White Petrolatum
Pharmaceutical Premium
Pharmaceutical Excipient

White Petrolatum

High-purity pharmaceutical White Petrolatum manufactured to meet stringent USP and EP specifications for ointment applications. Our White Petrolatum provides excellent protective properties with superior ointment base characteristics for topical pharmaceutical formulations.

  • USP/EP Pharmaceutical Grade
  • Superior Ointment Properties
  • Excellent Protective Properties
  • Enhanced Stability
  • Consistent Quality
  • Ultra-Low Impurities

Technical Specifications

Chemical Name: Petrolatum, White
CAS Number: 8009-03-8
Physical State: White to off-white semi-solid
Melting Point: 38-60°C
Congealing Point: 36-58°C
Viscosity (60°C): 7-14 cSt
Penetration (25°C): 115-175 dmm
Acid Value: ≤0.5 mg KOH/g
Saponification Value: ≤5 mg KOH/g
Sulfur Compounds: ≤0.002%
Polycyclic Aromatics: ≤5 ppm
Heavy Metals: ≤5 ppm
Water Content: ≤0.5%
Storage Conditions: Store at room temperature
Packaging Options: 5kg, 25kg pharmaceutical containers

Applications

Ointment Base
Topical Formulations
Protective Barrier
Skin Moisturizer
Pharmaceutical Excipient
Ophthalmic Ointments
Baby Care Products
Wound Care
Dermatological Applications
Soft Gel Capsules
Tablet Coating
USP/EP Applications

Industry-Specific Grades

DRAVYOM offers specialized White Petrolatum grades tailored for specific pharmaceutical and cosmetic requirements, ensuring optimal performance and regulatory compliance across diverse topical and ointment applications.

USP Grade (United States Pharmacopeia)
Melting Point: 38-60°C Acid Value: ≤0.5 mg KOH/g Heavy Metals: ≤5 ppm Application: FDA-compliant formulations
EP Grade (European Pharmacopoeia)
Congealing Point: 36-58°C Penetration: 115-175 dmm Polycyclic Aromatics: ≤5 ppm Application: EU regulatory submissions
Ophthalmic Grade
Sterility: Compliant Particulate Matter: <25 µm Endotoxin: ≤0.5 EU/g Application: Eye ointments
Cosmetic Grade
Consistency: Optimized Color: White Odor: Odorless Application: Cosmetic formulations

Quality Standards

DRAVYOM's White Petrolatum is manufactured under stringent quality control protocols, meeting international pharmaceutical standards including USP, EP specifications. Our pharmaceutical-grade production ensures consistent performance and regulatory compliance.

ISO 9001:2015 Certified Manufacturing
USP/EP Grade Specifications
Pharmaceutical Grade Quality
Advanced Purity Testing
Protective Barrier Properties
Moisture Retention
Comprehensive COA
Pharmaceutical Grade Packaging

Advanced Chemical Properties & Performance

Pharmaceutical Grade White Petrolatum exhibits exceptional chemical properties essential for topical applications. Its purified hydrocarbon composition and precise specification ensure reliable performance in demanding pharmaceutical formulations and dermatological treatment systems.

Chemical Properties
Molecular Composition: C₁₅H₃₂ to C₅₀H₁₀₂ (mixture)
Molecular Weight: 300-700 g/mol
Melting Point: 38-54°C
Density: 0.85-0.87 g/cm³
Physical Properties
Appearance: White, odorless, translucent mass
Solubility: Insoluble in water
Consistency: Semi-solid at room temperature
Viscosity: 38-75 cSt at 40°C
Pharmaceutical Performance
Occlusive Effect: Excellent moisture barrier
Spreading: Good spreadability
Compatibility: Inert with most APIs
Penetration: Enhances drug penetration
Purity Specifications
Purification Level: Pharmaceutical Grade
Aromatic Hydrocarbons: ≤1%
Heavy Metals: ≤10 ppm
Sulfur Compounds: ≤10 ppm
Stability Properties
Shelf Life: 5 years (unopened)
Photostability: Stable under normal light
Temperature Stability: Stable 15-25°C
Oxidation Resistance: Excellent stability

Performance Characteristics

Detailed performance metrics demonstrate Pharmaceutical Grade White Petrolatum superiority in topical applications with exceptional functionality, stability, and reproducibility across diverse pharmaceutical procedures and dermatological protocols.

Barrier Function

Protection: Superior moisture barrier

Prevents transepidermal water loss
Occlusive Properties

Coverage: 95% occlusion efficiency

Enhanced hydration retention
Spreadability

Application: Smooth spreading properties

Excellent user experience
Thermal Stability

Range: Stable across temperature variations

Consistent formulation performance
Batch Uniformity

Variation: Consistent physical properties

Reliable pharmaceutical grade quality
Long-term Stability

5 years shelf life with maintained properties

Extended pharmaceutical grade integrity

Safety Information

Generally recognized as safe (GRAS) pharmaceutical excipient with extensive safety data. Non-irritating and hypoallergenic for most users. Handle with standard laboratory precautions including appropriate protective equipment. Avoid inhalation of heated vapors and ensure proper ventilation during processing.

