Description

Tiquizium is a synthetic organic compound with specific pharmacological activity, identified by CAS No. 149755-23-7. It serves as a key intermediate or active ingredient in the development of specialized pharmaceutical formulations. This compound is primarily utilized by research institutions and pharmaceutical manufacturers focused on creating new therapeutic agents.

Application

• Pharmaceutical Intermediate: A critical building block in the synthesis of novel drug candidates, particularly in early-stage research and development.
• Active Pharmaceutical Ingredient (API) Development: Used in the formulation and process development for potential new medications.
• Biochemical Research: Employed in laboratory studies to investigate specific biological pathways and mechanisms of action.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for custom synthesis projects under cGMP conditions.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method validation in pharmaceutical analysis.

Basic Information

Product Name	Tiquizium
CAS No.	149755-23-7
Molecular Formula	C21H29N3O2S
Molecular Weight	387.54 g/mol
Synonyms	TIQUIZIUM; Tiquizium Bromide; 3-(Di-2-thienylmethylene)-8-methyl-8-azabicyclo[3.2.1]octane; 8-Methyl-3-[(2-thienyl)(2-thienyl)methylene]-8-azabicyclo[3.2.1]octane; 8-Azabicyclo[3.2.1]octane, 8-methyl-3-[(2-thienyl)(2-thienyl)methylene]-; Tiquizium (base); UNII-9LHU78OQFD
EINECS	Contact for details

Quality Control

Our Tiquizium is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling via HPLC and other validated methods, to ensure it meets the stringent requirements for pharmaceutical research and development. A detailed Certificate of Analysis (COA) is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (typically 15-25°C). Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 0.5%
Heavy Metals	≤ 20 ppm

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