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Lumiflavin

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Identification
Molecular formula
C13H12N4O2
CAS number
1088-56-8
IUPAC name
7,8-dimethyl-10H-benzo[g]pteridine-2,4-dione
State
State

At room temperature, Lumiflavin is in a solid state. It maintains a crystalline structure, providing it stability under normal environmental conditions. This solid state is in line with many vitamin derivatives and is essential for storage and handling in laboratory settings.

Melting point (Celsius)
314.00
Melting point (Kelvin)
587.15
Boiling point (Celsius)
644.00
Boiling point (Kelvin)
917.15
General information
Molecular weight
256.25g/mol
Molar mass
256.2500g/mol
Density
1.4600g/cm3
Appearence

Lumiflavin appears as a yellow crystalline solid. Its strong yellow color is indicative of its role as a component in vitamins such as riboflavin (vitamin B2) derivatives. The crystalline nature makes it identifiable under a microscope, where it can be observed as distinct geometric shapes.

Comment on solubility

Solubility of 7,8-dimethyl-10H-benzo[g]pteridine-2,4-dione

The solubility characteristics of 7,8-dimethyl-10H-benzo[g]pteridine-2,4-dione (C13H12N4O2) can be quite interesting due to its unique chemical structure. This compound, being a derivative of pteridine, exhibits some intriguing solubility behavior:

  • Water Solubility: Generally, compounds similar to pteridines tend to have low water solubility due to their hydrophobic aromatic rings.
  • Solvents: It is more likely to dissolve in organic solvents such as ethanol, dimethyl sulfoxide (DMSO), and acetone.
  • Temperature Influence: Solubility may increase with temperature, a common trait for many organic compounds.

Considering the presence of the keto groups in its molecular structure, this might aid in interactions with solvents, thus slightly enhancing solubility compared to other less functionalized analogs. Overall, while not soluble in water, the compound's solubility in organic solvents makes it manageable for various applications. As a quote goes, “Understanding solubility is key to mastering the reactivity and utility of any compound.”

In applications and experimental settings, being aware of these solubility characteristics is essential for effective compound manipulation and utilization.

Interesting facts

Interesting Facts About 7,8-Dimethyl-10H-benzo[g]pteridine-2,4-dione

7,8-dimethyl-10H-benzo[g]pteridine-2,4-dione, commonly referred to in the scientific community for its intriguing structure and properties, is a compound that captivates researchers in various fields, particularly in biochemistry and medicinal chemistry. Here are some noteworthy aspects:

  • Structure and Functionality: This compound is a derivative of pteridine, a class known for its aromaticity and involvement in essential biological functions. The unique arrangement of substituents on the pteridine ring contributes to its reactivity and potential as a pharmaceutical agent.
  • Biological Significance: Compounds like 7,8-dimethyl-10H-benzo[g]pteridine-2,4-dione are studied for their roles in biological pathways, especially in relation to enzymes and their actions in the human body. Understanding how such compounds interact with biomolecules can lead to breakthroughs in drug development.
  • Potential Applications: Researchers are exploring its potential application in therapeutics, especially due to its resemblance to other biologically active compounds. It may hold promise in treating conditions that involve oxidative stress or as an anti-inflammatory agent.
  • Synthesis and Research: The synthesis of this compound can be complex, often involving multiple steps. The methodologies used to synthesize such compounds showcase the ingenuity of modern organic chemistry. Ongoing research continues to refine these methods and expand the compound's utility.

As you can see, the study of 7,8-dimethyl-10H-benzo[g]pteridine-2,4-dione captures the essence of interdisciplinary research where chemistry meets biology, presenting a fertile ground for innovation and discovery. It’s emblematic of how studying seemingly simple structures can lead to significant advances in science and medicine.