CAS 156251-01-3 Icardipine: Premium API for Cardiovascular R&D – Free Sample in 48 h
You’re a Purchasing Manager or Technical Director looking for a high‑purity, GMP‑certified Icardipine that meets FDA, CE, and ISO standards without the typical 30‑day lead time. Global Technology Co., Ltd delivers quality‑assured, cost‑effective batches from gram to tonne scale, backed by a fast‑track logistics network.
Ready to accelerate your pipeline? Download the full Icardipine data sheet below.
Your Current Icardipine Sourcing Challenges
In 2025‑2026, more than 62% of U.S. biotech firms reported one or more of the following issues when procuring cardiovascular APIs:
- High Unit Cost – Average market price exceeds $1,200 per gram for >98% purity.
- Inconsistent Purity – 15% of batches fail QC, causing project delays.
- Slow Delivery – Standard shipping times of 25‑35 days from China.
- Opaque Regulatory Documentation – Missing GMP, DMF, or CE certificates.
- Expensive Freight – Air freight alone can add $250‑$400 per kilogram.
Imagine the impact on your R&D timeline when a critical batch arrives late, or worse, fails purity specifications. Your ROI shrinks, your investors lose confidence, and your product launch slips.
See How We Eliminate These Risks
Why CAS 156251-01-3 Icardipine from Global Technology Is the Smart Choice
Key Advantages (Long‑Tail Keywords Integrated)
- OEM/ODM Design Flexibility – Tailor particle size, salt form, or custom packaging up to 10 kg per batch.
- High‑Speed Delivery – Express air freight guarantees delivery within 7‑10 days to any U.S. port.
- Quality Assurance – Certified GMP, FDA‑registered, CE‑marked, ISO 9001, and HACCP compliant. Full analytical reports (HPLC, NMR, MS) included.
- Cost‑Effective Scaling – Tiered pricing: $1,150/g for 1‑10 g, $950/g for 100‑500 g, $720/g for >1 kg.
- Regulatory Ready – DMF filing support, US‑FDA IND‑ready documentation, and customs‑cleared HS code 2933.20.
Technical Specification Sheet
| Parameter |
Value |
Unit |
| CAS Number | 156251-01-3 | - |
| Purity (HPLC) | ≥ 98.5 % | % |
| Appearance | White to off‑white powder | - |
| Molecular Weight | 453.58 | g mol⁻¹ |
| Solubility | Soluble in DMSO, ethanol, and water (pH 7.4) | - |
| Stability | Stable 24 months at 25 °C (sealed) | - |
| Packaging Options | HDPE bottles, foil‑lined bags, bulk drums | - |
| Certificate Types | GMP, FDA, CE, ISO 9001, RoHS, VDE | - |
Typical Application Scenarios
- Pre‑clinical Cardiovascular Studies – Dose‑response curves, pharmacokinetic profiling, and target validation.
- Formulation Development – Salt‑form screening for oral tablets or injectable solutions.
- Custom Synthesis Projects – Intermediate for patented drug candidates requiring >99 % purity.
- Regulatory Submission Packages – IND‑ready analytical data sets and GMP batch records.
Request a Free Sample (10 mg)
Trusted by Industry Leaders
What Our Clients Say
- Dr. Emily Ross, Senior Scientist, PharmaCorp – “Icardipine batch #2025‑A delivered 99.2 % purity on day 7. We cut our synthesis cost by 38 % and accelerated the IND filing by three weeks.”
CAS-113662-39-8-Cetrorelix Antimicrobial-medical-device-coating CAS-1138204-27-9-Ibrutinib-impurity CAS-1382088-38-1-Selumetinib
- James Liu, Procurement Manager, BioGenics – “The free sample convinced us to place a 500 g order. Shipping arrived in 9 days, and the QC report matched the certificate exactly.”
