Tinidazole
Pharmaceutical Premium
Pharmaceutical API

Tinidazole

High-purity pharmaceutical grade Tinidazole manufactured to meet stringent USP/EP specifications for pharmaceutical formulations and research applications. Our pharmaceutical grade material delivers exceptional purity and consistency for critical pharmaceutical manufacturing.

  • USP/EP Grade Specifications
  • High Purity (≥99.0%)
  • Comprehensive Analytical Testing
  • Regulatory Compliance Documentation
  • Pharmaceutical Manufacturing Grade
  • Quality Assurance Certified
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Technical Specifications

Chemical Formula: C8H13N3O4S
CAS Number: 19387-91-8
Molecular Weight: 247.27 g/mol
Physical State: White to off-white crystalline powder
Purity (HPLC): ≥99.0% (USP/EP Grade)
Loss on Drying: ≤0.5%
Residue on Ignition: ≤0.1%
Heavy Metals (as Pb): ≤10 ppm
Related Substances: ≤1.0% (total impurities)
Particle Size: D90 ≤ 100 μm
pH (1% solution): 5.0-7.0
Solubility: Slightly soluble in water
Storage Conditions: Store at room temperature, protect from light
Shelf Life: 3 years from date of manufacture
Packaging Options: 25g, 50g, 100g pharmaceutical containers

Applications

Antiprotozoal Therapy
Oral Tablet Formulations
Capsule Formulations
Suspension Formulations
Anti-Infective Therapy
Amoebiasis Treatment
Trichomonas Infections
Giardiasis Treatment
Parasitology Research
Generic Formulations
Regulatory Submissions
Reference Standards

Industry-Specific Grades

DRAVYOM offers specialized Tinidazole grades tailored for specific antiprotozoal pharmaceutical requirements, ensuring optimal performance and regulatory compliance across diverse anti-infective therapeutic applications.

USP Grade (United States Pharmacopeia)
Purity: ≥99.0% (HPLC) Related Substances: ≤1.0% Heavy Metals: ≤10 ppm Application: FDA-compliant formulations
EP Grade (European Pharmacopoeia)
Purity: ≥99.0% (HPLC) Loss on Drying: ≤0.5% pH: 5.0-7.0 (1% solution) Application: EU regulatory submissions
Antiprotozoal Grade
Purity: ≥99.5% (HPLC) Antimicrobial Activity: Verified Bioavailability: Optimized Application: Anti-infective medications
Suspension Grade
Purity: ≥99.8% (HPLC) Particle Size: Controlled Stability: Verified Application: Oral suspension formulations

Quality Standards

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

ISO 9001:2015 Certified Manufacturing
USP/EP Grade Specifications
≥99.0% HPLC Purity
Advanced Antimicrobial Testing
Antiprotozoal Activity Verified
Batch-to-Batch Consistency
Comprehensive COA
Pharmaceutical Grade Packaging

Advanced Chemical Properties & Performance

Pharmaceutical Grade Tinidazole exhibits exceptional chemical properties essential for antimicrobial applications. Its nitroimidazole antiprotozoal composition and precise specification ensure reliable performance in demanding pharmaceutical formulations and infection treatment systems.

Chemical Properties
Molecular Formula: C₈H₁₃N₃O₄S
Molecular Weight: 247.27 g/mol
Melting Point: 127-130°C
LogP (Octanol/Water): 0.26
Physical Properties
Appearance: White to off-white crystalline powder
Solubility: Slightly soluble in water
pH (saturated solution): 4.5-6.5
Bulk Density: 0.5-0.7 g/cm³
Pharmaceutical Performance
Bioavailability: ~100% (oral)
Half-life: 12-14 hours
Protein Binding: 12%
Mechanism: DNA synthesis inhibitor
Purity Specifications
Assay (HPLC): ≥ 99.0%
Related Substances: ≤ 0.5%
Heavy Metals: ≤ 20 ppm
Residual Solvents: Within ICH limits
Stability Properties
Shelf Life: 3 years (unopened)
Photostability: Stable under normal light
Temperature Stability: Stable 15-25°C
Humidity Stability: Store ≤60% RH

Performance Characteristics

Detailed performance metrics demonstrate Pharmaceutical Grade Tinidazole superiority in antimicrobial applications with exceptional functionality, stability, and reproducibility across diverse pharmaceutical procedures and infection treatment protocols.

Antimicrobial Efficacy

Potency: Broad-spectrum antiprotozoal activity

Superior pathogen elimination
Duration of Action

Time: 12-14 hour half-life

Extended therapeutic coverage
Bioavailability

Absorption: ~100% oral bioavailability

Complete therapeutic levels
Formulation Stability

Range: Stable in standard formulations

Consistent performance across dosage forms
Batch Uniformity

Variation: ±0.5% between production batches

Exceptional pharmaceutical grade consistency
Long-term Stability

3 years shelf life with maintained potency

Extended pharmaceutical grade integrity

Safety Information

Prescription pharmaceutical with established safety profile in antimicrobial therapy. Generally well-tolerated antiprotozoal agent. Handle with standard laboratory precautions including appropriate protective equipment. Avoid inhalation of powder and ensure proper ventilation during processing.

