Phenolphthalein

CAS No. 77-09-8

Phenolphthalein( Phenolphthalein | Euchessina | Phthalimetten | Chocolax | Espotabs )

Catalog No. M15915 CAS No. 77-09-8

An acid-base indicator which is colorless in acid solution, but turns pink to red as the solution becomes alkaline. It is used medicinally as a cathartic.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
500MG 38 In Stock
1G 45 In Stock

Biological Information

  • Product Name
    Phenolphthalein
  • Note
    Research use only, not for human use.
  • Brief Description
    An acid-base indicator which is colorless in acid solution, but turns pink to red as the solution becomes alkaline. It is used medicinally as a cathartic.
  • Description
    An acid-base indicator which is colorless in acid solution, but turns pink to red as the solution becomes alkaline. It is used medicinally as a cathartic.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Phenolphthalein | Euchessina | Phthalimetten | Chocolax | Espotabs
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    Other Indications
  • Indication
    ——

Chemical Information

  • CAS Number
    77-09-8
  • Formula Weight
    318.33
  • Molecular Formula
    C20H14O4
  • Purity
    >98% (HPLC)
  • Solubility
    Water: 400 mg/L
  • SMILES
    O=C1OC(C2=CC=C(O)C=C2)(C3=CC=C(O)C=C3)C4=CC=CC=C14
  • Chemical Name
    3,3-Bis(4-hydroxyphenyl)-2-benzofuran-1-one

Shipping & Storage Information

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

Reference

1.Uesawa Y, et al. Arch Toxicol. 2007 Mar;81(3):163-8.
molnova catalog
related products
  • V9302

    V-9302 (V9302) is a competitive antagonist of transmembrane glutamine flux that selectively and potently targets the amino acid transporter ASCT2 (IC50: 9.6 uM).

  • 5,6-dibromo-1H-indol...

    5,6-dibromo-1H-indole-3-carboxylic acid is a marine derived natural products found in Smenospongia sp.

  • BAY-179

    BAY-179 is a potent, selective, and species cross-reactive complex I inhibitor used for cancer research.