Ethanol
Pharmaceutical Premium
Pharmaceutical Excipient

Ethanol

High-purity pharmaceutical Ethanol manufactured to meet stringent USP and EP specifications for solvent applications. Our Ethanol provides excellent solvent properties with superior purity standards for pharmaceutical extraction and formulation processes.

  • USP/EP Pharmaceutical Grade
  • Ultra-Pure Quality
  • Excellent Solvent Properties
  • Enhanced Purity Standards
  • Consistent Quality
  • Low Water Content
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Technical Specifications

Chemical Formula: C2H5OH
CAS Number: 64-17-5
Molecular Weight: 46.07 g/mol
Purity (GC): ≥99.8% (pharmaceutical grade)
Physical State: Clear, colorless liquid
Water Content (Karl Fischer): ≤0.2%
Residue on Evaporation: ≤0.001%
Heavy Metals (as Pb): ≤5 ppm
Aldehydes (as Acetaldehyde): ≤10 ppm
Storage Conditions: Store in cool, dry place (15-25°C)
Packaging Options: 1L, 5L, 25L pharmaceutical containers

Applications

Pharmaceutical Solvent Applications
Tincture and Extract Manufacturing
Oral Liquid Formulations
API Extraction & Purification
Chemical Synthesis Reactions
Pharmaceutical Research
Manufacturing Processes
Quality Control Testing
Regulatory Compliance
Analytical Method Development
Bioanalytical Applications
Reference Standard Applications

Industry-Specific Grades

DRAVYOM offers specialized Ethanol grades tailored for specific pharmaceutical requirements, ensuring optimal performance and regulatory compliance across diverse solvent and extraction applications.

USP Grade (Pharmaceutical)
Purity: ≥99.8% (GC) Water Content: ≤0.2% Heavy Metals: ≤5 ppm Application: Pharmaceutical formulations
EP Grade (European Pharmacopoeia)
Purity: ≥99.8% (pharmaceutical) Aldehydes: ≤10 ppm Residue on Evaporation: ≤0.001% Application: European market compliance
Absolute Grade
Purity: ≥99.9% (analytical) Water Content: ≤0.1% Anhydrous Quality Application: Anhydrous reactions
GMP Grade
Purity: ≥99.9% (pharmaceutical) Endotoxins: ≤0.25 EU/mL Microbial Limits: Compliant Application: Sterile formulations

Quality Standards

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

cGMP Certified Manufacturing
USP/EP Grade Specifications
≥99.8% 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 Ethanol exhibits exceptional chemical properties essential for pharmaceutical solvent applications. Its ultra-pure composition and precise molecular structure ensure reliable performance in demanding pharmaceutical formulations and research applications.

Analytical Properties
Solubility (Water): Miscible in all proportions
LogP (octanol/water): -0.31
pKa: 15.9
Molecular Weight: 46.07 g/mol
Physical Properties
Appearance: Clear colorless liquid
Boiling Point: 78.37°C
Density: 0.789 g/mL at 20°C
Viscosity: 1.2 cP at 20°C
Pharmaceutical Performance
Solvent Properties: Excellent for organic compounds
Extraction Efficiency: High for botanical extracts
Antimicrobial Activity: Effective at >70% concentration
Volatility: Rapid evaporation
Purity Specifications
Assay (GC): ≥99.8%
Water Content: ≤0.2% (Karl Fischer)
Aldehydes: ≤10 ppm
Residue on Evaporation: ≤5 mg/100 mL
Stability Properties
Shelf Life: 5 years (unopened)
Light Sensitivity: Minimal photodegradation
Temperature Stability: Stable at room temperature
Oxidation Resistance: Good under nitrogen

Performance Characteristics

Detailed performance metrics demonstrate pharmaceutical grade Ethanol superiority in solvent applications with exceptional extraction efficiency, antimicrobial activity, and reproducibility across diverse pharmaceutical processes.

Solvent Power

Excellent solubility for organic compounds

Wide range of applications
Extraction Efficiency

Superior botanical extraction capability

High active compound recovery
Stability Profile

Chemical stability: Excellent under storage conditions

Maintains quality for 5 years
Antimicrobial Activity

Effective antimicrobial at >70% concentration

Preservative properties
Batch Reproducibility

Variation: ±0.05% between batches

Consistent performance
Volatility

Rapid evaporation for processing

Easy residue removal

Safety Information

Flammable pharmaceutical solvent requiring specialized handling protocols. Well-established safety profile for pharmaceutical applications. Handle with appropriate fire safety precautions and ensure proper GMP environmental controls. Monitor for vapor accumulation and maintain adequate ventilation during processing.

