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Indanazoline Hydrochloride CAS NO 56601-85-5


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CAS No.:56601-85-5

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Indanazoline Hydrochloride is a high-purity pharmaceutical intermediate and active pharmaceutical ingredient (API) with significant therapeutic relevance. Its primary value lies in its role as a key building block for the synthesis of advanced pharmaceutical compounds, particularly those targeting specific receptor pathways. This compound is essential for manufacturers and research institutions in the pharmaceutical, biotechnology, and fine chemical sectors engaged in the development and production of specialized active ingredients.

Application

  • Pharmaceutical Intermediate: A critical precursor in the multi-step synthesis of complex drug molecules and novel therapeutic agents.
  • Active Pharmaceutical Ingredient (API): Serves as the core active component in formulated pharmaceutical products, subject to strict Good Manufacturing Practice (GMP) standards.
  • Biochemical Research: Used as a reference standard and investigational compound in pharmacological studies and receptor binding assays.
  • Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for custom synthesis projects and scale-up production.
  • Analytical Standard: Provides a high-purity benchmark for quality control laboratories performing HPLC, LC-MS, or NMR analysis.

Basic Information

Product Name Indanazoline Hydrochloride
CAS No. 56601-85-5
Molecular Formula C16H15N3O • HCl
Molecular Weight 317.77 g/mol
Synonyms Indanazoline HCl; 2-[(4,5-Dihydro-1H-imidazol-2-yl)methyl]-2,3-dihydro-1H-inden-1-one hydrochloride; Indanazolinium chloride; 1H-Inden-1-one, 2,3-dihydro-2-[(4,5-dihydro-1H-imidazol-2-yl)methyl]-, hydrochloride; (RS)-Indanazoline hydrochloride
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Quality Control

Our Indanazoline Hydrochloride is manufactured under a quality management system and undergoes rigorous analytical testing to ensure batch-to-batch consistency and high purity. Specifications are designed to meet the demanding requirements of pharmaceutical applications. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with each shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and light-sensitive; containers must be kept tightly sealed after opening to minimize exposure to atmospheric moisture and light.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to structure
Identification (HPLC) Retention time matches reference standard
Assay (HPLC) ≥98.5%
Water Content (KF) ≤1.0%
Residue on Ignition ≤0.1%
Heavy Metals ≤20 ppm
Related Substances (HPLC) Individual impurity ≤0.5%; Total impurities ≤1.5%

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

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