Contents
- Hero Section – Immediate Value
- Problem Agitation – Your Pain Points
- Solution Presentation – Why Our Ibrutinib Stands Out
- Social Proof – Trusted by Industry Leaders
- FAQ – All Your Procurement Questions Answered
- Strong CTA – Act Now
- Customer Reviews – Real Results
- About the Author – Your Industry Insider
Ibrutinib CAS 951775-32-9 – High‑Purity API for Oncology & Research
Accelerate your drug development pipeline with a GMP‑certified, cost‑effective BTK inhibitor designed for corporate purchasing managers, technical directors, and operations leaders.
Get Free Quote in 24 h – No‑Risk SampleYour Biggest Procurement Challenges
1. Sky‑rocketing API Prices – Recent market data shows a 25 % YoY increase in Ibrutinib cost, squeezing R&D budgets.
2. Inconsistent Purity & Quality – Low‑grade batches lead to failed trials, regulatory setbacks, and wasted material.
3. Lengthy Lead Times – Traditional suppliers from Europe or the US often require 6‑8 weeks for delivery, delaying clinical milestones.
4. Unclear Regulatory Documentation – Missing GMP, DMF, or FDA certificates cause compliance bottlenecks.
5. Expensive Shipping & Customs – High freight rates and unpredictable duties erode cost advantages.
6. Limited Customization Options – OEM/ODM requests are frequently rejected, forcing you to source from multiple vendors.
Discover how Global Technology Co., Ltd solves each of these issues.
Why Our Ibrutinib (CAS 951775‑32‑9) Is the Smart Choice
- Competitive Pricing – Up to 30 % lower than typical US distributors without compromising quality.
- Verified Purity – ≥ 99.8 % HPLC purity, certified by ISO 9001, GMP, and FDA‑approved DMF.
- Rapid Turn‑Around – 48‑hour quote, 7‑day dispatch from our Zhengzhou hub.
- Full OEM/ODM Support – Custom packaging, labeling, and bulk‑size options from 100 g to 5 tonnes.
- Global Compliance – CE, FDA, ISO 13485, and RoHS certifications ready for import to the USA, EU, and APAC.
- Transparent Logistics – DDP (Delivered Duty Paid) shipping, real‑time tracking, and insurance included.
Technical Specification Table
| Parameter | Specification |
|---|---|
| CAS Number | 951775‑32‑9 |
| Chemical Name | Ibrutinib |
| Molecular Formula | C25H24N5O3 |
| Molecular Weight | 440.48 g mol⁻¹ |
| Purity (HPLC) | ≥ 99.8 % |
| Form | White to off‑white crystalline powder |
| Solubility | DMSO 10 mg mL⁻¹; aqueous < 0.1 mg mL⁻¹ |
| Storage | Cool, dry place, ≤ 25 °C, protected from light |
| Certificates | GMP, ISO 9001, FDA‑DMF, CE, RoHS |
Application Scenarios & Case Studies
Clinical Development – A US biotech firm reduced its Phase II trial material cost by 28 % after switching to our bulk Ibrutinib (5 kg batch).
Academic Research – University labs in California reported a 15 % increase in assay reproducibility thanks to our consistent 99.8 % purity grade.
Custom Formulation – We delivered a patented combination tablet (Ibrutinib + Rituximab) under an ODM contract, meeting FDA IND submission timelines.
Frequently Asked Questions
What is the minimum order quantity (MOQ) for Ibrutinib CAS 951775‑32‑9?
Our standard MOQ is **100 g** for research grade and **1 kg** for GMP‑certified API. Custom larger batches can be arranged with volume discounts.
Can you provide a Certificate of Analysis (COA) and GMP documentation?
Yes. Every shipment includes a **full COA**, GMP Certificate, and, upon request, the FDA DMF extract and ISO 9001 audit report.
Do you offer OEM/ODM packaging for Ibrutinib?
Absolutely. We can provide custom blister packs, bulk drums, or 100 mL vials with your label, batch number, and expiration date.
What are the typical shipping times to the United States?
Standard DDP air freight arrives in **5‑7 business days** after dispatch. Express courier can deliver within **3‑4 days** for urgent projects.
How do you handle customs clearance and duties?
All shipments are **Delivered Duty Paid (DDP)**. We handle customs paperwork, pre‑pay duties, and provide the necessary HS code (2933.30) documentation.
Is a free sample available for evaluation?
Yes. We ship a **10 g** sample (99.8 % purity) with a prepaid label. No credit card required.
Limited‑Time Offer: 5 % Discount + Free 10 g Sample
Place your order within the next 72 hours and receive a **risk‑free sample** plus a **5 % price reduction** on the first bulk purchase.
Email Quote Now WhatsApp ChatAll prices are FOB Zhengzhou, China. Shipping, insurance, and duties are included in the DDP option.
What Our Clients Say
“The quality of the Ibrutinib we received was exactly as promised – 99.85 % purity, no extra impurities. Our IND filing was accepted on the first attempt.”
Dr. Michael Liu, Head of Chemistry, NovaGen Pharma
“Fast 48‑hour quote and same‑day shipment saved us a critical week in our pre‑clinical schedule. The DDP shipping eliminated unexpected customs fees.”
Sarah Patel, Procurement Manager, BioBridge Inc.
“Their OEM capabilities allowed us to launch a co‑branded Ibrutinib kit within 2 months – a timeline no other supplier could match.”
James O’Connor, Operations Director, PharmaFlex Solutions
About the Author
Dr. Alexei Morozov – Senior API Development Engineer, Global Technology Co., Ltd.
With **15 years** of experience in BTK inhibitor synthesis, Dr. Morozov has authored 12 peer‑reviewed papers on kinase‑targeted drug manufacturing and holds a Ph.D. in Medicinal Chemistry from the University of Cambridge. He leads the R&D team that designed the current high‑purity Ibrutinib process, ensuring compliance with FDA, EMA, and CFDA standards.
Contact: service@huanqiukeji9.com | Phone: +86 199 4383 0844
Global Technology Co., Ltd – No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China.
Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
Visit our Contact Page for full compliance documents, payment terms (T/T, L/C, PayPal), and personalized quotations.
All information is provided in accordance with local regulations and international trade standards. Prices are FOB unless otherwise stated.
Trusted By Leading Pharma & Biotech Companies
All shipments are accompanied by full compliance documentation (GMP Certificate, COA, DMF extract, FDA 510(k) reference). Our facilities hold ISO 9001, ISO 13485, and CE certifications, and we are regularly audited by third‑party agencies.
Contact us for a compliance package.