Sodium Phosphate
High-purity pharmaceutical Sodium Phosphate manufactured to meet stringent USP and EP specifications for buffering applications. Our Sodium Phosphate provides excellent buffering properties with superior pH control for various pharmaceutical formulations.
- USP/EP Pharmaceutical Grade
- Superior Buffering Properties
- Excellent pH Control
- Enhanced Stability
- Consistent Quality
- Ultra-Low Impurities
Technical Specifications
Applications
Industry-Specific Grades
DRAVYOM offers specialized Sodium Phosphate grades tailored for specific pharmaceutical and laboratory applications, ensuring optimal buffering performance and regulatory compliance across diverse stabilization requirements.
USP Grade (United States Pharmacopeia)
EP Grade (European Pharmacopoeia)
Injectable Grade
Buffer Grade
Quality Standards
DRAVYOM's Sodium Phosphate is manufactured under stringent quality control protocols, meeting international pharmaceutical standards including USP, EP specifications. Our buffer-grade production ensures consistent performance and regulatory compliance.
Advanced Chemical Properties & Performance
Pharmaceutical Grade Sodium Phosphate exhibits exceptional chemical properties essential for buffering and pH control applications. Its potent phosphate buffering structure and superior stability characteristics ensure reliable performance in demanding pharmaceutical formulation and processing systems.
Molecular Properties
Physical Properties
Pharmaceutical Properties
Quality Specifications
Stability Properties
Performance Characteristics
Detailed performance metrics demonstrate Sodium Phosphate superiority in buffering applications with exceptional pH control, osmotic regulation, and solubility enhancement across diverse pharmaceutical formulation and processing systems.
Phosphate Buffering
Strong phosphate buffer system
Excellent pH control capabilitiesOsmotic Control
High osmotic contribution
Effective osmolality adjustmentHigh Solubility
Excellent water solubility
Easy incorporation in formulationsSolubility Enhancement
Improves drug solubility
Enhanced bioavailability potentialRegulatory Status
USP/EP grade pharmaceutical excipient
Global regulatory acceptanceInjectable Compatible
Suitable for injectable formulations
Parenteral formulation useSafety Information
Generally recognized as safe (GRAS) pharmaceutical excipient requiring standard handling protocols. Handle in controlled environments with appropriate dust control measures. Use proper personal protective equipment and follow established safety protocols for phosphate materials.
Storage & Handling
Store in tightly closed containers in a cool, dry place away from direct sunlight. Maintain controlled room temperature storage and ensure protection from moisture to preserve buffering capacity and pharmaceutical quality.
Chemical Mechanisms & Reaction Pathways
Sodium Phosphate exhibits specific buffering and pharmaceutical excipient mechanisms essential for drug formulation and stability. Its molecular structure enables effective pH control and ionic strength regulation with predictable pharmaceutical responses.
Buffering System
Dibasic phosphate buffering with physiological pH range
pH stability assuranceIonic Strength Control
Controlled electrolyte balance for pharmaceutical formulations
Formulation stabilitySolubility Enhancement
Improved dissolution characteristics for active pharmaceuticals
Enhanced bioavailabilityStabilization Effects
Prevents degradation and maintains pharmaceutical integrity
Extended shelf lifeRegulatory Compliance & Documentation
Comprehensive regulatory compliance ensures global pharmaceutical access with complete documentation packages supporting international drug development and manufacturing standards.
USP Specifications
United States Pharmacopeia pharmaceutical standards compliance
EP Standards
European Pharmacopoeia specifications for pharmaceutical quality
ICH Guidelines
International Conference on Harmonization standards compliance
GMP Certification
Good Manufacturing Practices certified production facility
DMF Support
Drug Master File documentation for regulatory submissions
CEP Available
Certificate of Suitability to European Pharmacopoeia monographs
Technical Support & Value-Added Services
DRAVYOM's pharmaceutical development team provides comprehensive formulation support, regulatory assistance, and technical services to optimize pharmaceutical performance in your specific drug development applications.
Formulation Development
- Dosage form optimization support
- Stability testing guidance
- Bioavailability enhancement
- Custom formulation development
Analytical Services
- Method development and validation
- Impurity profiling and identification
- Stability indicating methods
- Dissolution testing support
Regulatory Support
- Regulatory submission assistance
- DMF preparation and maintenance
- Pharmacovigilance support
- Global registration strategy
Supply Solutions
- Pharmaceutical supply chain management
- Cold chain logistics
- Custom packaging solutions
- Global distribution network
Environmental Impact & Sustainability
Our pharmaceutical production emphasizes environmental responsibility through sustainable manufacturing practices, green chemistry principles, and comprehensive environmental impact management for pharmaceutical operations.
Green Chemistry
Sustainable synthetic routes with minimal environmental impact
Water Management
Advanced wastewater treatment and recycling systems
Clean Production
Energy-efficient synthesis with emission controls
Safe Disposal
Comprehensive pharmaceutical waste management protocols
ISO 14001
Environmental management system certified production
Sustainable Packaging
Recyclable pharmaceutical packaging solutions
Manufacturing Excellence & Quality Control
DRAVYOM's state-of-the-art pharmaceutical manufacturing facility employs advanced synthesis technology and continuous monitoring systems to ensure consistent pharmaceutical quality and performance across all production batches.
Production Process
Advanced synthesis and purification in GMP-controlled clean-room environment
Multi-stage purification for pharmaceutical grade qualityQuality Testing
Comprehensive testing protocol including purity, potency, and impurity profiling
HPLC, GC-MS, and spectroscopic analysisQuality Systems
ISO 9001:2015 and GMP quality management systems
Continuous improvement and validation protocolsPackaging Control
Pharmaceutical-grade packaging with controlled atmosphere
Contamination prevention and stability protectionMarket Applications & Performance Data
Comprehensive pharmaceutical development data demonstrating effectiveness across diverse therapeutic applications with quantified performance metrics and clinical validation support.
Pharmaceutical Development
Research Applications
Commercial Manufacturing
DRAVYOM Competitive Advantages
Pharmaceutical Excellence
Consistently exceeds pharmacopeial specifications with superior purity and pharmaceutical performance
Reliable Supply
Guaranteed pharmaceutical availability with strategic inventory and GMP production scheduling
Development Expertise
Dedicated pharmaceutical development team provides formulation and regulatory support
Regulatory Assurance
Complete regulatory packages with DMF support and global registration assistance
Global Standards
International compliance with USP, EP, and ICH standards for worldwide market access
Partnership Approach
Collaborative relationships with pharmaceutical companies and custom development services