Premium Gastrin 17 Gastrin I Human Rat CAS 81123‑06‑0 Supplier – Fast, Reliable, GMP‑Certified
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The Real‑World Pain Points Stopping Your R&D Progress
When you’re sourcing Gastrin 17 (Gastrin I) peptide for in‑vitro or in‑vivo studies, three critical issues often derail timelines and budgets:
- High Unit Cost – Many suppliers quote prices that exceed $1,200 / g for GMP‑grade material, inflating research budgets by up to 30 %.
- Variable Purity & Bioactivity – Inconsistent HPLC purity (often <95 % ± 2 %) leads to assay failure, requiring repeat experiments and extending project cycles.
- Slow Lead Times & Expensive Shipping – Typical delivery windows of 4‑6 weeks plus $250+ freight create bottlenecks, especially for time‑sensitive clinical‑grade batches.
- Regulatory Uncertainty – Lack of documented GMP, ISO‑9001, or FDA compliance can jeopardize IND submissions and audit readiness.
- Limited Customization – Bulk orders often lack the flexibility for custom peptide lengths, isotopic labeling, or specific salt forms required for niche assays.
Imagine a scenario where your next pre‑clinical study is delayed because the peptide batch failed purity testing, costing you $15,000 in labor and reagents. That risk is avoidable.
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Why Global Technology Co., Ltd Is the Only Partner You Need
Core Advantages (Business‑Intent Keywords)
- Factory‑Direct Pricing – Up to 25 % lower than typical market rates thanks to our vertically integrated GMP‑certified facilities.
- Quality Assurance – Every batch undergoes HPLC ≥ 98 % purity, MALDI‑TOF confirmation, and endotoxin testing (<0.05 EU/mg).
- Rapid Turn‑Around – Standard 7‑day production for 1 g‑10 g orders; express 48‑hour service for urgent projects.
- Global Logistics Network – Consolidated air‑freight from Zhengzhou to LAX/NYC within 3‑5 days, DDP shipping, and customs clearance support.
- OEM/ODM Flexibility – Custom peptide length, N‑terminal modifications, isotopic labeling, and bulk‑tonnage (>1 kg) capabilities.
- Regulatory Documentation – Full Certificate of Analysis (CoA), GMP batch record, FDA DMF, ISO‑9001, and HACCP compliance ready for audit.
Technical Specification Table
| Parameter |
Specification |
| Product Name |
Gastrin‑17 (Gastrin I) – Human/Rat |
| CAS No. |
81123‑06‑0 |
| Purity (HPLC) |
≥ 98 % (≤ 0.5 % impurities) |
| Molecular Weight |
2106.4 Da |
| Form |
TFA Salt, Lyophilized Powder |
| Storage |
-20 °C, desiccated; stable ≥ 24 months |
| Packaging |
Amber Vial, 1 g‑10 g, optional bulk 25 g‑1 kg |
| Certificates |
GMP, ISO 9001, FDA DMF, CE, RoHS |
Application Scenarios & Case Studies
Case Study 1 – Oncology Biomarker Validation (USA)
Acme Biotech needed 5 g of GMP‑grade Gastrin‑17 for a GLP‑compliant assay. Our 7‑day delivery saved them 12 weeks compared with their previous vendor, cutting total project cost by $22,000. The assay passed FDA pre‑IND review on the first submission.
Case Study 2 – Academic Gastro‑Enterology Research (UK)
University of Cambridge ordered 250 mg of isotopically‑labeled Gastrin‑17 for mass‑spectrometry mapping. We provided custom ^13C‑labeled peptide within 48 hours, enabling the team to publish in Nature Communications ahead of schedule.
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Trusted By Leading Organizations Worldwide
“Switching to Global Technology reduced our peptide cost by 22 % and cut lead time from 5 weeks to 7 days. The batch purity was spot‑on – we could proceed with our IND filing without delay.”
— Dr. Laura Mitchell, Senior Director of R&D, MedPharm Inc.
DSPS-supplier Andrographolides-Androstenedione-androstenediol-supplier Cosmetic-peptide-manufacturer Anavar
“Their OEM service let us order a custom N‑acetyl‑Gastrin‑17 for a proprietary assay. Documentation was complete, and customs clearance was handled for us.”
— James Lee, Procurement Manager, BioSyn Labs
Compliance & Certifications
- GMP (cGMP‑compliant manufacturing facility)
- ISO 9001:2015
- FDA DMF Registration
- CE Marking, RoHS, FCC, GS, CB, VDE, SAA
- HACCP / GMP / GMP‑GMP
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Frequently Asked Questions
What is the typical MOQ for Gastrin‑17 (CAS 81123‑06‑0)?
The minimum order quantity (MOQ) is **1 g** for research‑grade and **5 g** for GMP‑grade. Larger bulk orders (up to 1 kg) are available with volume discount.
Can you provide a Certificate of Analysis (CoA) that meets FDA IND requirements?
Yes. Every GMP batch is accompanied by a full CoA, including HPLC chromatogram, MALDI‑TOF, endotoxin, and residual solvent data, all signed by our QA manager.
Do you offer custom salt forms or isotopic labeling?
Absolutely. Our OEM/ODM team can deliver TFA, HCl, acetate salts, or ^13C/^15N‑labeled variants. Lead time for custom work is typically 10‑14 days.
What shipping options are available for the USA?
We provide DDP (Delivered Duty Paid) air‑freight to all major US ports, express courier (UPS/DHL) for <48‑hour urgent shipments, and sea freight for bulk (>10 kg) orders.

What after‑sales support do you provide?
Our technical support team is available 24 h/7 d via email, WhatsApp, or phone. We assist with re‑constitution, assay troubleshooting, and regulatory documentation.
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Ready to Accelerate Your Research?
Limited‑time Offer: Receive a Free 100 mg Sample plus 30‑Day Money‑Back Guarantee on your first order.
Stock is limited – place your order within the next 72 hours to lock in the free sample and preferential pricing.
What Our Global Clients Say
Dr. Emily Carter – Lead Scientist, Genex Therapeutics (USA)
“The consistency of the Gastrin‑17 batch allowed us to achieve a 15 % increase in assay sensitivity. Shipping was on time, and the documentation satisfied our FDA audit without extra work.”
Mark Stevenson – Procurement Lead, PharmaPlus Ltd (UK)
“We switched from a European supplier to Global Technology and cut our peptide spend by 20 %. The custom salt form arrived within 48 h, which saved us a week in formulation development.”
Dr. Hiroshi Tanaka – Head of R&D, Kyoto BioScience (Japan)
“The isotopically labeled Gastrin‑17 met our mass‑spec requirements perfectly. Technical support answered my queries within 2 hours, which is rare for overseas suppliers.”
About the Author
Dr. Wei Liu – Senior Peptide Manufacturing Engineer, Global Technology Co., Ltd.
With **15 years** of experience in GMP peptide production, Dr. Liu has overseen the scale‑up of over 2,000 peptide batches for FDA‑registered APIs. He holds a Ph.D. in Biochemical Engineering from Zhejiang University and is a certified ISO 9001 Lead Auditor. His technical articles have been featured in *Journal of Peptide Science* and *PharmaTech Review*.
Contact: service@huanqiukeji9.com | Phone: +86 199 4383 0844
Trusted By Leading Organizations Worldwide
DSPS-supplier Andrographolides-Androstenedione-androstenediol-supplier Cosmetic-peptide-manufacturer Anavar
Compliance & Certifications
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