API's
Active Pharmaceutical Ingredients
Active Pharmaceutical Ingredients
API
BP / USP
C16H22ClNO2
(RS)-1-(Isopropylamino)-3-(1-naphthyloxy)propan-2-ol hydrochloride
318-98-9
295.81 g/mol
Naphthoxypropanolamine derivative
Antihypertensive agent
| Appearance | White to off-white crystalline powder |
|---|---|
| Solubility | Freely soluble in water, methanol, and ethanol; slightly soluble in chloroform; insoluble in ether |
| Melting Point | 163–166°C |
| pH (1% aqueous solution) | 4.5 – 6.5 |
Propranolol Hydrochloride is a non-selective beta-adrenergic receptor blocker used for hypertension, angina pectoris, cardiac arrhythmias, and anxiety-related tachycardia. It remains a cost-effective cornerstone therapy in cardiovascular care.
Propranolol competitively blocks beta-1 (β1) and beta-2 (β2) adrenergic receptors, reducing heart rate, myocardial contractility, and cardiac output, while suppressing sympathetic nervous system stimulation. This results in lower blood pressure and decreased cardiac workload.
| Attribute | Why Salius Pharma Is a Good Choice |
|---|---|
| Quality Certification | WHO GMP, ISO 9001:2015, FDA audited facilities |
| Affordability & Generic Access | Cost competitive generics for global supply |
| Export Experience | Proven track record of supplying globally |
When you order from Salius Pharma, you receive more than just a product — you receive a complete, professionally prepared package that meets international regulatory and quality expectations.
We ensure prompt and reliable shipping worldwide. Delivery times vary depending on destination, order volume, and regulatory requirements.
7 to 21 business days from dispatch, depending on your location.
Manufactured under WHO-GMP and ICH Q7 guidelines with validated synthesis and impurity profiling to meet pharmacopeial standards.
Yes. We offer micronized and non-micronized grades tailored for tablets, capsules, and liquid dosage forms to ensure desired dissolution properties.
Our API is registered and supplied across LATAM, MENA, CIS, and Southeast Asia with CTD/ACTD dossiers and full analytical documentation.
Each batch is packed in HDPE drums with double PE liners, optionally nitrogen-flushed for stability. Shipments follow GDP with COA, MSDS, and TDS enclosed.
Each lot undergoes in-process monitoring, HPLC and GC assays, moisture and stability testing (Zone IVa/IVb) to ensure consistent purity and potency.
Yes. DMF open parts, stability data, and specifications are available prior to commercial agreement for evaluation and registration support.
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Whether you need Active Pharmaceutical Ingredients (APIs), finished formulations, or regulatory support,
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Any patented products are excluded from our offerings in regions where such patents are currently in force.