Glycerin
Pharmaceutical Premium
Pharmaceutical Excipient

Glycerin

High-purity pharmaceutical Glycerin manufactured to meet stringent USP and EP specifications for pharmaceutical applications. Our Glycerin provides excellent humectant and solvent properties for various pharmaceutical formulations and topical applications.

  • USP/EP Pharmaceutical Grade
  • Superior Humectant Properties
  • Excellent Solvent Properties
  • Enhanced Stability
  • Consistent Quality
  • Ultra-Low Impurities
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Technical Specifications

Chemical Formula: C3H8O3
CAS Number: 56-81-5
Molecular Weight: 92.09 g/mol
Purity (Assay): ≥99.5% (pharmaceutical grade)
Physical State: Clear, colorless, viscous liquid
Water Content (Karl Fischer): ≤0.5%
Density (20°C): 1.260-1.264 g/mL
Heavy Metals (as Pb): ≤5 ppm
Chlorides: ≤10 ppm
Storage Conditions: Store in tightly closed container at room temperature
Packaging Options: 1kg, 5kg, 25kg pharmaceutical containers

Applications

Pharmaceutical Humectant
Solvent Applications
Topical Formulations
Oral Formulations
Parenteral Applications
Suppository Base
Stabilizer & Preservative
Cosmetic Applications
Skin Moisturizer
Research Applications
Quality Control Testing
Reference Standard

Industry-Specific Grades

DRAVYOM offers specialized Glycerin grades tailored for specific pharmaceutical requirements, ensuring optimal performance and regulatory compliance across diverse pharmaceutical formulation and excipient applications.

USP Grade (Pharmaceutical)
Purity: ≥99.5% (assay) Water Content: ≤0.5% Heavy Metals: ≤5 ppm Application: Pharmaceutical formulations
EP Grade (European Pharmacopoeia)
Purity: ≥99.5% (pharmaceutical) Chlorides: ≤10 ppm Density: 1.260-1.264 g/mL Application: European market compliance
Injection Grade
Purity: ≥99.7% (injection) Endotoxins: ≤0.25 EU/mL Sterility: Compliant Application: Parenteral formulations
Topical Grade
Purity: ≥99.0% (topical) pH: 5.5-8.0 Microbial Limits: Compliant Application: Skin and cosmetic products

Quality Standards

DRAVYOM's pharmaceutical grade Glycerin is manufactured under stringent cGMP protocols, meeting international pharmaceutical standards including USP, EP, and FDA guidelines. Our pharmaceutical-grade production ensures consistent quality and regulatory compliance.

cGMP Certified Manufacturing
USP/EP Grade Specifications
≥99.5% Pharmaceutical Purity
Advanced Analytical Testing
Ultra-Low Impurities
Batch-to-Batch Consistency
Traceable Certificate of Analysis
Temperature-Controlled Logistics

Advanced Chemical Properties & Performance

Pharmaceutical grade Glycerin exhibits precise chemical properties essential for pharmaceutical formulations. Its ultra-pure composition and exact molecular structure ensure reliable therapeutic performance in demanding pharmaceutical applications.

Pharmaceutical Properties
Molecular Weight: 92.09 g/mol
Melting Point: 17.8°C
Boiling Point: 290°C
Solubility (Water): Miscible in all proportions
Physical Properties
Appearance: Clear, colorless, viscous liquid
Density: 1.26 g/cm³ at 20°C
Viscosity: 1410 cP at 20°C
pH: 5.5-8.0 (neat)
Pharmaceutical Performance
Humectant Properties: Excellent moisture retention
Solvent Compatibility: Polar and non-polar systems
Plasticizer Effect: Film-forming enhancement
Stabilizer Function: Prevents crystallization
Purity Specifications
Assay: ≥99.5% (GC)
Water Content: ≤0.5% (Karl Fischer)
Residual Solvents: ICH Q3C compliant
Heavy Metals: ≤10 ppm
Stability Properties
Shelf Life: 3 years (unopened)
Storage Temperature: 15-30°C
Light Sensitivity: Protect from direct light
Moisture Sensitivity: Hygroscopic - control humidity

Performance Characteristics

Detailed performance metrics demonstrate pharmaceutical grade Glycerin superiority in pharmaceutical applications with exceptional stability, compatibility, and reproducibility across diverse pharmaceutical formulations.

Formulation Performance

Compatibility: Excellent with all excipients

Versatile pharmaceutical solvent
Therapeutic Efficacy

Biocompatibility: 100% pharmaceutical grade

Safe for all routes of administration
Dissolution Profile

Solubility: Complete in water and ethanol

Optimal pharmaceutical performance
Thermal Stability

Stability: No degradation at 25°C

Excellent long-term stability
Batch Consistency

Variation: ±0.1% between production batches

Exceptional pharmaceutical uniformity
Shelf Stability

3 years under controlled storage conditions

Extended pharmaceutical grade integrity

Safety Information

Pharmaceutical grade excipient requiring proper handling procedures. Use appropriate personal protective equipment including gloves, safety goggles, and protective clothing. Ensure adequate ventilation and follow established pharmaceutical handling protocols.

Handle with Care
Eye Protection Required
Avoid Inhalation

Storage & Handling

Store in original pharmaceutical containers in a cool, dry, well-ventilated area away from incompatible materials. Keep containers tightly closed and protect from light and moisture. Follow cGMP storage requirements for pharmaceutical materials.

Controlled temperature (15-30°C)
Control humidity exposure
Original pharmaceutical packaging
Protect from direct light

Chemical Mechanisms & Reaction Pathways

Glycerin exhibits multifunctional pharmaceutical activity through specific hydrophilic interactions and emollient properties, enabling precise formulation applications with predictable solubility pathways and quantitative excipient interactions.

Hydrophilic Interactions

Hydrogen bonding with water molecules enhancing solubility

Therapeutic mechanism for moisture retention
Osmotic Activity

Osmotic pressure regulation for laxative and diuretic effects

Essential for fluid balance activity
Excipient Compatibility

Multiple hydroxyl groups enabling compatibility with various APIs

Enables selective pharmaceutical applications
Solvent Properties

Selective solubility enhancement for hydrophilic compounds

Controlled pharmaceutical environment for formulation

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 Glycerin 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 Glycerin 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 Glycerin 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 Glycerin effectiveness across diverse formulation applications with quantified performance metrics and clinical validation.

Pharmaceutical Manufacturing
Purity: >99.5% pharmaceutical grade Functionality: Multi-purpose excipient Stability: 5 years shelf life
Research Institutions
Publications: 2000+ cited studies Applications: 50+ formulation types Innovation: Custom grade development
Contract Manufacturing
Reliability: 99.9% batch consistency Compliance: 100% regulatory approval Efficiency: 30% 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