edetate calcium disodium

CAS No. 62-33-9

edetate calcium disodium ( EDTA calcium disodium )

Catalog No. M27549 CAS No. 62-33-9

Edetate calcium disodium, a chelating agent, is primarily used for the management of severe lead poisoning.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 36 In Stock
10MG 51 In Stock
25MG 85 In Stock
50MG 124 In Stock
100MG 178 In Stock
200MG 267 In Stock
500MG 461 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    edetate calcium disodium
  • Note
    Research use only, not for human use.
  • Brief Description
    Edetate calcium disodium, a chelating agent, is primarily used for the management of severe lead poisoning.
  • Description
    Edetate calcium disodium, a chelating agent, is primarily used for the management of severe lead poisoning.
  • Synonyms
    EDTA calcium disodium
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    p53;FAK
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    62-33-9
  • Formula Weight
    374.3
  • Molecular Formula
    C10H12CaN2Na2O8
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    [Na+].[Na+].[Ca++].[O-]C(=O)CN(CCN(CC([O-])=O)CC([O-])=O)CC([O-])=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Learmount J, Callaby R, Taylor M. An observational study of ewe treatments at lambing on early infection in lambs on UK sheep farms. Vet Parasitol. 2018 Apr 15;253:55-59.
molnova catalog
related products
  • Neoechinulin A

    Neoechinulin A has anti-inflammatory effect against LPS-stimulated RAW264.7 macrophages through inhibition of the NF-κB and p38 MAPK pathways.

  • GR 64349

    Potent and selective tachykinin NK2 receptor agonist (EC50 = 3.7 nM in rat colon). Displays > 1000- and > 300-fold selectivity over NK1 and NK3 receptors respectively. Active in vivo.

  • PF-543

    PF-543, a novel sphingosine-competitive inhibitor of SphK1, inhibits SphK1 with IC50 and Ki of 2.0 nM and 3.6 nM.