Ornithine Aspartate (L-ornithine L-aspartate salt) is a premium pharmaceutical intermediate designed for high-efficacy therapeutic applications. As a critical component in the synthesis of advanced pharmaceutical products, this compound is essential for organizations seeking high-purity biochemical precursors to support metabolic and hepatic health treatments.
Manufactured by Kunxiangda, a leading China-based supplier, our Ornithine Aspartate is produced under strict GMP certifications and CFDA approvals. By leveraging a robust R&D infrastructure and advanced custom synthesis capabilities, we ensure that every batch meets the rigorous standards required by global biotech firms, universities, and pharmaceutical research institutions.
Detailed Parameters
| Product Name | Ornithine Aspartate | CAS Number | 3230-94-2 |
|---|---|---|---|
| Molecular Formula | C9H18N3O6 | Molecular Weight | 264.256 |
| Synonym 1 | L-Ornithine-L-aspartate | Synonym 2 | L-Ornithine Aspartate |
| Chemical Class | Pharmaceutical Intermediate | Certification | GMP Certified / CFDA Approved |
| Supply Scale | Grams to Tons | Application | API Synthesis / Research |
Key Advantages
GMP Compliance
Strict adherence to GMP and CFDA standards ensures pharmaceutical-grade quality and safety.
Scalable Production
Flexible manufacturing capacity ranging from milligram laboratory scales to multi-ton industrial batches.
Custom Synthesis
Expert R&D team available for custom synthesis of complex intermediates and specialized chemicals.
High Purity
Advanced purification processes guarantee high-assay reference compounds and API precursors.
R&D Driven
Continuous innovation through collaboration with universities and innovative biotech organizations.
Competitive Pricing
Optimized production chains allow us to offer premium intermediates at highly competitive market prices.
Product Gallery
Management Platforms
Inventory Control
Real-time tracking of bulk raw materials and finished pharmaceutical intermediates.
Quality Assurance
Rigorous multi-stage testing protocols to ensure CFDA and GMP compliance.
Order Monitoring
End-to-end visibility from custom synthesis request to final product delivery.
Compliance Audits
Systematic documentation and auditing for international regulatory alignment.
Supply Logistics
Specialized chemical transport ensuring stability and purity during transit.
Synthesis Tracking
Precise monitoring of R&D milestones for custom-designed pharmaceutical agents.
Investment Return Comparison
| Service Tier | Standard Grade | Kunxiangda Premium | Custom Synthesis |
|---|---|---|---|
| Purity Level | 98% Average | 99.5%+ Guaranteed | Tailored Specs |
| Compliance | Basic ISO | GMP & CFDA Approved | Full Documentation |
| Lead Time | Long/Variable | Optimized/Fast | Project Based |
| Scale Flexibility | Fixed Lots | Gram to Ton | Lab to Plant |
| R&D Support | None | Dedicated Team | Co-Development |
Frequently Asked Questions
It is primarily used as an active pharmaceutical ingredient (API) or intermediate in the production of drugs targeting hepatic disorders and metabolic support.
Yes, we hold GMP certification and CFDA approval, ensuring our products meet international pharmaceutical standards.
Absolutely. We have a professional in-house R&D team specializing in the custom synthesis of advanced intermediates and special chemicals.
Our production capabilities are highly scalable, allowing us to supply quantities ranging from a few grams for research to multiple tons for commercial production.
We serve a diverse global clientele, including pharmaceutical corporations, biotech firms, universities, and independent research institutions.
We utilize specialized pharmaceutical-grade packaging and temperature-controlled logistics to maintain the chemical integrity and purity of our products.
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