6151-22-0 Usage
Explanation
The compound is named based on its structure, which includes a benzene ring with four carboxylic acid groups and two water molecules.
Explanation
The molecular formula represents the number of carbon (C), hydrogen (H), and oxygen (O) atoms in the compound.
Explanation
The compound consists of a benzene ring with four carboxylic acid groups (-COOH) attached to it, and it also contains two water molecules (H2O) as part of its structure.
Explanation
The term "dihydrate" indicates that the compound has two water molecules associated with it, which are typically coordinated to the carboxylic acid groups.
Explanation
Due to its versatile chemical structure and properties, 1,2,4,5-Benzenetetracarboxylic acid, dihydrate is used in various industries, including the production of coordination compounds, organic synthesis, polymer manufacturing, and as a component in pharmaceuticals and dyes.
Explanation
The compound exhibits acidic properties due to the presence of carboxylic acid groups. It also has the ability to form coordination complexes with metal ions and can undergo various chemical reactions, such as esterification and decarboxylation.
Explanation
The dihydrate form of the compound is soluble in water and other polar solvents due to the presence of polar carboxylic acid groups and water molecules.
Explanation
1,2,4,5-Benzenetetracarboxylic acid, dihydrate is generally stable under normal conditions, such as room temperature and pressure. However, it may decompose or react under extreme conditions, such as high temperatures or in the presence of strong acids or bases.
Explanation
The compound can form crystalline structures, which are important for its characterization and applications in various industries.
Explanation
As with many chemicals, 1,2,4,5-Benzenetetracarboxylic acid, dihydrate should be handled with care, as it may cause irritation to the skin, eyes, or respiratory system if not properly managed. It is essential to follow safety guidelines and use appropriate protective equipment when working with 1,2,4,5-Benzenetetracarboxylic acid, dihydrate.
Structure
Benzene ring with four carboxylic acid groups and two water molecules
Dihydrate Form
Contains two water molecules
Applications
Coordination compounds, organic synthesis, polymers, pharmaceuticals, and dyes
Chemical Properties
Acidity, coordination ability, and reactivity
Solubility
Soluble in water and polar solvents
Stability
Stable under normal conditions
Crystallography
Forms crystalline structures
Safety
Handle with care due to potential irritant properties
Check Digit Verification of cas no
The CAS Registry Mumber 6151-22-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,5 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6151-22:
(6*6)+(5*1)+(4*5)+(3*1)+(2*2)+(1*2)=70
70 % 10 = 0
So 6151-22-0 is a valid CAS Registry Number.
6151-22-0Relevant academic research and scientific papers
Process for producing aromatic polycarboxylic acid
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, (2008/06/13)
Aromatic polycarboxylic acids are produced in high yield by oxidation of polyalkyl-substituted aromatic aldehydes or polyalkyl-substituted aromatic carboxylic acids with molecular oxygen in water as a solvent in the presence of metal ions of manganese or cerium and a bromine ion-liberating compound as a catalyst, while keeping an oxygen concentration of effluent gas from reactor at least at 3%.