Prescription Only
Antimicrobial Active
Well Tolerated

Storage & Handling

Store in original sealed containers in a cool, dry, well-ventilated area away from light and moisture. Keep containers tightly closed and protect from degradation. Use appropriate pharmaceutical handling procedures and ensure proper environmental controls for stability management.

Cool storage (15-25°C)
Low humidity (≤60% RH)
Normal light exposure acceptable
Original sealed containers

Chemical Mechanisms & Reaction Pathways

Pharmaceutical Grade Tinidazole exhibits potent nitroimidazole antimicrobial properties through DNA disruption mechanisms enabling effective treatment of anaerobic infections and parasitic diseases with selective targeting.

DNA Disruption

Nitro reduction creates reactive intermediates that damage microbial DNA

Selective toxicity against anaerobic organisms
Antiprotozoal Action

Specific activity against protozoan parasites

Effective against Giardia, Trichomonas, and Entamoeba
Anaerobic Specificity

Selective activation in oxygen-poor environments

Minimal effect on aerobic host cells
Resistance Prevention

Multiple target sites reduce resistance development

Sustained antimicrobial efficacy

Regulatory Compliance & Documentation

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

USP Specifications

United States Pharmacopeia API standards compliance

EP Standards

European Pharmacopoeia specifications for pharmaceutical manufacturing

FDA Approved

FDA approved antimicrobial API with comprehensive safety data

WHO Listed

World Health Organization Essential Medicine status

DMF Documentation

Drug Master File with comprehensive manufacturing and safety data

cGMP Certified

Current Good Manufacturing Practice with antimicrobial API standards

Technical Support & Value-Added Services

DRAVYOM's antimicrobial API team provides comprehensive development support, formulation optimization assistance, and regulatory services for anti-infective drug manufacturing with specialized microbiology expertise.

API Development
  • Antimicrobial formulation support
  • Bioavailability enhancement studies
  • Stability optimization protocols
  • Combination therapy development
Analytical Services
  • Certificate of Analysis with antimicrobial testing
  • Polymorphic form characterization
  • Impurity profiling and identification
  • Dissolution study support
Regulatory Support
  • Antimicrobial drug documentation
  • Regulatory filing assistance
  • Clinical trial support
  • Resistance monitoring protocols
Supply Solutions
  • Consistent API supply chains
  • Temperature-controlled logistics
  • Emergency supply protocols
  • Global distribution network

Environmental Impact & Sustainability

Our Pharmaceutical Grade Tinidazole production emphasizes environmental responsibility through green chemistry principles, sustainable synthetic pathways, and comprehensive environmental impact management for API manufacturing.

Green Synthesis

Optimized synthetic routes with minimal environmental impact

Solvent Recovery

Advanced solvent recycling and waste minimization

Clean Production

Energy-efficient synthesis with emission controls

Water Treatment

Advanced wastewater treatment and recycling systems

ISO 14001

Environmental management system certified production

Safe Disposal

Responsible pharmaceutical waste management protocols

Manufacturing Excellence & Quality Control

DRAVYOM's state-of-the-art antimicrobial API manufacturing facility employs advanced synthetic technology and continuous monitoring systems to ensure consistent Pharmaceutical Grade Tinidazole quality and therapeutic efficacy.

Production Process

Advanced multi-step synthesis with pharmaceutical-grade intermediates

Controlled synthesis for optimal purity and yield
Quality Testing

26-point pharmaceutical testing protocol including antimicrobial testing

HPLC verification and microbiology-specific testing
Quality Systems

cGMP compliance with antimicrobial API manufacturing standards

Continuous improvement and process validation
API Packaging

Specialized packaging with moisture and light protection

Stability maintenance and contamination prevention

Market Applications & Performance Data

Comprehensive clinical and pharmaceutical data demonstrating Pharmaceutical Grade Tinidazole effectiveness across diverse antimicrobial applications with quantified therapeutic metrics and resistance profiles.

Parasitic Infections
Efficacy: 85-95% cure rate Spectrum: Broad antiprotozoal activity Duration: Extended half-life advantage
Anaerobic Infections
Penetration: Excellent tissue distribution Activity: Potent anaerobic coverage Safety: Favorable side effect profile
Treatment Regimens
Dosing: Once or twice daily regimens Compliance: Improved patient adherence Combinations: Synergistic therapy options

DRAVYOM Competitive Advantages

Superior Purity

Consistently exceeds pharmacopeial specifications with optimal polymorphic control and impurity profile

Reliable Supply

Guaranteed availability with strategic inventory management and antimicrobial API expertise

API Expertise

Specialized antimicrobial API manufacturing with comprehensive development support

Quality Assurance

Enhanced testing protocols with complete documentation and regulatory compliance

Global Standards

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

Partnership Approach

Collaborative relationships with antimicrobial pharmaceutical companies and development support