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Lignocaine n-Oxide CAS NO 2903-45-9


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CAS No.:2903-45-9

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Lignocaine n-Oxide is a specific chemical derivative of the widely used local anesthetic lidocaine. This compound is primarily utilized as a key intermediate in advanced pharmaceutical synthesis and research. It is essential for manufacturers and R&D laboratories in the pharmaceutical and fine chemical sectors developing new anesthetic agents or studying metabolic pathways. The product is supplied to meet the stringent purity requirements of these applications.

Application

  • Pharmaceutical Intermediate: A crucial building block in the synthesis of novel local anesthetic agents and related pharmaceutical compounds.
  • Metabolite Reference Standard: Used in analytical laboratories as a reference standard for the identification and quantification of lidocaine metabolites in pharmacological and toxicological studies.
  • Biochemical Research: Employed in research to study the metabolism, mechanism of action, and structure-activity relationships (SAR) of aminoamide local anesthetics.
  • Fine Chemical Synthesis: Serves as a specialized intermediate for the preparation of more complex, targeted molecules in medicinal chemistry projects.
  • Quality Control: Used by API (Active Pharmaceutical Ingredient) manufacturers for in-process testing and method development.

Basic Information

Product Name Lignocaine n-Oxide
CAS No. 2903-45-9
Molecular Formula C14H22N2O2
Molecular Weight 250.34 g/mol
Synonyms Lidocaine N-Oxide; 2-(Diethylamino)-N-(2,6-dimethylphenyl)acetamide N-Oxide; Lignocaine Oxide; Lidocaine 1-Oxide; Diethylglycinexylidide N-Oxide; Xylocaine N-Oxide; NSC 526046
EINECS 220-829-5

Quality Control

Our Lignocaine n-Oxide is produced under a strict quality management system. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. We provide a detailed Certificate of Analysis (COA) with key parameters including assay, related substances, and identification. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates, ensuring reliability for your critical synthesis and research applications.

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 White to off-white crystalline powder
Identification (IR) Conforms to structure
Assay (HPLC) ≥ 98.0%
Related Substances (HPLC) Total impurities ≤ 2.0%
Loss on Drying ≤ 0.5%
Residue on Ignition ≤ 0.1%

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

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