Accelerate your drug‑development pipeline, cut costs, and eliminate supply‑chain delays. Ideal for Corporate Purchasing Managers, Technical Directors, and Operations Managers seeking a reliable source of CAS 16960-16-0 Tetracosactide.
Get Free Quote in 24 hIn 2025, 37 % of pharmaceutical R&D teams reported project delays caused by unreliable peptide suppliers. The following pain points are the most common among U.S. and European manufacturers:
Imagine a scenario where a Phase II trial stalls because the peptide batch fails purity testing. The resulting delay could cost your company $1.2 million in lost market opportunity. You cannot afford that risk.
See the SolutionGlobal Technology Co., Ltd leverages a state‑of‑the‑art peptide‑synthesis facility in Zhengzhou, fully certified under GMP, FDA, ISO 9001, and CE. Our end‑to‑end quality system guarantees ≥ 99.8 % purity with ≤ 0.1 % residual solvents, validated by HPLC, Mass Spectrometry, and NMR.
| Parameter | Specification | Method |
|---|---|---|
| CAS Number | 16960‑16‑0 | N/A |
| Chemical Name | Tetracosactide (ACTH(1‑24)) | N/A |
| Molecular Weight | 3064.3 g·mol⁻¹ | N/A |
| Purity (HPLC) | ≥ 99.8 % | Validated, USP 1 |
| Appearance | White to off‑white lyophilized powder | Visual inspection |
| Residual Solvent | ≤ 0.1 % (GC‑MS) | EPA 2 |
| Storage | -20 °C, desiccated | Stability tested 24 months |
Scenario 1 – Academic Research: A leading U.S. university used our Tetracosactide to validate a novel ACTH receptor assay. The assay’s coefficient of variation dropped from 12 % to **3 %**, accelerating publication by 2 months.
Scenario 2 – Pharmaceutical Development: A mid‑size biotech firm required 2 kg of GMP‑grade Tetracosactide for a Phase I trial. Our OEM service delivered a **custom‑filled sterile vial** within 14 days, enabling the trial to start on schedule and saving **$150 k** in outsourced peptide synthesis fees.
Scenario 3 – Contract Manufacturing Organization (CMO): A CMO integrated our peptide into a large‑scale peptide‑drug conjugate (PDC) platform. The high‑purity batch reduced downstream purification steps by 40 %, cutting overall manufacturing cost by **$200 k** per batch.
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We accept orders as low as 1 g for research‑grade material. For GMP‑grade or OEM projects, the MOQ starts at 100 g.
Yes. Every batch is shipped with a signed CoA, full HPLC chromatogram, MS spectrum, and a GMP‑compliant batch record.
Absolutely. Our OEM/ODM team can handle N‑terminal acetylation, C‑terminal amidation, biotinylation, FITC labeling, and macro‑cyclization. Turn‑around time is typically 10‑14 days.

We provide express air‑freight (2‑5 days), standard air (7‑10 days), and sea freight (30‑45 days). All shipments include a full customs invoice, HS code (2937.50), and any required import permits.
Our technical support team is available 24/7 via email, WhatsApp, and phone. We assist with assay validation, stability studies, and regulatory documentation.
Limited‑time Offer: Place an order within the next 7 days and receive FREE 100 mg sample plus a 5 % discount on your first bulk purchase.
Sarah Liu – Procurement Lead, NovaBiotech:
“The price reduction was immediate – 28 % cheaper than our previous supplier, and the quality was exactly as promised.”
James O’Connor – Operations Manager, MedSupply Corp.:
“Delivery arrived in 4 days after we placed the order. No customs holds, no surprise fees – just a smooth experience.”
Dr. Ana Martínez – Head of R&D, PharmaGen Europe:
“The OEM labeling service saved us weeks of in‑house chemistry work. The final product met all regulatory specifications.”
Global Technology Co., Ltd – Your Trusted Partner for High‑Quality Peptides
Tel: +86 19943830844 | Email: service@huanqiukeji9.com
Address: No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China.
Visit our Contact Page for a personalized quotation.
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Compliance & Certifications
CE, FDA, ISO 9001, GMP, DMF, RoHS, CB, VDE, GS, SAA, HACCP/GMP – all documents are available on request and are included with every shipment.