Description

6-Bromo-N,n-Dimethylpyridine-3-Sulfonamide is a high-purity, advanced pharmaceutical intermediate and versatile chemical building block. Its molecular structure, featuring a brominated pyridine core and a dimethylsulfonamide group, makes it a critical synthon for constructing complex molecules in medicinal chemistry. This compound is essential for research and development chemists, process chemists, and manufacturers in the pharmaceutical, agrochemical, and specialty chemical industries seeking to develop new active ingredients.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of novel drug candidates, particularly in kinase inhibitor and other small molecule therapeutic programs.
• Agrochemical Synthesis: Used in the research and development of new herbicides, fungicides, and insecticides, leveraging its halogenated heterocyclic structure.
• Ligand and Catalyst Development: Serves as a precursor for creating specialized ligands used in metal-catalyzed cross-coupling reactions and other catalytic processes.
• Material Science Research: Employed in the development of organic electronic materials, dyes, and photoactive compounds.
• Chemical Biology Probes: Utilized as a scaffold for developing molecular probes to study biological pathways and enzyme functions.
• Custom Synthesis and Contract Manufacturing: A vital starting material for custom synthesis houses and CDMOs (Contract Development and Manufacturing Organizations) serving global clients.

Basic Information

Product Name	6-Bromo-N,n-Dimethylpyridine-3-Sulfonamide
CAS No.	1216077-29-0
Molecular Formula	C7H9BrN2O2S
Molecular Weight	265.13 g/mol
Synonyms	6-Bromo-N,N-dimethylpyridine-3-sulfonamide; 3-Pyridinesulfonamide, 6-bromo-N,N-dimethyl-; 6-Bromo-N,N-dimethyl-3-pyridinesulfonamide; 6-Bromo-N,N-dimethylnicotinamide sulfonamide; 6-Bromo-3-(N,N-dimethylsulfamoyl)pyridine; 1216077-29-0
EINECS	Contact for details

Quality Control

Our 6-Bromo-N,n-Dimethylpyridine-3-Sulfonamide is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC, NMR, and mass spectrometry, to ensure identity, purity, and consistency. A comprehensive Certificate of Analysis (COA) detailing all specifications is provided with every shipment. We support cGMP (current Good Manufacturing Practice) standards for pharmaceutical applications and can provide documentation to meet the regulatory requirements of our global partners.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at a controlled room temperature (typically 15-25°C). Keep away from incompatible materials such as strong oxidizing agents, strong acids, and strong bases. For long-term storage, consider storing under an inert atmosphere to maintain optimal purity.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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