Isoprenaline hydrochloride

盐酸异丙肾上腺素

Also known as: Isoproterenol hydrochloride, DL-Isoprenaline hydrochloride, DL-Isoproterenol hydrochloride, N-Isopropyl-DL-noradrenaline hydrochloride, (±)-Isoproterenol hydrochloride, 4-[1-hydroxy-2-(isopropylamino)ethyl]benzene-1,2-diol hydrochloride, Isuprel, Norisodrine hydrochloride

Isoprenaline hydrochloride (CAS 51-30-9) is a compound in the Organic Acids category listed in the Jingsj chemical database. It has the molecular formula C11H18ClNO3 and a molecular weight of 247.719 g/mol. It is also known as Isoproterenol hydrochloride, DL-Isoprenaline hydrochloride and DL-Isoproterenol hydrochloride. Key properties include a melting point of 165-175 °C (dec.)(lit.), a boiling point of 417.5ºC at 760 mmHg, a density of 1.324 g/cm3 and a flash point of 179.7ºC. It is classified under GHS with signal word Warning and hazard statements H315 — Causes skin irritation, H319 — Causes serious eye irritation and H335 — May cause respiratory irritation. No supplier offers are currently listed; request a quote. Record last updated Aug 21, 2026.

CAS No.
51-30-9
Jingsj CID
J-15603-5
Molecular Formula
C11H18ClNO3
Chinese Name
盐酸异丙肾上腺素
Molecular Weight
247.719 g/mol
Category
Organic Acids
Last updated
8/21/2026

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Physicochemical Properties

Melting Point165-175 °C (dec.)(lit.)
Boiling Point417.5ºC at 760 mmHg
Density1.324 g/cm3
Flash Point179.7ºC
Exact Mass247.097519
PSA72.72000
LogP2.32210
StabilityStable, but may be air and light sensitive. Incompatible with strong oxidizing agents.
Additional PropertySoluble

GHS Safety & Compliance

IrritantSignal word: Warning
  • H315 — Causes skin irritation
  • H319 — Causes serious eye irritation
  • H335 — May cause respiratory irritation

Activity & Biological Data

TargetBeta-adrenergic receptor[1]
Additional Information[1]. Degerman E, et al. Evidence that insulin and isoprenaline activate the cGMP-inhibited low-K m cAMP phosphodiesterase in rat fat cells by phosphorylation. Proc Natl Acad Sci U S A. 1990 Jan;87(2):533-7 [2]. Vannucci SJ, et al. Cell surface accessibility of GLUT4 glucose transporters in insulin-stimulated rat adipose cells. Modulation by isoprenaline and adenosine. Biochem J. 1992 Nov 15;288 (Pt 1):325-30. [3]. Delpy E, et al. Effects of cyclic GMP elevation on isoprenaline-induced increase in cyclic AMP and relaxation in rat aortic smooth muscle: role of phosphodiesterase 3. Br J Pharmacol. 1996 Oct;119(3):471-8. [4]. Muller FU, et al. Isoprenaline stimulates gene transcription of the inhibitory G protein alpha-subunit Gi alpha-2 in rat heart. Circ Res. 1993 Mar;72(3):696-700. [5]. Lei M, et al. Modulation of delayed rectifier potassium current, iK, by isoprenaline in rabbit isolated pacemaker cells. Exp Physiol. 2000 Jan;85(1):27-35.

Frequently Asked Questions

What is the CAS number of Isoprenaline hydrochloride?

The CAS number of Isoprenaline hydrochloride is 51-30-9.

What are the molecular formula and molecular weight of Isoprenaline hydrochloride?

Isoprenaline hydrochloride has molecular formula C11H18ClNO3 and molecular weight 247.719 g/mol.

Is Isoprenaline hydrochloride hazardous?

Isoprenaline hydrochloride has GHS signal word Warning and hazard statements H315 — Causes skin irritation; H319 — Causes serious eye irritation; H335 — May cause respiratory irritation.

What are the upstream and downstream products of Isoprenaline hydrochloride?

For Isoprenaline hydrochloride, Upstream Products: Isoprenaline hydrochloride; Downstream Products: Isoprenaline hydrochloride, (-)-Isoproterenol hydrochloride.

Data compiled from public chemical databases and supplier catalogs; supplier offers are provided by suppliers.

Last updated:

How to cite: Jingsj. "Isoprenaline hydrochloride (CAS 51-30-9)". Jingsj Chemical Database. https://www.jingsj.com/compound/J-15603-5 (accessed 2026-10-28).

Data for reference only; verify specifications, grades and regulatory status with suppliers before purchase.