Epinephrine HCl

CAS No. 55-31-2

Epinephrine HCl ( Epinephrine hydrochloride; l-Adrenaline chloride )

Catalog No. M18798 CAS No. 55-31-2

Epinephrine HCl is a hormone and a neurotransmitter.

Purity : 98%

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
25MG 49 In Stock
50MG 72 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Epinephrine HCl
  • Note
    Research use only, not for human use.
  • Brief Description
    Epinephrine HCl is a hormone and a neurotransmitter.
  • Description
    Epinephrine HCl is a hormone, neurotransmitter, and medication. Epinephrine is normally produced by both the adrenal glands and certain neurons. It plays an important role in the fight-or-flight response by increasing blood flow to muscles, output of the heart, pupil dilation, and blood sugar. It does this by binding to alpha and beta receptors. It is found in many animals and some single cell organisms.
  • Synonyms
    Epinephrine hydrochloride; l-Adrenaline chloride
  • Pathway
    MAPK/ERK Signaling
  • Target
    ERK
  • Recptor
    Adrenergic Receptor
  • Research Area
    Others-Field
  • Indication
    ——

Chemical Information

  • CAS Number
    55-31-2
  • Formula Weight
    219.67
  • Molecular Formula
    C9H13NO3·HCl
  • Purity
    98%
  • Solubility
    ——
  • SMILES
    Cl.CNC[C@H](O)C1=CC=C(O)C(O)=C1
  • Chemical Name
    4-(1-hydroxy-2-(methylamino)ethyl)benzene-1,2-diol hydrochloride

Shipping & Storage Information

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

Reference

1. Berecek KH, et al. Am J Physiol, 1982, 242(4), H593-601.
molnova catalog
related products
  • GSK2656157

    GSK2656157 is an ATP-competitive and highly selective inhibitor of PERK with IC50 of 0.9 nM in a cell-free assay.

  • Muramyl dipeptide

    Muramyl dipeptide is a synthetic immunoreactive peptide, consisting of N-acetyl muramic acid attached to a short amino acid chain of L-Ala-D-isoGln.

  • FR 180204

    FR 180204 is a potent, selective, ATP-competitive ERK inhibitor with Ki of 0.31 and 0.14 uM for ERK1 and ERK2, respectively.