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Niclosamide Ethanolamine Salt CAS NO 1420-04-8


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CAS No.:1420-04-8

Grade:Pharmacy Grade

Content:99.0%

Brand:Customizable

Packaging:Customizable

Description

Niclosamide Ethanolamine Salt is the ethanolamine salt form of the anthelmintic compound niclosamide, offering enhanced solubility and stability for formulation. This compound is a critical active pharmaceutical ingredient (API) valued for its potent molluscicidal and anti-parasitic properties. It is primarily required by manufacturers in the pharmaceutical and agrochemical industries for producing targeted treatments.

Application

  • Pharmaceutical API: Core ingredient in the formulation of anthelmintic medications for human and veterinary use.
  • Molluscicide Production: Key component in commercial products designed for controlling snail populations in agriculture and aquaculture to prevent parasitic diseases.
  • Veterinary Formulations: Used in treatments for tapeworm and other parasitic infections in livestock and companion animals.
  • Public Health Programs: Employed in large-scale disease control initiatives targeting schistosomiasis and fascioliasis transmission vectors.
  • Research & Development: Serves as a reference standard and active compound in pharmacological and parasitological studies.
  • Intermediate Synthesis: Utilized as a starting material or intermediate for further chemical synthesis of specialized derivatives.

Basic Information

Product Name Niclosamide Ethanolamine Salt
CAS No. 1420-04-8
Molecular Formula C13H8Cl2N2O4 • C2H7NO
Molecular Weight 327.12 (Niclosamide) + 61.08 (Ethanolamine) = 388.20 g/mol (approx.)
Synonyms Niclosamide Monoethanolamine Salt; 2',5-Dichloro-4'-nitrosalicylanilide Ethanolamine Salt; 5-Chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide compound with 2-aminoethanol (1:1); Yomesan® (trade name); Bayluscid® (trade name); Clonitralid; Ethanolamine Niclosamate
EINECS 215-811-7

Quality Control

Our Niclosamide Ethanolamine Salt is manufactured under a strict quality management system. It undergoes rigorous analytical testing to ensure it meets high-purity standards suitable for pharmaceutical and agrochemical applications. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with each batch to ensure traceability and compliance.

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). Keep away from incompatible materials.

Specification

Item Specification
Appearance Yellow to yellowish-brown crystalline powder
Identification (IR) Conforms to reference spectrum
Assay (HPLC) 98.0% - 102.0% (on anhydrous basis)
Water Content (KF) ≤ 2.0%
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.

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