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Mabuterol Hydrochloride CAS NO 95656-55-6


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CAS No.:95656-55-6

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Mabuterol Hydrochloride CAS NO 95656-55-6 is a selective β-2 adrenergic receptor agonist, a key pharmaceutical intermediate and active ingredient. This compound matters for its critical role in the synthesis of advanced bronchodilator medications, offering a pathway to targeted therapeutic development. It is primarily needed by pharmaceutical manufacturers and research institutions focused on developing treatments for respiratory conditions such as asthma and chronic obstructive pulmonary disease (COPD).

Application

  • Pharmaceutical Intermediate: Primary use in the synthesis of advanced bronchodilator drugs and respiratory therapeutics.
  • Active Pharmaceutical Ingredient (API): Serves as the core active component in formulated respiratory medications.
  • Biochemical Research: Used as a reference standard and tool compound in pharmacological studies of β-2 adrenergic receptors.
  • Veterinary Medicine Development: Potential application in developing treatments for respiratory ailments in animals.
  • Process Development & Scale-up: Employed in R&D for optimizing synthetic routes and manufacturing processes.
  • Analytical Standard: Serves as a high-purity standard for quality control and method validation in analytical laboratories.

Basic Information

Product Name Mabuterol Hydrochloride
CAS No. 95656-55-6
Molecular Formula C13H19Cl2N3O2
Molecular Weight 328.21 g/mol
Synonyms Mabuterol HCl; 4-Amino-α-[(tert-butylamino)methyl]-3,5-dichlorobenzyl alcohol hydrochloride; 3,5-Dichloro-α-[[(1,1-dimethylethyl)amino]methyl]-4-hydroxybenzenemethanamine hydrochloride; Mabuterol HCL; Mabuterol Hydrochloride (USP); Mabuterol Monohydrochloride; Mabuterol HCl (JP)
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Quality Control

Our Mabuterol Hydrochloride is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC for purity, identification by IR and NMR spectroscopy, and tests for residual solvents and related substances to ensure compliance with pharmaceutical-grade standards. Certificates of Analysis (COA) detailing all specifications are available upon request.

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 to prevent moisture absorption. Keep away from incompatible materials.

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%
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Heavy Metals ≤ 20 ppm

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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Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.