Description

Tripelennamine Citrate is the citrate salt form of the first-generation ethylenediamine-class H1-antihistamine. This compound is valued for its reliable antagonistic activity against histamine H1 receptors, making it a key intermediate in pharmaceutical research and development. It is primarily utilized by manufacturers and research institutions in the life sciences sector for developing therapeutic agents and conducting pharmacological studies.

Application

• Pharmaceutical Intermediate: Serves as a critical building block in the synthesis of antihistamine APIs (Active Pharmaceutical Ingredients).
• Pharmacological Research: Used in preclinical studies to investigate histamine receptor pathways and allergic response mechanisms.
• Reference Standard: Employed as an analytical standard in quality control laboratories for method development and validation.
• Chemical Synthesis: Acts as a starting material or intermediate for the preparation of more complex therapeutic molecules.

Basic Information

Product Name	Tripelennamine Citrate
CAS No.	6138-56-3
Molecular Formula	C16H21N3·C6H8O7
Molecular Weight	447.46 g/mol
Synonyms	Pyribenzamine Citrate; N-Benzyl-N',N'-dimethyl-N-2-pyridylethylenediamine Citrate; 2-[(Benzyl)(2-dimethylaminoethyl)amino]pyridine Citrate; Tripelemin Citrate; PBZ Citrate; Tripelennamine Acid Citrate
EINECS	Contact for details

Quality Control

Our Tripelennamine Citrate is produced under a rigorous quality management system. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. A Certificate of Analysis (COA) detailing specifications such as assay, related substances, and residual solvents is provided with every shipment to support your quality assurance protocols.

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). The material is hygroscopic (moisture-sensitive); keep the container tightly sealed when not in use.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥98.0%
Related Substances (HPLC)	Total impurities ≤2.0%
Loss on Drying	≤1.0%
Residue on Ignition	≤0.1%

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