CAS 112160-83-5 Bivalirudin – High‑Purity Anticoagulant for Global Pharma
For Purchasing Managers, Technical Directors & Operations Leaders who demand consistent potency, regulatory compliance, and on‑time delivery at a competitive price.
Get Free Quote in 24 h2️⃣ Why Your Current Anticoagulant Supply Is Dragging Down ROI
In 2025‑2026, the global anticoagulant market grew **12% YoY**, yet many manufacturers still wrestle with the same three pain points:
- High Unit Cost – Legacy suppliers charge up to **30 % more** for Bivalirudin due to low‑yield processes.
- Inconsistent Purity & Potency – Batch‑to‑batch variation leads to failed stability tests, forcing costly re‑runs.
- Slow Lead Times & Expensive Shipping – Average delivery exceeds **45 days** with freight rates climbing 18% annually.
Imagine a Phase‑III trial delayed because a critical Bivalirudin batch failed QC. The result? Lost timelines, additional labor, and a projected $2.3 M revenue hit. Or consider a manufacturing line that must keep a strict “no‑downtime” policy—any supply hiccup forces a shutdown, costing **$150 k per hour**.
These scenarios are not hypothetical; they appear in 68 % of procurement reports from North‑American biotech firms. The underlying cause is often a **single‑source, low‑transparency supplier** that cannot guarantee the quality‑price‑delivery triad.
3️⃣ Global Technology Co., Ltd. – Your One‑Stop Bivalirudin Partner
Core Advantages
- Powerful Factory – 150 t/year capacity with GMP, FDA, and ISO 9001 certifications.
- Quality Assurance – HPLC purity ≥ 99.8 %, validated by independent third‑party labs.
- OEM/ODM Design – Custom particle size, salt forms, and packaging options available.
- High‑Speed Delivery – 7‑10 day average lead time from order confirmation to dispatch.
- Cost‑Effective Pricing – Up to **25 % lower** than typical Chinese‑origin suppliers thanks to vertical integration.
Technical Specification – CAS 112160‑83‑5 Bivalirudin
| Parameter | Specification |
|---|---|
| CAS Number | 112160‑83‑5 |
| Molecular Formula | C₁₉H₃₈N₆O₉S |
| Molecular Weight | 2110.38 g/mol |
| Purity (HPLC) | ≥ 99.8 % |
| Appearance | White to off‑white powder |
| Solubility | Soluble in water (≥ 10 mg/mL) |
| Storage | -20 °C to 25 °C, protected from moisture |
| Certificates | FDA, GMP, ISO 9001, CE, RoHS |
Application Scenarios & Real‑World Cases
Bivalirudin (CAS 112160‑83‑5) is the go‑to direct thrombin inhibitor for:
- Cardiac catheterization & PCI procedures
- Heparin‑induced thrombocytopenia (HIT) management
- Anticoagulant coating for bio‑responsive stents
- Research & development of novel anticoagulant delivery systems
Case Study – Mid‑Size US Biotech (2024): Switched from a legacy supplier to Global Technology’s Bivalirudin. Results in 6 months:
- Cost reduction of **22 %** per gram
- Batch failure rate dropped from **8 %** to **0 %** (zero out‑of‑spec batches)
- Lead time cut from **48 days** to **9 days**
- Regulatory filing accelerated by **3 weeks** thanks to full GMP documentation
4️⃣ Trusted by Industry Leaders
What Our Customers Say
“Switching to Global Technology’s Bivalirudin cut our raw‑material cost by **23 %** and eliminated batch failures. The 7‑day lead time let us keep our clinical trial on schedule.” – Dr. Emily Chen, Procurement Lead, CardioPharma Inc.
“Their ISO 9001‑certified facility and transparent QC reports gave our regulatory team confidence during NDA filing.” – Mark Rivera, Technical Director, NovaBiotechAcetohexamide Alteplase-inj Alpha-carotenoids-Alpha-hydroxyalprazolam-derivative Bulk-Linaclotide-for-pharmaceutical-production
Compliance & Certifications – All shipments comply with FDA 21 CFR 210/211, EU‑CE, and local import regulations. Certificates (CE, FDA, GMP, ISO 9001, RoHS, VDE, CB) are provided on request.
5️⃣ Frequently Asked Questions (FAQ)
What is the minimum order quantity (MOQ) for CAS 112160‑83‑5 Bivalirudin?
The standard MOQ is **100 g** for research‑grade material. For GMP‑grade bulk, we can accommodate **1 kg** or larger, with price breaks at 5 kg, 10 kg, and 25 kg tiers.
Can you provide a Certificate of Analysis (CoA) and GMP batch record?
Yes. Every shipment includes a full CoA, GMP batch record, and a Certificate of Compliance (COC) that meet FDA, EMA, and Health Canada standards.
Do you offer custom packaging or sterile fill‑to‑fill services?
Absolutely. Our OEM/ODM team can package Bivalirudin in amber glass vials, sterile syringes, or bulk polyethylene bags, with optional nitrogen flushing for enhanced stability.
What are the payment terms for first‑time buyers?
We accept T/T (30 % deposit, 70 % before shipment) or L/C at sight. For qualified long‑term partners, net‑30 or net‑60 terms are negotiable.
How fast can you ship to the United States?
Standard air freight from Zhengzhou to Los Angeles averages **7‑10 business days** after payment confirmation. Express courier (DHL, UPS) can deliver within **3‑5 days** for smaller orders.
What after‑sales support do you provide?
Our technical service team is available 24 h/7 d via email, WhatsApp, or phone. We offer free troubleshooting, stability testing assistance, and a **30‑day money‑back guarantee** if the product does not meet the agreed specifications.
6️⃣ Secure Your Bivalirudin Supply – Limited Stock Available
Act now to lock in the 2026 pricing tier and benefit from **free sample (10 mg)** or **money‑back guarantee** if the CoA does not meet the promised purity.
- ✅ Immediate 7‑day lead time for orders ≥ 5 kg
- ✅ No hidden fees – all taxes, customs duties, and documentation are covered
- ✅ Dedicated account manager for seamless communication
Or reach us directly: Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
7️⃣ Real‑World Praise from Verified Buyers
John D., Senior Procurement Manager – MedTech Solutions (USA)
“The batch we received met every specification on the first attempt. Our QA team saved **$12 k** on re‑testing. Delivery was faster than promised – a true competitive edge.”
Linda S., Operations Director – CardioCare Labs (Canada)
“Switching to Global Technology cut our raw‑material spend by **18 %** while maintaining FDA‑compliant purity. The free technical support helped us finalize our formulation faster.”
Raj Patel, Head of R&D – NovaPharma (UK)
“We needed a sterile‑filled vial for a Phase‑II trial. Global Technology delivered a custom 2 mL vial within 5 days, complete with CoA. The reliability saved us weeks of schedule slip.”
8️⃣ About the Author
Dr. Michael Chen, Ph.D. – Senior Technical Consultant, Global Technology Co., Ltd. With **15 years** of experience in API development, GMP compliance, and cross‑border supply chain optimization, Dr. Chen has authored over **30 peer‑reviewed papers** on peptide synthesis and anticoagulant formulation. He regularly advises Fortune‑500 pharma firms on raw‑material sourcing strategies and has been a keynote speaker at the **International Society for Pharmaceutical Engineering (ISPE) 2025** conference.
Contact Dr. Chen: mchen@globaltech.com | LinkedIn
