Description

Cytisine Nitrate Monohydrate is a high-purity alkaloid derivative, primarily valued for its potent pharmacological activity. This compound is a critical intermediate and active ingredient in the development of smoking cessation aids and other therapeutic agents. It is essential for research institutions, pharmaceutical manufacturers, and fine chemical suppliers focused on neuropharmacology and addiction treatment.

Application

• Pharmaceutical Intermediate: Key starting material for the synthesis of advanced smoking cessation therapeutics (e.g., varenicline analogs).
• Reference Standard: Used as a certified reference material (CRM) in analytical laboratories for quality control and method validation.
• Biochemical Research: Employed in studies targeting nicotinic acetylcholine receptors (nAChRs) for neurological and behavioral research.
• Active Pharmaceutical Ingredient (API): Serves as the core active component in the formulation of specific prescription medications.
• Process Development: Utilized in scaling up and optimizing synthetic routes within process chemistry and R&D departments.

Basic Information

Product Name	Cytisine Nitrate Monohydrate
CAS No.	6013-62-3
Molecular Formula	C11H14N2O • HNO3 • H2O
Molecular Weight	279.26 g/mol
Synonyms	Cytisine Nitrate Hydrate; Baptitoxine Nitrate Monohydrate; Sophorine Nitrate Monohydrate; Ulexine Nitrate Monohydrate; (1R,5S)-1,2,3,4,5,6-Hexahydro-1,5-methano-8H-pyrido[1,2-a][1,5]diazocin-8-one Nitrate Monohydrate
EINECS	Contact for details

Quality Control

Our Cytisine Nitrate Monohydrate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, residual solvent analysis, and identity confirmation (IR, NMR) to ensure it meets stringent specifications for pharmaceutical research and development. Certificates of Analysis (COA) are provided and available upon request.

Storage

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

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%
Water Content (KF)	4.0% - 7.0%
Residue on Ignition	≤0.1%
Heavy Metals	≤20 ppm
Related Substances (HPLC)	Total impurities ≤2.0%

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