Description

Risedremate Sodium is a high-purity pharmaceutical intermediate and active ingredient. This compound is critical for ensuring the efficacy and consistency of advanced therapeutic formulations. It is primarily utilized by research institutions and manufacturers in the pharmaceutical and biotechnology sectors for the development and production of novel drug substances.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of active pharmaceutical ingredients (APIs) for various therapeutic areas.
• Research & Development: Used in laboratory settings for pharmacological studies, metabolic pathway research, and the discovery of new drug candidates.
• Bioconjugation: Potential use in the development of antibody-drug conjugates (ADCs) and other targeted drug delivery systems.
• Process Chemistry: Employed in scale-up and optimization of manufacturing processes under current Good Manufacturing Practices (cGMP).
• Reference Standard: Serves as an analytical standard for quality control and regulatory compliance testing in pharmaceutical production.

Basic Information

Item	Detail
Product Name	Risedremate Sodium
CAS No.	329003-65-8
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Risedremate Sodium Salt; Sodium Risedremate; Risedremate Na; UNII-Contact for details; (Chemical IUPAC name - Contact for details)
EINECS	Contact for details

Quality Control

Our Risedremate Sodium is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets stringent specifications for identity, purity, and potency. A Certificate of Analysis (COA) documenting results from tests such as HPLC, NMR, and residual solvent analysis is provided with every shipment to guarantee traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (typically 15-25°C). This material is hygroscopic (moisture-sensitive) and should be handled under an inert atmosphere or in a dry environment to maintain stability.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference standard
Assay (HPLC)	≥98.0%
Related Substances (HPLC)	Total impurities ≤2.0%
Water Content (KF)	≤5.0%
Residual Solvents (GC)	Complies with ICH guidelines

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