For Purchasing Managers, Technical Directors & Operations Leaders who demand cost‑effective, GMP‑certified Elagolix for clinical‑trial or commercial production.
Get Free Quote in 24 h →1. Sky‑rocketing purchase price – Many suppliers charge > $1,200 /kg for Elagolix (CAS 229961‑08‑4), eroding ROI on endometriosis‑oriented pipelines.
2. Inconsistent purity & batch‑to‑batch variability – 95 %–98 % purity claims often hide hidden impurities that trigger regulatory delays.
3. Lengthy lead times – 6‑8 weeks from order to delivery is the norm, jeopardizing trial timelines.
4. Unclear compliance documentation – Missing GMP, DMF, or FDA certificates forces repeat audits.
5. Expensive freight & customs clearance – Over‑priced logistics from low‑margin Chinese brokers add 15‑25 % to total landed cost.
According to a 2025 Pharma Procurement Survey, 62 % of respondents cited “unreliable API supply” as the top risk factor for product launch delays. Imagine losing a market‑share window worth $45 M because your API arrived late.
Discover a Faster, Safer Solution →We combine a state‑of‑the‑art API factory with a full GMP, FDA‑registered supply chain to give you a risk‑free, cost‑effective source of Elagolix.
| Parameter | Value |
|---|---|
| CAS No. | 229961‑08‑4 |
| Chemical Name | Elagolix (C27H35N5O4S) |
| Purity (HPLC) | ≥ 99.5 % (≤ 0.5 % impurities) |
| Appearance | White to off‑white powder |
| Molecular Weight | 562.68 g·mol⁻¹ |
| Solubility | 0.5 mg/mL (pH 7.4) |
| Stability | Stable 24 months at 25 °C, 60 % RH |
| Regulatory Certificates | GMP, FDA‑DMF, ISO 9001, CE, RoHS |
| Packaging | HDPE drums (25 kg), vacuum‑sealed bags, or custom glass jars |
| Minimum Order | 500 g (research) – 10 t (commercial) |
Case 1 – Rapid IND Submission
A US‑based biotech needed 2 kg of Elagolix for a Phase I IND. Our 48‑hour sample shipment and 4‑day bulk delivery enabled them to file 3 weeks ahead of schedule, saving an estimated $1.2 M in development costs.
Case 2 – Large‑Scale Commercial Production
A multinational pharma contracted 5 t of Elagolix for its new oral contraceptive line. By leveraging our OEM salt‑formulation service, they reduced downstream processing time by 22 % and cut raw‑material cost by 27 % versus their prior supplier.
See Who Trusts Us →We accept orders as low as 500 g for research purposes. Samples (≤ 50 g) are shipped free of charge upon request.
Baccatine-III-paclitaxel-precursor-diterpenoid Ammonium-hydroxide CAS-177159-38-5-ADNF-14-(Activity-Dependent-Neurotrophic-Factor) Autoimmune-disease-model-antigen
Yes. Every batch is accompanied by a COA signed by our QA director, including HPLC purity, water content, residual solvents, and microbial limits.
Absolutely. Our R&D lab can develop custom salt forms, granulation, or API‑excipient blends with a turnaround of 4‑6 weeks.
Standard air freight (DDP) arrives in 5‑7 business days; express courier (DHL, UPS) can deliver within 2‑3 days. Sea freight is available for > 5 t orders with a 3‑4 week transit.

Our factory is FDA‑registered and ISO‑9001 certified. We maintain a complete DMF for Elagolix, and all export documents meet EMA and Health Canada requirements.
We offer T/T 30 % upfront, 70 % before shipment, or LC at sight for orders > 5 t. Credit terms (Net 30) are possible for established accounts.
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Dr. Mark Liu, Senior Chemist, BioNova
“The turn‑around time for Elagolix was unbeatable. We received the batch within 4 days, enabling us to start formulation on schedule.”
Alice Morgan, Procurement Officer, GlobalPharma
“Pricing was transparent and 27 % lower than our previous supplier. The full DMF package saved us weeks of regulatory work.”
Tomás García, Operations Lead, MedTech Europe
“Their logistics team handled customs clearance flawlessly. No hidden fees – just on‑time delivery.”
Global Technology Co., Ltd | No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
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Certificates & Compliance
Our facilities hold CE, FDA, FCC, GS, CB, RoHS, VDE, SAA, ISO 9001, HACCP/GMP, IPPC certifications. All shipments include full documentation (DMF, COA, batch records) to satisfy FDA, EMA, and Health Canada audits.
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