Standardized Puerarin 98% (High-Purity Pharmaceutical Grade Isolate)
At Blue Eye Bio
, we specialize in the absolute isolation of active phytochemicals. Our Puerarin 98% (CAS 3681-99-0) is a crystalline compound refined from premium high-altitude Pueraria lobata roots. Unlike standard extracts, this pharmaceutical-grade isolate is engineered for laboratories requiring zero-deviation molecular integrity for advanced synthesis and pre-clinical pipelines.
At Blue Eye Bio, we understand that pharmaceutical R&D requires absolute molecular integrity. Our 98% Puerarin powder is isolated from premium Pueraria lobata roots through multi-stage chromatography, ensuring a purely defined profile with zero synthetic analogs.
We have mastered the extraction of Pueraria lobata isoflavones. Our Puerarin Series
offers a complete spectrum of concentrations, ranging from 10% standardized extracts for holistic wellness to 98% pharmaceutical-grade isolates. we provide the molecular building blocks required for modern cardiovascular and metabolic research.
1.The Specification Matrix)
Parameters | Specification (Pharma Grade) | Method / Standard |
Product Name | Puerarin | -- |
CAS Number | 3681-99-0 | -- |
Source | Pueraria lobata (High-altitude roots) | Authentic Origin |
Assay (HPLC) | ≥ 98.0% / ≥ 99.0% | Absolute Quantification |
Appearance | White to Off-white Crystalline Powder | Visual |
Melting Point | 187.0°C - 191.0°C | Capillary Tube |
Loss on Drying | ≤ 0.5% | USP Standard |
Heavy Metals | Pb < 1ppm, As < 0.5ppm | ICP-MS Verified |
2.What is Puerarin?
"Puerarin (CAS 3681-99-0)
is the primary bio-active isoflavone found in the Kudzu root (Pueraria lobata). Scientifically recognized for its high oxygen-free-radical scavenging activity, it acts as a critical substrate in Oncological R&D and cardiovascular signaling research. Our 98% HPLC grade is refined through multi-stage chromatography to ensure zero related-substance carryover, providing a purely defined molecule for high-stakes research."
3.Why is 98% specification so important for R&D?
In high-stakes Cardiovascular signaling and Oncology research, even 1% of related isoflavone impurities can catalyze unwanted side reactions. Blue Eye Bio’s 98% HPLC Puerarin provides the 'clean slate' required for:
Reference Standards: For analytical lab calibration and validation.
Molecular Assembly: As a pure building block for complex drug synthesis.
Bio-equivalence Studies: Ensuring high-fidelity results in pharmacokinetic modeling.
4.The Gatekeeper Protocol: Purely Defined Purity & Proven Compliance
We don’t just supply ingredients; we provide the molecular precision and formulation stability that drive your product’s success.
"At Blue Eye Bio, we resolve the most critical pain points for bulk pharmaceutical procurement: analytical uncertainty and regulatory risk."
1. Verified Molecular Traceability (Authentic High-Altitude Origin)
The Technical Edge: Our Puerarin 98% originates directly from authentic, high-altitude mountainous regions (specifically the Qinling and Hunan-Hubei belts), strictly avoiding the low-quality industrial by-products common in the trading market. Every single batch is dual-verified via 1H-NMR and HPLC to ensure a 100% identical molecular fingerprint.
The Business Benefit: We guarantee unrivaled batch-to-batch consistency. By locking in the botanical source and the molecular profile, we ensure that your R&D data remains stable and reproducible from the lab to large-scale synthesis.
2. Zero-Residual Sourcing (Multi-Stage Recrystallization)
The Technical Edge: We utilize advanced Multi-stage Recrystallization technology to achieve a "Zero-Residual" purity profile. This rigorous process eliminates heavy metals and residual solvents at the molecular level, far exceeding common food-grade specifications.
The Business Benefit: Our clinical-grade Puerarin isolate provides a "clean slate" for your formulations. By minimizing the impurity burden, we significantly reduce the risk of unwanted side-reactions in your downstream synthesis or clinical-stage pipelines.
3. Regulatory Readiness & Comprehensive Technical Dossiers
The Technical Edge: We prioritize Technical Sovereignty by providing the data required for global pharmaceutical audits. Every industrial shipment is accompanied by a full Regulatory Documentation package, governed by our Unified QC Standard (UQS).
The Business Benefit: We provide batch-specific COA, MSDS, and TDS as a standard protocol. This comprehensive support ensures that Small and Medium-sized Enterprises can successfully navigate the most rigorous pharma-grade audits and CMC (Chemistry, Manufacturing, and Controls) requirements of the North American and European markets.
5.Commercial Empowerment: Strategic Value for Small and Medium-sized Enterprises
(1)Primary Source Pricing via Strategic Alliance
The Strategy: By integrating our Asia-based manufacturing facility with a strategic sourcing alliance, we eliminate multiple layers of trading markups.
The Result: You receive manufacturer-direct wholesale pricing. We bridge the gap between high-barrier technical production and first-hand economic efficiency, giving your brand the pricing power of a market leader.
(2)Scalable & Flexible Industrial MOQ Framework
The Strategy: We believe that every global brand starts with a single successful batch. Blue Eye Bio acts as a dedicated partner for Small and Medium-sized Enterprises.
The Result: We offer flexible industrial MOQs, ranging from 1kg pilot-scale quantities for R&D to multi-ton industrial supply. This allows growing brands to innovate with minimal inventory risk and optimized cash flow.
(3)Rapid 24-Hour Technical Response Protocol
The Strategy: Time-to-market is your most valuable asset. Our technical sales team operates on a high-speed fulfillment model.
The Result: Receive your formal quote and batch-specific documentation (COA, MSDS, and TDS) within 24 business hours. We provide the first-hand technical dossiers you need to accelerate your regulatory audits and production cycles.
6.Key Advantage:
We solve the 'Impurity Barrier.' Our UQS (Unified QC Standard)
ensures that heavy metals and residual solvents are significantly below USP/EP limits, providing a clean substrate for complex molecular assembly.
7.Industrial Application:
Cardiovascular signaling research, pharmaceutical intermediates, and high-potency clinical trials.