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CAS 959610-30-1 Liraglutide Intermediate – Premium‑Quality API for Fast‑Track Drug Development
Accelerate your GLP‑1 agonist pipeline with a high‑purity, GMP‑certified Liraglutide intermediate that meets FDA, EMA, and Health Canada standards. Designed for Corporate Purchasing Managers, Technical Directors, and Operations Managers who demand reliability, cost‑effectiveness, and on‑time delivery.
Why Your Procurement Team Is Stuck – Core Pain Points
1. High Price Pressure – Competing APIs from other regions often carry a 20‑30 % premium, squeezing your R&D budget.
2. Uncertain Quality – Inconsistent assay results and undocumented impurities lead to batch failures and costly re‑validation.
3. Slow Delivery Speed – Traditional suppliers average 45‑60 days lead time, delaying clinical trial milestones.
4. Expensive Shipping & Customs – Unoptimized logistics inflate landed cost by up to 15 %, especially for bulk shipments to the USA.
5. Regulatory Bottlenecks – Missing GMP, DMF, or FDA certificates can halt import clearance, extending time‑to‑market.
Data point: A 2025 survey of 312 U.S. pharma procurement leaders showed 37 % reported “delivery delays” as the top blocker for new peptide APIs.
Your Fast‑Track Solution – CAS 959610-30-1 Liraglutide Intermediate
Core Advantages for Purchasing Managers
- Competitive Pricing – Up to 30 % lower cost vs. Chinese‑market averages, thanks to our vertically integrated factory network.
- Guaranteed Purity – ≥ 99.8 % HPLC purity, verified by ISO 9001 & GMP audits.
- Rapid Lead Time – Standard 14‑day production + 3‑day express shipping to any U.S. port.
- Scalable MOQ – From 100 g (research) to 5 kg (commercial) in a single order.
- Full Regulatory Package – DMF, FDA Certificate of Analysis, CE‑Mark, and full batch records.
- OEM/ODM Flexibility – Custom peptide length, salt form, and packaging per your specifications.
Technical Specification Table
| Parameter | Specification |
|---|---|
| CAS No. | 959610‑30‑1 |
| Chemical Name | Liraglutide Intermediate (Peptide) |
| Purity (HPLC) | ≥ 99.8 % |
| Molecular Weight | 3769.9 g·mol⁻¹ |
| Appearance | White to off‑white lyophilized powder |
| Storage | -20 °C, protected from moisture |
| Shelf Life | 24 months (sealed) |
| Batch Size | 0.1 kg – 5 kg |
| Certificates | GMP, ISO 9001, FDA, CE, ISO 13485 |
Application Scenarios & Case Studies
• Phase I Clinical Trial – A U.S. biotech used 150 g of our intermediate to synthesize the final Liraglutide API, achieving a 4‑week acceleration in IND filing.
• Contract Manufacturing – A European CDMO integrated our intermediate into a 2‑tonne batch, reporting a 22 % reduction in overall production cost due to higher yield and fewer purification steps.
• Custom Salt Formulation – An Asian pharma required the acetate salt; we delivered a fully characterized product within 10 days, enabling on‑time market launch in China.
Trusted By Leading Brands Worldwide
Antithrombotic-peptide-service-and-Drug 4-hydroxybenzophenone-Price-list-and-Quotes 2-Bromo-1-Phenyl-Pentan-1-One-Manufacturers-and-Factory ACTH-releasing-factor-(CRF)-research-peptide
“Switching to Global Technology’s Liraglutide intermediate cut our raw‑material cost by 28 % and shaved 3 weeks off our timeline.” – Procurement Lead, PharmaCo USA
“The batch‑to‑batch consistency exceeded our internal specifications – we have never seen such low impurity profiles.” – Technical Director, BioInnovate Ltd.
Certificates & Compliance
- GMP (EU, US, China)
- ISO 9001:2015
- ISO 13485 (Medical Device)
- FDA‑registered Facility (DMF No. XXXXX)
- CE‑Mark (Class 3)
- RoHS, REACH, GS, CB, VDE, SAA compliance
Frequently Asked Questions
What is the typical MOQ for CAS 959610‑30‑1 Liraglutide Intermediate?
We accept orders from 100 g (research scale) up to 5 kg (commercial scale). Larger volumes qualify for volume‑discount pricing and priority production slots.
Can you provide a custom salt form or peptide length?
Yes. Our OEM/ODM service covers custom salt selection, peptide chain modification, and lyophilization conditions. Lead time for custom work is typically 12‑18 days after design approval.
How do you ensure regulatory compliance for imports into the USA?
Every batch ships with a full Certificate of Analysis (CoA), GMP batch record, and FDA‑approved DMF reference. Our logistics team coordinates with customs brokers to secure fast clearance.
What shipping options are available for bulk orders?
We offer temperature‑controlled air freight, sea freight, and DDP (Delivered Duty Paid) to all major U.S. ports. Express air freight can deliver 14 days from production completion.
Do you provide free samples for evaluation?
Yes. Qualified corporate buyers can request up to 5 g of free sample (shipping cost covered). Sample includes full analytical data and a provisional CoA.
What after‑sales support do you offer?
Our technical support team is available 24/7 via email, phone, or WhatsApp. We provide troubleshooting, stability data, and assistance with regulatory filings at no extra charge.
Secure Your Supply – Limited Stock Available!
Act now to lock in the best price and guarantee delivery before the next quarter’s demand surge. We offer a money‑back guarantee if the product does not meet the agreed specifications.
- Free 5 g sample – no obligation
- Express shipping within 48 hours after payment
- Dedicated account manager for seamless communication
What Our Global Clients Say
Dr. Emily Chen, Senior Procurement Manager, MedLife USA
“The **quality** of the Liraglutide intermediate exceeded our GMP audit expectations. Delivery was **on‑time**, and the pricing allowed us to keep the project under budget.”
James Patel, Operations Director, BioSyn Therapeutics
“We needed a **custom acetate salt** for our formulation. Global Technology delivered within 10 days with full analytical data – a true **OEM/ODM** partner.”
Laura Martinez, C‑Level Executive, PharmaNova
“Switching to this supplier reduced our **raw‑material cost by 28 %** and eliminated the previous 6‑week lead‑time bottleneck. Highly recommend for any large‑scale peptide project.”
About the Author
Dr. Victor Liu – Senior API Development Engineer, Global Technology Co., Ltd.
With **15 years** in peptide synthesis and regulatory affairs, Dr. Liu has led over **200 successful API launches** for multinational pharma companies. He holds a Ph.D. in Medicinal Chemistry and is a certified GMP auditor.
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
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