Product Recommended
Toltrazuril
CAS No.
Appearance
Purity
Molecular Formula
Molecular Weight
Solubility
Synonyms
Table of Contents
Overview
Toltrazuril (CAS No. 69004-03-1) is a triazinetrione-class compound supplied as a white to off-white crystalline powder. It is widely used by veterinary pharmaceutical manufacturers as an active raw material during the development and production of various solid and liquid formulations.
The material shows good stability under typical processing conditions and maintains consistent particle morphology, making it suitable for blending, granulation, suspension preparation, and other common manufacturing steps in veterinary API formulation plants. Toltrazuril’s solid-state properties and impurity profile support reliable downstream processing and formulation design.
We supply Toltrazuril with controlled quality specifications to support industrial R&D, scale-up, and commercial production requirements.
Product Information
| Product Name | Toltrazuril |
| CAS No. | 69004-03-1 |
| Chemical Formula | C18H14F3N3O4S |
| Appearance | White or off-white crystalline powder |
| Assay (HPLC) | Not less than 98.0% |
| Melting Point | 192–196 °C |
| Identification | Infrared spectrum consistent with reference profile |
| Single Impurity | Not more than 0.20% |
| Total Impurities | Not more than 1.00% |
| Loss on Drying | Not more than 0.50% |
| Sulfated Ash | Not more than 0.10% |
| Heavy Metals | Not more than 10 ppm |
| Solubility | Practically insoluble in water; soluble in selected organic solvents |
| Packaging | 1 kg foil bag; 25 kg fiber drum or customized |
| Storage | Store in a tightly closed container, protected from moisture and light |
| Shelf Life | 24 months under recommended storage |
Technical Specifications
| Form | Crystalline powder |
| Color | White to off-white |
| Purity (HPLC) | ≥98.0% |
| Particle Characteristics | Available in standard or customized particle size ranges |
| Impurities | Total ≤1.0% |
| Residual Solvents | Meets in-house specification limits |
| Microbial Quality | Controlled according to internal standards for veterinary API raw materials |
Quality Assurance
Each batch of Toltrazuril is produced under controlled conditions and evaluated against internal quality specifications before release. Testing includes appearance, purity, impurity profile, and identification to ensure consistent suitability for formulation use in veterinary pharmaceutical manufacturing.
- Validated analytical methods used for key parameters
- Batch records and retained samples maintained for traceability
- Custom packaging and handling options available
- Samples can be arranged for laboratory evaluation
Applications
- Formulation Use: Toltrazuril is commonly utilized by veterinary pharmaceutical manufacturers as an API for developing solid products such as premix, granules, and powder-based preparations.
- Processing Behavior: The powder exhibits good stability and predictable flow characteristics during blending, mixing, and granulation, supporting efficient production workflows.
- Compatibility: Its crystalline structure and impurity limits enable consistent incorporation into multi-component formulations.
- R&D & Scale-up: Frequently used in formulation trials, performance studies, and optimization of manufacturing processes.
- Manufacturing Advantages: Suitable for plants requiring controlled particle size, robust stability, and reproducible quality parameters.
Product FAQ
What is Toltrazuril used for in the manufacturing process?
It is used as a veterinary API raw material in the production of solid and suspension-type formulations by pharmaceutical manufacturers.
Why is Toltrazuril suitable for solid formulation development?
Its stable crystalline nature and controlled impurity profile allow consistent processing during blending, granulation, and content uniformity control.
What purity specification is commonly required?
Manufacturers usually work with material that meets a minimum purity of 98.0% (HPLC), ensuring reliable performance during formulation.
Can Toltrazuril be customized for particle size?
Yes, particle size distribution can be adjusted to meet specific formulation or processing requirements.
What information is helpful when requesting a quotation?
Please indicate the required quantity, preferred packaging, particle size needs, and destination country to recommend suitable logistics arrangements.
Q1. How can I request a quotation or sample?
You can click the “Send Inquiry” button on this page or email us directly at [email protected].
Samples are available for most products, and our sales team will reply within 24 hours with detailed pricing and documentation .
Q2. What is the minimum order quantity (MOQ)?
The MOQ is 0.5 kg for most products.
For laboratory evaluation or small trial batches, smaller quantities can be arranged depending on stock availability.
Q3. What certifications do your products comply with?
Our GMP-certified partners operate under ISO, CEP, and FSC standards.
Each batch is supplied with a full set of COA, MSDS, and export documents to ensure quality traceability.
Q4. How long does delivery take?
Usually 3–7 working days for available stock and 2–3 weeks for customized specifications or large orders.
Q5. Which payment methods do you accept?
We accept T/T, L/C, and other agreed terms depending on the order volume and region.
Q6. Can you provide contract manufacturing or custom formulation support?
Yes. We cooperate with multiple GMP facilities to offer custom synthesis, formulation, and registration support for specific markets.
Packaging Information
Standard packing: 25 kg fiber drum or 1 kg foil bag
Double PE inner liner for moisture protection
Custom packaging available on request
Storage & Stability
Store in a cool, dry environment away from direct light. Shelf life 24 months under recommended conditions.
Transportation
Shipped by air, sea, or express according to customer preference. Dangerous goods comply with IATA/IMDG standards if applicable.
Our company and partner facilities hold valid GMP and ISO certificates issued by national authorities, ensuring that every batch meets strict quality and traceability standards required for international veterinary API markets.
You Might Also Like
Tylosin Tartrate Soluble Powder 50%
CAS No. None
Doxycycline Hyclate
CAS No. 24390-14-5
Tylosin Tartrate Powder
CAS No. 1405-54-5
Tilmicosin Phosphate
CAS No. 137330-13-3
Florfenicol
CAS No. 73231-34-2
Tiamulin Fumarate
CAS No. 55297-96-6