GRAS Status
Non-Toxic
Hypoallergenic

Storage & Handling

Store in original sealed containers in a cool, dry, well-ventilated area away from heat sources and direct sunlight. Keep containers tightly closed and protect from contamination. Use appropriate pharmaceutical handling procedures and ensure proper environmental controls for quality maintenance.

Cool storage (15-25°C)
Dry conditions
Protect from direct sunlight
Original sealed containers

Chemical Mechanisms & Reaction Pathways

Pharmaceutical Grade White Petrolatum exhibits exceptional barrier protection properties through refined hydrocarbon structure enabling effective skin protection with optimal occlusive characteristics and dermatological compatibility for topical applications.

Occlusive Barrier

Forms protective film reducing transepidermal water loss

Primary mechanism for skin hydration and protection
Skin Compatibility

Inert hydrocarbon matrix with minimal skin sensitization

Excellent tolerance in sensitive skin applications
Moisture Retention

Prevents water loss through semi-permeable barrier formation

Enhances skin healing and hydration
Drug Delivery

Vehicle for topical drug delivery systems

Enhances API penetration and stability

Regulatory Compliance & Documentation

Comprehensive regulatory compliance ensures global pharmaceutical market access with complete excipient documentation supporting international standards and topical drug manufacturing validations.

USP Specifications

United States Pharmacopeia excipient standards compliance

EP Standards

European Pharmacopoeia specifications for pharmaceutical manufacturing

FDA Approved

FDA approved pharmaceutical excipient with comprehensive safety data

Global Approval

International regulatory compliance for topical applications

DMF Documentation

Drug Master File with comprehensive manufacturing and safety data

cGMP Certified

Current Good Manufacturing Practice with pharmaceutical excipient standards

Technical Support & Value-Added Services

DRAVYOM's dermatology excipient team provides comprehensive development support, formulation optimization assistance, and regulatory services for topical drug manufacturing with specialized dermatological expertise.

Formulation Development
  • Topical formulation support
  • Rheological optimization studies
  • Stability enhancement protocols
  • Drug delivery system development
Analytical Services
  • Certificate of Analysis with dermatological testing
  • Physicochemical characterization
  • Impurity profiling and identification
  • Compatibility study support
Regulatory Support
  • Topical drug documentation
  • Regulatory filing assistance
  • Safety assessment support
  • Post-market surveillance
Supply Solutions
  • Consistent excipient supply chains
  • Temperature-controlled logistics
  • Emergency supply protocols
  • Global distribution network

Environmental Impact & Sustainability

Our Pharmaceutical Grade White Petrolatum production emphasizes environmental responsibility through sustainable refining processes, renewable energy utilization, and comprehensive environmental impact management for excipient manufacturing.

Clean Refining

Advanced refining processes with minimal environmental impact

Sustainable Sourcing

Responsible sourcing and waste minimization practices

Energy Efficiency

Energy-efficient production with emission controls

Water Conservation

Advanced water treatment and recycling systems

ISO 14001

Environmental management system certified production

Carbon Neutral

Carbon-neutral production with renewable energy

Manufacturing Excellence & Quality Control

DRAVYOM's state-of-the-art pharmaceutical excipient manufacturing facility employs advanced refining technology and continuous monitoring systems to ensure consistent Pharmaceutical Grade White Petrolatum quality and safety.

Refining Process

Advanced multi-stage refining with pharmaceutical-grade specifications

Controlled processing for optimal purity and consistency
Quality Testing

18-point pharmaceutical testing protocol including dermatological safety

Comprehensive verification and safety testing
Quality Systems

cGMP compliance with pharmaceutical excipient manufacturing standards

Continuous improvement and process validation
Excipient Packaging

Specialized packaging with contamination protection

Stability maintenance and purity preservation

Market Applications & Performance Data

Comprehensive clinical and pharmaceutical data demonstrating Pharmaceutical Grade White Petrolatum effectiveness across diverse topical applications with quantified dermatological metrics and safety profiles.

Barrier Protection
TEWL Reduction: 95% reduction in water loss Hydration: Improved skin moisture retention Protection: Enhanced barrier function
Dermatological Safety
Sensitization: Minimal allergic potential Irritation: Non-irritating to sensitive skin Compatibility: Excellent with active ingredients
Pharmaceutical Applications
Ointments: Base for topical formulations Drug Delivery: Enhanced API stability Wound Care: Protective barrier applications

DRAVYOM Competitive Advantages

Superior Purity

Consistently exceeds pharmacopeial specifications with optimal refinement and purity control

Reliable Supply

Guaranteed availability with strategic inventory management and excipient expertise

Excipient Expertise

Specialized pharmaceutical excipient manufacturing with comprehensive topical development support

Quality Assurance

Enhanced testing protocols with complete documentation and regulatory compliance

Global Standards

International compliance with USP, EP, and topical drug regulations worldwide

Partnership Approach

Collaborative relationships with dermatological pharmaceutical companies and development support