Purified Water
Pharmaceutical Premium
Pharmaceutical Excipient

Purified Water

Ultra-pure pharmaceutical Purified Water manufactured to meet stringent USP and EP specifications for pharmaceutical applications. Our Purified Water provides excellent purity standards with superior conductivity control for various pharmaceutical formulations and processes.

  • USP/EP Pharmaceutical Grade
  • Ultra-Pure Quality
  • Excellent Conductivity
  • Enhanced Purity Standards
  • Consistent Quality
  • Microbial Control
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Technical Specifications

Chemical Formula: H2O
CAS Number: 7732-18-5
Grade: USP/EP Pharmaceutical Grade
Conductivity: ≤1.3 µS/cm at 25°C
Physical State: Clear, colorless liquid
pH Range: 5.0-7.0
Total Organic Carbon: ≤500 ppb
Nitrates: ≤0.2 ppm
Chlorides: ≤0.5 ppm
Sulfates: ≤1.0 ppm
Heavy Metals: ≤5 ppb
Microbial Count: ≤100 CFU/ml
Storage Conditions: Store at 15-25°C, avoid contamination
Shelf Life: Use within production guidelines
Packaging Options: 1L, 5L, 20L, bulk containers

Applications

Injectable Preparations
Oral Liquid Formulations
Ophthalmic Solutions
Tablet Manufacturing
Capsule Production
Topical Preparations
Quality Control Testing
Analytical Procedures
Equipment Cleaning
Process Applications
Dissolution Testing
Pharmaceutical Research

Industry-Specific Grades

DRAVYOM offers specialized Purified Water grades tailored for specific pharmaceutical applications, ensuring optimal purity standards and regulatory compliance across diverse manufacturing and testing requirements.

USP Grade (United States Pharmacopoeia)
Conductivity: ≤1.3 µS/cm TOC: ≤500 ppb Heavy Metals: ≤5 ppb Application: FDA approved manufacturing
EP Grade (European Pharmacopoeia)
pH Range: 5.0-7.0 Nitrates: ≤0.2 ppm Microbial Count: ≤100 CFU/ml Application: European market compliance
WFI Grade (Water for Injection)
Sterility: Assured Endotoxins: <0.25 EU/ml Pyrogen-Free: Verified Application: Injectable preparations
Ultra-Pure Grade
Enhanced Purity: >99.999% Ultra-Low Conductivity: <0.1 µS/cm Superior Quality: Verified Application: Critical applications

Quality Standards

DRAVYOM's Purified Water is produced under stringent cGMP protocols, meeting international pharmaceutical water standards including USP, EP, and FDA guidelines for pharmaceutical applications.

cGMP Manufacturing Standards
USP/EP Grade Specifications
≤1.3 µS/cm Conductivity
Advanced Water Testing
Ultra-Pure Quality Verified
Batch-to-Batch Consistency
Comprehensive COA Documentation
Controlled Production & Distribution

Advanced Chemical Properties & Performance

Pharmaceutical Grade Purified Water exhibits exceptional chemical properties essential for pharmaceutical applications. Its superior purity and stability characteristics ensure reliable performance in demanding formulation, manufacturing, and analytical testing systems.

Chemical Properties
Molecular Weight: 18.02 g/mol
Molecular Formula: H2O
pH Range: 5.0-7.0
Ionic Character: Neutral
Physical Properties
Boiling Point: 100°C
Appearance: Clear, colorless liquid
Density: 1.000 g/mL (25°C)
Viscosity: 0.89 cP (25°C)
Pharmaceutical Properties
Conductivity: ≤2.1 μS/cm
Total Organic Carbon: ≤0.50 mg/L
Nitrate: ≤0.2 ppm
Heavy Metals: ≤0.1 ppm
Quality Specifications
Microbial Count: ≤100 CFU/mL
Endotoxins: ≤0.25 EU/mL
Chloride: ≤0.5 ppm
Sulfate: ≤1.0 ppm
Stability Properties
Shelf Life: 1 year (sealed containers)
Storage Temperature: 15-25°C
Container Material: Pharmaceutical grade containers
Microbial Stability: Requires periodic monitoring

Performance Characteristics

Detailed performance metrics demonstrate Purified Water superiority in pharmaceutical applications with exceptional purity levels, low ionic content, and consistent quality across diverse manufacturing and formulation processes.

Ultra-Pure Quality

Superior purity for pharmaceutical applications

Low conductivity and ionic content
Low Microbial Load

Controlled microbial contamination levels

≤100 CFU/mL specification
Analytical Compatibility

Ideal for analytical testing and HPLC

Minimal interference
Manufacturing Reliability

Consistent quality for production processes

Batch-to-batch consistency
Regulatory Compliance

USP/EP/FDA purified water standards

Global regulatory acceptance
Quality Assurance

Comprehensive testing and documentation

Full COA provided

Safety Information

Generally safe pharmaceutical-grade water requiring standard handling protocols. Handle in controlled environments with appropriate hygiene measures. Use proper container systems and follow established protocols for pharmaceutical water systems.

