Fluoren-9-amine, also known as 9-aminofluorene, is an organic compound characterized by its structure, which consists of a fluorene backbone with an amino group (-NH2) attached at the 9-position. This compound is typically a white to pale yellow solid at room temperature and is known for its aromatic properties due to the presence of fused benzene rings. Fluoren-9-amine is soluble in organic solvents such as ethanol and acetone but has limited solubility in water. It is primarily used in organic synthesis and as an intermediate in the production of dyes, pharmaceuticals, and other chemical compounds. Additionally, fluoren-9-amine has been studied for its potential mutagenic properties, making it of interest in toxicology and environmental chemistry. Safety precautions should be taken when handling this compound, as it may pose health risks upon exposure. Overall, fluoren-9-amine is a significant compound in both industrial applications and research contexts.

Fluoren-9-amine

525-03-1: 9-Amino-9H-fluorene, 9-Aminofluorene, Fluoren-9-amine, Fluoren-9-amine(7CI,8CI), Fluoren-9-ylamine, Iem 2117, 9H-Fluoren-9-amine

9H-FLUOREN-9-AMINE

9H-Fluoren-9-amine

9H-Fluoren-9-Amine

9H-Fluoren-9-amine hydrochloride is a protonated and fluorinated derivative of 9H-fluoren. It is an amide with a quaternary ammonium salt group. 9H-Fluoren-9-amine hydrochloride is used as a fluorescence probe for oligosaccharides and inorganic compounds, such as metal ions and transition metals. 
The fluorescence properties of this compound are related to the bond cleavage of the imine function. The nitrogen atom undergoes protonation and forms the corresponding ammonium salt under acidic conditions. The resulting amine can then be quantified using spectrometric methods or by mass spectrometry.

CAS 525-03-1: Fluoren-9-amine

9H-FLUOREN-9-AMINE

Ref: IN-DA00DE4Y

9H-Fluoren-9-amine

Ref: 10-F065053

9H-Fluoren-9-Amine

Ref: 54-OR1024615

9H-Fluoren-9-amine hydrochloride

Ref: 3D-FF131190