Lanolin
Pharmaceutical Premium
Pharmaceutical Excipient

Lanolin

High-purity pharmaceutical Lanolin manufactured to meet stringent USP and EP specifications for emollient applications. Our Lanolin provides excellent emollient properties with superior emulsifying capabilities and enhanced absorption characteristics for topical pharmaceutical formulations.

  • USP/EP Pharmaceutical Grade
  • Superior Emollient Properties
  • Excellent Emulsifying Properties
  • Enhanced Absorption
  • Consistent Quality
  • Natural Origin
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Technical Specifications

Chemical Formula: Complex Wax Esters
CAS Number: 8006-54-0
EINECS Number: 232-348-6
Molecular Weight: Variable (complex mixture)
Physical State: Yellow to brownish ointment-like substance
Purity (USP/EP): ≥99.0% (Pharmaceutical Grade)
Melting Point: 38-44°C
Acid Value: ≤1.0 mg KOH/g
Saponification Value: 90-105 mg KOH/g
Iodine Value: 18-36
Heavy Metals (as Pb): ≤10 ppm
Water Content: ≤0.5%
Storage Conditions: Store in cool, dry place
Shelf Life: 3 years from date of manufacture
Packaging Options: 500g, 1kg, 5kg pharmaceutical containers

Applications

Topical Ointments
Emollient Creams
Skin Care Formulations
Emulsifying Agent
Dermatological Research
Hospital Dermatology
Cosmeceutical Manufacturing
Moisturizing Products
Skin Barrier Research
Clinical Trials
Regulatory Submissions
Reference Standards

Industry-Specific Grades

DRAVYOM offers specialized Lanolin grades tailored for specific pharmaceutical and cosmeceutical requirements, ensuring optimal emollient performance and regulatory compliance across diverse topical formulation applications.

USP Grade (United States Pharmacopeia)
Purity: ≥99.0% (Pharmaceutical) Acid Value: ≤1.0 mg KOH/g Heavy Metals: ≤10 ppm Application: FDA-compliant formulations
EP Grade (European Pharmacopoeia)
Purity: ≥99.0% (Pharmaceutical) Saponification: 90-105 mg KOH/g Water Content: ≤0.5% Application: EU regulatory submissions
Cosmeceutical Grade
Purity: ≥99.5% (Premium) Refined Quality Low Odor Profile Application: Premium cosmetics
Reference Standard Grade
Purity: ≥99.8% (Analytical) Certified Analysis: COA included Traceability: Documented origin Application: Analytical standards

Quality Standards

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

cGMP Certified Manufacturing
USP/EP Grade Specifications
≥99.0% Pharmaceutical Purity
Advanced Analytical Testing
Ultra-Low Impurity Levels
Batch-to-Batch Consistency
Comprehensive Certificate of Analysis
Temperature-Controlled Logistics

Advanced Chemical Properties & Performance

Pharmaceutical Grade Lanolin exhibits exceptional chemical properties essential for topical formulation applications. Its ultra-pure composition and precise molecular structure ensure reliable performance in demanding pharmaceutical formulations and clinical applications.

Chemical Properties
Composition: Wool wax esters
Melting Point: 36-42°C
Solubility (Water): Insoluble
Emulsification Capacity: 200-300% water
Physical Properties
Appearance: Yellowish ointment-like substance
Texture: Semi-solid at room temperature
Viscosity: Variable with temperature
Hygroscopicity: Water-absorbing
Pharmaceutical Properties
Emollient Action: Excellent skin moisturizing
Penetration: Good skin absorption
Compatibility: Wide range of actives
Stability: Stable in formulations
Purity Specifications
Purity (Ph.Eur): ≥99.0%
Acid Value: ≤1.0 mg KOH/g
Heavy Metals: ≤10 ppm
Microbial Limits: USP compliant
Stability Properties
Shelf Life: 3 years (unopened)
Storage Temperature: Below 25°C
Light Sensitivity: Protect from light
Oxidation Resistance: Good antioxidant stability

Performance Characteristics

Detailed performance metrics demonstrate Lanolin superiority in topical pharmaceutical applications with exceptional emollient properties, formulation compatibility, and clinical efficacy across diverse dermatological treatment protocols.

Emollient Efficacy

Superior moisturizing capacity verified

Excellent skin hydration
Formulation Stability

Stable in diverse formulation matrices

Excellent compatibility
Emulsification Performance

200-300% water incorporation capacity

Outstanding emulsifying properties
Temperature Stability

Stable across formulation temperatures

Robust processing conditions
Batch Consistency

≤2% variation between batches

Excellent manufacturing reproducibility
Dermatological Compatibility

Well-tolerated in sensitive applications

Skin-friendly formulations

Safety Information

Handle with appropriate pharmaceutical safety protocols. Use personal protective equipment including safety glasses, gloves, and lab coats. Ensure adequate ventilation and avoid dust generation. Store away from incompatible materials and follow standard pharmaceutical handling procedures.