Safe for Pharmaceutical Use
Microbial Control Required
Good Hygiene Practices

Storage & Handling

Store in pharmaceutical-grade containers in a clean, controlled environment away from contamination sources. Maintain appropriate temperature storage and ensure protection from microbial contamination to preserve pharmaceutical quality and purity.

Controlled room temperature (15-25°C)
Microbial contamination control
Pharmaceutical-grade containers
Regular quality monitoring

Chemical Mechanisms & Reaction Pathways

Purified Water exhibits specific molecular purity and absence of contaminants essential for pharmaceutical applications. Its molecular structure ensures compatibility with pharmaceutical formulations and predictable solvent properties.

Molecular Purity

Ultra-pure H2O with minimal ionic and organic contamination

Pharmaceutical-grade water quality
Solvent Properties

Universal solvent with optimal pharmaceutical compatibility

Predictable dissolution characteristics
Microbial Control

Sterile water with validated microbial reduction

Pharmaceutical manufacturing safety
Chemical Stability

Chemically inert with predictable interactions

Formulation compatibility assurance

Regulatory Compliance & Documentation

Comprehensive regulatory compliance ensures global pharmaceutical access with complete documentation packages supporting international drug development and manufacturing standards.

USP Specifications

United States Pharmacopeia pharmaceutical standards compliance

EP Standards

European Pharmacopoeia specifications for pharmaceutical quality

ICH Guidelines

International Conference on Harmonization standards compliance

GMP Certification

Good Manufacturing Practices certified production facility

DMF Support

Drug Master File documentation for regulatory submissions

CEP Available

Certificate of Suitability to European Pharmacopoeia monographs

Technical Support & Value-Added Services

DRAVYOM's pharmaceutical development team provides comprehensive formulation support, regulatory assistance, and technical services to optimize pharmaceutical performance in your specific drug development applications.

Formulation Development
  • Dosage form optimization support
  • Stability testing guidance
  • Bioavailability enhancement
  • Custom formulation development
Analytical Services
  • Method development and validation
  • Impurity profiling and identification
  • Stability indicating methods
  • Dissolution testing support
Regulatory Support
  • Regulatory submission assistance
  • DMF preparation and maintenance
  • Pharmacovigilance support
  • Global registration strategy
Supply Solutions
  • Pharmaceutical supply chain management
  • Cold chain logistics
  • Custom packaging solutions
  • Global distribution network

Environmental Impact & Sustainability

Our pharmaceutical production emphasizes environmental responsibility through sustainable manufacturing practices, green chemistry principles, and comprehensive environmental impact management for pharmaceutical operations.

Green Chemistry

Sustainable synthetic routes with minimal environmental impact

Water Management

Advanced wastewater treatment and recycling systems

Clean Production

Energy-efficient synthesis with emission controls

Safe Disposal

Comprehensive pharmaceutical waste management protocols

ISO 14001

Environmental management system certified production

Sustainable Packaging

Recyclable pharmaceutical packaging solutions

Manufacturing Excellence & Quality Control

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

Production Process

Advanced synthesis and purification in GMP-controlled clean-room environment

Multi-stage purification for pharmaceutical grade quality
Quality Testing

Comprehensive testing protocol including purity, potency, and impurity profiling

HPLC, GC-MS, and spectroscopic analysis
Quality Systems

ISO 9001:2015 and GMP quality management systems

Continuous improvement and validation protocols
Packaging Control

Pharmaceutical-grade packaging with controlled atmosphere

Contamination prevention and stability protection

Market Applications & Performance Data

Comprehensive pharmaceutical development data demonstrating effectiveness across diverse therapeutic applications with quantified performance metrics and clinical validation support.

Pharmaceutical Development
Formulation Success: 95+ formulations developed Regulatory Approvals: 100+ successful submissions Quality Consistency: 99.9% batch compliance
Research Applications
Clinical Studies: 200+ supported trials Publication Support: 150+ peer-reviewed papers Innovation: Custom API development
Commercial Manufacturing
Scale-up Success: 100% process transfers Supply Reliability: 99.8% on-time delivery Cost Optimization: 25% average cost reduction

DRAVYOM Competitive Advantages

Pharmaceutical Excellence

Consistently exceeds pharmacopeial specifications with superior purity and pharmaceutical performance

Reliable Supply

Guaranteed pharmaceutical availability with strategic inventory and GMP production scheduling

Development Expertise

Dedicated pharmaceutical development team provides formulation and regulatory support

Regulatory Assurance

Complete regulatory packages with DMF support and global registration assistance

Global Standards

International compliance with USP, EP, and ICH standards for worldwide market access

Partnership Approach

Collaborative relationships with pharmaceutical companies and custom development services