CAS 959610-54-9 Liraglutide Intermediate – Premium Quality, Fast Delivery, OEM/ODM Ready
For Corporate Purchasing Managers, Technical Directors & Operations Leaders seeking reliable peptide intermediates at competitive prices.
Get Free Quote in 24 hIntroduction to CAS 959610‑54‑9 Liraglutide Intermediate
CAS 959610‑54‑9 Liraglutide Intermediate is a high‑purity peptide precursor used worldwide for the synthesis of the anti‑obesity and type‑2 diabetes drug Liraglutide (brand name Victoza®, Saxenda®). As the demand for GLP‑1 analogues surges—projected to grow at a CAGR of 13% through 2032—pharmaceutical developers, contract manufacturing organizations (CMOs), and biotech startups are scrambling for reliable, GMP‑grade intermediates that meet stringent regulatory standards.
Our Global Technology Co., Ltd. has invested heavily in state‑of‑the‑art peptide synthesis lines, partnered with GMP‑certified domestic manufacturers, and secured FDA‑registered DMF dossiers. This enables us to deliver CAS 959610‑54‑9 Liraglutide Intermediate in batches ranging from 5 g to 2 tonnes, with a guaranteed purity of ≥ 98.5% (HPLC) and endotoxin levels < 0.1 EU/mg. The product is supplied as a lyophilized powder, sealed under nitrogen, and shipped in UN 3373‑compliant containers.
Why does this matter to you? As a purchasing manager, you balance three critical variables: cost per milligram, lead‑time, and compliance risk. Traditional suppliers in China often quote low prices but compromise on batch‑to‑batch consistency, resulting in costly re‑work downstream. European or US‑based vendors may guarantee quality but charge a premium that erodes ROI, especially for early‑stage programs with tight budgets.
Our solution bridges that gap. By leveraging a vertically integrated supply chain—raw material sourcing, peptide chain assembly, purification, and final packaging—we keep unit cost down 12‑18% while maintaining ISO 9001 & GMP compliance. Moreover, our high‑speed logistics network (air‑freight hub in Zhengzhou + strategic partners in Los Angeles, Rotterdam, and Singapore) guarantees delivery within 10‑14 business days to most major ports, a dramatic improvement over the industry average of 25‑45 days.
Below you will find a deep dive into the exact specifications, the regulatory landscape, and how our product can accelerate your development timeline while protecting your bottom line.
Key Benefits at a Glance
- High Purity: ≥ 98.5% (HPLC), ≤ 0.1 EU/mg endotoxin
- Scalable Supply: 5 g – 2 t batch sizes
- Regulatory Ready: GMP, ISO 9001, FDA‑registered DMF
- Fast Lead‑Time: 10‑14 days to most global ports
- Cost‑Effective: 12‑18% lower than typical EU/US sources
Contact us now to receive a free technical data sheet and a complimentary sample (≤ 100 mg) shipped within 48 hours.
2. Core Pain Points in Peptide Procurement
Even with the market’s growth, many organizations still encounter the same three‑fold barrier:
- High Price & Hidden Fees – Suppliers quote low base prices but tack on exorbitant shipping, customs brokerage, and quarantine fees, inflating total cost by 25‑40%.
- Inconsistent Quality & Documentation – Variability in purity, residual solvents, and missing batch certificates cause delays in IND submissions and increase the risk of FDA holds.
- Slow Delivery & Unreliable Logistics – Average transit times exceed 30 days, and many vendors lack real‑time tracking, leading to production line stoppages.
Data from a 2025 industry survey (n = 312) shows that 68% of purchasing managers cite “delivery uncertainty” as the top reason for switching suppliers. Moreover, 54% reported “quality re‑work” costing an average of $45,000 per batch.
3. Why Global Technology’s Liraglutide Intermediate Is the Smart Choice
Our product addresses each pain point with a concrete, measurable advantage:
- Transparent Pricing Model – No hidden surcharges. All logistics, customs, and handling fees are disclosed up‑front. Save up to 30% on total landed cost.
- Full GMP Documentation Package – Includes Certificate of Analysis (CoA), Batch Manufacturing Record (BMR), Material Safety Data Sheet (MSDS), and FDA‑registered DMF reference number.
- Rapid Production Cycle – Our dedicated peptide line can complete a 500 g batch in 7 days, with QC completed in an additional 2 days.
- Customizable Scale‑Up – Whether you need 10 g for early‑stage screening or 1 t for commercial manufacturing, we provide a seamless scale‑up pathway without re‑qualifying the intermediate.
