CAS No. 148849-67-6

Batch: Purity:99.74
Ivabradine HCl Chemical Structure
Chemical Structure
Check the Ivabradine HCl product page for in-depth specifications, including solubility, stock solutions, MOA, and working concentrations.

Chemical Information

IUPAC Name 3-[3-[[(7S)-3,4-dimethoxy-7-bicyclo[4.2.0]octa-1,3,5-trienyl]methyl-methylamino]propyl]-7,8-dimethoxy-2,5-dihydro-1H-3-benzazepin-4-one;hydrochloride
CAS Number 148849-67-6
Molecular Formula

C27H36N2O5.HCl

Molecular Weight (MW) 505.05
SMILES CN(CCCN1CCC2=CC(=C(C=C2CC1=O)OC)OC)CC3CC4=CC(=C(C=C34)OC)OC.Cl
InChIKey HLUKNZUABFFNQS-ZMBIFBSDSA-N

Ordering Information

Biological Activity

Ivabradine HCl is a selective hyperpolarization-activated cyclic nucleotide-gated (HCN) channel blocker that selectively inhibits the cardiac pacemaker If current. By targeting HCN channels in the sinoatrial node, it suppresses spontaneous diastolic depolarization and slows the pacemaker firing rate without altering cardiac contractility or ventricular repolarization pathways. This selective mechanism reduces heart rate through precise modulation of cardiac ionic currents. [1]

How to Prepare Stock Solution?

Concentration Volume Mass
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Solubility

Batch:
All in vitro solubility values are batch-tested experimental data (non-literature values).
Solvent Solubility & Note
DMSO 101 mg/mL (199.98 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO. The recommended stock concentration is 10 mM in DMSO.)
Ethanol 101 mg/mL
Water 82 mg/mL
FAQ
Q: Why does a DMSO stock precipitate in media/saline?
A: It is caused by unheated aqueous media (supersaturation), local solvent shock, or incorrect mixing sequence.
How to fix it?
  • Preheat media/saline to 37°C.
  • Mix rapidly (pipette/vortex) upon addition.
  • For complex mixes, always add the aqueous phase last.
  • Re-dissolve minor precipitates with a 37°C water bath and sonication (≤30 min).

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Note: Technical data last updated: Sep 1, 2026.