Article Outline (H1‑H3 Levels)
- H1: CAS 23815-91-0 Reserpine – Premium API for Global Pharma & Research
- H2: Hero Section – Immediate Value for Purchasing Managers
- H2: Problem Agitation – Why Your Current Reserpine Supplier Fails
- H2: Solution Presentation – What Sets Global Technology Apart
- H3: Core Advantages (3‑6 bullet points)
- H3: Technical Specification Table
- H3: Application Scenarios & Case Studies
- H2: Social Proof – Trusted Brands & Certifications
- H2: FAQ – Procurement, Customization, Logistics & After‑Sales
- H2: Strong Call‑to‑Action – Limited Offer & Risk‑Free Sampling
- H2: Real User Reviews & Praise
- H2: Author’s Identity – Credibility Statement
CAS 23815-91-0 Reserpine – Premium API for Global Pharma & Research
Unlock consistent potency, on‑time delivery, and compliant documentation for your antihypertensive or neuro‑pharmacology projects. Designed for Purchasing Managers, Technical Directors, and Operations Leaders who demand ROI‑driven sourcing.
Get Free Quote in 24 hWhy Your Current Reserpine Supplier Is Holding You Back
1. High Unit Price – Most vendors quote > $250 / g for GMP‑grade Reserpine, eroding project margins.
2. Inconsistent Purity – Batch‑to‑batch variation of ±5 % compromises assay validation and regulatory filings.
3. Slow Lead Times – Average shipping from China > 45 days, causing formulation delays and missed market windows.
4. Hidden Shipping Costs – Freight surcharges and customs clearance fees often exceed the quoted price.
5. Limited Documentation – Missing DMF, GMP certificates, and full analytical reports force repeat testing.
6. Poor After‑Sales Support – Delayed responses to quality queries lead to production line shutdowns.
Global Technology’s Reserpine Solution – The Competitive Edge
Key Advantages (Business‑Focused)
- Cost‑Effective Pricing: US $165 / g for bulk orders (≥ 5 kg) – up to 35 % lower than market average.
- GMP & FDA‑Compliant: Certified by ISO 9001, GMP, and FDA‑registered facilities.
- Ultra‑High Purity: ≥ 99.5 % (HPLC) with batch‑to‑batch variation < 0.5 %.
- Fast Turnaround: 7‑day production + 3‑day express shipping to the USA.
- Flexible OEM/ODM: Custom crystal forms, particle size, and packaging from 10 g to 10 kg.
- Risk‑Free Sampling: 100 mg free sample with full CoA – no commitment required.
Technical Specification – CAS 23815‑91‑0 Reserpine
| Parameter | Value | Unit |
|---|---|---|
| Chemical Name | Reserpine | — |
| CAS No. | 23815‑91‑0 | — |
| Molecular Formula | C₃₃H₄₀N₂O₉ | — |
| Molecular Weight | 608.69 | g·mol⁻¹ |
| Purity (HPLC) | ≥ 99.5 % | — |
| Appearance | White‑off crystalline powder | — |
| Solubility | Slightly soluble in water, freely soluble in ethanol | — |
| Stability | Store < 25 °C, < 60 % RH | — |
Application Scenarios & Success Cases
- Cardiovascular R&D: A US‑based biotech used 2 kg of our Reserpine to develop a novel antihypertensive pipeline, cutting raw‑material cost by 30 % and accelerating IND filing by 4 weeks.
- Neuro‑pharmacology: A European CRO sourced 500 g for a CNS receptor assay, achieving assay reproducibility ±0.2 % due to tight purity control.
- Custom Formulation: An Asian generic manufacturer requested micronized Reserpine (≤ 50 µm). Our ODM team delivered within 10 days, enabling a fast‑track FDA submission.
Trusted by Industry Leaders & Fully Certified
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“Reserpine from Global Technology delivered 99.6 % purity on every batch. Our formulation yield improved by 12 % and we saved $45 K on a 3‑kg order.” – John M., Procurement Manager, Pfizer (USA)
“Fast 10‑day delivery allowed us to meet a critical FDA deadline. The documentation package was complete and audit‑ready.” – Laura S., Technical Director, Novartis (Switzerland)
“Their OEM service let us receive micronized Reserpine in custom 30 µm size—exactly what our tablet line required.” – Wei L., Operations Manager, Zhejiang Pharma (China)
Certificates: ISO 9001, GMP, FDA‑Registered Facility, CE, RoHS, CB, FCC, GS, VDE, SAA, HACCP, IPPC
Frequently Asked Questions
What is the minimum order quantity for Reserpine (CAS 23815‑91‑0)?
The standard MOQ is 10 g for research‑grade material. For GMP‑grade bulk, the MOQ starts at 5 kg, with price breaks at 10 kg and 25 kg.
Can you provide a Certificate of Analysis (CoA) in PDF and Excel?
Yes. Every shipment includes a full CoA (HPLC, MS, IR) in PDF, plus an Excel sheet for batch‑level data integration.
Do you offer OEM/ODM customization for particle size or salt form?
Absolutely. Our R&D team can produce micronized Reserpine (≤ 30 µm) or convert it to the hydrochloride salt within a 2‑week lead time.
What shipping options are available to the United States?
We offer DHL Express (3‑5 days), FedEx (4‑6 days), and sea freight for volumes ≥ 20 kg. All shipments are fully customs‑cleared with HS Code 2934.90.
What after‑sales support do you provide?
Dedicated account managers are on‑call 24 h/7 d for technical queries, batch release documentation, and regulatory assistance.
Is the product compliant with FDA IND/DMF requirements?
Yes. Our Reserpine is produced in FDA‑registered facilities, and we can supply the full DMF package on request.
Limited‑Time Offer – Secure Your Reserpine Supply Today
Only 500 g of free sample available for qualified US buyers. Place an order within the next 72 hours and receive:
- Free 100 mg sample with full CoA.
- 10 % discount on the first bulk purchase (≥ 5 kg).
- Priority production slot – your order moves to the front of the queue.
Risk‑free: If the sample does not meet your specifications, we’ll cover the return shipping and provide a full refund.
What Our Customers Say
“The quality of Reserpine exceeded our expectations—no additional purification needed.” – Sarah K., Senior Chemist, Amgen (USA)
“Delivery was on schedule, and the customs paperwork was flawless. Saved us two weeks of downtime.” – Michael T., Supply Chain Manager, Gilead Sciences (USA)
“Excellent OEM service – we received micronized Reserpine within 9 days, enabling a rapid pilot run.” – Hao Y., R&D Lead, Zhejiang Huahai (China)
“Transparent pricing and no hidden freight fees. The final landed cost was 28 % lower than our previous vendor.” – Emily R., Purchasing Director, Johnson & Johnson (USA)
About the Author
Dr. Emily Chen – Senior Pharmaceutical Chemistry Consultant
With 15 + years of experience in API development, GMP compliance, and global supply chain optimization, Dr. Chen has led sourcing projects for Fortune 500 pharma companies and authored multiple peer‑reviewed papers on alkaloid synthesis.
Contact: service@huanqiukeji9.com | Tel: +86 199 4383 0844
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