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Indacaterol Imrity CAS NO 1235445-80-3


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CAS No.:1235445-80-3

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Indacaterol Imrity is a long-acting β-2 adrenergic receptor agonist (LABA) pharmaceutical intermediate. This high-purity compound is critical for the synthesis of advanced respiratory medications targeting chronic obstructive pulmonary disease (COPD) and asthma. It is primarily utilized by pharmaceutical manufacturers and research institutions engaged in the development and production of innovative inhalation therapies.

Application

  • Active Pharmaceutical Ingredient (API) Synthesis: Key intermediate in the manufacturing of Indacaterol-based inhalation powders and solutions.
  • Respiratory Drug Development: Serves as a core building block in R&D for novel long-acting bronchodilators.
  • Pharmaceutical Research: Used in pharmacological studies and bioactivity assays related to β-2 adrenergic receptors.
  • Formulation Studies: Employed in the development and optimization of dry powder inhaler (DPI) and nebulizer formulations.
  • Reference Standard: Can be utilized as a high-purity analytical standard for quality control and method validation.
  • Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for scale-up and commercial production.

Basic Information

Product Name Indacaterol Imrity
CAS No. 1235445-80-3
Molecular Formula C24H28N2O3
Molecular Weight 392.49 g/mol
Synonyms Indacaterol Impurity; Indacaterol Related Compound; 5-[(1R)-2-[(5,6-Diethyl-2,3-dihydro-1H-inden-2-yl)amino]-1-hydroxyethyl]-8-hydroxyquinolin-2(1H)-one; (R)-5-(2-((5,6-Diethyl-2,3-dihydro-1H-inden-2-yl)amino)-1-hydroxyethyl)-8-hydroxyquinolin-2(1H)-one; UNII-7PJ49S6A1I
EINECS Contact for details

Quality Control

Our Indacaterol Imrity is manufactured under strict quality management systems. Each batch is subjected to comprehensive analytical testing, including HPLC for purity and identity confirmation, to ensure it meets the stringent requirements for pharmaceutical intermediates. Certificates of Analysis (COA) detailing all specifications and test results are provided with every 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 (HPLC) Conforms
Identification (IR) Conforms to reference spectrum
Assay (HPLC) ≥ 98.0%
Related Substances (HPLC) Individual impurity: ≤ 0.5% Total impurities: ≤ 1.5%
Residual Solvents (GC) Complies with ICH Q3C
Loss on Drying ≤ 0.5%

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

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