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2-Chloro-n-Piperidin-4-Yl-Isonicotinamide Hydrochloride CAS NO 1353951-89-9


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CAS No.:1353951-89-9

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

2-Chloro-n-Piperidin-4-Yl-Isonicotinamide Hydrochloride is a high-purity chemical building block and advanced pharmaceutical intermediate. This compound is critical for research and development in medicinal chemistry, particularly in the synthesis of novel therapeutic agents. It is primarily utilized by pharmaceutical R&D laboratories, contract research organizations (CROs), and fine chemical manufacturers focused on developing new drug candidates.

Application

  • Pharmaceutical Intermediate: A key building block in the synthesis of complex molecules for drug discovery and development programs.
  • Medicinal Chemistry Research: Used in structure-activity relationship (SAR) studies and the creation of targeted compound libraries.
  • API Synthesis: Serves as a precursor in the multi-step synthesis of potential Active Pharmaceutical Ingredients (APIs).
  • Biochemical Tool Compound: May be utilized in biochemical assays and as a probe for investigating biological pathways and target validation.
  • Custom Synthesis: Employed by fine chemical suppliers for the custom manufacturing of specialized compounds for clients.
  • Academic Research: Used in university and institutional laboratories for advanced organic synthesis and pharmacological studies.

Basic Information

Product Name 2-Chloro-n-Piperidin-4-Yl-Isonicotinamide Hydrochloride
CAS No. 1353951-89-9
Molecular Formula C11H15ClN3O • HCl
Molecular Weight 278.17 g/mol
Synonyms 2-Chloro-N-(piperidin-4-yl)isonicotinamide hydrochloride; 2-Chloro-N-(4-piperidinyl)isonicotinamide monohydrochloride; 4-Piperidinamine, N-(2-chloro-4-pyridinyl)carbonyl-, hydrochloride (1:1); Isonicotinamide, 2-chloro-N-4-piperidinyl-, hydrochloride; 1353951-89-9; UNII-8JQ7H0S6P9; 8JQ7H0S6P9
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Quality Control

Our 2-Chloro-n-Piperidin-4-Yl-Isonicotinamide Hydrochloride is manufactured under strict quality control protocols to ensure batch-to-batch consistency and high purity. We adhere to cGMP (current Good Manufacturing Practice) standards where applicable for pharmaceutical intermediates. Each batch is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles, 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 (typically 15-25°C). This product is hygroscopic (moisture-sensitive) and should be handled in a dry environment to prevent degradation.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to structure
Identification (HPLC) Conforms to reference standard
Assay (HPLC) ≥ 98.0%
Water Content (KF) ≤ 1.0%
Residue on Ignition ≤ 0.1%
Heavy Metals ≤ 20 ppm
Related Substances (HPLC) Individual impurity ≤ 0.5%; Total impurities ≤ 1.5%

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

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