Description

Enolicam is a high-purity pharmaceutical intermediate and active ingredient, identified by CAS NO 59755-82-7. This compound is critical for the synthesis of advanced non-steroidal anti-inflammatory drugs (NSAIDs) and other therapeutic agents. It is primarily required by pharmaceutical manufacturers and advanced research institutions engaged in drug development and production.

Application

• Key intermediate in the synthesis of Piroxicam and related enolic acid class NSAIDs.
• Active Pharmaceutical Ingredient (API) for anti-inflammatory and analgesic formulations.
• Precursor in the research and development of novel COX-2 inhibitors.
• Reference standard for analytical method development and quality control in pharmaceutical laboratories.
• Building block for specialized fine chemicals and advanced organic synthesis.
• Used in academic and industrial research for studying structure-activity relationships (SAR) in medicinal chemistry.

Basic Information

Product Name	Enolicam
CAS No.	59755-82-7
Molecular Formula	C₁₅H₁₃N₃O₄S
Molecular Weight	331.35 g/mol
Synonyms	4-Hydroxy-2-methyl-N-(2-pyridinyl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide; Piroxicam Intermediate; CP-16171; Felden Intermediate; 2H-1,2-Benzothiazine-3-carboxamide, 4-hydroxy-2-methyl-N-2-pyridinyl-, 1,1-dioxide; Enolic Acid of Piroxicam; 4-Hydroxy-1,1-dioxo-2-methyl-1,2-dihydro-1λ⁶,2-benzothiazine-3-carboxylic acid 2-pyridylamide
EINECS	Contact for details

Quality Control

Our Enolicam is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, IR for identification, and residual solvent analysis, to ensure it meets stringent pharmaceutical-grade specifications. Certificates of Analysis (COA) are provided with every shipment, and we support compliance with cGMP, ICH Q7, and relevant pharmacopoeial standards.

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 nature, the container must be kept tightly sealed to exclude moisture. Keep away from incompatible materials.

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
Residual Solvents (GC)	Complies with ICH Q3C guidelines

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