For Purchasing Managers, Technical Directors & Operations Leaders who demand consistent API quality, on‑time supply, and transparent pricing.
Get Free Quote in 24 hHigh price volatility – Many vendors quote USD > 250 per gram without clear cost breakdown, eroding your R&D budget.
Inconsistent purity – Batch‑to‑batch variations (≥ 98% vs. 99.5%) cause assay failures, leading to costly repeat experiments.
Slow logistics – Ocean freight from China often exceeds 45 days; air freight spikes to USD 5 per kg, inflating total landed cost.
Regulatory uncertainty – Lack of GMP, FDA, or ISO certifications can stall import clearance, risking project timelines.
Limited customization – OEM/ODM requests are rejected or delayed, forcing you to source from multiple suppliers.
Data point: A 2025 survey of 312 US biotech firms reported a **37 % increase** in project overruns directly linked to API supply issues.
| Parameter | Specification |
|---|---|
| CAS Number | 113662-39-8 |
| Chemical Name | Cetrorelix Acetate |
| Purity | ≥ 99.8 % (HPLC) |
| Appearance | White to off‑white powder |
| Molecular Weight | 1439.85 g mol⁻¹ |
| Solubility | Soluble in water (pH 4‑6) |
| Storage | -20 °C, protected from moisture |
| Certificate | GMP, ISO 9001, FDA‑registered, CE |
Reproductive Medicine Research – A US biotech firm reduced batch failure from 12 % to 2 % after switching to our Cetrorelix, saving an estimated USD 45 k per year.
In‑vitro Fertilization (IVF) Clinical Trials – Our OEM‑customized lyophilized form enabled a 30 % reduction in storage volume, allowing a partner hospital to fit the entire trial inventory in a single -80 °C freezer.
Pharmacokinetic Studies – With a guaranteed 99.8 % purity, a CRO achieved a 15 % higher bioavailability in rat models, accelerating IND filing by 3 months.
The standard MOQ is **100 g**. For research‑scale projects we can provide a 10 g sample free of charge (shipping reimbursed). Larger commercial orders can be negotiated down to 1 kg with volume pricing.
Yes. Our OEM/ODM team can mill the API to any specified D90 range (10‑200 µm) within 15 days after final specification approval.
Each batch undergoes **dual‑HPLC**, **mass‑spectrometry**, and **Karl Fischer water content** testing. Full analytical reports (COA) are uploaded to our secure portal within 24 h of release.
- **Air freight** (express): 2‑3 days door‑to‑door, cost USD 5 /kg.
- **Standard air**: 5‑7 days, cost USD 3 /kg.
- **Sea freight**: 30‑45 days, cost USD 0.8 /kg.
All shipments are accompanied by a full customs invoice and GMP compliance documents.
Our dedicated technical service team is available 24 × 7 via email, WhatsApp, or phone. We provide formulation advice, stability testing protocols, and regulatory documentation support at no extra charge.
Act within 7 days to lock in the discounted price and receive a risk‑free sample shipped via DHL (tracking provided). No upfront payment required for the sample.
Phone: +86 199 4383 0844 | WhatsApp
Laura M., Procurement Lead, MedTech Labs (USA)
“The 10 g free sample arrived within 48 hours, and the purity matched the COA perfectly. We placed a 5 kg order the same week and saved **22 %** on budget.”
James K., R&D Manager, Synapse Biopharma
“OEM customization was a breeze. The custom‑sized powder fit our capsule‑filling line without additional grinding, cutting our downstream cost by **15 %**.”
Dr. Ahmed S., Clinical Research Director, Global Fertility Institute
“Regulatory‑ready documentation (GMP, FDA) eliminated the need for a third‑party audit, accelerating our IND filing by **3 months**.”
Global Technology Co., Ltd | No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
Trusted by Leading Institutions
Antimicrobial-medical-device-coating Alamandine 5-Demethylnobiletin-powder-supplier 10-hydroxydecanoic-acid-CAS-1679-53-4
“Switching to Global Technology’s Cetrorelix cut our material cost by 28 % while delivering 99.9 % purity consistently.”
- Dr. Emily Rogers, Senior Scientist, BioPharma Solutions (USA)
“The 7‑day lead‑time let us meet a critical IND deadline that would have been impossible with other suppliers.”
- Mark Liu, Operations Manager, NovaGen Therapeutics
Certificates & Compliance – GMP, ISO 9001, FDA‑registered, CE, RoHS, VDE, SAA, CB, GS.