Sodium Benzoate
High-purity pharmaceutical Sodium Benzoate manufactured to meet stringent USP and EP specifications for preservative applications. Our Sodium Benzoate provides excellent antimicrobial activity with broad-spectrum effectiveness for various pharmaceutical and oral formulations.
- USP/EP Pharmaceutical Grade
- Superior Preservative Properties
- Excellent Antimicrobial Activity
- Enhanced Stability
- Consistent Quality
- Ultra-Low Impurities
Technical Specifications
Applications
Industry-Specific Grades
DRAVYOM offers specialized Sodium Benzoate grades tailored for specific pharmaceutical and food preservation requirements, ensuring optimal antimicrobial performance and regulatory compliance across diverse application areas.
USP Grade (United States Pharmacopeia)
EP Grade (European Pharmacopoeia)
Preservative Grade
Food Grade
Quality Standards
DRAVYOM's Sodium Benzoate is manufactured under stringent quality control protocols, meeting international pharmaceutical standards including USP, EP specifications. Our preservative-grade production ensures consistent performance and regulatory compliance.
Advanced Chemical Properties & Performance
Pharmaceutical Grade Sodium Benzoate exhibits exceptional chemical properties essential for preservation applications. Its potent antimicrobial structure and superior stability characteristics ensure reliable performance in demanding pharmaceutical preservation and buffering formulations.
Molecular Properties
Physical Properties
Pharmaceutical Properties
Quality Specifications
Stability Properties
Performance Characteristics
Detailed performance metrics demonstrate Sodium Benzoate superiority in preservation applications with exceptional antimicrobial efficacy, broad-spectrum activity, and stability across diverse pharmaceutical formulation and preservation systems.
Antimicrobial Activity
Broad-spectrum antimicrobial efficacy
Effective against bacteria, yeast, and moldspH Dependent
Most effective in acidic pH range
Optimal activity at pH 2.5-4.0High Solubility
Excellent water solubility
Easy incorporation in aqueous formulationsHeat Stability
Stable under processing temperatures
Maintains activity during manufacturingRegulatory Status
FDA/GRAS approved preservative
Global regulatory acceptanceCost Effective
Economical preservation solution
Low use levels requiredSafety Information
Generally recognized as safe (GRAS) pharmaceutical preservative requiring standard handling protocols. Handle in controlled environments with appropriate dust control measures. Use proper personal protective equipment and follow established safety protocols for preservative 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 antimicrobial efficacy and pharmaceutical quality.
Chemical Mechanisms & Reaction Pathways
Sodium Benzoate exhibits specific antimicrobial preservative mechanisms essential for pharmaceutical preservation. Its molecular structure enables effective microbial growth inhibition with predictable preservation therapeutic responses.
Antimicrobial Action
Benzoic acid release and microbial membrane disruption
Broad-spectrum preservationpH-Dependent Activity
Optimal antimicrobial effectiveness at acidic pH ranges
Enhanced preservation efficiencyMicrobial Selectivity
Effective against bacteria, yeasts, and molds
Comprehensive microbial controlPreservation Effects
Extended shelf life and product stability
Pharmaceutical quality assuranceRegulatory 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