Description

2-Amino-6-Fluorobenzenesulfonamide is a specialized aromatic sulfonamide derivative characterized by its distinct amino and fluorine substituents. This compound serves as a high-value intermediate in the synthesis of complex molecules, particularly in the pharmaceutical sector where its structure is leveraged for developing new active ingredients. It is primarily required by R&D chemists and process development scientists in the pharmaceutical, agrochemical, and advanced material industries for creating novel compounds with targeted biological or physical properties.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of novel drug candidates, particularly those targeting enzymes where the sulfonamide moiety is pharmacologically active.
• Agrochemical Research: Used in the development of new herbicides and fungicides, leveraging the bioactivity of the sulfonamide group.
• Chemical Synthesis: Serves as a versatile precursor for further functionalization, enabling the creation of libraries of compounds for high-throughput screening.
• Material Science: Potential intermediate in the synthesis of specialty polymers or dyes where fluorine and sulfonamide groups impart specific properties like stability or solubility.
• Bioconjugation & Probe Development: The amino group allows for coupling reactions, making it useful for creating fluorescent probes or affinity labels for biochemical research.

Basic Information

Product Name	2-Amino-6-Fluorobenzenesulfonamide
CAS No.	1161930-99-9
Molecular Formula	C6H7FN2O2S
Molecular Weight	190.20 g/mol
Synonyms	6-Fluoro-2-aminobenzenesulfonamide; 2-Amino-6-fluorobenzene-1-sulfonamide; Benzenesulfonamide, 2-amino-6-fluoro-; 6-Fluoroanthranilamide-2-sulfonamide; 2-Fluoro-6-aminobenzenesulfonamide; 1-Amino-3-fluoro-4-sulfamoylbenzene (tautomeric form); 6-Fluoro-2-sulfamoylaniline
EINECS	Contact for details

Quality Control

Our 2-Amino-6-Fluorobenzenesulfonamide is produced under a strict quality management system. Every batch undergoes comprehensive analytical testing including HPLC, NMR, and MS to ensure identity, purity, and consistency. We provide a detailed Certificate of Analysis (COA) with each shipment, documenting critical parameters such as assay and impurity profiles. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates, ensuring reliability for your most demanding synthesis applications.

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 nature, the container must be kept tightly sealed to minimize exposure to atmospheric moisture. Keep away from incompatible materials.

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)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Single Unknown Impurity (HPLC)	≤ 0.5%
Total Impurities (HPLC)	≤ 2.0%

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