Description

Atropine Salicylate is a pharmaceutical-grade salt formed from the combination of atropine and salicylic acid. This compound is valued for its anticholinergic and analgesic properties, making it a critical intermediate in the synthesis of specialized pharmaceutical formulations. It is primarily utilized by manufacturers in the pharmaceutical and fine chemical industries for research, development, and production.

Application

• Pharmaceutical Intermediate: Key starting material or active ingredient in the synthesis of antispasmodic and mydriatic medications.
• Research & Development: Used in biochemical and pharmacological research to study muscarinic acetylcholine receptor antagonists.
• Fine Chemical Synthesis: Serves as a building block for creating more complex molecules with targeted therapeutic effects.
• Analytical Reference Standard: Employed as a high-purity standard in quality control laboratories for HPLC, GC, or other analytical methods.

Basic Information

Product Name	Atropine Salicylate
CAS No.	5908-95-2
Molecular Formula	C24H27NO6
Molecular Weight	425.48 g/mol
Synonyms	Atropine Salicylate; Atropine 2-hydroxybenzoate; Atropine Salicylate Salt; DL-Hyoscyamine Salicylate; Tropine Tropate Salicylate; (±)-Hyoscyamine Salicylate; 8-Methyl-8-azabicyclo[3.2.1]oct-3-yl 3-hydroxy-2-phenylpropanoate 2-hydroxybenzoate
EINECS	227-616-3

Quality Control

Our Atropine Salicylate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. A detailed Certificate of Analysis (COA) confirming identity, purity, and impurity profiles is provided with every shipment.

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 product is hygroscopic (moisture-sensitive) and light-sensitive; therefore, containers must be kept tightly sealed and away from moisture and direct light exposure.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥98.0%
Loss on Drying	≤1.0%
Residue on Ignition	≤0.1%
Heavy Metals	≤20 ppm
Related Substances (HPLC)	Total impurities ≤2.0%

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