Description

Tiludronic Acid CAS NO 89987-06-4 is a potent bisphosphonate compound belonging to the class of drugs used to regulate bone metabolism. This active pharmaceutical ingredient (API) is valued for its targeted action in inhibiting osteoclast-mediated bone resorption. It is primarily required by pharmaceutical manufacturers for the formulation of medications treating bone disorders such as Paget's disease and osteoporosis in veterinary and human medicine.

Application

• Pharmaceutical API: Core active ingredient in prescription medications for treating Paget's disease of bone.
• Osteoporosis Management: Used in the development of therapeutic agents to prevent and treat bone loss and fractures.
• Veterinary Pharmaceuticals: Incorporated into treatments for bone resorptive disorders in animals, particularly in equine medicine.
• Research & Development: Serves as a critical reference standard and biochemical tool in metabolic bone disease research.
• Formulation Development: Used in the development of various dosage forms, including tablets and injectables.

Basic Information

Product Name	Tiludronic Acid
CAS No.	89987-06-4
Molecular Formula	C7H9ClNO7P2S
Molecular Weight	361.60 g/mol
Synonyms	Tiludronate; Tiludronic Acid Disodium; (4-Chlorophenyl)thio-methylene-1,1-bisphosphonic Acid; SR-41319; CAS 89987-06-4; Tiludronate Disodium; Tiludronic Acid Monohydrate
EINECS	Contact for details

Quality Control

Our Tiludronic Acid is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical use. Certificates of Analysis (COA) documenting identity, purity, and impurity profiles are provided with every shipment to ensure traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption, which can affect stability.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference standard
Assay (HPLC)	≥ 98.0%
Water Content (KF)	≤ 2.0%
Heavy Metals	≤ 20 ppm
Residue on Ignition	≤ 0.5%
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 2.0%

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