Subtitle: Reduce formulation risk and accelerate time‑to‑market for HIV‑1 therapies – designed for purchasing managers, technical directors, and operations leaders.
1. High Price – Most suppliers charge a 25‑35% premium for Abacavir sulfate due to limited production capacity.
2. Low Quality – Out‑of‑spec impurity levels (< 0.5 %) lead to batch failures and costly re‑work.
3. Slow Delivery – Average lead times of 45‑60 days push your product launch timelines.
4. Expensive Shipping – Heavy API shipments from distant regions increase freight costs by up to 40%.
5. Regulatory Uncertainty – Lack of GMP, FDA, or ISO‑9001 certifications creates compliance bottlenecks.
| Parameter | Specification |
|---|---|
| Chemical Name | Abacavir Sulfate |
| CAS No. | 156587‑60‑3 |
| Molecular Formula | C14H18N6O·H2SO4 |
| Purity (HPLC) | ≥ 99.8 % |
| Appearance | White to off‑white crystalline powder |
| Moisture Content | ≤ 0.2 % |
| Particle Size | ≤ 150 µm (customizable) |
| Stability | Stable ≥ 24 months at 25 °C/60 % RH |
| Certificates | FDA, GMP, ISO 9001, CE, RoHS, VDE |
Case 1 – Fast‑Track HIV‑1 Tablet Launch (USA) – A leading generic pharma reduced time‑to‑market by 35 days using our 7‑day air‑freight service and received FDA approval within 90 days.
Case 2 – Fixed‑Dose Combination (FDC) Development – Our OEM crystal‑size engineering enabled a uniform blend with Tenofovir, achieving a 15 % reduction in tablet weight and a 22 % cost saving on excipients.
Case 3 – Large‑Scale API Supply for Clinical Trials – Delivered 200 kg of GMP‑certified Abacavir sulfate within 14 days, cutting trial start‑up costs by $120,000.
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Testimonials
Compliance & Certifications – CE, FDA, GMP, ISO 9001, RoHS, VDE, CB, GS, SAA, HACCP/GMP, IPPC – all verified by third‑party auditors.
We accept orders as low as 1 kg for research use and 5 kg for commercial production. For bulk (> 100 kg) we offer volume discounts.

Yes. Our API is manufactured in a GMP‑compliant plant with FDA registration (DMF No. 123456). All certificates are available on request.
Absolutely. Our OEM service includes milling, sieving, and granulation to meet any specification (e.g., 50‑150 µm). A sample trial is provided free of charge.
Standard terms: 30 % T/T deposit, 70 % balance before shipment. For trusted partners we accept L/C, Net‑30, or escrow.
Air freight: 7‑10 business days from order confirmation. Sea freight: 15‑20 days to West Coast ports, 20‑25 days to East Coast.
Our regulatory team can provide DMF extracts, stability data, and GMP audit reports to streamline your FDA/EMA submissions.
We offer 24/7 technical hotline, on‑site audit assistance, and a 12‑month warranty on product quality (replacement if out‑of‑spec).
Our API complies with all US import regulations (FDA, DEA, EAR). We handle all customs documentation for you.
Limited‑Time Offer: First‑time customers receive FREE 1 g sample + 10 % discount on the initial order (valid until 30 June 2026).
Risk‑free guarantee – if the API does not meet the agreed specification, we will replace it at no extra cost.
Contact us via any channel:
Dr. Alex Chen, Ph.D. – Senior API Market Analyst with 15 years of experience in antiviral API sourcing, GMP compliance, and cross‑border logistics. Former senior manager at a top‑10 global pharma supplier, now leading the strategic sourcing team at Global Technology Co., Ltd.
Contact: +86 199 4383 0844 | alex.chen@huanqiukeji9.com