Flammable
Professional Use
Adequate ventilation required

Storage & Handling

Store in original containers in a cool, dry, well-ventilated area away from heat sources and ignition. Keep containers tightly closed and maintain pharmaceutical-grade environmental controls. Use appropriate fire safety measures and explosion-proof equipment.

Cool storage (15-25°C)
Away from heat sources
Adequate ventilation
GMP handling required

Chemical Mechanisms & Reaction Pathways

Ethanol exhibits pharmaceutical solvent properties through excellent miscibility with water and organic compounds, providing optimal dissolution characteristics for drug formulation, extraction processes, and pharmaceutical manufacturing.

Solvent Properties

Excellent miscibility with water and organic solvents

Versatile pharmaceutical solvent
Extraction Medium

Effective for botanical and pharmaceutical extractions

High extraction efficiency
Antiseptic Activity

Antimicrobial properties for topical applications

Broad-spectrum antimicrobial
Formulation Aid

Enhances drug solubility and bioavailability

Pharmaceutical co-solvent

Regulatory Compliance & Documentation

Comprehensive regulatory compliance ensures pharmaceutical excipient manufacturing access with complete documentation packages supporting international standards and pharmaceutical solvent applications.

USP Standards

United States Pharmacopeia pharmaceutical excipient specifications

EP Monograph

European Pharmacopoeia specifications for pharmaceutical ethanol

Pharmaceutical GMP

Good Manufacturing Practices for pharmaceutical excipients

ICH Guidelines

International excipient regulatory compliance

Excipient DMF

Drug Master File for pharmaceutical excipient applications

Safety Documentation

Comprehensive pharmaceutical safety documentation

Technical Support & Value-Added Services

DRAVYOM's pharmaceutical excipient team provides comprehensive formulation support, quality testing, and regulatory services for Ethanol pharmaceutical applications.

Solvent Formulation
  • Pharmaceutical solvent optimization
  • Extraction process development
  • Co-solvent system design
  • Custom solvent blending
Analytical Services
  • Pharmaceutical grade purity analysis
  • Residual solvent testing
  • Water content determination
  • Method validation support
Regulatory Support
  • Excipient regulatory filing
  • DMF preparation and maintenance
  • International compliance guidance
  • Pharmaceutical documentation
Supply Solutions
  • Pharmaceutical excipient supply chain
  • Custom packaging solutions
  • Global distribution network
  • Emergency pharmaceutical supply

Environmental Impact & Sustainability

Our Ethanol production emphasizes environmental responsibility through sustainable pharmaceutical manufacturing practices, renewable sourcing, and comprehensive environmental impact management.

Renewable Sourcing

Produced from renewable agricultural materials

Water Conservation

Advanced water treatment and recycling systems

Clean Production

Energy-efficient distillation processes

Waste Reduction

Comprehensive pharmaceutical waste management

ISO 14001

Environmental management system certification

Sustainable Practices

Carbon-neutral manufacturing initiatives

Manufacturing Excellence & Quality Control

DRAVYOM's pharmaceutical excipient manufacturing facility employs advanced distillation technology and continuous monitoring systems to ensure consistent Ethanol quality and pharmaceutical performance.

Pharmaceutical GMP

Pharmaceutical grade manufacturing in controlled environment

Multi-stage distillation for pharmaceutical purity
Quality Testing

Comprehensive testing including assay, impurities, and water content

GC verification and pharmaceutical analysis
Quality Systems

ISO 9001:2015 quality management with pharmaceutical compliance

Continuous improvement and excipient validation
Pharmaceutical Packaging

Pharmaceutical-grade containers with tamper-evident seals

Contamination prevention and stability protection

Market Applications & Performance Data

Comprehensive pharmaceutical data demonstrating Ethanol effectiveness as pharmaceutical excipient with quantified performance metrics and formulation validation data.

Pharmaceutical Formulations
Solubility: Excellent miscibility with water and organics Stability: Stable under pharmaceutical conditions Compatibility: Excellent with various excipients
Pharmaceutical Applications
Solvent: Proven pharmaceutical solvent systems Extraction: Effective botanical extraction medium Antiseptic: Well-established topical antiseptic
Manufacturing Performance
Purity: >99.5% pharmaceutical grade Water Content: <0.5% pharmaceutical specification Consistency: 99.9% batch-to-batch reproducibility

DRAVYOM Competitive Advantages

Pharmaceutical Excellence

Superior pharmaceutical grade with proven solvent performance and regulatory compliance

Reliable Supply

Guaranteed pharmaceutical supply with strategic inventory management

Excipient Expertise

Dedicated pharmaceutical excipient team with specialized formulation support

Regulatory Compliance

Complete pharmaceutical documentation with international compliance

Global Standards

International pharmaceutical compliance with USP, EP, and ICH guidelines

Partnership Approach

Collaborative pharmaceutical relationships with specialized services