Description

Lornoxicam is a potent non-steroidal anti-inflammatory drug (NSAID) belonging to the oxicam class, widely recognized for its analgesic and anti-inflammatory properties. Its primary commercial value lies in its effectiveness in managing moderate to severe pain and inflammation, offering a critical active pharmaceutical ingredient (API) for pharmaceutical formulations. This compound is essential for manufacturers in the global pharmaceutical industry developing prescription medications for conditions such as osteoarthritis, rheumatoid arthritis, and postoperative pain.

Application

• Pharmaceutical API: Primary use as the active ingredient in solid oral dosage forms (tablets, capsules) for pain and inflammation management.
• Analgesic Formulations: Development of prescription-strength analgesic drugs targeting acute and chronic pain conditions.
• Anti-inflammatory Medications: Key component in drugs designed to reduce inflammation associated with musculoskeletal disorders.
• Postoperative Care: Used in medications prescribed for pain relief following surgical procedures.
• R&D and Reference Standard: Serves as a high-purity chemical reference standard in analytical laboratories and pharmaceutical research.
• Generic Drug Manufacturing: Critical for producers of generic pharmaceutical products containing lornoxicam.

Basic Information

Product Name	Lornoxicam
CAS No.	70374-39-9
Molecular Formula	C13H10ClN3O4S2
Molecular Weight	371.82 g/mol
Synonyms	Chlortenoxicam; 6-Chloro-4-hydroxy-2-methyl-N-2-pyridinyl-2H-thieno[2,3-e]-1,2-thiazine-3-carboxamide 1,1-dioxide; Ro 13-9297; TS-110; Xefo; Telos
EINECS	Contact for details

Quality Control

Our Lornoxicam is manufactured under strict quality management systems to ensure it meets the high standards required for pharmaceutical applications. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling via advanced techniques like HPLC. We provide Certificates of Analysis (COA) with each shipment, detailing compliance with in-house specifications aligned with major pharmacopeial guidelines. Our commitment to cGMP (current Good Manufacturing Practice) principles ensures consistent quality, traceability, and reliability for our global B2B partners.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed to prevent degradation from atmospheric moisture. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to almost white crystalline powder
Identification (IR)	Conforms
Identification (HPLC)	Conforms
Assay (HPLC)	98.0% - 102.0%
Related Substances (HPLC)	Total impurities ≤ 1.0% Any individual impurity ≤ 0.5%
Loss on Drying	≤ 1.0%
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.