Dihydroxyaminobenzamidine | Solubility of Things

Identification

Molecular formula

C₇H₉N₃O₂

CAS number

586-81-2

IUPAC name

4-(dihydroxyamino)-N-imino-benzamide

State

At room temperature, dihydroxyaminobenzamidine is in a solid state. It is generally stable and does not evaporate, making it suitable for various laboratory applications.

Melting point (Celsius)

182.00

Melting point (Kelvin)

455.00

Boiling point (Celsius)

305.00

Boiling point (Kelvin)

578.00

General information

Molecular weight

167.17g/mol

Molar mass

167.1660g/mol

Density

1.3400g/cm³

Appearence

Dihydroxyaminobenzamidine typically appears as a crystalline solid. The compound is usually white to off-white in color, depending on purity and specific conditions.

Comment on solubility

Solubility of 4-(dihydroxyamino)-N-imino-benzamide

4-(dihydroxyamino)-N-imino-benzamide, with its unique structural features, exhibits varying solubility characteristics that are of significant interest in both scientific and industrial applications. Below are key points regarding its solubility:

Polar Nature: The presence of hydroxyl groups (-OH) contributes to the polar nature of the compound, likely enhancing its solubility in polar solvents, such as water.
Hydrogen Bonding: The potential for intramolecular and intermolecular hydrogen bonding is notable, as this can influence solubility by stabilizing interactions with solvent molecules.
pH Dependency: Its solubility might be affected by pH changes in a solution; typically, compounds with amino and hydroxyl groups can form protonated or deprotonated species, altering solubility profiles.
Solvent Compatibility: Besides water, the compound may exhibit solubility in various organic solvents, especially those that can engage in hydrogen bonding.

In summary, the solubility of 4-(dihydroxyamino)-N-imino-benzamide can be described as:

Potentially high in polar environments due to hydrogen bonding capabilities.
Variable in response to changes in pH, impacting its overall solubility behavior.

Understanding the solubility characteristics is crucial for applications in pharmaceuticals, where solubility influences bioavailability and formulation strategies.

Interesting facts

Interesting Facts About 4-(Dihydroxyamino)-N-imino-benzamide

The compound 4-(Dihydroxyamino)-N-imino-benzamide is an intriguing member of the benzamide family, with applications and implications that extend into various fields of chemistry and biochemistry.

Key Features and Applications

Potential Therapeutic Uses: This compound is researched for its potential as a pharmacological agent, particularly in the realm of anti-cancer therapies. Its structure suggests possible interactions with biological systems that could inhibit tumor growth.
Functional Groups: The presence of both dihydroxyamino and imino groups suggests this compound may participate in interesting chemical reactions, including hydrogen bonding and nucleophilic attack, making it a valuable point of investigation in synthetic chemistry.
Research Interest: Due to its unique structure, it has attracted attention in materials science for the development of novel polymers and coatings that could exhibit enhanced properties.

Scientific Relevance

The ^{aminobenzamide} derivatives are significant due to their roles in biochemistry, particularly in the development of enzymatic inhibitors. The structural features of 4-(dihydroxyamino)-N-imino-benzamide allow it to act as an essential lead compound for developing more complex molecules with positive biological effects.

Fun Fact

“Chemistry is the study of matter, but I prefer to see it as the study of change.” This famous quote reflects the nature of compounds like 4-(dihydroxyamino)-N-imino-benzamide, which embody the potential for transformation both chemically and biologically, expanding our understanding of therapeutic agents.

Overall, the study of 4-(dihydroxyamino)-N-imino-benzamide opens doors to explorations in medicinal chemistry and synthetic biology, making it a compound well worth further examination.