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Salbutamol Sulfate CAS NO 39971-61-4


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CAS No.:39971-61-4

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Salbutamol Sulfate CAS NO 39971-61-4 is a selective β2-adrenergic receptor agonist widely recognized for its bronchodilatory effects. This active pharmaceutical ingredient (API) is critical for the formulation of respiratory medications that provide rapid relief from bronchospasm. It is essential for pharmaceutical manufacturers developing treatments for asthma, chronic obstructive pulmonary disease (COPD), and other respiratory conditions requiring immediate symptom management.

Application

  • Primary Pharmaceutical API: Core active ingredient in metered-dose inhalers (MDIs), dry powder inhalers (DPIs), and nebulizer solutions for asthma and COPD.
  • Tablet and Syrup Formulations: Used in oral dosage forms for the management and prevention of exercise-induced bronchoconstriction.
  • Veterinary Medicine: Employed in veterinary practice for the treatment of bronchoconstrictive conditions in animals.
  • Research and Development: Serves as a key reference standard and building block in pharmacological research for new respiratory therapeutics.
  • Compounding Pharmacy: Utilized by specialized pharmacies for preparing customized medication formulations for patients with specific needs.

Basic Information

Product Name Salbutamol Sulfate
CAS No. 39971-61-4
Molecular Formula C26H44N2O10S
Molecular Weight 576.71 g/mol
Synonyms Albuterol Sulfate; Salbutamol Sulphate; Ventolin® (brand name); Aironir; Aerolin; Asmavent; Proventil; (RS)-4-[2-(tert-Butylamino)-1-hydroxyethyl]-2-(hydroxymethyl)phenol sulfate
EINECS 254-692-5

Quality Control

Our Salbutamol Sulfate is manufactured under strict quality systems to meet the rigorous standards of the global pharmaceutical industry. We ensure compliance with major pharmacopoeial specifications, including USP, EP, and BP monographs. Every batch is supported by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles, confirming its suitability for use as a pharmaceutical active ingredient.

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 low-humidity environment to prevent degradation.

Specification

Item Specification
Appearance White or almost white, crystalline powder
Identification (IR) Conforms
Identification (HPLC) Retention time corresponds to reference standard
Assay (HPLC) 98.0% - 102.0% (on anhydrous basis)
Water (KF) ≤ 5.0%
Related Substances (HPLC) Individual impurity: ≤ 0.5% Total impurities: ≤ 2.0%
Sulfate 15.0% - 17.5%
Residue on Ignition ≤ 0.1%
Heavy Metals ≤ 20 ppm
Microbial Limits Meets EP/USP requirements

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

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