Cabazitaxel API
Pharmaceutical Oncology
Oncology API

Cabazitaxel

High-purity pharmaceutical grade Cabazitaxel API manufactured to meet stringent USP/EP specifications for cancer chemotherapy formulations. Our pharmaceutical grade API delivers exceptional purity and consistency for critical oncology drug manufacturing applications.

  • USP/EP Grade Quality Standards
  • High Purity ≥99.0% (HPLC)
  • Comprehensive Analytical Documentation
  • Regulatory Compliance Support
  • cGMP Manufacturing Standards
  • Pharmaceutical Grade Packaging
Request Quote Technical Support

Technical Specifications

Chemical Formula: C45H57NO14
CAS Number: 183133-96-2
Molecular Weight: 835.94 g/mol
Purity (HPLC): ≥99.0% (pharmaceutical grade)
Physical State: White to off-white crystalline powder
Water Content (Karl Fischer): ≤0.5%
Residue on Ignition: ≤0.1%
Heavy Metals (as Pb): ≤10 ppm
Related Substances: ≤1.0% total impurities
Storage Conditions: Store in cool, dry place (2-8°C)
Packaging Options: 100mg, 1g pharmaceutical vials

Applications

Cancer Chemotherapy Drug Manufacturing
Oncology Formulations
Injectable Pharmaceutical Products
API Synthesis & Development
Taxane Inhibitor Research
Pharmaceutical Research
Oncology Drug Manufacturing
Quality Control Testing
Regulatory Compliance
Clinical Trial Materials
Bioanalytical Method Development
Reference Standard Applications

Industry-Specific Grades

DRAVYOM offers specialized Cabazitaxel grades tailored for specific pharmaceutical requirements, ensuring optimal performance and regulatory compliance across diverse oncology drug manufacturing applications.

USP Grade (Pharmaceutical)
Purity: ≥99.0% (HPLC) Water Content: ≤0.5% Heavy Metals: ≤10 ppm Application: Pharmaceutical formulations
EP Grade (European Pharmacopoeia)
Purity: ≥99.0% (pharmaceutical) Related Substances: ≤1.0% Residue on Ignition: ≤0.1% Application: European market compliance
Research Grade
Purity: ≥98.0% (analytical) Water Content: ≤1.0% Particle Size: Controlled Application: R&D, method development
GMP Grade
Purity: ≥99.5% (pharmaceutical) Endotoxins: ≤2.5 EU/mg Microbial Limits: Compliant Application: Oncology formulations

Quality Standards

DRAVYOM's pharmaceutical grade Cabazitaxel 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
≥99.0% Pharmaceutical Purity
Advanced Analytical Testing
Comprehensive Impurity Control
Batch-to-Batch Consistency
Complete Documentation Package
Temperature-Controlled Logistics

Advanced Chemical Properties & Performance

Pharmaceutical grade Cabazitaxel exhibits exceptional chemical properties essential for oncological applications. Its ultra-pure composition and precise molecular structure ensure reliable performance in demanding pharmaceutical formulations and research applications.

Analytical Properties
Solubility (Water): Practically insoluble
LogP (octanol/water): 4.6
pKa: Not applicable
UV λmax: 230 nm
Physical Properties
Melting Point: 174-178°C
Bulk Density: 0.3-0.5 g/mL
Crystalline Form: White to off-white crystalline powder
Hygroscopicity: Non-hygroscopic
Pharmaceutical Performance
Bioavailability: 100% (intravenous)
Protein Binding: 89-92%
Half-life: 95 hours
Elimination: Hepatic metabolism
Purity Specifications
Assay (HPLC): ≥99.0%
Related Substances: ≤1.0% total
Water Content: ≤0.5% (Karl Fischer)
Residue on Ignition: ≤0.1%
Stability Properties
Shelf Life: 2 years (unopened)
Light Sensitivity: Protect from light
Temperature Stability: Store 2-8°C
Container Compatibility: Amber glass vials

Performance Characteristics

Detailed performance metrics demonstrate pharmaceutical grade Cabazitaxel superiority in oncological applications with exceptional microtubule stabilization, antitumor efficacy, and reproducibility across diverse pharmaceutical formulations and cancer therapeutic protocols.

