Tolazoline

CAS No. 59-98-3

Tolazoline( Vasimid | Benzalolin | Divascol | Pridazole | Priscol | Priscoline )

Catalog No. M27407 CAS No. 59-98-3

Tolazoline, a non-selective competitive α-adrenergic receptor antagonist, is used as a vasodilator to treat spasms of peripheral blood vessels.

Purity : >98% (HPLC)

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

Biological Information

  • Product Name
    Tolazoline
  • Note
    Research use only, not for human use.
  • Brief Description
    Tolazoline, a non-selective competitive α-adrenergic receptor antagonist, is used as a vasodilator to treat spasms of peripheral blood vessels.
  • Description
    Tolazoline, a non-selective competitive α-adrenergic receptor antagonist, is used as a vasodilator to treat spasms of peripheral blood vessels. It has also been used successfully as an antidote to reverse the severe peripheral vasoconstriction as a result of overdose with certain 5-HT2A agonist drugs.
  • In Vitro
    Tolazoline (Imidaline) can be synthesized by the heterocyclation of the ethyl ester of iminophenzylacetic acid with ethylene diamine, which forms the desired product. The structure of Tolazoline (Imidaline) is strikingly similar to α-adrenergic agonists, which are antiedema sympathomimetics.
  • In Vivo
    ——
  • Synonyms
    Vasimid | Benzalolin | Divascol | Pridazole | Priscol | Priscoline
  • Pathway
    Angiogenesis
  • Target
    Adrenergic Receptor
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    59-98-3
  • Formula Weight
    160.22
  • Molecular Formula
    C10H12N2
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    C(C1=NCCN1)c1ccccc1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Shotton DM, et, al. Amino-acid sequence of porcine pancreatic elastase and its homologies with other serine proteinases. Nature. 1970 Feb 28;225(5235):802-6.
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