An adrenergic receptor agonist
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(±)-Epinephrine (hydrochloride)

Item No. 21245

Technical Information
Formal Name
4-[1-hydroxy-2-(methylamino)ethyl]-1,2-benzenediol, monohydrochloride
CAS Number
329-63-5
Synonyms
  • (±)-Adrenaline
  • DL-Adrenaline
  • DL-Epinephrine
Molecular Formula
C9H13NO3 • HCl
Formula Weight
Purity
≥95%
Formulation
A crystalline solid
DMF: 20 mg/mlDMSO: 20 mg/mlPBS (pH 7.2): 5 mg/ml
λmax
225, 282 nm
SMILES
OC1=C(O)C=CC(C(O)CNC)=C1.Cl
InChi Code
InChI=1S/C9H13NO3.ClH/c1-10-5-9(13)6-2-3-7(11)8(12)4-6;/h2-4,9-13H,5H2,1H3;1H
InChi Key
ATADHKWKHYVBTJ-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    (±)-Epinephrine is a natural neurotransmitter that is released from the adrenal medulla and activates adrenoceptors (Kis = 15, 735, and 3,970 nM for α1A-, β2-, and β1-adrenergic receptors, respectively).1,2,3 Through these receptors, (±)-epinephrine may induce either contraction or relaxation of vascular smooth muscle, depending on adrenoceptor subtype expression.3 Formulations containing (±)-epinephrine have been used in the emergency treatment of severe allergic reactions and the induction and maintenance of mydriasis during intraocular surgery.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Rothman, R.B., Vu, N., Partilla, J.S., et alIn vitro characterization of ephedrine-related stereoisomers at biogenic amine transporters and the receptorome reveals selective actions as norepinephrine transporter substrates. J. Pharmacol. Exp. Ther. 307(1), 138-145 (2003).

    2. Hoffmann, C., Leitz, M.R., Oberdorf-Maass, S., et alComparative pharmacology of human β-adrenergic receptor subtypes—characterization of stably transfected receptors in CHO cells. N.-S. Arch. Pharmacol. 369(2), 151-159 (2004).

    3. Ahles, A., and Englehardt, S. Polymorphic variants of adrenoceptors: Pharmacology, physiology, and role in disease. Pharmacol. Rev. 66(3), 598-637 (2014).