Pirarubicin 72496-41-4 99% Purity Medicine Grade API for Pharmaceutical Manufacturing
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Pirarubicin 72496-41-4 99% Purity Medicine Grade API for Pharmaceutical Manufacturing

<p>Ensure consistent pharmaceutical manufacturing quality with our <strong>Pirarubicin 72496-41-4</strong> API, a reliable medicine grade solution that meets stringent industry standards. This orange-red crystalline powder delivers 99% purity, supporting precise formulation and reducing batch variability for pharmaceutical production.</p><ul><li>Medicine grade API with non-volatile solid form, ideal for stable storage and processing</li><li>Produced under controlled conditions with a monthly capacity of 20kg, ensuring steady supply for your manufacturing needs</li><li>Packaged in secure cardboard drums or cartons to maintain integrity during transport and storage</li></ul>

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Ensure consistent pharmaceutical manufacturing quality with our Pirarubicin 72496-41-4 API, a reliable medicine grade solution that meets stringent industry standards. This orange-red crystalline powder delivers 99% purity, supporting precise formulation and reducing batch variability for pharmaceutical production.

  • Medicine grade API with non-volatile solid form, ideal for stable storage and processing
  • Produced under controlled conditions with a monthly capacity of 20kg, ensuring steady supply for your manufacturing needs
  • Packaged in secure cardboard drums or cartons to maintain integrity during transport and storage

描述

FOR INDUSTRIAL AND LABORATORY RESEARCH USE ONLY. NOT FOR DIRECT HUMAN CONSUMPTION, THERAPEUTIC OR HOUSEHOLD USE.
For industrial manufacturing and laboratory research purposes only.

Product Specifications

Parameter Value
Product Name Pirarubicin
CAS Number 72496-41-4
Grade Standard Medicine Grade
Assay More Than 99%
Appearance Orange-Red Crystalline Powder
State Solid
Volatile Not Volatile
Packaging Cardboard Drums or Cartons
Specification gram, kilogram
Origin China
HS Code 2934999099
Production Capacity 20kg/Month

Overcoming API Supply Challenges: Reliable Pirarubicin 72496-41-4 for Pharmaceutical R&D

Consistency in active pharmaceutical ingredients directly impacts research reproducibility and manufacturing efficiency. In our 10+ years serving pharmaceutical labs and production facilities across 50+ countries, we’ve witnessed countless projects delayed by API purity fluctuations, batch-to-batch variability, and unreliable supply chains—issues that compromise both timeline and research integrity.

A Stable Source of High-Purity Pirarubicin API

Our Pirarubicin 72496-41-4 addresses these critical challenges with pharmaceutical-grade quality and consistent supply. As a solid medicine grade chemical with 99% purity, it meets the stringent requirements of pharmaceutical manufacturing and laboratory research, supported by our monthly production capacity of 20kg to ensure uninterrupted material availability.

Key Applications in Pharmaceutical Development

This orange-red crystalline powder serves as a critical raw material in pharmaceutical manufacturing API processes, particularly in the synthesis and formulation stages of research and development. Its consistent composition makes it suitable for analytical method development, stability testing, and small-scale pilot production—applications strictly limited to industrial and laboratory environments.

Why Purity and Physical Properties Matter in API Selection

The 99% purity level of our Pirarubicin minimizes interference from impurities, reducing the risk of non-specific reactions in research assays. Its solid, non-volatile nature ensures stable handling and storage, while the orange-red crystalline structure allows for easy visual identification and quality verification. These characteristics collectively contribute to reliable experimental results and streamlined manufacturing workflows, where even minor compositional variations can lead to significant process deviations.

The Value of Reliable API Sourcing for Pharmaceutical Operations

Choosing a consistent, high-purity API like our Pirarubicin 72496-41-4 mitigates the risks associated with substandard raw materials—including failed batch runs, wasted resources, and extended project timelines. Unlike suppliers with inconsistent quality control, our strict production standards ensure each batch meets the same pharmaceutical-grade specifications, translating to predictable performance and long-term cost efficiency for pharmaceutical manufacturing API projects.

Our Quality Assurance Commitment

Every batch of Pirarubicin undergoes comprehensive testing before release, including purity analysis and physical property verification. We provide a complete Certificate of Analysis with each shipment, detailing critical parameters to confirm compliance with your requirements. Our production process adheres to strict industrial standards, and we maintain full traceability from raw material sourcing to final packaging. Should any specification fail to meet agreed standards, we offer prompt replacement or refund to ensure your research and production continuity.

Certificate of Analysis & Documentation

Each order includes a batch-specific Certificate of Analysis (COA) and Material Safety Data Sheet (MSDS). For research transparency, detailed testing records can be requested using your order number, and additional technical documentation is available upon request to support regulatory compliance and internal quality control processes.

Storage & Handling

  • Store in a cool, dry, well-ventilated area, sealed and away from direct sunlight.
  • Keep away from incompatible materials, food and feed sources.
  • Handle with appropriate personal protective equipment (gloves, goggles, lab coat).
  • Follow good industrial hygiene practices. Avoid inhalation and skin contact.
  • Refer to MSDS for detailed storage and safety instructions.

Streamlined Ordering Process for Pharmaceutical Ingredients

Initiate your order by inquiring about current availability and specifications. We can provide samples for preliminary evaluation, followed by bulk ordering once requirements are confirmed. All shipments include the necessary documentation to facilitate your receiving and quality control processes, ensuring a smooth transition from order to application in your pharmaceutical research or manufacturing workflow.

Frequently Asked Questions

Q: What is the shelf life of Pirarubicin under proper storage conditions?

A: When stored as recommended (cool, dry, sealed, away from sunlight), the product maintains stability for 24 months from the date of manufacture. Specific batch expiration dates are provided on the Certificate of Analysis.

Q: Can this product be used directly in finished pharmaceutical products for human use?

A: No. This product is supplied FOR INDUSTRIAL AND LABORATORY RESEARCH USE ONLY. It is not intended for direct human consumption, therapeutic applications, or household use.

Q: What documentation is provided with each shipment?

A: Each order includes a batch-specific Certificate of Analysis (COA) and Material Safety Data Sheet (MSDS). Additional technical documents can be requested prior to ordering.

Q: Do you offer custom packaging or specification options?

A: While standard packaging is in cardboard drums or cartons with gram/kilogram specifications, custom packaging requests can be evaluated based on order volume. Contact our sales team for specific requirements.

Q: How is product purity verified?

A: Purity is determined through quantitative analysis methods as part of our quality control process, with results documented in the batch-specific COA provided with each shipment.

Usage Notice: Supplied exclusively for industrial manufacturing and laboratory research purposes. The buyer is fully responsible for complying with all local laws, regulations and safety requirements for its use.

Technical Specifications

Specifications will be provided upon inquiry.

Safety & Storage Information

⚠️ Handling Notice

Always handle chemical products with appropriate personal protective equipment (PPE). Refer to the Safety Data Sheet (SDS) for complete safety information before use.

Available Documents

Certificate of Analysis (COA)
Request
Safety Data Sheet (SDS/MSDS)
Request
Technical Data Sheet (TDS)
Request
Regulatory Compliance Report
Request

Documents are available upon request. Contact us for immediate access.

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