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Azaperol CAS NO 2804-05-9
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CAS No.:2804-05-9
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Azaperol is a potent sedative and tranquilizer belonging to the butyrophenone class of neuroleptic agents. This compound is of significant commercial importance for its reliable and rapid calming effects in veterinary medicine, particularly for managing aggressive behavior and facilitating handling. It is primarily utilized by manufacturers of veterinary pharmaceuticals and large-scale animal farming operations for the safe restraint of swine and other livestock during transport, medical procedures, and management.
Application
- Veterinary Sedation: Primary use for the sedation and tranquilization of pigs to minimize stress and prevent injury during handling, transport, or veterinary interventions.
- Animal Restraint: Facilitates safe and humane restraint of aggressive or large animals for diagnostic procedures, hoof trimming, or minor surgeries.
- Pre-Anesthetic Medication: Used as a pre-medication agent to calm animals prior to the induction of general anesthesia, reducing the required dose of anesthetic agents.
- Stress Reduction in Livestock: Administered to manage acute stress episodes in livestock, improving animal welfare and preventing physical damage caused by panic.
- Veterinary Pharmaceutical Formulation: Serves as the active pharmaceutical ingredient (API) in injectable solutions and other formulations for veterinary use.
- Research & Development: Used in pharmacological and toxicological studies within veterinary science and comparative medicine research.
Basic Information
| Product Name | Azaperol |
| CAS No. | 2804-05-9 |
| Molecular Formula | C19H23FN2O |
| Molecular Weight | 314.40 g/mol |
| Synonyms | Stresnil; Azaperone; R-1929; 1-(4-Fluorophenyl)-4-[4-(2-pyridinyl)-1-piperazinyl]-1-butanone; 4'-Fluoro-4-[4-(2-pyridinyl)-1-piperazinyl]butyrophenone; Azaporone; Suicalm |
| EINECS | 220-548-1 |
Quality Control
Our Azaperol is manufactured under strict quality management systems to ensure batch-to-batch consistency and reliability. We provide material that meets high-purity standards suitable for pharmaceutical formulation. Comprehensive testing includes identification, assay, and impurity profiling. A Certificate of Analysis (COA) detailing all specifications and test results is provided with each shipment to support your quality assurance protocols.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive); keep the container tightly sealed in a dry environment to prevent degradation.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to reference spectrum |
| Identification (HPLC) | Retention time corresponds to reference standard |
| Assay (HPLC) | 98.0% - 102.0% (on anhydrous basis) |
| Water Content (KF) | ≤ 1.0% |
| Residue on Ignition | ≤ 0.1% |
| Related Substances (HPLC) | Individual impurity ≤ 0.5%; Total impurities ≤ 1.5% |
| Heavy Metals | ≤ 20 ppm |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
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