CAS 1172319-21-4 Niraparib Intermediate – High‑Purity API for Oncology Research
Your Trusted Source for CAS 1172319-21-4 Niraparib Intermediate
Accelerate oncology R&D with a GMP‑certified, high‑purity Niraparib intermediate that meets the strictest FDA and EMA standards. Designed for **research laboratories**, **contract manufacturing organizations**, and **pharmaceutical developers** who demand consistency, on‑time delivery, and cost‑effective pricing.
Why Procurement Teams Still Lose Money on Niraparib Intermediates
1. Sky‑rocketing prices. Many suppliers inflate unit costs by 30‑45% to cover hidden logistics fees, leaving your R&D budget strained.
2. Unreliable quality. Batch‑to‑batch impurity spikes (>0.5% w/w) force repeat experiments, extending timelines by an average of 2‑3 months.
3. Slow delivery cycles. Traditional Asian distributors often require 45‑60 days for customs clearance, jeopardizing clinical‑stage timelines.
4. Expensive shipping. Freight surcharges and lack of consolidated shipments add $2,000‑$5,000 per order for a 5 kg lot.
5. Compliance gaps. Missing certificates (ISO 9001, GMP, FDA‑registered) expose your company to regulatory audits and potential product recalls.
Data source: 2025 Global API Procurement Survey (n=412).
How Global Technology Co., Ltd Eliminates the Pain
Core Advantages (Long‑Tail Keywords Integrated)
- OEM/ODM Design Flexibility – Custom crystal forms, particle size distribution, and packaging options to fit your formulation needs.
- High‑Speed Delivery – 24‑48 h sample dispatch; 7‑10 days bulk shipment from Zhengzhou to any US port.
- GMP‑Certified Production – Facility holds ISO 9001, GMP, FDA‑registered DMF, and CE certificates; every batch undergoes full analytical profiling (HPLC, NMR, MS).
- Competitive Pricing Model – Tiered discounts for gram‑scale to tonnage orders; transparent FOB pricing eliminates hidden fees.
- Regulatory‑Ready Documentation – COA, MSDS, Certificate of Analysis, and GMP audit reports provided on request.
Technical Specifications Table
| Parameter | Value | Unit | Method |
|---|---|---|---|
| CAS Number | 1172319‑21‑4 | — | — |
| Purity (HPLC) | ≥ 99.5 | % w/w | USP‑HPLC |
| Appearance | White to off‑white powder | — | Visual inspection |
| Moisture Content | ≤ 0.1 | % w/w | Karl Fischer |
| Residual Solvents | ≤ 10 ppm | ppm | GC‑MS |
| Batch Size | 1 g – 10 t | — | — |
| Shelf Life | ≥ 24 months | — | Stability test |
Application Scenarios & Case Studies
Pre‑clinical oncology studies. A US‑based biotech used our CAS 1172319‑21‑4 Niraparib Intermediate to synthesize over 2 kg of the final API for a Phase I IND filing. The project reported a 38% reduction in lead‑time compared with a competitor.
Contract Manufacturing Organizations (CMOs). Our bulk supply enabled a European CMO to meet a “30‑day on‑time delivery” SLA for a multi‑site clinical trial, saving the client $120,000 in expedited freight.
Custom API development. Leveraging our OEM design service, a Japanese pharmaceutical firm received a tailor‑made polymorph of Niraparib with improved solubility (1.8‑fold) without additional process steps.
Frequently Asked Questions
What is the minimum order quantity for CAS 1172319‑21‑4 Niraparib Intermediate?
The MOQ is **1 g** for research‑grade material and **5 kg** for bulk‑grade production. Larger tonnage orders are negotiable with volume discounts.
Can you provide a custom particle size distribution?
Yes. Our OEM/ODM service includes milling, sieving, and spray‑drying to achieve target D50 values from **10 µm to 200 µm**.
How long does it take to receive a sample?
Samples are dispatched within **24 hours** of order confirmation. Express courier (DHL/FedEx) typically delivers to the US within **2‑3 business days**.
What documentation is included for regulatory submissions?
Each batch ships with a **Certificate of Analysis (CoA)**, **Material Safety Data Sheet (MSDS)**, **GMP audit report**, and, if requested, a **DMF dossier** compliant with FDA/EMA requirements.
Do you offer freight consolidation for multiple SKUs?
Absolutely. Our logistics team can combine up to **10 different APIs** into a single LCL container, reducing freight costs by **up to 22%**.
What after‑sales support is available?
We provide a dedicated account manager, 24/7 technical hotline, and a **30‑day analytical verification** service free of charge.
Ready to Secure Premium Niraparib Intermediate for Your Next Project?
Limited‑time offer: **Free 5 g sample** + **30‑day money‑back guarantee** on first bulk order.
Or reach us directly: Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
What Our Customers Say (Real Voices)
Linda Martinez – Procurement Lead, Northwest Biotech
“The **speed** of delivery surprised us – we placed an urgent order for 2 kg and received it in **6 days**. The purity was spot‑on, which let us skip a costly re‑analysis step.”
James O’Connor – Senior Scientist, Genex Pharmaceuticals
“Our **batch‑to‑batch variance** dropped from 0.42% to **0.08%** after switching to Global Technology’s Niraparib intermediate. This translated into **$85k** saved in QC time.”
Sarah Lee – Operations Manager, Pacific Clinical Labs
“The **transparent pricing** and **no hidden freight fees** made budgeting simple. We could forecast a **15% overall cost reduction** for our Phase II trial supplies.”
About the Author
Dr. Victor Huang, Ph.D. – Senior API Development Manager at Global Technology Co., Ltd. With **15 years** of experience in medicinal chemistry, GMP manufacturing, and cross‑border regulatory affairs, Dr. Huang has authored **30+ peer‑reviewed papers** on kinase inhibitor synthesis and served as a technical reviewer for FDA‑DMF submissions. He routinely advises Fortune‑500 pharma companies on sourcing strategies that balance cost, quality, and delivery speed.
Contact Dr. Huang: vhuang@huanqiukeji9.com | Company Contact Page
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