4-Methylumbelliferone chloride | Solubility of Things

Identification

Molecular formula

C₁₂H₁₅ClN₁O₃

CAS number

3785-01-1

IUPAC name

(7-hydroxy-2-methyl-4-oxo-chromen-8-yl)methyl-dimethyl-ammonium;chloride

State

At room temperature, 4-Methylumbelliferone chloride is in a solid state.

Melting point (Celsius)

203.00

Melting point (Kelvin)

476.15

Boiling point (Celsius)

285.00

Boiling point (Kelvin)

558.15

General information

Molecular weight

255.73g/mol

Molar mass

255.7250g/mol

Density

1.2000g/cm³

Appearence

4-Methylumbelliferone chloride appears as a crystalline powder. It is typically white or off-white in color. Due to its chemical structure, it may exhibit fluorescence under ultraviolet light.

Comment on solubility

Solubility of (7-hydroxy-2-methyl-4-oxo-chromen-8-yl)methyl-dimethyl-ammonium; chloride

The solubility of the compound (7-hydroxy-2-methyl-4-oxo-chromen-8-yl)methyl-dimethyl-ammonium chloride is influenced by various factors including its ionic nature and structural characteristics. As an ammonium salt, its solubility can be summarized as follows:

Solvent: This compound is typically soluble in polar solvents, such as water or methanol, due to the presence of the ammonium group, which interacts favorably with polar molecules.
Temperature: Like many salts, the solubility of this compound generally increases with higher temperatures. This is a common behavior for ionic compounds.
pH Sensitivity: The solubility may also be affected by the pH of the solution, as protonation or deprotonation can influence the compound's ionic state and therefore its solubility.
Concentration: At higher concentrations, solubility may exhibit saturation, where no additional compound dissolves, indicating the limits of solubility.

In conclusion, the solubility of (7-hydroxy-2-methyl-4-oxo-chromen-8-yl)methyl-dimethyl-ammonium chloride is typically favorable in aqueous solutions and is subject to variations based on the factors mentioned. Understanding these parameters is crucial for practical applications such as formulation chemistry and drug delivery systems.

Interesting facts

Exploring (7-hydroxy-2-methyl-4-oxo-chromen-8-yl)methyl-dimethyl-ammonium;chloride

This intriguing compound, commonly recognized for its structural features and biological relevance, is more than just a name—a treasure trove of scientific inquiry! Here are some engaging facts that highlight its significance in the world of chemistry:

Key Component of Natural Products: The compound is derived from flavonoids, a class of compounds widely known for their antioxidant properties. Flavonoids have been extensively studied for their potential health benefits.
Ammonium Ion's Role: The dimethylammonium group in this compound enhances its solubility in water and biological systems, making it a promising candidate for various applications in pharmaceuticals.
Versatile Applications: Variants of this compound are utilized in fields like cosmetics, food additives, and colorants due to their ability to absorb UV light, thereby protecting against harmful radiation.
Biological Activity: Studies suggest that the compound exhibits anti-inflammatory and antimicrobial properties, which could pave the way for new therapeutic agents.
Chemical Synthesis: The synthesis of this compound involves intricate organic chemistry techniques, highlighting the beauty and complexity of chemical reactions. Understanding its formation aids in developing more efficient synthetic methods.

Ultimately, (7-hydroxy-2-methyl-4-oxo-chromen-8-yl)methyl-dimethyl-ammonium;chloride exemplifies how certain compounds bridge gaps between chemistry and biology, yielding significant implications for the development of modern therapeutics. As stated by renowned chemist Marie Curie, "Nothing in life is to be feared, it is only to be understood." This compound invites us to delve deeper into its mysteries!

Synonyms

8-(Dimethylamino)methyl-7-hydroxy-2-methylchromone hydrochloride

17544-17-1

CHROMONE, 8-(DIMETHYLAMINO)METHYL-7-HYDROXY-2-METHYL-, HYDROCHLORIDE