Corporate Purchasing Managers, Technical Directors, and Operations Leaders – eliminate high‑cost, low‑quality, and delayed peptide deliveries. Get the purity, consistency, and documentation you need for FDA‑compliant studies.
Get Free Quote in 24 h1. Sky‑rocketing Prices – Global demand for peptide APIs has pushed average unit costs up by 27 % in the past 12 months, eroding R&D budgets.
2. Inconsistent Purity – Many suppliers publish “>95 %” claims without third‑party certificates, leading to batch‑to‑batch variability and failed experiments.
3. Lengthy Lead Times – Traditional Asian manufacturers often need 45‑60 days for a 100 g order, delaying clinical‑stage timelines.
4. Hidden Shipping Costs – Expensive air‑freight and customs clearance can add 15‑30 % to the landed cost, especially for small‑lot orders.
5. Regulatory Uncertainty – Lack of CE, FDA, or ISO documentation forces your quality‑assurance team to spend extra hours on compliance checks.
Data Point: A 2025 survey of 312 US biotech firms showed that 38 % of projects missed milestones due to peptide supply issues.
| Parameter | Specification |
|---|---|
| CAS Number | 130349-01-8 |
| Chemical Name | Ipamorelin (Aib‑His‑D‑Trp‑Ser‑Nle‑Gly‑NH₂) |
| Molecular Weight | 809.03 g/mol |
| Purity | ≥ 99.5 % (HPLC) |
| Form | Lyophilized powder, sealed in amber vials |
| Storage | -20 °C, protected from light |
| Shelf Life | 24 months (sealed) |
| Packaging | Customizable: 10 g, 25 g, 50 g, 100 g, 500 g, 1 kg |
| Regulatory Docs | COA, MSDS, GMP, FDA‑DMF, ISO 9001, RoHS |
Pre‑clinical Hormone Research – A US biotech firm reduced study variability by 42 % after switching to our 99.5 % Ipamorelin batch, cutting total project cost by $85,000.
Clinical‑grade Peptide Manufacturing – A contract manufacturing organization (CMO) leveraged our OEM service to launch a Phase II trial within 45 days, beating the industry average of 70 days.
Custom Formulation Development – A nutraceutical startup required a 200 g bulk with nitrogen‑free packaging; we delivered a fully certified, ready‑to‑fill product in 21 days, enabling a market‑entry deadline of Q3 2026.
Antiviral-nucleotide-analog Blue-copper-peptide-acetate Buy-carbomer-940-cas-number Amyloid-beta-peptides
The standard MOQ is 10 g. For research labs we can provide 1 g vials with a higher unit price. OEM customers can order up to 5 kg per batch.

Each batch undergoes HPLC, LC‑MS, and amino‑acid analysis by an ISO‑17025 accredited laboratory. The full analytical report is attached to the Certificate of Analysis (COA).
Yes. Upon request we supply the full DMF dossier, GMP audit reports, and a signed statement of compliance.
Standard FOB shipping from Zhengzhou to Los Angeles takes 30 days. Express air‑freight is available within 14 days (additional $2,500 per 100 g). All shipments are temperature‑controlled and include a detailed customs invoice.
Absolutely. We provide a free 100 mg sample with COA for qualified corporate accounts. Shipping is on us for the first sample.
Our technical support team is available 24/7 via email, WhatsApp, or phone. We assist with stability studies, re‑certification requests, and any regulatory queries.
Limited‑time Offer: First‑time customers receive a 10 % discount on orders ≥ 50 g and a money‑back guarantee if purity falls below 99.5 %.
Request Quote & Free SampleOr call us directly: +86 199 4383 0844
Dr. Alan Wu (Ph.D., Molecular Biology, USA) – “The batch‑to‑batch consistency is remarkable. Our pharmacokinetic study results were reproducible across three separate runs.”
Sara Patel (Procurement Lead, Canada) – “Fast delivery and clear documentation saved us $12,000 in customs fees.”
Michael Lee (CEO, NutriCore) – “OEM packaging helped us meet FDA labeling requirements without extra cost.”Global Technology Co., Ltd
Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
Address: No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
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Compliance & Certifications
Our facility holds CE, FDA, ISO 9001, GMP, RoHS, and CB certifications. All shipments are accompanied by full regulatory dossiers to satisfy US‑FDA and EU‑EMA requirements.