Antazoline hydrochloride

CAS No. 2508-72-7

Antazoline hydrochloride ( 2-(N-Benzylanilinomethyl)-2-imidazoline Hydrochloride )

Catalog No. M13739 CAS No. 2508-72-7

Antazoline hydrochloride is a first generation antihistamine, binding to the histamine H1 receptor and blocking the action of endogenous histamine.

Purity : >98%(HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
50MG 38 In Stock
100MG 53 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Antazoline hydrochloride
  • Note
    Research use only, not for human use.
  • Brief Description
    Antazoline hydrochloride is a first generation antihistamine, binding to the histamine H1 receptor and blocking the action of endogenous histamine.
  • Description
    Antazoline hydrochloride is a first generation antihistamine, binding to the histamine H1 receptor and blocking the action of endogenous histamine.
  • Synonyms
    2-(N-Benzylanilinomethyl)-2-imidazoline Hydrochloride
  • Pathway
    GPCR/G Protein
  • Target
    Histamine Receptor
  • Recptor
    H1 receptor
  • Research Area
    Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    2508-72-7
  • Formula Weight
    301.82
  • Molecular Formula
    C17H19N3·HCl
  • Purity
    >98%(HPLC)
  • Solubility
    Ethanol: 4 mg/mL (13.25 mM); Water: 14 mg/mL (46.38 mM); DMSO: 40 mg/mL (132.53 mM)
  • SMILES
    Cl.C(N(CC1=CC=CC=C1)C1=CC=CC=C1)C1=NCCN1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Milhaud D, et al. Neuroscience, 2003, 120(2), 475-484.
molnova catalog
related products
  • Clemastine fumarate

    Clemastine Fumarate is a selective histamine H1 receptor antagonist with IC50 of 3 nM.

  • Calcium carbonate

    Calcium Carbonate is the carbonic salt of calcium (CaCO3).

  • JNJ 39220675

    JNJ 39220675 is potent and selective, brain penetrant H3 antagonist with Ki of 1.4 nM, pA2 of 9.42 for hH3.