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3-Spiral Indole-4-Piperidine CAS NO 19136-10-8


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CAS No.:19136-10-8

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

3-Spiral Indole-4-Piperidine is a high-purity, advanced pharmaceutical intermediate characterized by its unique fused heterocyclic structure. This compound matters for its critical role as a sophisticated building block in modern medicinal chemistry, enabling the synthesis of complex molecules with targeted biological activity. Pharmaceutical R&D teams and fine chemical manufacturers need it for developing new therapeutic agents, particularly in central nervous system (CNS) and oncology research pipelines.

Application

  • Pharmaceutical Intermediate: A key precursor in the synthesis of novel drug candidates targeting specific receptors.
  • Medicinal Chemistry Research: Serves as a versatile scaffold for constructing complex molecular libraries in drug discovery programs.
  • CNS Drug Development: Used in the research and development of potential therapeutics for neurological and psychiatric disorders.
  • Oncological Agent Synthesis: Employed as a building block for creating potential small-molecule inhibitors and targeted cancer therapies.
  • Chemical Biology Probes: Utilized in the design of tool compounds for studying biological pathways and protein function.
  • Contract Research & Manufacturing (CRAM): Supplied to organizations engaged in custom synthesis and process development for clinical trial materials.

Basic Information

Product Name 3-Spiral Indole-4-Piperidine
CAS No. 19136-10-8
Molecular Formula C13H14N2
Molecular Weight 198.26 g/mol
Synonyms 3-Spiroindole-4-piperidine; 4-Piperidine-3-spiroindole; 1,2,3,4-Tetrahydrospiro[cyclopenta[b]indole-3,4'-piperidine]; Spiro[indole-3,4'-piperidine]; 19136-10-8; 3-Spiro(cyclopenta[b]indole)piperidine; Tetrahydrospiro(cyclopentaindole-3,4-piperidine)
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Quality Control

Our 3-Spiral Indole-4-Piperidine is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. Production adheres to cGMP guidelines where applicable, and each lot is supported by a comprehensive Certificate of Analysis (COA). The QC process includes rigorous identity confirmation, purity assessment, and impurity profiling to meet the exacting standards of pharmaceutical development.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (15-25°C). Keep the container sealed to protect from moisture and contamination.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to reference spectrum
Purity (HPLC) ≥ 98.0%
Loss on Drying ≤ 0.5%
Residue on Ignition ≤ 0.1%
Heavy Metals ≤ 10 ppm

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

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