Activates the PI3K/AKT pathway and promotes self-renewal of hESCs via cell-cycle progression and protein translation. Also potentiates the TGFβ pathway, priming hESCs toward the endoderm lineage. Stimulates angiogenesis in HUVEC cells. Relaxes mouse aortic vessels. Functions as an anorexigenic hormone through activation of the AVP and CRH neurons in the PVN.

  • Licochalcone E

    Licochalcone E is a potential LXRβ agonist.