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Methylene blue

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Identification
Molecular formula
C16H18N3SCl
CAS number
61-73-4
IUPAC name
1,1'-[(Z)-azinomethylylidynenitrilo]bis(2-methylpyrrolidinium) 4-methylbenzenesulfonate
State
State

At room temperature, methylene blue is typically found as a solid in the form of a dark green powder. Its solutions are characteristically deep blue.

Melting point (Celsius)
100.00
Melting point (Kelvin)
373.00
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.00
General information
Molecular weight
319.85g/mol
Molar mass
319.8520g/mol
Density
1.1900g/cm3
Appearence

Methylene blue appears as a dark green crystalline powder which yields a blue solution when dissolved in water. It is often used as a dye and has a characteristic deep blue color.

Comment on solubility

Solubility of 1,1'-[(Z)-azinomethylylidynenitrilo]bis(2-methylpyrrolidinium) 4-methylbenzenesulfonate

The solubility of 1,1'-[(Z)-azinomethylylidynenitrilo]bis(2-methylpyrrolidinium) 4-methylbenzenesulfonate can be considered quite interesting due to its unique structure and composition. Let's explore some key points regarding its solubility:

  • Solvent Compatibility: This compound is likely soluble in polar solvents, particularly water and alcohols, due to the presence of the sulfonate group, which enhances hydrophilicity.
  • pH Influence: The solubility may be affected by pH levels; under acidic conditions, the protonation of functional groups can enhance solubility.
  • Temperature Effects: Increased temperatures generally lead to higher solubility for many salts and polar compounds, and this may also apply to our compound.
  • Concentration Factors: As with many compounds, the solubility limits will vary widely depending on concentration—saturation points may need to be experimentally determined.

In summary, while the specific solubility data for this compound may not be readily available, it is reasonable to expect that its solubility characteristics will be influenced by factors such as solvent polarity, pH levels, and temperature, making it an intriguing subject for further study.

Interesting facts

Interesting Facts about 1,1'-[(Z)-azinomethylylidynenitrilo]bis(2-methylpyrrolidinium) 4-methylbenzenesulfonate

The compound 1,1'-[(Z)-azinomethylylidynenitrilo]bis(2-methylpyrrolidinium) 4-methylbenzenesulfonate is a fascinating example in the world of organic chemistry, showcasing the complexity and diversity of chemical structures. Here are some intriguing points regarding this compound:

  • Multifunctionality: This compound exhibits multiple functional groups that contribute to its unique reactivity, making it a subject of interest for synthetic chemists.
  • Research Potential: Due to its nitrogen-containing structure, it may find applications in the development of novel materials or pharmaceuticals, especially in areas involving drug discovery and design.
  • Quaternary Ammonium Structure: The presence of 2-methylpyrrolidinium moieties indicates that this compound could display interesting ionic properties, potentially making it useful in electrochemistry.
  • Environmental Chemistry: The sulfonate group attached to the aromatic system can enhance water solubility, which is significant when considering the compound's behavior in environmental contexts.

As researchers continue to explore new chemical compounds, the ability to synthesize and manipulate complex structures such as this one exemplifies the innovative possibilities within the field of chemistry. The journey of studying compounds like this often leads to unexpected applications and discoveries!

