Description

Gallamine Triethiodide is a quaternary ammonium neuromuscular blocking agent with the CAS registry number 65-29-2. This compound is a critical pharmaceutical intermediate and research chemical, primarily valued for its role in the study and development of neuromuscular pharmacology. It is essential for researchers and manufacturers in the pharmaceutical and life sciences sectors who require high-purity reference standards and active pharmaceutical ingredients (APIs).

Application

• Pharmaceutical Intermediate: Serves as a key building block in the synthesis of specialized neuromuscular blocking agents and related therapeutic compounds.
• Research & Development: Used extensively in pharmacological studies as a reference standard for investigating neuromuscular junction function and the mechanisms of non-depolarizing muscle relaxants.
• Biochemical Research: Employed in in vitro and ex vivo experiments to study cholinergic receptors and the competitive inhibition of acetylcholine.
• Veterinary Medicine: Historically used and studied for muscle relaxation during surgical procedures in animal models.
• Quality Control Standards: Utilized as a certified reference material (CRM) in analytical laboratories for method development and validation in pharmaceutical QC.
• Academic Studies: A standard compound in university and institutional labs for teaching and advanced research in physiology and anesthesiology.

Basic Information

Product Name	Gallamine Triethiodide
CAS No.	65-29-2
Molecular Formula	C30H60I3N3O3
Molecular Weight	891.54 g/mol
Synonyms	Gallamine Triiodide; 1,2,3-Tris(2-diethylaminoethoxy)benzene Triethiodide; Benzenetriyltrioxy)tris(N,N-diethylethanaminium) Triiodide; Flaxedil; Relaxan; Syncurine; Gallamine; Gallamoni Triiodidum; 2,2',2''-[1,2,3-Benzenetriyltris(oxy)]tris[N,N-diethylethanaminium] Triiodide
EINECS	200-607-7

Quality Control

Our Gallamine Triethiodide is produced and tested under a strict quality management system. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency, meeting the stringent requirements for pharmaceutical research and development. A detailed Certificate of Analysis (COA) is provided with every shipment, confirming compliance with in-house specifications. We support compliance with global regulatory frameworks, including cGMP where applicable.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥ 98.0%
Loss on Drying	≤ 2.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0%
Single Unknown Impurity	≤ 0.5%

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