Description

Suxethonium Bromide is a quaternary ammonium neuromuscular blocking agent. This compound is a critical intermediate in the synthesis of pharmaceutical actives, particularly in the development of short-acting muscle relaxants. It is primarily utilized by research institutions and pharmaceutical manufacturers engaged in the development and production of anesthetic and neuromuscular blocking agents.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of neuromuscular blocking agents used in surgical anesthesia.
• Research & Development: Used in biochemical and pharmacological research to study neuromuscular junction physiology and drug-receptor interactions.
• Reference Standard: Serves as a certified reference material (CRM) for analytical method development and quality control in pharmaceutical labs.
• Active Pharmaceutical Ingredient (API) Synthesis: Employed in the multi-step synthesis of complex pharmaceutical molecules requiring a short-duration depolarizing agent structure.

Basic Information

Product Name	Suxethonium Bromide
CAS No.	111-00-2
Molecular Formula	C14H30Br2N2O4
Molecular Weight	426.21 g/mol
Synonyms	Succinylcholine Bromide; Suxamethonium Bromide; 2,2'-[(1,4-Dioxo-1,4-butanediyl)bis(oxy)]bis[N,N,N-trimethylethanaminium] Dibromide; Brevidil Bromide; Bromure de Suxamethonium; Brometo de Suxametonio; Suxamethonii Bromidum
EINECS	203-822-5

Quality Control

Our Suxethonium Bromide is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling, to ensure it meets stringent specifications for pharmaceutical intermediates. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and batch-to-batch consistency.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥98.0%
Water Content (KF)	≤2.0%
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.