Description

3,4-Dihydro-7-Hydroxy-1-(2-Piperidinopropyl)Carbostyril is a high-purity synthetic organic compound belonging to the carbostyril class, serving as a crucial advanced pharmaceutical intermediate. Its value lies in its role as a key building block for the synthesis of complex active pharmaceutical ingredients (APIs), particularly in therapeutic areas requiring specific receptor targeting. This compound is essential for research institutions and manufacturers in the pharmaceutical and fine chemical industries engaged in developing new drug candidates and scaling up production processes.

Application

• Pharmaceutical Intermediate: Primary use as a critical building block in the synthesis of novel drug candidates, particularly those targeting neurological or cardiovascular systems.
• API Synthesis: Key precursor in the multi-step manufacturing process of complex Active Pharmaceutical Ingredients (APIs).
• Medicinal Chemistry Research: Used in R&D laboratories for structure-activity relationship (SAR) studies and lead optimization.
• Process Development: Serves as a standard or starting material for developing and optimizing scalable synthetic routes in pilot plants.
• Reference Standard: Can be supplied as a high-purity analytical standard for quality control and method validation in pharmaceutical analysis.
• Fine Chemical Production: Utilized in the synthesis of other specialized fine chemicals and complex organic molecules.

Basic Information

Product Name	3,4-Dihydro-7-Hydroxy-1-(2-Piperidinopropyl)Carbostyril
CAS No.	98067-16-4
Molecular Formula	C₁₇H₂₄N₂O₂
Molecular Weight	288.39 g/mol
Synonyms	7-Hydroxy-1-(2-piperidinopropyl)-3,4-dihydrocarbostyril; 1-(2-Piperidinopropyl)-7-hydroxy-3,4-dihydro-2(1H)-quinolinone; 7-Hydroxy-1-[2-(1-piperidinyl)propyl]-3,4-dihydro-2(1H)-quinolinone; Carbostyril 98067-16-4; DHPC Intermediate; 3,4-Dihydro-7-hydroxy-1-(2-piperidinopropyl)-2(1H)-quinolinone
EINECS	Contact for details

Quality Control

Our 3,4-Dihydro-7-Hydroxy-1-(2-Piperidinopropyl)Carbostyril is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC for purity, to ensure it meets the high standards required for pharmaceutical intermediate applications. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment. We support compliance with cGMP and ICH guidelines for pharmaceutical development.

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). Keep the container tightly sealed to protect from moisture. Store away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Conforms to reference
Assay (HPLC)	≥98.0%
Related Substances (HPLC)	Total impurities ≤2.0%
Loss on Drying	≤0.5%
Residue on Ignition	≤0.1%

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