Description

4,5,6,7-Tetrahydro-1H-Pyrazolo[3,4-C]Pyridine Hcl is a high-purity pharmaceutical intermediate and heterocyclic building block of significant importance in modern organic synthesis. This compound is valued for its role as a key precursor in the research and development of novel active pharmaceutical ingredients (APIs), particularly in central nervous system (CNS) and oncology therapeutic areas. It is primarily sought after by pharmaceutical R&D laboratories, contract research and manufacturing organizations (CROs/CMOs), and fine chemical suppliers engaged in advanced medicinal chemistry.

Application

• Pharmaceutical Intermediate: A critical building block for the synthesis of novel drug candidates, especially in neurological and psychiatric disorder research.
• Medicinal Chemistry Research: Used in structure-activity relationship (SAR) studies and lead optimization for developing new therapeutic agents.
• API Synthesis: Serves as a core scaffold in the multi-step synthesis of complex Active Pharmaceutical Ingredients (APIs).
• Biochemical Tool Compound: Utilized in biochemical assays and as a reference standard in pharmacological studies.
• Contract Manufacturing: Supplied to CROs and CMOs for custom synthesis and scale-up projects under GMP or non-GMP conditions.
• Academic Research: Employed in university and institutional laboratories for exploratory organic synthesis and heterocyclic chemistry.

Basic Information

Product Name	4,5,6,7-Tetrahydro-1H-Pyrazolo[3,4-C]Pyridine Hcl
CAS No.	879668-17-4
Molecular Formula	C7H12ClN3
Molecular Weight	173.64 g/mol
Synonyms	1H-Pyrazolo[3,4-c]pyridine, 4,5,6,7-tetrahydro-, hydrochloride; 4,5,6,7-Tetrahydro-1H-pyrazolo[3,4-c]pyridine hydrochloride; 879668-17-4; Pyrazolopyridine hydrochloride derivative; Tetrahydro-pyrazolopyridine HCl; 1H-Pyrazolo[3,4-c]pyridine, 4,5,6,7-tetrahydro-, monohydrochloride
EINECS	Contact for details

Quality Control

Our 4,5,6,7-Tetrahydro-1H-Pyrazolo[3,4-C]Pyridine Hcl is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC for purity, NMR and IR for structural confirmation, and residual solvent analysis, to ensure it meets the high standards required for pharmaceutical R&D. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment to guarantee traceability and batch-to-batch consistency.

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 in a dry environment to prevent moisture absorption, which can affect stability and handling properties. For long-term storage, consider using desiccants.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (NMR)	Conforms to structure
Assay (HPLC)	≥ 98.0%
Purity (HPLC)	≥ 97.0%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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