Ensure consistent medical production quality with our Ciprofloxacin 99% Purity Solid Pharmaceutical Chemical (CAS 85721-33-1), designed to stabilize your supply chain and reduce cost variability. This high-purity solid meets stringent pharmaceutical standards, with a precise melting point of 255-257°C ensuring reliable formulation results for medical applications.
- 99% purity guarantee minimizes batch-to-batch differences, streamlining your manufacturing process
- Available in 25kg foil-alum bags or 250kg drums, optimized for bulk ordering and long-term storage
- Backed by our large warehousing center for steady availability, even for ton-level requirements
Description
For industrial manufacturing and laboratory research purposes only.
Product Specifications
| Parameter | Value |
|---|---|
| Product Name | Ciprofloxacin |
| CAS Number | 85721-33-1 |
| Purity | >99% |
| Purity Degree | 99% |
| State | Solid |
| Molecular Formula | C17h18fn3o3 |
| Melting Point | 255-257°c |
| Boiling Point | 581.8±50.0 °c at 760 Mmhg |
| Packing | 25kgs |
| Transport Package | by Foil – Alum Bag or Paper Drum |
| Specification | 250kg/drum Or 1, 250kg/IBC |
| Origin | Hangzhou |
| HS Code | 3004909090 |
| Production Capacity | 20t/Year |
Addressing Purity Instability and Supply Challenges with Ciprofloxacin 85721-33-1
We’ve witnessed countless production delays caused by erratic raw material quality—from batch-to-batch purity fluctuations disrupting synthesis processes to unexpected supply shortages halting laboratory research. In the fine chemical industry, these inconsistencies don’t just affect timelines; they compromise the integrity of your entire operation.
A Stable and Reliable Chemical Supply Solution
Our Ciprofloxacin 99% purity solid pharmaceutical chemical (CAS 85721-33-1) is engineered to resolve these challenges. Backed by a large warehousing center and stable supply chain system, we ensure consistent availability from kilogram to ton-level orders, supporting both small-scale research and large-volume industrial production with the reliability your operations demand.
Typical Industrial Applications
This high purity ciprofloxacin serves as a critical intermediate in industrial chemical synthesis and laboratory research processes. Its consistent composition makes it valuable for analytical standard development, process validation studies, and specialty chemical manufacturing—applications where precise molecular structure and impurity control are paramount for reliable results.
Why Key Specifications Matter
The 99% purity level of our ciprofloxacin minimizes interference from impurities, ensuring cleaner reaction pathways and more accurate research outcomes. Its defined melting point (255-257°C) provides a reliable quality control benchmark for batch consistency, while the boiling point of 581.8±50.0°C at 760 mmHg aids in process optimization for distillation or thermal stability studies. The solid state ensures ease of handling and storage compared to liquid alternatives, reducing spillage risks and simplifying dosage measurement in industrial settings.
What You Gain With Our Product
Choosing our ciprofloxacin 85721-33-1 means eliminating the hidden costs of substandard materials—reduced yield losses from副反应, fewer failed experiments due to impurity interference, and minimized production downtime from supply disruptions. Our adherence to strict quality control protocols ensures compliance with industrial chemical standards, while our competitive pricing structure delivers long-term cost stability in a volatile market.
Why You Can Trust Us
Our 10+ years of experience in chemical manufacturing and supply chain management is reflected in our rigorous quality assurance process. Each production batch undergoes comprehensive testing, and we maintain a production capacity of 20t/year to ensure consistent supply even for large-scale requirements. With a customer base spanning 50+ countries and 10000+ industrial clients, our track record speaks to our commitment to reliability and product integrity.
Certificate of Analysis & Documentation
Every shipment includes a detailed Certificate of Analysis (COA) specific to the batch, providing complete transparency of quality parameters. Material Safety Data Sheets (MSDS) are also included to support your safety and compliance protocols, with additional documentation available upon request for regulatory submissions or internal quality audits.
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.
How to Place Your Order
Initiate your procurement process by submitting your required quantity and specifications for a personalized quotation. We can arrange sample provision for qualification testing prior to full-scale orders, ensuring the product meets your specific requirements. Our standard transaction process ensures clear communication at every stage, from order confirmation to delivery and post-sales support.
Frequently Asked Questions
Q: What is the shelf life of your ciprofloxacin product?
A: Shelf life information is provided on the product label and COA, typically 24 months from manufacturing date when stored under recommended conditions.
Q: Can this product be used for pharmaceutical or food applications?
A: No. This product is supplied FOR INDUSTRIAL AND LABORATORY RESEARCH USE ONLY. NOT FOR DIRECT HUMAN CONSUMPTION, THERAPEUTIC OR HOUSEHOLD USE.
What documentation is provided with each shipment?
A: Each shipment includes a Certificate of Analysis (COA) and Material Safety Data Sheet (MSDS) specific to the batch.
Q: Do you offer custom packaging options?
A: Yes, shipping marks can be arranged according to customer requirements, with standard packaging available in 25kgs, 250kg/drum, or 1250kg/IBC options.
Q: How is product purity verified?
A: Purity is determined through comprehensive analytical testing as specified in the COA, ensuring compliance with the stated 99% purity standard.







