CAS 945-30-2

1,4-Benzenedicarboxylic acid, 2,5-diamino-

Description:

1,4-Benzenedicarboxylic acid, 2,5-diamino- is an organic compound characterized by its dual functional groups: carboxylic acid and amino groups. This compound features a benzene ring with two carboxylic acid groups (-COOH) located at the 1 and 4 positions, and two amino groups (-NH2) at the 2 and 5 positions. The presence of these functional groups imparts both acidic and basic properties, making it a versatile compound in various chemical reactions. It is typically a solid at room temperature and may exhibit solubility in polar solvents due to its ability to form hydrogen bonds. This compound is often used in the synthesis of polymers, dyes, and pharmaceuticals, owing to its ability to participate in condensation reactions and form complex structures. Additionally, its structural features allow for potential applications in materials science and biochemistry. Safety precautions should be observed when handling this substance, as it may pose health risks if ingested or inhaled.

Formula: C₈H₈N₂O₄

2,5-Diaminoterephthalic acid

CAS: 945-30-2

Formula: C₈H₈N₂O₄

Purity: 95%

Color and Shape: Solid

Molecular weight: 196.1601

Ref: IN-DA0032ZY

2,5-Diaminoterephthalic acid

CAS: 945-30-2

2,5-Diaminoterephthalic acid

Purity: 97%

Molecular weight: 196.16g/mol

Ref: 54-OR73794

2,5-Diaminoterephthalic acid

CAS: 945-30-2

Formula: C₈H₈N₂O₄

Purity: 95%

Molecular weight: 196.162

Ref: 10-F336513

2,5-Diaminoterephthalic Acid

Controlled Product

CAS: 945-30-2

Formula: C₈H₈N₂O₄

Color and Shape: Neat

Molecular weight: 196.16

Ref: TR-D270920

2,5-Diaminoterephthalic acid

CAS: 945-30-2

2,5-Diaminoterephthalic acid is a synthetic organic compound that is used as a building block for the synthesis of polyamides. It has been shown to have high salt adsorption properties and low detection limits for certain analytes. 2,5-Diaminoterephthalic acid has also been found to have photocatalytic activity and can be used in the treatment of cancer. This chemical reacts with nitro groups on nucleophilic attack to form the carcinogenic nitrosamine. The formation rate of this nitrosamine depends on the presence of methoxy groups and nitrogen atoms in 2,5-diaminoterephthalic acid.

Formula: C₈H₈N₂O₄

Purity: Min. 95%

Molecular weight: 196.16 g/mol

Ref: 3D-FD145461