Description

Carbinoxamine Maleate Salt is a pharmaceutically active compound, specifically an ethanolamine-class antihistamine. This high-purity chemical is essential for research and development in the pharmaceutical sector, where precise and reliable active pharmaceutical ingredients (APIs) are critical. It is primarily utilized by pharmaceutical manufacturers and research institutions for the development and production of antihistamine formulations.

Application

• Pharmaceutical API: Primary use as an active pharmaceutical ingredient in antihistamine medications.
• Clinical Research: Used in preclinical and clinical studies to investigate antihistaminic effects and therapeutic efficacy.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method validation in laboratories.
• Formulation Development: Key component in the R&D of solid dosage forms (e.g., tablets) and other drug delivery systems.
• Biochemical Research: Tool compound for studying histamine H1 receptor antagonism and related physiological pathways.

Basic Information

Product Name	Carbinoxamine Maleate Salt
CAS No.	3505-38-2
Molecular Formula	C16H19ClN2O · C4H4O4
Molecular Weight	406.86 g/mol
Synonyms	Carbinoxamine Maleate; Histex; CLC; Clistin; 2-[(4-Chlorophenyl)(pyridin-2-yl)methoxy]-N,N-dimethylethanamine (Z)-butenedioate; Allergefon; Carbinoxamini Maleas; Polistin
EINECS	Contact for details

Quality Control

Our Carbinoxamine Maleate Salt is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling, to ensure it meets high-grade pharmaceutical standards. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and compliance.

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 (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to 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)	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.