Subtitle: Accelerate your oncology pipeline, lower cost per gram, and guarantee GMP‑grade quality – engineered for Purchasing Managers, Technical Directors, and Operations Leaders.
When you are responsible for a multi‑million‑dollar drug development program, any delay or quality issue translates directly into lost market share and inflated ROI calculations. Below are the three most common pain points we hear from corporate purchasing teams across the United States:
According to a 2025 Pharma Procurement Survey, 42% of respondents postponed clinical‑phase trials due to unreliable API sourcing. Imagine the cost of a 6‑month delay – it can exceed $10 million.
Global Technology Co., Ltd combines a powerful factory network with strict quality assurance to deliver the most cost‑effective, high‑purity Avadomide (CC‑122) on the market. Below are the core advantages you gain when you choose us as your API partner:
| Parameter | Value |
|---|---|
| CAS Number | 1580555‑26‑5 |
| Chemical Name | Avadomide (CC‑122) |
| Purity (HPLC) | ≥ 99.5 % |
| Appearance | White to off‑white crystalline powder |
| Molecular Formula | C22H23N5O2S |
| Molecular Weight | 409.48 g·mol⁻¹ |
| Solubility | Soluble in DMSO, DMF; sparingly soluble in water |
| Stability | Stable 2 years at –20 °C (protected from moisture) |
Scenario 1 – Early‑Stage Oncology Research
A U.S. biotech firm needed 5 g of Avadomide for a pre‑clinical mouse model. By sourcing from Global Technology, they received a 99.7 % pure batch within 10 days, cutting their study timeline by 40 % and saving $12,000 in material costs.
Scenario 2 – GMP Clinical‑Phase Manufacturing
A Phase II contract manufacturing organization (CMO) required 2 kg of GMP‑grade Avadomide. Our on‑site GMP facility delivered the material in 18 days, complete with a full regulatory dossier, enabling the CMO to file an IND amendment without delay.
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Compliance & Certifications
All Avadomide (CC‑122) shipments are accompanied by CE, FDA, ISO 9001, GMP, and RoHS certificates. Our facilities also hold CB, FCC, and VDE approvals, ensuring seamless import into the U.S., EU, and Asian markets.
Q1: What is the minimum order quantity for CAS 1580555-26-5 Avadomide (CC‑122)?
A: We accept orders as low as **1 g** for research use, and **100 g** for GMP‑grade bulk. Larger volumes (tonnage) are available with volume discounts.
Q2: Is the Avadomide supplied with a full regulatory dossier?

A: Yes. Every batch includes a Certificate of Analysis, MSDS, GMP audit report, and a **DMF‑ready** dossier for IND submissions.
Q3: Can you provide custom salt forms or isotopic labeling?
A: Absolutely. Our OEM/ODM team can develop custom salts, deuterated analogues, or bulk‑scale synthesis up to **5 tonnes** per year.
Q4: What are the payment terms for U.S. corporate buyers?
A: We accept **T/T 30 % advance, 70 % upon shipment**, with letters of credit (L/C) also accepted for orders over $50,000.
Q5: How do you handle shipping and customs clearance?
A: We partner with DHL and UPS for **door‑to‑door** service, provide all import documentation, and offer **FOB** or **CIF** terms based on your preference.
Q6: What after‑sales support is available?
A: Our technical service team offers **24/7 email support**, free re‑analysis if purity deviates > 0.2 %, and a **money‑back guarantee** for any non‑conformity.
Urgency: Only **200 g** of our promotional stock remain at the discounted price of **$2,950 / g** (regular $3,200 / g). Offer expires **July 15 2026**.
Risk‑Mitigation: Receive a **free 0.5 g sample** and a **full‑refund guarantee** if the batch fails to meet the COA specifications.
Contact Options:
Dr. Michael Zhang, Ph.D. – Senior API Development Manager at Global Technology Co., Ltd, with 15 years of experience in API scale‑up, GMP compliance, and cross‑border pharmaceutical logistics. Dr. Zhang has authored three peer‑reviewed papers on heterocyclic drug synthesis and serves on the advisory board of the International Society for Pharmaceutical Engineering (ISPE).
Contact: service@huanqiukeji9.com | Phone: +86 199 4383 0844
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