Description

Bendazac L-Lysine is a non-steroidal anti-inflammatory drug (NSAID) salt, combining the active pharmaceutical ingredient bendazac with the essential amino acid L-lysine to enhance solubility and bioavailability. This compound is valued for its anti-inflammatory and analgesic properties, making it a critical intermediate in advanced pharmaceutical synthesis. It is primarily required by manufacturers in the pharmaceutical industry for the development of ophthalmic solutions and topical formulations targeting inflammatory conditions.

Application

• Active Pharmaceutical Ingredient (API) for anti-inflammatory and analgesic medications.
• Key Intermediate in the synthesis of ophthalmic drugs for treating cataracts and ocular inflammation.
• Formulation Component in topical creams and gels for dermatological applications.
• Research & Development chemical for pharmacological studies and new drug discovery.
• Reference Standard for quality control and analytical testing in pharmaceutical laboratories.

Basic Information

Product Name	Bendazac L-Lysine
CAS No.	81919-14-4
Molecular Formula	C19H27N3O5
Molecular Weight	377.44 g/mol
Synonyms	Bendazac Lysinate; L-Lysine Bendazac Salt; 1-[Benzyl(1H-indazol-3-yl)acetyl]-L-lysine; Bendazac Lysine Salt; Bendazac Mono-L-Lysine Salt; AF 983; Bendazac Lysine; Bendazac L-Lysine Salt
EINECS	Contact for details

Quality Control

Our Bendazac L-Lysine is manufactured under strict quality management systems to ensure high purity and batch-to-batch consistency. The product is suitable for use in pharmaceutical applications and is tested against rigorous in-house specifications. A comprehensive Certificate of Analysis (COA), detailing purity, identity, and impurity profiles, 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 a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.5%
Water Content (KF)	≤ 2.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 1.5% Any single impurity ≤ 0.5%

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