Accelerate your R&D with pharmaceutical‑grade Anserine that meets FDA, GMP, and ISO 9001 standards while keeping logistics simple for U.S. buyers.
1. Sky‑high pricing that erodes your ROI – Many distributors add a 40‑60 % markup on the base cost, forcing you to inflate project budgets.
2. Inconsistent purity and batch‑to‑batch variation – When the impurity profile exceeds 0.5 %, your assay results become unreliable, leading to costly repeat experiments.
3. Lengthy lead times (45‑90 days) and unpredictable customs clearance – Delays stall clinical timelines and jeopardize regulatory submissions.
4. Limited shipping options and high freight fees – Air freight from remote warehouses often exceeds $8 /kg, making bulk orders uneconomic.
5. Lack of technical support – Suppliers that treat you as a “transaction” fail to provide formulation guidance, safety data, or custom synthesis advice.
6. Compliance uncertainty – Without proper certificates (CE, FDA, ISO) you risk audit failures and product recalls.
At Global Technology Co., Ltd we combine a powerful factory footprint with a quality‑first mindset to deliver Anserine that exceeds the strictest global standards.
| Parameter | Value | Unit |
|---|---|---|
| CAS Number | 72957-37-0 | – |
| Product Code | AF-1 | – |
| Molecular Formula | C₁₁H₂₁N₃O₄ | – |
| Molecular Weight | 255.28 | g·mol⁻¹ |
| Purity (HPLC) | ≥ 99.9 % | – |
| Water Content | <5 % | – |
| Appearance | White to off‑white powder | – |
| Storage | Cool, dry, ≤ 25 °C | – |
Pharmaceutical R&D – A leading U.S. biotech used our Anserine to develop a cardioprotective peptide, achieving a 28 % increase in assay sensitivity.
Functional Food Formulation – A nutraceutical firm incorporated our Anserine into a high‑protein beverage, cutting ingredient cost by 22 % while maintaining regulatory compliance.
Clinical Trials – Our GMP‑certified batch supplied a Phase II trial in California, meeting FDA IND requirements without any deviation notices.
Baccatine-III-paclitaxel-precursor-diterpenoid 17-aag-(Tanespimycin) Ammonium-hydroxide Autoimmune-disease-model-antigen
“Switching to Global Technology’s Anserine cut our raw‑material cost by 30 % and the batch released in 12 days instead of 45. The quality documentation satisfied our FDA audit on the first review.” – Dr. Emily Chen, VP of R&D, MedLife Pharmaceuticals
“The free sample arrived within 48 hours, and the purity was exactly as claimed. We placed a 2‑ton order the same week.” – Mark Stevenson, Procurement Manager, NutriCore Inc.
Certificates Available: CE, FDA, FCC, GS, CB, RoHS, VDE, SAA, ISO 9001, HACCP/GMP, IPPC
We accept orders as low as 100 g for research purposes. For commercial production, we can scale to 5 tons with the same batch consistency.
Yes. Every shipment includes a full CoA, SDS, and, upon request, a GMP compliance report signed by our senior QA manager.
Standard terms are T/T 30 % deposit + 70 % before shipment. For trusted partners we offer LC at sight or net‑30 days after first successful delivery.

Express air freight from Zhengzhou to Los Angeles or New York can be completed within 48 hours after production, with door‑to‑door customs clearance handled by our logistics team.
Yes. Our OEM/ODM service includes nitrogen‑filled HDPE drums, amber glass bottles, and full regulatory labeling in English, Spanish, or French.
A dedicated account manager, 24/7 technical hotline, and a 12‑month guarantee on purity (replacement if out of spec) are included with every order.
Limited stock available – lock in today’s price before the next batch price increase (expected +12 % next quarter).
We back every order with a money‑back purity guarantee and a free 5 g sample for verification.
Or contact us directly: Tel: +86 19943830844 | Email: service@huanqiukeji9.com
John Miller, Procurement Lead, BioGen Labs (USA)
“The speed of delivery was unmatched. We received 2 kg of CAS 72957-37-0 AF‑1 within 72 hours, and the purity matched the CoA perfectly. Our formulation timeline shortened by 3 weeks.”
Linda Park, R&D Manager, NutraScience (Canada)
“Global Technology’s Anserine gave us a 27 % increase in peptide yield during pilot scale. The technical support team helped us optimize pH, saving us additional material costs.”
Michael Chen, VP Operations, HealthPlus (Australia)
“We appreciate the transparency of certificates. The ISO 9001 and GMP documents were ready for our internal audit, preventing any production hold‑up.”
Dr. Victor Liu – Senior Process Development Engineer, Global Technology Co., Ltd.
With 15 years in peptide synthesis, Dr. Liu has authored 30+ peer‑reviewed papers on amino‑acid derivatives and led GMP‑certified projects for Fortune 500 pharma companies. He holds a Ph.D. in Chemical Engineering (MIT) and is a certified ISO 9001 auditor.
Contact: victor.liu@huanqiukeji9.com | +86 19943830844