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Methylene blue

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Identification
Molecular formula
C16H18N3SCl
CAS number
61-73-4
IUPAC name
trimethyl-[2-[[4-[4-[2-(trimethylammonio)ethylsulfamoyl]phenyl]phenyl]sulfonylamino]ethyl]ammonium;diiodide
State
State
Methylene blue exists as an odorless solid at room temperature, usually handled as a powder.
Melting point (Celsius)
100.00
Melting point (Kelvin)
373.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
319.85g/mol
Molar mass
319.8520g/mol
Density
1.1500g/cm3
Appearence
Methylene blue is a solid that appears as a dark green powder at room temperature. When dissolved, typically in water, it forms a deep blue solution, which is characteristic of its name.
Comment on solubility

Solubility of Trimethyl-[2-[[4-[4-[2-(trimethylammonio)ethylsulfamoyl]phenyl]phenyl]sulfonylamino]ethyl]ammonium Diiodide

The solubility of Trimethyl-[2-[[4-[4-[2-(trimethylammonio)ethylsulfamoyl]phenyl]phenyl]sulfonylamino]ethyl]ammonium;diiodide is influenced by several factors, particularly its ionic nature and the presence of functional groups in its structure.

Key Points About Solubility:

  • Ionic Compounds: Being a quaternary ammonium salt, this compound tends to be soluble in polar solvents, such as water.
  • Temperature Dependence: Solubility generally increases with temperature. Thus, heating the solvent may enhance the dissolution of the compound.
  • Solvent Choice: It is likely to have lower solubility in non-polar solvents due to the absence of significant interaction with the solvent's molecules.
  • Interactions with Water: The presence of sulfonyl and ammonium groups can lead to favorable interactions with water, potentially increasing solubility.

As a result, this compound is predicted to be soluble in aqueous solutions, and its solubility may be enhanced by the formation of hydrogen bonds and ionic interactions. Overall, understanding the solubility behavior of such compounds is crucial for their application in various chemical and biological systems.

Interesting facts

Interesting Facts about Trimethyl-[2-[[4-[4-[2-(trimethylammonio)ethylsulfamoyl]phenyl]phenyl]sulfonylamino]ethyl]ammonium;diiodide

The compound known as trimethyl-[2-[[4-[4-[2-(trimethylammonio)ethylsulfamoyl]phenyl]phenyl]sulfonylamino]ethyl]ammonium;diiodide is a fascinating member of the class of quaternary ammonium compounds. Here are some engaging facts about this unique chemical:

  • Complex Structure: This compound has a highly intricate structure that features multiple aromatic rings and functional groups. Its complexity makes it a subject of interest in organic and medicinal chemistry.
  • Biological Applications: Compounds like this are often investigated for their biological activities. Many quaternary ammonium compounds have been noted for their antimicrobial properties, making them potential candidates for use in pharmaceuticals or as disinfectants.
  • Unique Functional Groups: The presence of sulfonamide and sulfamoyl groups contributes to the compound's functional versatility. These groups can enhance solubility and alter reactivity, leading to a variety of chemical transformations.
  • Interactions in Solutions: The diiodide counterion plays a critical role in how the compound interacts in solution. Ionic interactions can lead to unique solubility profiles and can influence the compound's behavior in biological systems.

As a chemistry student or scientist, exploring such compounds can open avenues for research into new materials and biological entities. Their intricate structures often lead to unexpected properties and potential applications in real-world chemistry.

Remember, as you dive deeper into the world of chemical compounds, each one tells a story and plays a role in the intricate tapestry of science!

Synonyms
Disufene
Disufen
5184-79-2
HB 72
KHB 72
XB-72
AMMONIUM, (4,4'-BIPHENYLYLENEBIS(SULFONYLIMINOETHYLENE))BIS(TRIMETHYL-, DIIODIDE
(4,4'-Biphenylylenebis(sulfonyliminoethylene))bis(trimethylammonium iodide)
Ethanaminium, 2,2'-((1,1'-biphenyl)-4,4'-diylbis(sulfonylimino))bis(N,N,N-trimethyl-, diiodide
trimethyl-[2-[[4-[4-[2-(trimethylazaniumyl)ethylsulfamoyl]phenyl]phenyl]sulfonylamino]ethyl]azanium;diiodide
DTXSID70966169
2,2'-[[1,1'-Biphenyl]-4,4'-diylbis(sulfonylazanediyl)]bis(N,N,N-trimethylethan-1-aminium) diiodide