Description

Oxethazaine is a potent local anesthetic agent belonging to the amino ester class, widely recognized for its surface anesthetic properties. Its primary commercial value lies in its specialized use as a key active pharmaceutical ingredient (API) in formulations designed to relieve gastrointestinal discomfort and pain. This compound is essential for manufacturers in the pharmaceutical industry developing topical anesthetics and specific gastrointestinal medications. Oxethazaine CAS NO 126-27-2 is supplied to meet the stringent quality demands of global API production.

Application

• Primary Active Pharmaceutical Ingredient (API) in topical anesthetic creams, gels, and sprays.
• Key component in formulations for symptomatic relief of gastritis, esophagitis, and peptic ulcers.
• Used in oral pharmaceutical suspensions and lozenges designed for local numbing effects.
• Intermediate in the synthesis of more complex anesthetic and pharmaceutical compounds.
• Research and development applications within medicinal chemistry and pharmacology.

Basic Information

Product Name	Oxethazaine
CAS No.	126-27-2
Molecular Formula	C28H40N2O4
Molecular Weight	468.63 g/mol
Synonyms	Oxetacaine; Oxethazine; 2,2'-(2-Hydroxyethylimino)bis[N-(1,1-dimethyl-2-phenylethyl)-N-methylacetamide]; Mucaine; Strocain; Win-12267; Oxethazaine Hydrochloride (salt form); Oxetacainum
EINECS	204-780-5

Quality Control

Our Oxethazaine is manufactured under strict quality management systems to ensure it meets the high-purity standards required for pharmaceutical applications. Each batch is subjected to comprehensive analytical testing, including identity confirmation, purity assay, and impurity profiling. A detailed Certificate of Analysis (COA) is provided with every shipment, documenting compliance with agreed specifications. We support compliance with cGMP, ICH Q7, and other relevant pharmacopeial guidelines (USP/EP) as required.

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. For long-term storage, consider conditions under an inert atmosphere to maintain stability.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference standard
Assay (HPLC)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.5%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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