Propylparaben
High-purity pharmaceutical Propylparaben manufactured to meet stringent USP and EP specifications for preservative applications. Our Propylparaben provides excellent antimicrobial activity with broad-spectrum effectiveness for pharmaceutical and cosmetic 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 Propylparaben grades tailored for specific pharmaceutical applications, ensuring optimal preservative efficacy and regulatory compliance across diverse formulation requirements.
USP Grade (United States Pharmacopoeia)
EP Grade (European Pharmacopoeia)
Injectable Grade
High Purity Grade
Quality Standards
DRAVYOM's Propylparaben is manufactured under stringent cGMP protocols, meeting international pharmaceutical excipient standards including USP, EP, and FDA guidelines for preservative applications.
Advanced Chemical Properties & Performance
Pharmaceutical Grade Propylparaben exhibits exceptional chemical properties essential for preservation applications. Its potent antimicrobial structure and superior stability characteristics ensure reliable performance in demanding pharmaceutical preservation systems.
Molecular Properties
Physical Properties
Pharmaceutical Properties
Quality Specifications
Stability Properties
Performance Characteristics
Detailed performance metrics demonstrate Propylparaben superiority in preservation applications with exceptional antimicrobial activity, broad-spectrum efficacy, and lipophilic advantage across diverse pharmaceutical formulation systems.
Antimicrobial Activity
Potent activity against bacteria, yeasts, and molds
Broad-spectrum preservationLipophilic Advantage
Enhanced activity in oil-based formulations
Superior creams and ointments preservationpH Stability
Stable preservation across wide pH range
Versatile formulation compatibilityHeat Stability
Stable under processing conditions
Manufacturing compatibilityRegulatory Status
USP/EP/FDA approved preservative
Global regulatory acceptanceSynergistic Effect
Enhanced activity with methylparaben
Optimized preservative systemsSafety Information
Generally recognized as safe (GRAS) pharmaceutical preservative requiring standard handling protocols. Handle in controlled environments with appropriate ventilation systems. 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
Propylparaben exhibits specific antimicrobial mechanisms through cell membrane disruption and enzyme inhibition pathways essential for pharmaceutical preservation. Its molecular structure enables broad-spectrum antimicrobial activity with predictable preservative efficacy.
Antimicrobial Action
Cell membrane disruption and enzyme inhibition mechanisms
Broad-spectrum antimicrobial activityMetabolic Pathways
Hydrolysis to p-hydroxybenzoic acid and n-propanol
Predictable clearance mechanismsFormulation Stability
Chemical stability across pH ranges and temperatures
Preservative efficacy maintenanceSynergistic Effects
Enhanced antimicrobial activity with methylparaben
Optimized preservative systemsRegulatory 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