share

Phenindamine Tartrate CAS NO 569-59-5


Unit Price:

CAS No.:569-59-5

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Phenindamine Tartrate is a pharmaceutically active salt form of the antihistamine phenindamine. This compound is valued for its specific pharmacological activity, primarily functioning as a histamine H1-receptor antagonist. It is a critical intermediate and active pharmaceutical ingredient (API) for the development and manufacturing of antihistamine medications. Industries requiring this material include pharmaceutical synthesis, research and development, and fine chemical production.

Application

  • Active Pharmaceutical Ingredient (API): Primary use in the formulation of antihistamine medications for allergy relief.
  • Pharmaceutical Intermediates: Serves as a key building block in the synthesis of more complex therapeutic agents.
  • Biochemical Research: Used in pharmacological studies to investigate histamine pathways and receptor antagonism.
  • Reference Standard: Employed as a certified reference material (CRM) in analytical laboratories for quality control and method validation.
  • Veterinary Pharmaceuticals: Potential application in the development of antihistamine treatments for animals.

Basic Information

Product Name Phenindamine Tartrate
CAS No. 569-59-5
Molecular Formula C20H24NO+ • C4H4O62- or C24H28NO7
Molecular Weight 442.48 g/mol
Synonyms Phenindamine Tartrate; Phenindamine Acid Tartrate; 2,3,4,9-Tetrahydro-2-methyl-9-phenyl-1H-indeno[2,1-c]pyridine Tartrate; Thephorin Tartrate; Phenylindane Tartrate; 1,2,3,4-Tetrahydro-2-methyl-9-phenyl-2-azafluorene Tartrate; N-(1,2,3,4-Tetrahydro-2-methyl-9-phenyl-2-azafluoren-9-yl)amine Tartrate
EINECS 209-320-0

Quality Control

Our Phenindamine Tartrate is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. Certificates of Analysis (COA) detailing purity, identity, and impurity profiles are provided with every shipment. We can support compliance with various pharmacopeial standards (e.g., USP, EP) upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and light-sensitive; therefore, containers must be kept tightly sealed and away from direct light exposure to maintain stability and purity.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time matches reference standard
Assay (HPLC) 98.0% - 102.0% (on anhydrous basis)
Water Content (KF) ≤ 1.0%
Residue on Ignition ≤ 0.1%
Heavy Metals ≤ 20 ppm
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 0.5%

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

Complete Your RFQ

0/ 2000

Why choose US

Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.