Natural Origin
Wear Gloves
Potential Allergen

Storage & Handling

Store in original pharmaceutical-grade containers in a cool, dry, well-ventilated area. Keep containers tightly closed and protect from direct sunlight and oxidation. Use appropriate pharmaceutical storage equipment and ensure proper environmental controls for optimal product stability.

Store below 25°C
Protect from oxidation
Original container storage
Protect from light

Chemical Mechanisms & Reaction Pathways

Lanolin exhibits exceptional skin protection properties through natural lipid barrier enhancement and moisture retention, enabling precise dermatological applications with predictable biocompatibility pathways and quantitative skin barrier restoration.

Lipid Barrier Enhancement

Natural cholesterol and fatty acid complex mimicking skin lipids

Therapeutic mechanism for skin barrier repair
Moisture Retention

Occlusive and humectant properties for sustained hydration

Essential for dermatological formulations
Biocompatibility

Natural compatibility with human skin lipid composition

Enables selective therapeutic applications
Drug Delivery Enhancement

Improved penetration of active pharmaceutical ingredients

Controlled therapeutic environment for topical treatment

Regulatory Compliance & Documentation

Comprehensive regulatory compliance ensures global pharmaceutical market access with complete documentation packages supporting international standards and therapeutic method validations.

USP Grade Specifications

United States Pharmacopeia pharmaceutical grade standards compliance

EP Monograph Standard

European Pharmacopoeia standard for pharmaceutical specifications

IP Grade Available

Indian Pharmacopoeia specifications for pharmaceutical analysis

ICH Guidelines

International Conference on Harmonisation pharmaceutical compliance

Method Validation

Supported pharmaceutical method validation documentation

SDS Documentation

Multi-language Safety Data Sheets (16 sections, GHS compliant)

Technical Support & Value-Added Services

DRAVYOM's pharmaceutical development team provides comprehensive formulation support, stability testing, and regulatory services to optimize Lanolin performance in your specific pharmaceutical applications.

Formulation Development
  • Pharmaceutical formulation optimization support
  • Stability testing guidance
  • Bioavailability and bioequivalence studies
  • Custom pharmaceutical procedures
Analytical Services
  • Certificate of Analysis verification
  • Custom purity analysis
  • Impurity profiling and identification
  • Method validation support
Technical Support
  • Pharmaceutical troubleshooting consultation
  • Storage and handling guidance
  • Safety training and protocols
  • cGMP best practices
Supply Solutions
  • Consistent batch scheduling
  • Emergency supply arrangements
  • Custom packaging options
  • Global distribution network

Environmental Impact & Sustainability

Our Lanolin production emphasizes environmental responsibility through sustainable manufacturing practices, waste minimization, and comprehensive environmental impact management for pharmaceutical operations.

Waste Minimization

Optimized production with minimal waste generation

Water Treatment

Advanced wastewater treatment and recycling systems

Clean Production

Energy-efficient synthesis with emission controls

Safe Disposal

Comprehensive guidance for pharmaceutical waste management

ISO 14001

Environmental management system certified production

Container Recycling

Pharmaceutical container return and recycling programs

Manufacturing Excellence & Quality Control

DRAVYOM's state-of-the-art pharmaceutical manufacturing facility employs advanced purification technology and continuous monitoring systems to ensure consistent Lanolin quality and performance across all production batches.

Production Process

Advanced synthesis and purification in controlled cGMP environment

Multi-stage purification for pharmaceutical grade quality
Quality Testing

Comprehensive analytical testing protocol including purity, impurities, and stability

HPLC verification and spectroscopic analysis
Quality Systems

ISO 9001:2015 quality management with cGMP compliance

Continuous improvement and method validation
Packaging Control

Pharmaceutical grade containers with controlled atmosphere packaging

Light protection and contamination prevention

Market Applications & Performance Data

Comprehensive pharmaceutical data demonstrating Lanolin effectiveness across diverse dermatological applications with quantified performance metrics and clinical validation.

Pharmaceutical Manufacturing
Purity: >98% pharmaceutical grade Bioavailability: >90% in formulations Stability: 3 years shelf life
Research Institutions
Publications: 200+ cited studies Clinical Trials: 15+ ongoing studies Innovation: Dermatological therapy development
Contract Manufacturing
Reliability: 99.9% batch consistency Compliance: 100% regulatory approval Efficiency: 20% cost reduction

DRAVYOM Competitive Advantages

Superior Purity

Consistently exceeds pharmacopeia specifications with ultra-low impurities and exceptional pharmaceutical performance

Reliable Supply

Guaranteed availability with strategic inventory management and pharmaceutical-grade production scheduling

Pharmaceutical Expertise

Dedicated pharmaceutical development team provides formulation and regulatory support

Quality Assurance

Traceable certificates with comprehensive analytical data and stability studies

Global Standards

International compliance with USP, EP, and ICH guidelines for worldwide acceptance

Partnership Approach

Collaborative relationships with pharmaceutical manufacturers and custom development services