Tranexamic Acid Powder (TXA-99)

£50,000.00

Tranexamic Acid Powder (TXA-99) is a high-purity active pharmaceutical ingredient (API) valued for its reliable antifibrinolytic properties and broad pharmaceutical applications. It is widely used in the formulation of hemostatic and bleeding-control medicines across healthcare markets. Competitive Advantage: TXA-99 offers consistent purity, batch-to-batch quality, and dependable supply for pharmaceutical manufacturers seeking scalable, specification-driven sourcing.

Description

1. Product Overview

Tranexamic Acid Powder (TXA-99) is a high-purity pharmaceutical-grade active ingredient used primarily in formulations designed to control excessive bleeding and support hemostatic applications. With a target purity of 99%, it provides consistent performance and reliable formulation characteristics for pharmaceutical manufacturers and healthcare product developers. Its established functionality, scalability, and broad pharmaceutical relevance make it a strategically important raw material for global sourcing programs.

2. Key Specifications & Technical Characteristics

  • Chemical Name: Tranexamic Acid
  • CAS Number: 1197-18-8
  • Chemical Formula: C₈H₁₅NO₂
  • Purity: ≥99%
  • Grade: Pharmaceutical / industrial bulk grade, subject to applicable specification
  • Physical Form: Fine crystalline powder
  • Color: White to off-white
  • Solubility: Soluble in water
  • Packaging Options: 25 kg bags/drums; customized bulk packaging available
  • Shelf Life: Typically 24–36 months when stored under recommended conditions
  • Storage: Keep tightly sealed in a cool, dry, well-ventilated environment and protected from moisture

3. Core Industrial Applications

  • Pharmaceutical Manufacturing: Used as an active pharmaceutical ingredient (API) in formulations intended for antifibrinolytic and hemostatic applications.
  • Healthcare Products: Suitable for incorporation into tablets, capsules, injectable formulations, and other pharmaceutical dosage forms subject to regulatory requirements.
  • Contract Manufacturing: Supports large-scale API procurement for pharmaceutical producers and contract manufacturing organizations.
  • Formulation Development: Its high purity and consistent physical characteristics facilitate standardized formulation and production processes.
  • Operational Advantages: Reliable assay consistency can support batch-to-batch reproducibility, efficient processing, and reduced formulation variability compared with lower-purity raw materials.

4. Competitive Advantages

  • Quality Consistency: ≥99% purity specification supports dependable pharmaceutical manufacturing and formulation control.
  • Supply Reliability: Suitable for structured bulk procurement and recurring industrial supply programs.
  • Logistics Capability: Bulk packaging and container-scale shipment options support international sourcing requirements.
  • Price Competitiveness: High-volume procurement enables commercially attractive cost structures for pharmaceutical manufacturers.
  • Sustainability: Efficient bulk packaging and consolidated transportation can help optimize material handling and logistics efficiency.
  • Technical Documentation: Certificate of Analysis (CoA), specification sheets, Safety Data Sheet (SDS), and other quality documentation can be provided subject to supplier and regulatory requirements.

5. Commercial & Supply Information

  • Minimum Order Quantity (MOQ): BULK 20 MT
  • Loading Capacity: Approximately 20 MT per standard 20-foot container, subject to packaging configuration, applicable weight restrictions, and shipping requirements

Additional information

Price

per MT

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