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Salbutamon Hydrochloride CAS NO 41489-89-8


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CAS No.:41489-89-8

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Salbutamon Hydrochloride is a high-purity pharmaceutical intermediate and active ingredient, essential for the synthesis of specialized therapeutic agents. Its consistent quality and reliable supply are critical for manufacturers requiring precise chemical building blocks in regulated environments. This compound is primarily utilized by the pharmaceutical and advanced research sectors for the development and production of active pharmaceutical ingredients (APIs).

Application

  • Pharmaceutical Intermediate: A key building block in the synthesis of active pharmaceutical ingredients (APIs) for respiratory and other therapeutic areas.
  • Research & Development: Used in laboratory settings for pharmacological studies, metabolic pathway research, and the development of new drug candidates.
  • Reference Standard: Serves as a high-purity analytical standard for quality control and method validation in pharmaceutical analysis.
  • Chemical Synthesis: Employed in organic synthesis for the introduction of specific functional groups in complex molecule construction.

Basic Information

Product Name Salbutamon Hydrochloride
CAS No. 41489-89-8
Molecular Formula C13H21NO3 • HCl
Molecular Weight 275.77 g/mol (as hydrochloride salt)
Synonyms Salbutamol Hydrochloride; Albuterol Hydrochloride; (±)-Salbutamol Hydrochloride; 2-(tert-Butylamino)-1-(4-hydroxy-3-hydroxymethylphenyl)ethanol hydrochloride; Ventolin Hydrochloride (as API); AH-3365; (±)-α-[(tert-Butylamino)methyl]-4-hydroxy-m-xylene-α,α'-diol hydrochloride
EINECS Contact for details

Quality Control

Our Salbutamon Hydrochloride is manufactured under strict quality management systems to ensure it meets the high standards required for pharmaceutical applications. Each batch undergoes comprehensive analytical testing, including identification, assay, and impurity profiling. Certificates of Analysis (COA) detailing all test results are provided and can be tailored to meet specific pharmacopoeial requirements such as USP or EP.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed after opening to prevent moisture absorption, which can affect stability and handling properties.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time corresponds to reference standard
Assay (HPLC) 98.0% - 102.0% (on anhydrous basis)
Water Content (KF) ≤ 1.0%
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.

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

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