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Ethacridine lactate monohydrate

CAS No. 6402-23-9

Ethacridine lactate monohydrate( Rivanol monohydrate | Ethodin )

Catalog No. M15434 CAS No. 6402-23-9

Ethacridine lactate monohydrate is an aromatic organic compound based on acridine used as an antiseptic agent.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    Ethacridine lactate monohydrate
  • Note
    Research use only, not for human use.
  • Brief Description
    Ethacridine lactate monohydrate is an aromatic organic compound based on acridine used as an antiseptic agent.
  • Description
    Ethacridine lactate monohydrate is an aromatic organic compound based on acridine used as an antiseptic agent.(In Vitro):Acrinol is effective against S. aureus including MRSA, with the MICs ranging from 100-200 μg/mL. The MIC of Acrinol for Eschericia coli is 200-800 μg/mL, and it is over 1,600 μg/mL for Proteus vulgaris and Proteus mirabilis.(In Vivo):Ethacridine lactate can be used for termination of pregnancy.
  • In Vitro
    Acrinol is effective against S. aureus including MRSA, with the MICs ranging from 100-200 μg/mL. The MIC of Acrinol for Eschericia coli is 200-800 μg/mL, and it is over 1,600 μg/mL for Proteus vulgaris and Proteus mirabilis.
  • In Vivo
    Ethacridine lactate can be used for termination of pregnancy.
  • Synonyms
    Rivanol monohydrate | Ethodin
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    Infection
  • Indication
    ——

Chemical Information

  • CAS Number
    6402-23-9
  • Formula Weight
    361.4
  • Molecular Formula
    C18H23N3O5
  • Purity
    >98% (HPLC)
  • Solubility
    Water: 5 mg/mL (13.83 mM); DMSO: 72 mg/mL (199.23 mM)
  • SMILES
    CC(O)C(O)=O.NC1=CC2=NC3=CC=C(OCC)C=C3C(N)=C2C=C1.[H]O[H]
  • Chemical Name
    7-ethoxyacridine-3,9-diamine 2-hydroxypropanoate hydrate

Shipping & Storage Information

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

Reference

1. Junka A, et al. Int Wound J, 2013.
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