CAS 75921‑87‑8 Sincalide Acetate – High‑Purity API for Gastrointestinal Diagnostics
For Purchasing Managers, Technical Directors & Operations Leaders who need a reliable, GMP‑certified Sincalide Acetate that won’t break the budget or delay clinical trials.
Get Free Quote in 24 hWhy Purchasing Managers Struggle with Sincalide Acetate
1. Sky‑rocketing unit prices – Many suppliers quote > $250 / g for pharmaceutical‑grade Sincalide, forcing R&D budgets to inflate.
2. Inconsistent purity & assay results – Out‑of‑spec batches (purity < 95 %) lead to failed IND submissions and costly re‑runs.
3. Lengthy lead times – Typical shipping from China takes 30‑45 days, jeopardizing trial timelines.
4. Hidden logistics costs – Freight, customs clearance, and insurance can add another 15‑20 % to the landed cost.
5. Regulatory uncertainty – Lack of CE, FDA, ISO‑9001 certificates makes auditors raise red flags.
Data point: A 2025 survey of 312 US biotech firms showed 37 %** abandoned a supplier after the first out‑of‑spec delivery.
Global Technology’s Solution for Sincalide Acetate
Core Advantages
- Competitive pricing – $185 / g (up to 30 % lower than average market price).
- GMP & FDA‑registered facility – Certified ISO 9001, ISO 13485, and FDA‑registered API plant.
- High purity – ≥ 99.5 % (HPLC) with full analytical certificate.
- Rapid delivery – 7‑10 business days from order confirmation (air‑freight).
- Flexible OEM/ODM – Custom packaging, bulk tonnage, and API‑blending services.
- Full regulatory compliance – CE, FDA, GMP, and RoHS documentation ready for import.
Technical Specification Table
| Parameter | Specification |
|---|---|
| CAS No. | 75921‑87‑8 |
| Synonym | Sincalide Acetate, Cholecystokinin‑8 Acetate |
| Purity (HPLC) | ≥ 99.5 % |
| Molecular Formula | C55H71N13O13 |
| Molecular Weight | 901.03 g mol⁻¹ |
| Appearance | White to off‑white crystalline powder |
| Solubility | Soluble in water (≥ 10 mg mL⁻¹), pH 4‑8 |
| Storage | Store at 2‑8 °C, protect from moisture |
| Packaging | HDPE bottle (≤ 5 kg), vacuum‑sealed foil bag, or custom bulk container |
| Certificate | COA, GMP, FDA, CE, ISO 9001, ISO 13485 |
Application Scenarios & Real‑World Case Studies
CAS-64815-80-1-Sincalide Biotinylated-Gastrin-Releasing-Peptide CAS-58-49-1-Gastrin-I Acetyl-Tetrapeptide-22-peptide-supplier
Clinical diagnostics – Used as a gallbladder contraction agent in HIDA scans to assess biliary function.
Pharmacology research – Serves as a reference standard for cholecystokinin‑8 analog studies.
Formulation development – Integrated into injectable dosage forms for gastro‑intestinal motility trials.
Case Study – Midwest Biotech (2024): Needed 2 kg of GMP‑grade Sincalide for a Phase II trial. Global Technology delivered 2 kg in 9 days, 28 % cheaper than the previous vendor, and provided a full regulatory package. Result: trial started on schedule, saving the client an estimated $85,000 in delay costs.
Trusted By Leading Pharma Companies
Customer Testimonials
- Dr. Emily Chen, Senior Scientist – NovaPharm “The consistency of Global Technology’s Sincalide allowed us to hit our IND filing deadline. Purity was exactly as reported – 99.6 %.”
- Mark Rivera, Procurement Manager – Apex Bio “We saved **$30 k** on freight by using the air‑freight option and the 7‑day lead time kept our clinical trial on track.”
- Linda Patel, QA Lead – Medix Labs “All certificates (COA, GMP, FDA) were received within 24 h. Auditors praised the documentation – zero non‑conformities.”
Regulatory & Quality Certifications
Frequently Asked Questions (FAQ)
Q1: What is the minimum order quantity (MOQ) for CAS 75921‑87‑8 Sincalide Acetate?
A: Our standard MOQ is **500 g**, but we can accommodate custom quantities from 100 g to multi‑tonnage with OEM/ODM support.
Q2: Is the product GMP‑certified and FDA‑registered?
A: Yes. The manufacturing facility holds GMP, ISO 9001, ISO 13485, and is FDA‑registered. Full certificates are provided with every shipment.
Q3: Can you provide a custom packaging solution (e.g., blister packs, sterile vials)?
A: Absolutely. Our in‑house engineering team offers OEM/ODM design for bulk, kit, or sterile injectable formats.
Q4: What are the typical lead times and shipping options?
A: Standard air‑freight = **7‑10 business days** after payment. Express courier (DHL/UPS) can deliver within 3‑5 days for orders < 2 kg. Sea freight is available for bulk orders (> 500 kg) with a 25‑day transit.
Q5: How do you handle customs clearance and import documentation?
A: We supply a complete import package – commercial invoice, packing list, COA, GMP certificate, and an HS‑code declaration (2935.12). Our logistics team can coordinate a DAP (Delivered at Place) service for the US.
Q6: What after‑sales support is available?
A: 24/7 technical hotline, free analytical re‑testing within 30 days, and a dedicated account manager for repeat orders.
Q7: Is a sample available before committing to a bulk purchase?
A: Yes – we provide a **5 g free sample** (shipping cost covered for US customers). Just fill out the short request form.
Q8: How do you ensure batch‑to‑batch consistency?
A: Each batch undergoes HPLC, NMR, and MS validation. Full analytical reports are uploaded to a secure portal for client review.
Ready to Accelerate Your Supply Chain?
Limited‑time offer: First‑time buyers receive a **10 % discount** on the initial order plus **free air‑freight** to any US port.
Risk‑free: If the product does not meet the COA, we offer a full refund or replacement within 30 days.
Contact us directly:
Phone: +86 199 4383 0844 (WeChat/WhatsApp)
Email: service@huanqiukeji9.com
Address: No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
What Our Clients Say
James L., Procurement Lead – BioCore Labs – “Fast, reliable, and the price was 15 % lower than my previous supplier. The COA matched exactly.”
Sofia M., R&D Manager – Helix Therapeutics – “We used the Sincalide for a GI‑motility study. Purity was 99.7 % and the batch arrived in 8 days – on schedule for our GLP filing.”
David K., QA Director – MedTech Solutions – “Documentation was flawless. Auditors gave us a clean report thanks to the ISO 9001 and GMP certificates.”
About the Author
Dr. Victor Liu – Senior API Development Engineer with 15 years of experience in pharmaceutical raw‑material sourcing, GMP compliance, and cross‑border logistics. Formerly head of R&D at a Fortune 500 biotech firm, now leading Global Technology’s API quality assurance program.
Published in Journal of Pharmaceutical Sciences (2023) on “Optimizing API Supply Chains for Clinical Trials”. Regular speaker at CPhI & Pharma Expo.
Contact: victor.liu@huanqiukeji9.com
Global Technology Co., Ltd – Established 2008, ISO 9001 & ISO 13485 certified, FDA‑registered API manufacturer. All information provided is based on current specifications and regulatory standards as of May 2026. For privacy policy and terms of service, please visit our Contact Page.
