Description

Tricyclo[3.3.1.13,7]Decane-1-Acetic Acid, 3-[5-Chloro-4-(Cyclopropylamino)-6-Oxo-1(6H)-Pyridazinyl]- is a high-purity, advanced pharmaceutical intermediate with a complex polycyclic structure. This compound is critical for the synthesis of novel active pharmaceutical ingredients (APIs) targeting specific therapeutic pathways. It is primarily sought by research institutions and pharmaceutical manufacturers engaged in the development of new chemical entities, particularly in the areas of oncology and central nervous system (CNS) disorders.

Application

• Pharmaceutical Intermediate: Serves as a key building block in the synthesis of proprietary drug candidates, especially those with complex molecular architectures.
• Research & Development (R&D): Used in medicinal chemistry for structure-activity relationship (SAR) studies and lead optimization in drug discovery programs.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for the cGMP production of clinical trial materials and commercial APIs.
• Oncology Drug Development: Potential precursor in the synthesis of targeted cancer therapies due to its specific heterocyclic and amine functional groups.
• Chemical Reference Standard: Utilized as a high-purity analytical standard for quality control and method development in analytical laboratories.

Basic Information

Product Name	Tricyclo[3.3.1.13,7]Decane-1-Acetic Acid, 3-[5-Chloro-4-(Cyclopropylamino)-6-Oxo-1(6H)-Pyridazinyl]-
CAS No.	899386-23-3
Molecular Formula	C19H24ClN3O3
Molecular Weight	377.86 g/mol
Synonyms	3-[5-Chloro-4-(cyclopropylamino)-6-oxo-1,6-dihydropyridazin-1-yl]tricyclo[3.3.1.13,7]decane-1-acetic acid; 1-Adamantaneacetic acid, 3-[5-chloro-4-(cyclopropylamino)-6-oxo-1(6H)-pyridazinyl]-; 899386-23-3; Adamantyl-pyridazinone derivative; CP-AD Acid Derivative; API Intermediate 899386; Chlorocyclopropylamino Pyridazinone Adamantane Acetic Acid
EINECS	Contact for details

Quality Control

Our Tricyclo[3.3.1.13,7]Decane-1-Acetic Acid derivative is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation, to ensure it meets the stringent requirements for pharmaceutical R&D and cGMP manufacturing. Certificates of Analysis (COA) with detailed chromatographic data are provided for every shipment, ensuring full traceability and compliance with your internal quality standards.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (typically 15-25°C). This material may be hygroscopic; therefore, the container should be kept tightly sealed in a dry environment to prevent moisture uptake.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Any single impurity ≤ 0.5%
Total Impurities	≤ 2.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Water Content (KF)	≤ 0.5%

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