Description

Ampiroxicam is a non-steroidal anti-inflammatory drug (NSAID) prodrug and a key pharmaceutical intermediate. Its primary value lies in its conversion to the active metabolite piroxicam, offering a favorable pharmacokinetic profile for therapeutic use. This compound is essential for manufacturers in the pharmaceutical industry developing long-acting anti-inflammatory and analgesic formulations. Ampiroxicam CAS NO 99464-64-9 is critical for producing medications targeting conditions such as osteoarthritis and rheumatoid arthritis.

Application

• Pharmaceutical Active Ingredient (API): Serves as a prodrug for the synthesis of piroxicam, a potent NSAID.
• Anti-inflammatory Drug Manufacturing: A crucial intermediate in the production of long-acting oral medications for chronic inflammatory diseases.
• Analgesic Formulations: Used in the development of prescription-strength pain relief drugs.
• Veterinary Medicine: Applied in the creation of anti-inflammatory treatments for animals.
• Research & Development: Utilized in preclinical and clinical studies for novel NSAID delivery systems and efficacy testing.
• Reference Standard: Serves as a high-purity standard for quality control and analytical testing in regulatory compliance.

Basic Information

Product Name	Ampiroxicam
CAS No.	99464-64-9
Molecular Formula	C20H21N3O7S2
Molecular Weight	503.53 g/mol
Synonyms	4-Hydroxy-2-methyl-N-(5-methyl-3-isoxazolyl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide; Ampiroxicam; CP-65703; Piroxicam prodrug; Ampyrox; Ampirox; Ampiroxicamum; 2H-1,2-Benzothiazine-3-carboxamide, 4-hydroxy-2-methyl-N-(5-methyl-3-isoxazolyl)-, 1,1-dioxide
EINECS	Contact for details

Quality Control

Our Ampiroxicam is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC for purity and identity confirmation, to ensure it meets high-grade pharmaceutical standards. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing all specified parameters. Our quality commitment aligns with cGMP principles to support our clients' regulatory requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (typically 15-25°C). Keep away from heat and incompatible materials. The product is light-sensitive and should be stored away from light as indicated by its chemical properties.

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)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.5% Any single impurity ≤ 0.5%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.