Description

Tetrazolast Meglumine [Usan] is a pharmaceutical-grade salt form of the active compound Tetrazolast, developed for enhanced solubility and stability in medicinal formulations. This compound is of significant interest for its targeted pharmacological activity and is a critical intermediate in advanced therapeutic research and development. It is primarily required by pharmaceutical R&D laboratories, contract manufacturing organizations (CMOs), and academic institutions engaged in developing novel therapeutic agents.

Application

• Pharmaceutical Intermediate: Serves as a key building block in the synthesis of advanced active pharmaceutical ingredients (APIs) for clinical research.
• Preclinical & Clinical Research: Used in formulation studies for injectable or oral dosage forms during drug discovery and development phases.
• Reference Standard: Employed as a high-purity analytical standard in quality control (QC) and quality assurance (QA) laboratories for method development and validation.
• Biochemical Research: Utilized in pharmacological studies to investigate specific receptor interactions and metabolic pathways.
• Process Development: Acts as a model compound for scaling up synthesis and purification processes in pilot plants.

Basic Information

Product Name	Tetrazolast Meglumine [Usan]
CAS No.	133008-33-0
Molecular Formula	C15H21N5O5 • C7H17NO5
Molecular Weight	543.55 g/mol
Synonyms	Tetrazolast Meglumine; Tetrazolast meglumine salt; 1-Deoxy-1-(methylamino)-D-glucitol Tetrazolast; USAN Tetrazolast Meglumine; Tetrazolast N-Methylglucamine Salt; Meglumine Tetrazolast; Tetrazolast (USAN) Meglumine; Tetrazolast compound with 1-deoxy-1-(methylamino)-D-glucitol (1:1)
EINECS	Contact for details

Quality Control

Our Tetrazolast Meglumine is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity suitable for research applications. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles. We adhere to cGMP guidelines where applicable, and our quality protocols are designed to meet the stringent requirements of pharmaceutical development.

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 (moisture-sensitive) nature, the container must be kept tightly sealed in a dry environment to prevent degradation. For long-term storage, consider using desiccants.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Water Content (KF)	≤ 2.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%

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