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Venostatin CAS NO 56575-31-6


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CAS No.:56575-31-6

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Venostatin is a high-purity pharmaceutical intermediate and active ingredient, identified by CAS NO 56575-31-6. This compound is critical for ensuring the efficacy and consistency of advanced therapeutic formulations. It is primarily utilized by manufacturers in the pharmaceutical and biotechnology sectors for the development and production of specialized medications.

Application

  • Key intermediate in the synthesis of novel pharmaceutical actives.
  • Research and development of vascular and circulatory system therapeutics.
  • Production of reference standards for analytical and quality control laboratories.
  • Formulation of clinical trial materials for new drug applications.
  • Manufacturing of high-value fine chemicals and specialty APIs.
  • Biochemical research involving enzyme inhibition studies.

Basic Information

Product Name Venostatin
CAS No. 56575-31-6
Molecular Formula C13H16N2O3S
Molecular Weight 280.34 g/mol
Synonyms Venostatin; 56575-31-6; 7-(2-Aminoethyl)-4-methyl-2H-1,3-benzothiazin-2-one; Troxerutin Impurity; Troxerutin Related Compound A; Venoruton Impurity; Hydroxyethylrutoside Impurity
EINECS Contact for details

Quality Control

Our Venostatin is manufactured under strict quality management systems. Every batch undergoes comprehensive analytical testing to ensure it meets the high-purity standards required for pharmaceutical applications. A Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with each shipment to guarantee traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at 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.

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%
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Water Content (KF) ≤ 1.0%
Residue on Ignition ≤ 0.1%

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

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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

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