Mineral Oil
High-purity pharmaceutical Mineral Oil manufactured to meet stringent USP and EP specifications for emollient applications. Our Mineral Oil provides excellent emollient properties with superior lubricating characteristics for various pharmaceutical and topical formulations.
- USP/EP Pharmaceutical Grade
- Superior Emollient Properties
- Excellent Lubricating Properties
- Enhanced Stability
- Consistent Quality
- Ultra-Low Impurities
Technical Specifications
Applications
Industry-Specific Grades
DRAVYOM offers specialized Mineral Oil grades tailored for specific pharmaceutical emollient requirements, ensuring optimal performance and regulatory compliance across diverse topical formulation applications.
USP Grade (United States Pharmacopeia)
EP Grade (European Pharmacopoeia)
Light Mineral Oil Grade
Reference Standard Grade
Quality Standards
DRAVYOM's Mineral Oil is manufactured under stringent quality control protocols, meeting international pharmaceutical standards including USP, EP, and cGMP specifications. Our pharmaceutical-grade production ensures consistent performance and regulatory compliance.
Advanced Chemical Properties & Performance
Mineral Oil exhibits exceptional emollient properties essential for pharmaceutical applications. Its ultra-pure composition and precise viscosity characteristics ensure reliable performance in demanding topical and oral formulations.
Molecular Properties
Physical Properties
Pharmaceutical Performance
Purity Specifications
Stability Properties
Performance Characteristics
Detailed performance metrics demonstrate Mineral Oil superiority in pharmaceutical applications with exceptional emollient properties, stability, and reproducibility across diverse topical and oral formulations.
Emollient Properties
Viscosity: 34.5-42.5 cSt
Superior skin conditioningPurity
USP/EP: ≥99.0% purity
Pharmaceutical grade qualityStability
Indefinite shelf life
Long-term pharmaceutical integrityThermal Stability
Working range: -10 to 80°C
Stable during processingBatch Reproducibility
Variation: ±0.5% between batches
Consistent lot-to-lot performanceShelf Stability
Indefinite under proper storage
Extended pharmaceutical grade integritySafety Information
Pharmaceutical grade emollient requiring standard handling. Handle with appropriate protective equipment in controlled environments. Avoid prolonged skin contact and inhalation. Follow cGMP guidelines for pharmaceutical excipients and ensure proper waste disposal procedures.
Storage & Handling
Store in original sealed containers in a cool, dry, well-ventilated area away from extreme temperatures. Keep containers tightly closed and protect from contamination. Use appropriate containment measures for pharmaceutical excipient handling.
Chemical Mechanisms & Reaction Pathways
Mineral Oil exhibits unique lubricating and protective properties through non-polar molecular interactions and barrier formation mechanisms, enabling precise pharmaceutical applications with excellent biocompatibility and chemical inertness.
Barrier Formation
Creates protective hydrophobic barrier on skin surfaces
Prevents moisture loss and external contaminationLubrication Properties
Reduces friction through molecular film formation
Excellent lubricating properties for pharmaceutical applicationsChemical Inertness
Non-reactive with pharmaceutical ingredients and biological systems
Stable excipient with minimal interactionsSolvent Properties
Dissolves lipophilic compounds and aids in formulation
Carrier for oil-soluble pharmaceutical ingredientsRegulatory Compliance & Documentation
Comprehensive regulatory compliance ensures global pharmaceutical access with complete documentation packages supporting international standards and pharmaceutical excipient regulatory requirements.
USP-NF Specifications
United States Pharmacopeia-National Formulary pharmaceutical grade standards compliance
EP Standards
European Pharmacopoeia specifications for pharmaceutical excipients
FDA Approved
Food and Drug Administration approved for pharmaceutical applications
IPEC Guidelines
International Pharmaceutical Excipients Council quality standards
CEP Certificate
Certificate of Suitability to European Pharmacopoeia Monograph
Safety Documentation
Complete safety and toxicological data package
Technical Support & Value-Added Services
DRAVYOM's formulation science team provides comprehensive excipient application support, pharmaceutical grade guidance, and technical solutions to optimize Mineral Oil performance in your pharmaceutical formulations.
Formulation Development
- Topical formulation optimization
- Ointment and cream formulation
- Capsule fill formulation guidance
- Solubility enhancement strategies
Analytical Services
- Pharmaceutical grade verification
- Purity and contaminant analysis
- Viscosity and flow property testing
- Stability testing programs
Technical Support
- Pharmaceutical excipient troubleshooting
- cGMP compliance guidance
- Quality control method development
- Regulatory documentation support
Supply Solutions
- Multiple pharmaceutical grades available
- Flexible packaging configurations
- Bulk pharmaceutical supply
- Global excipient distribution network
Environmental Impact & Sustainability
Our Mineral Oil production emphasizes environmental responsibility through sustainable pharmaceutical manufacturing practices, refined processing techniques, and comprehensive environmental impact management.
Refined Processing
Advanced refining techniques minimize environmental impact
Water Treatment
Advanced pharmaceutical wastewater treatment and recycling systems
Resource Efficiency
Optimized processing with minimal pharmaceutical waste generation
Safe Disposal
Comprehensive guidance for pharmaceutical waste management
ISO 14001
Environmental management system certified pharmaceutical production
Carbon Footprint
Optimized logistics and regional sourcing strategies
Manufacturing Excellence & Quality Control
DRAVYOM's specialized pharmaceutical excipient manufacturing facility employs advanced refining technology and continuous monitoring systems to ensure consistent Mineral Oil quality and purity across all production batches.
Production Process
Advanced refining and purification in pharmaceutical environment
Multi-stage distillation for pharmaceutical grade qualityQuality Testing
Comprehensive analytical testing including purity and contaminant analysis
GC-MS verification and pharmaceutical grade testingQuality Systems
ISO 9001:2015 quality management with pharmaceutical excipient certification
Specialized pharmaceutical excipient quality systemsPackaging Control
Pharmaceutical-grade containers with contamination prevention
Maintains purity and prevents degradationMarket Applications & Performance Data
Comprehensive pharmaceutical development data demonstrating Mineral Oil effectiveness across diverse formulation applications with quantified performance metrics and pharmaceutical grade validations.
Pharmaceutical Applications
Formulation Benefits
Manufacturing Performance
DRAVYOM Competitive Advantages
Pharmaceutical Grade Quality
Consistently exceeds USP-NF specifications with exceptional purity and pharmaceutical performance
Reliable Supply
Guaranteed availability with pharmaceutical inventory management and multiple grade production capabilities
Formulation Expertise
Dedicated pharmaceutical formulation team provides excipient optimization guidance
Quality Assurance
Comprehensive certificates with complete analytical data and pharmaceutical documentation
Global Standards
International compliance with USP-NF, EP, and IPEC specifications for worldwide pharmaceutical acceptance
Partnership Approach
Collaborative relationships with pharmaceutical manufacturers and custom grade development services