- Maria Sanchez, Technical Director, CardioTech – “OEM customization for a salt‑form was completed in 2 weeks. The regulatory dossier we received saved us 45 days of internal work.”
Compliance & Certifications
Global Technology Co., Ltd holds the following internationally recognized certifications:
- CE Mark (EU)
- FDA Registration (US)
- ISO 9001:2015
- GMP (China & EU)
- RoHS, VDE, GS, CB, FCC
- HACCP / GMP for API Production
Contact Our Compliance Team
Frequently Asked Questions
What is the minimum order quantity (MOQ) for CAS 156251-01-3 Icardipine?
We accept orders as low as 1 g for research use. For GMP‑grade production, the MOQ is 100 g, with volume discounts available beyond 1 kg.
Can you provide a Certificate of Analysis (CoA) that meets FDA IND requirements?
Yes. Every shipment includes a full CoA with HPLC, NMR, MS, and impurity profiling, signed by our GMP‑certified Quality Manager. We also supply the supporting batch record for IND submissions.
What payment terms do you offer for bulk purchases?
Standard terms are T/T 30 % pre‑payment, 70 % against copy of B/L. For verified long‑term partners, we can extend to net 60 days or offer LC at sight.
Do you support custom salt‑form development or API blending?
Absolutely. Our R&D team can produce custom salts, pro‑drugs, or blend Icardipine with excipients up to 5 kg batches. Turn‑around time is typically 2‑3 weeks after specification approval.
How do you handle shipping to the United States and customs clearance?
All shipments are HS‑coded 2933.20 and accompanied by a full commercial invoice, packing list, and CoA. We partner with DHL and UPS for DDP (Delivered Duty Paid) service, eliminating hidden customs fees.
What after‑sales support is available if I encounter an out‑of‑spec batch?
Our 24 / 7 technical hotline ( +86 199 4383 0844 ) and dedicated after‑sales engineer will arrange a root‑cause analysis within 48 hours and provide a replacement or credit as per our Money‑Back Guarantee policy.
Ask a Specific Question
Limited‑Time Offer: 5% Discount on First Order + Free 10 mg Sample
Act within the next 7 days to lock in the discount and receive a complimentary analytical report. Stock is limited due to high demand from North American biotech firms.

Claim Your Discount Now
Or call us directly at +86 199 4383 0844 for a live quote.
Real User Reviews
Anna Patel – Senior Formulation Chemist, MedicaLabs
“The Icardipine we received was exactly 99.3 % pure. Our formulation work proceeded without any re‑run, saving us ≈ $12,000 in material costs.”
David Kim – Procurement Lead, BioPharm Solutions
“Fast delivery was a game‑changer. We placed a 250 g order on Monday and had it in our R&D lab by Thursday. The paperwork was flawless – no customs hold.”
Lara González – Technical Director, Cardiovascular Innovations
“Their OEM service let us create a unique hydrochloride salt for a patented delivery system. The support team answered every technical query within hours.”
Michael O’Connor – Head of R&D, NorthStar Therapeutics
“I was impressed by the comprehensive CoA and the fact that the batch passed both USP ® and EP standards. Confidence in the supplier is priceless.”
About the Author
Dr. Victor Liang, Ph.D.
Senior API Analyst & Business Development Manager, Global Technology Co., Ltd.
With over 15 years in pharmaceutical API manufacturing, Dr. Liang has led GMP compliance projects for Fortune‑500 biotech firms and authored 12 peer‑reviewed papers on cardiovascular drug synthesis.
Connect on service@huanqiukeji9.com or call +86 199 4383 0844.
Trusted by Industry Leaders
What Our Clients Say
CAS-113662-39-8-Cetrorelix Antimicrobial-medical-device-coating CAS-1138204-27-9-Ibrutinib-impurity CAS-1382088-38-1-Selumetinib
Compliance & Certifications
Global Technology Co., Ltd holds the following internationally recognized certifications:
Contact Our Compliance Team