Description

Dipivaloylisoproterenol is a synthetic chemical intermediate of significant importance in the pharmaceutical industry. This compound is valued for its role as a key precursor in the synthesis of specialized active pharmaceutical ingredients (APIs). It is primarily utilized by research institutions and manufacturers engaged in the development and production of advanced therapeutic agents, particularly within the cardiovascular and respiratory domains.

Application

• Pharmaceutical Intermediate: A critical building block in the synthesis of complex drug molecules and active pharmaceutical ingredients (APIs).
• Research & Development: Used in laboratory settings for pharmacological studies and the development of new therapeutic compounds.
• Cardiovascular Drug Synthesis: Serves as a precursor in the manufacturing of agents targeting heart and circulatory system conditions.
• Respiratory Drug Synthesis: Employed in the production chain for medications designed to treat asthma and other pulmonary disorders.
• Chemical Reference Standard: Can be utilized as a high-purity standard for analytical method development and quality control testing.

Basic Information

Product Name	Dipivaloylisoproterenol
CAS No.	65114-85-4
Molecular Formula	C18H27NO5
Molecular Weight	337.41 g/mol
Synonyms	Dipivaloyl Isoproterenol; Isoproterenol Dipivalate; 3,4-Dipivaloyloxy-α-[(isopropylamino)methyl]benzyl Alcohol; 1-(3,4-Bis(pivaloyloxy)phenyl)-2-(isopropylamino)ethanol; DIPI; Isoproterenol Di-pivalate Ester
EINECS	Contact for details

Quality Control

Our Dipivaloylisoproterenol is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing to ensure it meets high-purity standards suitable for pharmaceutical research and development. Certificates of Analysis (COA) detailing purity, identity, and impurity profiles are available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed to minimize exposure to atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%

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