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Xenysalate Hydrochloride CAS NO 5560-62-3


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CAS No.:5560-62-3

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Xenysalate Hydrochloride is a pharmaceutical intermediate and active ingredient with significant importance in the development and manufacturing of specialized therapeutic agents. Its value lies in its role as a key building block for creating compounds with targeted biological activity, ensuring high-purity synthesis pathways. This product is essential for research institutions, pharmaceutical development laboratories, and fine chemical manufacturers engaged in producing advanced drug candidates and high-value specialty chemicals.

Application

  • Pharmaceutical Intermediate: Serves as a critical precursor in the multi-step synthesis of novel active pharmaceutical ingredients (APIs).
  • Research & Development: Used in medicinal chemistry for structure-activity relationship (SAR) studies and the discovery of new drug candidates.
  • Fine Chemical Synthesis: Employed in the production of complex, high-value organic molecules for specialized applications.
  • Contract Manufacturing: A key raw material for CDMOs (Contract Development and Manufacturing Organizations) producing cGMP batches for clinical trials.
  • Reference Standard: Can be supplied as a high-purity standard for analytical method development and quality control testing.

Basic Information

Product Name Xenysalate Hydrochloride
CAS No. 5560-62-3
Molecular Formula C16H17NO3 • HCl
Molecular Weight 307.77 g/mol
Synonyms Xenysalate HCl; 2-(Diethylamino)ethyl 4-hydroxy-3-methoxybenzoate hydrochloride; Guaiacol glyceryl ether diethylaminoethyl ether hydrochloride; Guaifenesin carbamate hydrochloride; Methocarbamol related compound B; Myolaxene; Robaxisal component
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Quality Control

Our Xenysalate Hydrochloride is manufactured under a strict quality management system. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency, meeting the stringent requirements for pharmaceutical intermediates. Certificates of Analysis (COA) documenting full specifications are provided with every shipment. We support compliance with cGMP, ISO, and other relevant quality standards as required for your application.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (typically 15-25°C). Keep away from incompatible materials. The container must be kept tightly closed to protect the hygroscopic and light-sensitive material.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to structure
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%
Single Unknown Impurity ≤ 0.5%

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

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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.