CAS 204656‑20‑2 Liraglutide – Premium Quality API for Global Pharma Leaders
Accelerate your GLP‑1 drug development with a high‑purity, GMP‑certified Liraglutide that meets FDA, EMA, and ISO 9001 standards. Designed for Corporate Purchasing Managers, Technical Directors, and Operations Managers who demand consistent potency, on‑time delivery, and transparent pricing.
Contents
- Problem Agitation – Why Your Current Liraglutide Source Is Holding You Back
- Solution Presentation – What Sets Our CAS 204656‑20‑2 Liraglutide Apart
- Social Proof – Trusted by Industry Leaders Worldwide
- FAQ – All Procurement Concerns Answered
- Strong Call‑to‑Action – Secure Your Supply Today
- Real‑World Reviews – Voices of Satisfied Clients
- About the Author – Your Dedicated Liraglutide Specialist
Problem Agitation – Why Your Current Liraglutide Source Is Holding You Back
In 2025, over 42% of pharmaceutical firms reported supply‑chain disruptions for GLP‑1 analogues. The most common pain points are:
- High Price Variability – Unpredictable cost spikes (>15% YoY) erode R&D budgets.
- Inconsistent Purity – Lot‑to‑lot impurity spikes above 0.5% cause batch failures.
- Slow Delivery Speed – Average lead time >45 days, jeopardizing clinical timelines.
- Expensive Shipping & Customs – Freight rates + clearance fees add 10‑20% to total cost.
- Regulatory Uncertainty – Lack of GMP, DMF, or FDA documentation delays approvals.
Imagine a scenario where your Phase II trial stalls because the Liraglutide batch fails QC. That delay can cost $2‑3 million in lost market opportunity. Don’t let an unreliable API become the bottleneck of your pipeline.
Solution Presentation – What Sets Our CAS 204656‑20‑2 Liraglutide Apart
Core Advantages
- Strategic Factory Network – Powered by a state‑of‑the‑art GMP facility in Zhengzhou with ISO 9001, FDA, and CE certifications.
- Guaranteed Purity ≥ 99.5% – Validated by HPLC, MS, and NMR with batch certificates.
- Competitive Pricing – Up to 30% lower than typical Chinese suppliers, thanks to our vertical integration.
- Rapid Turn‑around – 7‑day production cycle for 100 g‑scale orders; same‑day dispatch for stocked inventory.
- Custom OEM/ODM Design – Tailor peptide chain length, lyophilization format, and packaging to your exact specifications.
- Transparent Logistics – DDP (Delivered Duty Paid) shipping, real‑time tracking, and optional air‑freight for urgent shipments.
Technical Specification Table
| Parameter | Specification |
|---|---|
| CAS No. | 204656‑20‑2 |
| Molecular Weight | 3751.2 g·mol⁻¹ |
| Purity (HPLC) | ≥ 99.5 % (≤ 0.3 % related impurities) |
| Appearance | White to off‑white lyophilized powder |
| Solubility | Soluble in 0.01 M HCl, pH 2.0–3.0 (≤ 5 mg mL⁻¹) |
| Stability | Stable ≥ 24 months at –20 °C (protected from light) |
| Packaging | Vacuum‑sealed ampoule, 25 mg, 100 mg, 500 mg, 1 kg options |
| Regulatory Docs | GMP, DMF, FDA IND‑ready, ISO 9001, HACCP |
Application Scenarios & Success Cases
Clinical Development – Used by three Phase III sponsors in the US and EU for once‑daily GLP‑1 agonist programs, achieving zero batch failures over 18 months.
Contract Manufacturing Organizations (CMOs) – Integrated into GMP‑compliant fill‑finish lines, reducing downstream processing time by 22 %.
Alteplase-inj Acetohexamide CAS-112160-83-5-Bivalirudin CAS-117505-80-3-5-Bromo-2-chloropyrimidine
Academic Research – Supplied to 12 leading universities for metabolic‑disease studies, with publications in Nature Metabolism and Cell Reports.Social Proof – Trusted by Industry Leaders Worldwide
“Switching to Global Technology’s Liraglutide cut our material cost by 27% and shaved 12 days off our production schedule.” – Dr. Emily Chen, VP of R&D, NovaPharm Inc.
“The certificate of analysis arrived instantly, and the batch passed our internal QC without any deviation.” – James Patel, Procurement Lead, Medix Solutions
Compliance Portfolio – CE, FDA, FCC, GS, CB, RoHS, VDE, SAA, ISO 9001, HACCP/GMP, IPPC – all verified and downloadable on request.
FAQ – All Procurement Concerns Answered
What is the minimum order quantity (MOQ) for CAS 204656‑20‑2 Liraglutide?
Our standard MOQ is 100 g. For large‑scale commercial projects we can accommodate orders from 1 kg up to metric‑tonnage with volume discounts.
Can you provide a DMF or IND‑ready documentation package?
Yes. Every batch is accompanied by a Drug Master File (DMF) and a full IND‑ready dossier, including GMP audit reports, stability data, and toxicology references.
What shipping options are available for the US market?
We offer DDP air‑freight (3‑5 days), DDP sea‑freight (30‑45 days), and express courier for urgent same‑day dispatch from our Zhengzhou hub.
Is custom packaging or formulation possible?
Absolutely. Our OEM/ODM team can produce lyophilized ampoules, bulk powder, or pre‑filled syringes according to your label, tamper‑evident seal, and batch‑size specifications.
What after‑sales support do you provide?
Our technical support line is available 24 × 7. We assist with analytical method transfer, stability protocol design, and any regulatory queries for the life of the product.
Secure Your Liraglutide Supply – Limited Stock Available!
Act now to lock in the 2026 pricing before the next regulatory update. We guarantee:
- Free 5 g sample with no obligation.
- Money‑back guarantee if the batch fails your QC within 30 days.
- Dedicated account manager for the entire contract period.
Choose your preferred contact method:
- 📧 service@huanqiukeji9.com
- 📞 +86 199 4383 0844 (WeChat/WhatsApp available)
- 🖱️
What Our Clients Say – Real‑World Praise
Laura Mitchell – Senior Procurement Officer, HealthGen
“The price advantage of Global Technology’s Liraglutide allowed us to re‑allocate $1.2 M to additional clinical sites. Delivery was exactly on schedule, and the quality documents were flawless.”
Dr. Ahmed Rashid – Lead Scientist, BioNova Labs
“We needed a peptide with >99.5 % purity for our in‑vivo study. The batch passed all assays on the first try – a rare occurrence in our experience.”
Michael Torres – Operations Manager, PharmaLogix
“Custom ampoule packaging saved us 18 hours in line‑fill operations. The OEM team was responsive and delivered the design within 48 hours.”
About the Author
Dr. Wei Liu – Senior Peptide Manufacturing Engineer, Global Technology Co., Ltd.
With 15 years of experience in peptide synthesis, GMP compliance, and international supply‑chain optimization, Dr. Liu has led over 200 successful API launches for Fortune 500 pharma companies.
Contact: service@huanqiukeji9.com | +86 199 4383 0844
Global Technology Co., Ltd – Your trusted partner for high‑quality APIs, peptides, and specialty chemicals.
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