Description

Mivacurium CAS NO 106791-40-6 is a non-depolarizing neuromuscular blocking agent belonging to the benzylisoquinolinium class. It is valued for its rapid onset and short to intermediate duration of action, making it a critical agent for surgical muscle relaxation. This compound is primarily utilized in hospital and clinical settings by anesthesiologists and pharmaceutical manufacturers. Its reliable pharmacological profile supports controlled muscle paralysis during a variety of surgical procedures.

Application

• As an active pharmaceutical ingredient (API) in the formulation of injectable neuromuscular blocking agents.
• For use in general anesthesia to facilitate endotracheal intubation and provide skeletal muscle relaxation during surgery.
• In clinical research and pharmacological studies investigating neuromuscular transmission and blockade.
• For the development of generic pharmaceutical products within the anesthetic and muscle relaxant market.
• As a reference standard in analytical laboratories for quality control and method development.

Basic Information

Product Name	Mivacurium
CAS No.	106791-40-6
Molecular Formula	C58H80N2O14
Molecular Weight	1029.3 g/mol
Synonyms	Mivacurium Chloride; BW B1090U; Mivacron; (1R,1'R,2S,2'S)-2,2'-(3,11-Dioxo-4,10-dioxatridecamethylene)bis(1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-1-veratrylisoquinolinium) Dichloride; MiVacurio; 2,2'-(3,11-Dioxo-4,10-dioxatridecamethylene)bis(1,2,3,4-tetrahydro-6,7-dimethoxy-2-methyl-1-veratrylisoquinolinium) Dichloride
EINECS	Contact for details

Quality Control

Our Mivacurium is manufactured under strict quality management systems. Each batch is subjected to comprehensive analytical testing including identification, purity assay, and impurity profiling to ensure it meets high-grade pharmaceutical standards. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 5.0%
Related Substances (HPLC)	Individual impurity: ≤ 0.5% Total impurities: ≤ 2.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines

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