Description

Trimetaphan Camsilate is a ganglionic blocking agent and a short-acting, non-depolarizing neuromuscular blocking agent. This compound is primarily valued in medical and pharmaceutical research for its ability to induce controlled hypotension and as a tool for studying autonomic nervous system function. It is essential for researchers and manufacturers in the pharmaceutical industry, particularly those developing or testing cardiovascular drugs, anesthetics, and neurological agents. Trimetaphan Camsilate CAS NO 68-91-7 serves as a critical reference standard and active pharmaceutical ingredient (API) in specialized formulations.

Application

• Pharmaceutical API: Used as an active pharmaceutical ingredient in the formulation of injectable solutions for inducing controlled hypotension during surgical procedures.
• Research Chemical: A vital tool in pharmacological and physiological research for studying ganglionic transmission and autonomic nervous system blockade.
• Reference Standard: Serves as a high-purity certified reference material (CRM) for quality control and analytical method development in pharmaceutical laboratories.
• Neuromuscular Studies: Employed in preclinical research to investigate short-acting neuromuscular blockade and its mechanisms.
• Academic & Clinical Research: Utilized in university and hospital research settings for cardiovascular and anesthesiology studies.

Basic Information

Product Name	Trimetaphan Camsilate
CAS No.	68-91-7
Molecular Formula	C32H40N2O5S2
Molecular Weight	596.80 g/mol
Synonyms	Trimethaphan Camsylate; Trimethaphan Camsilate; Arfonad; Trimetaphan Camsylate; Trimetaphan Camphorsulfonate; (2S,3aS,4R,5R,7S,8aR)-5-(Diaminomethylideneamino)-2,3,3a,4,5,6,7,8,8a,9-decahydro-3a,8a-dihydroxy-7-methyl-3-methylene-1H-cyclopenta[b]naphthalene-4-carboxylic acid compound with (7,7-dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methanesulfonic acid; Ganglioplegic
EINECS	Contact for details

Quality Control

Our Trimetaphan Camsilate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical research and development. We provide Certificates of Analysis (COA) with detailed results for parameters including assay, related substances, and identification. Our quality commitment aligns with cGMP principles to ensure supply reliability and batch-to-batch consistency for our global B2B clients.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed in a dry environment to prevent degradation. For long-term storage, consider desiccants or inert atmosphere conditions.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 5.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Heavy Metals	≤ 20 ppm

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