Description

Xanthinol Nicotinate is a pharmaceutical-grade vasodilator compound that combines the properties of xanthinol and nicotinic acid. This product is valued for its role in improving peripheral and cerebral circulation by acting on the vascular system. It is primarily utilized in the formulation of prescription medications and advanced research applications within the pharmaceutical and life science sectors.

Application

• Active Pharmaceutical Ingredient (API) in vasodilator medications.
• Key intermediate in the synthesis of specialized cardiovascular drugs.
• Research chemical for studying peripheral and cerebral blood flow mechanisms.
• Component in clinical research for metabolic and vascular disorders.
• Raw material for compounding pharmacies requiring high-purity actives.
• Reference standard in analytical laboratories for quality control testing.

Basic Information

Product Name	Xanthinol Nicotinate
CAS No.	437-74-1
Molecular Formula	C13H21N3O4
Molecular Weight	283.33 g/mol
Synonyms	Xanthinol Niacinate; Xanthinol Nicotinate; 7-[2-Hydroxy-3-(2-hydroxyethyl)methylamino]propyl]theophylline nicotinate; Complamin; SK-331 A; Angioamin; Vedrin; Landrina; Sadamin; Xantinol Nicotinate
EINECS	207-119-9

Quality Control

Our Xanthinol Nicotinate is manufactured under strict quality management systems, ensuring it meets the high standards required for pharmaceutical applications. Each batch is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. We adhere to cGMP guidelines where applicable, and our quality protocols are designed to ensure batch-to-batch consistency and regulatory compliance for global markets.

Storage

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

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 (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.