Microtubule Binding

High affinity for β-tubulin subunits

Superior antitumor activity
Solution Stability

Stable in reconstituted form for 24 hours

Extended administration window
Bioavailability

100% intravenous bioavailability

Complete systemic exposure
Temperature Stability

Stable under refrigerated conditions

Consistent performance at 2-8°C
Batch Reproducibility

Variation: ±0.3% between batches

Exceptional lot-to-lot consistency
Shelf Stability

2 years under proper storage conditions

Extended pharmaceutical grade integrity

Safety Information

Cytotoxic compound requiring specialized handling protocols. Use appropriate personal protective equipment including chemotherapy-grade gloves, protective clothing, and work in designated cytotoxic preparation areas. Avoid skin contact, inhalation, and ensure proper disposal according to cytotoxic waste guidelines.

Cytotoxic
Carcinogen
Specialized Handling

Storage & Handling

Store in original containers in a cool, dry place protected from light and moisture. Requires refrigerated storage and specialized cytotoxic handling procedures. Use appropriate containment and ensure controlled temperature environment.

Store at 2-8°C (refrigerated)
Protect from light
Cytotoxic handling required
Secure storage required

Chemical Mechanisms & Reaction Pathways

Cabazitaxel exhibits antineoplastic properties through microtubule stabilization and mitotic arrest, enabling predictable anticancer therapeutic response with well-characterized pharmacokinetic and pharmacodynamic profiles.

Mechanism of Action

Microtubule stabilization and inhibition of mitosis

Targeted cancer cell cycle arrest
Metabolic Pathway

Hepatic metabolism via CYP3A4 and CYP2C8

Predictable drug interaction profile
Pharmacokinetics

Linear pharmacokinetics with 95-hour half-life

Suitable for three-weekly dosing
Elimination

Primarily hepatic metabolism and fecal excretion

Minimal renal elimination

Regulatory Compliance & Documentation

Comprehensive regulatory compliance ensures global pharmaceutical market access with complete documentation packages supporting international drug registration and regulatory submissions.

USP Monograph

United States Pharmacopeia specifications compliance

EP Standards

European Pharmacopoeia monograph requirements

cGMP Manufacturing

Current Good Manufacturing Practices compliance

ICH Guidelines

International Council for Harmonisation standards

DMF Support

Drug Master File documentation assistance

Audit Readiness

Regulatory inspection preparation and support

Technical Support & Value-Added Services

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

Formulation Development
  • Excipient compatibility studies
  • Stability testing protocols
  • Dissolution optimization
  • Bioavailability enhancement
Analytical Services
  • Method validation support
  • Impurity identification
  • Stability indicating methods
  • Pharmaceutical testing
Technical Support
  • Regulatory compliance guidance
  • Quality assurance protocols
  • Manufacturing process support
  • Documentation preparation
Supply Solutions
  • Pharmaceutical grade scheduling
  • Global regulatory shipping
  • Custom packaging options
  • Emergency supply protocols

Environmental Impact & Sustainability

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

Waste Minimization

Optimized synthesis with minimal pharmaceutical waste

Water Treatment

Advanced wastewater treatment and recycling systems

Clean Production

Energy-efficient synthesis with emission controls

Safe Disposal

Pharmaceutical waste management guidance

ISO 14001

Environmental management system certification

Green Chemistry

Sustainable pharmaceutical synthesis methods

Manufacturing Excellence & Quality Control

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

cGMP Production

Current Good Manufacturing Practices in controlled pharmaceutical environment

FDA and WHO-GMP certified facility
Quality Testing

Comprehensive pharmaceutical testing including identity, purity, and potency

USP/EP monograph compliance verification
Quality Systems

ISO 9001:2015 with pharmaceutical quality management

Continuous improvement and validation
Packaging Control

Pharmaceutical-grade packaging with moisture protection

Stability and contamination prevention

Market Applications & Performance Data

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

Pharmaceutical Formulations
Bioavailability: Parenteral administration Half-life: 95 hours prolonged exposure Stability: 2+ years refrigerated
Clinical Applications
Efficacy: 14.5% prostate cancer response Safety: Manageable hematological toxicity Dosage: 20-25 mg/m² standard dose
Manufacturing Data
Purity: >99.5% pharmaceutical grade Consistency: ±0.3% batch variation Yield: >95% synthesis efficiency

DRAVYOM Competitive Advantages

Pharmaceutical Excellence

Consistently exceeds USP/EP specifications with exceptional pharmaceutical quality and performance

Reliable Supply

Guaranteed pharmaceutical-grade availability with cGMP production scheduling

Development Expertise

Dedicated pharmaceutical development team providing formulation and regulatory support

Quality Assurance

Comprehensive COA with pharmaceutical testing and regulatory compliance documentation

Global Standards

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

Partnership Approach

Collaborative relationships with pharmaceutical companies and custom API development