Description

4-[1-Hydroxy-2-([1-Methylethyl]Amino)Butyl]-1,2-Benzenediol Methanesulfonate is a high-purity chemical intermediate and active pharmaceutical ingredient (API) salt form, known for its critical role in the synthesis of specific cardiovascular agents. This compound matters for its precise chemical structure, which is essential for achieving desired pharmacological activity and stability in final drug formulations. It is primarily needed by pharmaceutical manufacturers, research institutions, and fine chemical producers engaged in the development and production of advanced therapeutic agents.

Application

• Pharmaceutical Intermediate: Serves as a key building block in the synthesis of specific β-adrenergic receptor agonists and related cardiovascular drugs.
• Active Pharmaceutical Ingredient (API) Synthesis: Used in the final chemical steps to produce the methanesulfonate salt form of target APIs, enhancing stability and bioavailability.
• Biochemical Research: Employed in preclinical and pharmacological studies to investigate adrenergic pathways and receptor interactions.
• Reference Standard: Utilized as a high-purity analytical standard in quality control laboratories for method development and validation.
• Process Development: Applied in scaling up and optimizing synthetic routes within process chemistry and chemical engineering.

Basic Information

Product Name	4-[1-Hydroxy-2-([1-Methylethyl]Amino)Butyl]-1,2-Benzenediol Methanesulfonate
CAS No.	7279-75-6
Molecular Formula	C14H23NO6S
Molecular Weight	333.40 g/mol
Synonyms	Isoprenaline Mesylate; Isoproterenol Mesylate; Isoprenaline Methanesulfonate; Isoproterenol Methanesulfonate; 1-(3,4-Dihydroxyphenyl)-2-isopropylamino-1-butanol Methanesulfonate; DL-Isoproterenol Methanesulfonate; 3,4-Dihydroxy-α-[(isopropylamino)methyl]benzyl Alcohol Methanesulfonate
EINECS	Contact for details

Quality Control

Our 4-[1-Hydroxy-2-([1-Methylethyl]Amino)Butyl]-1,2-Benzenediol Methanesulfonate is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. Certificates of Analysis (COA) detailing identity, purity, and impurity profiles are provided and can be tailored to meet specific pharmacopeial (e.g., USP, EP) or customer requirements.

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). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥98.0%
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.