- Global Logistics Hub – Direct air‑freight from Zhengzhou to major ports, real‑time shipment tracking, and a 100% on‑time delivery guarantee.
Technical Specifications
| Parameter | Value | Unit | Compliance |
|---|---|---|---|
| Purity (HPLC) | ≥ 98.5 | % | USP, EP |
| Residual Solvents | ≤ 10 ppm | ppm | ICH Q3C |
| Endotoxin | ≤ 0.1 | EU/mg | Ph. Eur. |
| Moisture Content | ≤ 2.0 | % | ISO 17025 |
| Batch Size | 5 g – 2 t | — | Custom |
| Storage | -20 °C (dry) | — | Stability Tested 24 months |
| Regulatory Certificates | GMP, ISO 9001, FDA DMF, CE | — | Global |
All data points are verified by an independent third‑party laboratory (SGS, Eurofins, or Intertek). For a full analytical report, request a sample pack today.
Application Scenarios & Success Stories
Our CAS 959610‑54‑9 Liraglutide Intermediate has been integrated into multiple pipelines:
CAS-20126-59-4-Stephania-Tetranda-Extract-(Tetrandrine) CAS-2174-59-6-2-Diethylaminoethyl-chloride-hydrochloride CAS-90984-99-9-2-Bromo-1-phenyl-1-hexanone CAS-91050-39-4-Alarelin
- Phase I Clinical Development – A US biotech company reduced its IND filing timeline by 4 weeks using our ready‑to‑use batch (purity 99.1%).
- Contract Manufacturing Organization (CMO) – Delivered 250 kg of intermediate for a large‑scale commercial launch, achieving a 15% cost reduction versus previous supplier.
- Academic Research – Over 30 university labs worldwide have adopted our intermediate for GLP‑1 analogue studies, citing consistent assay results.
Get your case study PDF and see how you can replicate these results.
7. Frequently Asked Questions
What is the minimum order quantity (MOQ) for CAS 959610‑54‑9 Liraglutide Intermediate?
The standard MOQ is **5 g** for research use. For commercial scale, we can accommodate orders from **100 g up to 2 t** without additional setup fees.
Can the product be customized (e.g., salt form, isotopic labeling)?
Yes. We offer OEM/ODM services including **acetate, hydrochloride salts, and ^13C/^15N isotopic labeling**. Custom projects require a feasibility assessment and a non‑disclosure agreement.
How do you ensure batch‑to‑batch consistency?
Each batch undergoes a full analytical suite (HPLC, MS, NMR, endotoxin testing) performed by a **GLP‑certified laboratory**. Results are documented in a **Certificate of Analysis** linked to the batch’s unique serial number.
What are the shipping options and associated costs?
We provide **air‑freight (express, 3‑5 days)**, **sea‑freight (standard, 12‑18 days)**, and **courier (DHL, UPS, FedEx)**. All costs are disclosed in the quotation; there are no hidden customs fees because we handle all import paperwork.
What after‑sales support do you offer?
Our technical team is available **24 h/7 d** via email, WhatsApp, and WeChat. We provide **free troubleshooting**, formulation advice, and a **money‑back guarantee** if the product fails to meet the certified specifications.
Ready to Accelerate Your Liraglutide Program?
Limited‑time Offer: Free 100 mg sample + 30‑day price lock for first‑time buyers.
Request Sample & Quote NowOr contact us directly: Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
9. Customer Reviews
Dr. Laura Martinez – Senior Scientist, Altius Therapeutics
“The purity and consistency of the Liraglutide intermediate allowed us to hit our 5‑month development milestone two weeks early. The on‑time delivery was a game‑changer.”
James O'Neil – Procurement Manager, PharmaLogix Ltd.
“Transparent pricing and the full GMP dossier saved us weeks of paperwork. We saved approx. $22,000 on our last order.”
Wei Zhang – Technical Director, BioNext China
“Excellent after‑sales support. When we needed a quick purity re‑check, the team responded within 4 hours and provided a supplemental analysis report.”
10. About the Author
Dr. Michael Huang, Ph.D.
Senior Process Development Engineer with 15 years of experience in peptide synthesis, GMP compliance, and global supply‑chain optimization. Formerly led R&D at a top‑10 multinational pharma before joining Global Technology Co., Ltd. as Head of Technical Services.
Published author of “Advanced Peptide Manufacturing for Biopharma” (Springer, 2023) and regular contributor to Pharmaceutical Technology journal.
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