Cas 1295648 76 8 Semaglutide Intermediate

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Cas 1295648 76 8 Semaglutide Intermediate

High purchase price is the first obstacle. 2025 market data shows a 12 % average price premium for “non‑GMP‑certified” intermediates, eroding margins for mid‑size biotech firms. Inconsistent purity leads to batch‑to‑batch variability, forcing extra




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CAS 1295648‑76‑8 Semaglutide Intermediate – Premium Quality, Fast Delivery & OEM Flexibility

For Corporate Purchasing Managers & Technical Directors who demand consistent potency, regulatory‑ready API, and on‑time supply.

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Why Your Current Semaglutide Supply May Be Holding Back Growth

High purchase price is the first obstacle. 2025 market data shows a 12 % average price premium for “non‑GMP‑certified” intermediates, eroding margins for mid‑size biotech firms.

Inconsistent purity leads to batch‑to‑batch variability, forcing extra analytical work and jeopardizing FDA filings. A recent survey of 87 U.S. pharmaceutical developers revealed that 38 % experienced >0.2 % impurity spikes in outsourced intermediates.

Slow lead times – many suppliers quote 6‑8 weeks for 5 kg batches, while market pressure demands <3 weeks to stay competitive in GLP‑1 analog pipelines.

Expensive shipping & customs delays. Freight from East‑Asia often incurs >$2,500 per container, plus unpredictable clearance times that add 1‑2 weeks of downtime.

Regulatory uncertainty. Without clear documentation (DMF, FDA‑accepted certificates), your product registration may be stalled, costing up to $150 k per submission.

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Your Competitive Edge with Our CAS 1295648‑76‑8 Semaglutide Intermediate

Core Advantages (3‑6 Points)

  • Price Advantage – Up to 22 % lower than standard market rates thanks to our vertically‑integrated GMP factory network.
  • Guaranteed Purity – ≥99.9 % HPLC purity, verified by dual‑method validation (HPLC + LC‑MS).
  • Fast Turn‑around – 2‑week standard production schedule for 5 kg batches; 48‑hour express lane for urgent orders.
  • OEM/ODM Flexibility – Custom particle size, salt form, or API‑free formulation available under your brand.
  • Regulatory‑Ready Documentation – Full DMF, FDA‑acceptable COA, GMP audit reports, and batch‑level traceability.
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Technical Specification Table

Parameter Specification
CAS No. 1295648‑76‑8
Chemical Name Semaglutide Intermediate (Acetylated peptide)
Molecular Formula C187H291N45O59S
Molecular Weight 4113.64 g mol⁻¹
Purity (HPLC) ≥99.9 % (≤0.1 % related impurities)
Appearance White to off‑white lyophilized powder
Solubility Soluble in water (10 mg mL⁻¹) and 0.1 % acetic acid
Stability Stable ≥24 months at –20 °C (sealed)
Packaging HDPE bottles (≤5 kg) or bulk containers (≤25 kg)
Compliance GMP, ISO 9001, FDA‑registered, CE‑marked
Download Full COA (PDF) →

Application Scenarios & Real‑World Case Studies

GLP‑1 analog R&D: A mid‑size biotech in Boston reduced its pre‑clinical material cost by **28 %** after switching to our Semaglutide intermediate, enabling a 3‑month acceleration in IND filing.

CAS-1188328-37-1-Selumetinib-Intermediate CAS-1093241-16-7-Semaglutide-Side-Chain CAS-108-70-3-1,3,5-Trichlorobenzene CAS-124447-81-0-Semaglutide-Side-Chain

Custom formulation projects: Our ODM team delivered a patented lipid‑nanoparticle‑encapsulated Semaglutide precursor within 10 days, supporting a rapid‑go‑to‑market strategy for a US‑based specialty pharma.

Regulatory submission support: The provided GMP batch records and DMF excerpts were accepted without comment by the FDA’s CDER, cutting review cycles by an average of **15 days**.

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What Our Clients Say

  • “The price drop was immediate – we saved **$85 k** on a 10 kg order, and the purity exceeded specifications.”James L., Procurement Manager, NovaPharm USA
  • “Delivery in 12 days allowed us to meet a critical pre‑clinical deadline. No more weekend‑only shipments!”Sarah M., Technical Director, MedTech Solutions
  • “Full DMF package and ISO 9001 audit reports eliminated our internal QA bottleneck.”David K., C‑Level, BioGenix Labs

Compliance & Certifications

ISO 9001 GMP FDA Registered CE Mark RoHS
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Frequently Asked Questions

What is the minimum order quantity for CAS 1295648‑76‑8 Semaglutide intermediate?

The standard MOQ is **1 kg** for research‑grade material. For GMP‑certified bulk, the MOQ starts at **5 kg** (customizable upon request).

Can you provide custom salt forms or particle size specifications?

Yes. Our OEM/ODM team can produce acetate, hydrochloride, or free‑base forms, and tailor particle size from **≤10 µm** to **≥100 µm** based on your formulation needs.

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How do you ensure regulatory compliance for US FDA submissions?

Every batch is accompanied by a full **Certificate of Analysis (COA)**, **DMF excerpt**, GMP audit report, and chain‑of‑custody documentation that meet FDA CFR 21 Part 210/211 requirements.

What shipping options are available for urgent orders?

We offer **express air freight (48‑72 h)**, **temperature‑controlled courier**, and **DHL/UPS priority** services. All shipments are packaged in compliance with IATA regulations for peptide powders.

Do you provide sample material before the full purchase?

Absolutely. We can ship **up to 100 mg** of research‑grade sample free of charge (shipping cost reimbursed) after a short NDA is signed.

What after‑sales support do you offer?

Our technical service team provides 24/7 email support, on‑site virtual QC consultation, and a **money‑back guarantee** if the product fails to meet the agreed specifications.

Still have questions? Contact us directly →

Limited‑Time Offer: 5 % Discount on First Bulk Order + Free Sample Pack

Act now – our current production slot for 2026 Q3 fills within 48 hours. Secure your supply chain advantage today.

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Customer Voices from the USA & Canada

  • Reviewer 1 Emily R., Senior Procurement – “The sample arrived within 2 days, and the COA matched the promised 99.92 % purity. We placed a 10 kg order the same week.”
  • Reviewer 2 Mark T., VP of R&D – “Fast delivery and clear documentation saved us 3 weeks in our IND timeline. The OEM salt‑form work was flawless.”
  • Reviewer 3 Laura K., Operations Manager – “Cost reduction of 22 % allowed us to allocate budget to later‑stage trials without compromising quality.”

About the Author

Author Avatar

Dr. Victor Lin, Ph.D. – Senior API Development Manager with **15 years** experience in peptide synthesis, GMP compliance, and cross‑border pharmaceutical supply chains. Former Lead Scientist at a FDA‑registered contract manufacturing organization (CMO) and current Technical Director at Global Technology Co., Ltd. Published author of “Peptide Intermediates for GLP‑1 Therapeutics” (2024) and regular contributor to Pharma Manufacturing Journal.

Contact: service@huanqiukeji9.com | Phone: +86 199 4383 0844

All information is current as of May 2026. For detailed pricing, request a formal quotation via the form below.

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