Synonyms
2491-17-0
CME-CARBODIIMIDE
1-Cyclohexyl-3-(2-morpholinoethyl)carbodiimide metho-p-toluenesulfonate
EINECS 219-650-3
NSC 231596
1-Cyclohexyl 3-(2-morpholinoethyl)carbodiimide methotosylate
1-Cyclohexyl-3-(2-morpholinoethyl)carbodiimide methyl-p-toluenesulfonate
1-Cyclohexyl-3-(2-morpholinyl-(4)-ethyl)carbodiimide metho-p-toluenesulfonate
N-Cyclohexyl-N'-(beta-(4-methylmorpholinio)ethyl)carbodiimide p-toluenesulfonate
N-Cyclohexyl-N'-2-morpholinyl(4)ethylcarbodiimide methyl-p-toluenesulfonate
N-Cyclohexyl-N-(beta-(4-methylmorpholinium)ethyl)carbodiimide p-toluenesulfonate
N-Cyclohexyl-N'-beta-(4-methylmorpholinium)ethylcarbodiimide p-tolenesulfonate salt
4-(2-((Cyclohexylcarbonimidoyl)amino)ethyl)-4-methylmorpholinium toluene-p-sulphonate
4-[2-[(cyclohexylcarbonimidoyl)amino]ethyl]-4-methylmorpholinium toluene-p-sulphonate
Morpholinium, 4-(2-((cyclohexylimidocarbonyl)amino)ethyl)-4-methyl-, p-toluenesulfonate
Morpholinium, 4-(2-((cyclohexylcarbonimidoyl)amino)ethyl)-4-methyl-, 4-methylbenzenesulfonate (1:1)
Morpholinium, 4-(2-((cyclohexylcarbonimidoyl)amino)ethyl)-4-methyl-, salt with 4-methylbenzenesulfonic acid (1:1)
Morpholinium, 4-[2-[(cyclohexylcarbonimidoyl)amino]ethyl]-4-methyl-, salt with 4-methylbenzenesulfonic acid (1:1)
CME Carbodiimide
Carbodiimide, CME
Morpholinium, 4-[2-[(cyclohexylcarbonimidoyl)amino]ethyl]-4-methyl-, 4-methylbenzenesulfonate (1:1)
4-(2-((Cyclohexylimidocarbonyl)amino)ethyl)-4-methylmorpholinium
219-650-3
Morpholinium, 4-(2-((cyclohexylimidocarbonyl)amino)ethyl)-4-methyl-, p-toluenesulfonate (8CI)
Morpholinium, 4-2-(cyclohexylcarbonimidoyl)aminoethyl-4-methyl-, salt with 4-methylbenzenesulfonic acid (1:1)
Morpho CDI
4-(2-(((Cyclohexylimino)methylene)amino)ethyl)-4-methylmorpholin-4-ium 4-methylbenzenesulfonate
NSC231596
1-Cyclohexyl-3-[2-(4-methylmorpholino)ethyl]carbodiimide p-Toluenesulfonate
N-cyclohexyl-N'-(2-morpholinoethyl)carbodiimide methyl-p-toluenesulfonate
CMC [N-Cyclohexyl-N''-(2-morpholinoethyl)carbodiimide metho-p-toluenesulfonate]
1-cyclohexyl-3-(2-morpholinoethyl) carbodiimide metho-p-toluenesulfonate
N-Cyclohexyl-N'-(2-morpholinoethyl)carbodiimide metho-p-toluenesulfonate
102292-00-2
MFCD00011979
CHM (VAN)
Morpho-CDI
Morpho-CDI;CME-carbodiimide
SCHEMBL6533548
Morpholinium, p-toluenesulfonate
CHEMBL1789981
DTXSID60907344
AKOS015903467
CS-W014457
FC55888
HY-W013741
4-[2-[(Cyclohexylcarbonimidoyl)amino]ethyl]-4-methylmorpholinium p-toluenesulfonate
AS-11083
N-cyclohexyl-N-[2-(4-methyl-1-oxa-4-azoniacyclohex-4-yl)ethyl]methanediimine,4-methylbenzenesulfonic acid
NS00046864
D70774
Morpholinium, salt with 4-methylbenzenesulfonic acid (1:1)
1-cyclohexyl-3-(2-morpholinoethyl) carbodiimide metho p-toluenesulfonate
1-cyclohexyl-3-(2-morpholinoethyl)carbodiimide metho p-toluene sulfonate
1-cyclohexyl-3-(2-morpholinoethyl)carbodiimide metho-p-toluene sulfonate
1-Cyclohexyl-3-[2-(4-methylmorpholino)ethyl]carbodiimidep-Toluenesulfonate
1cyclohexyl-3-(2-morpholinoethyl)carbodiimide metho-p-toluenesulfonate
N-Cyclohexyl-N'-(2-morpholinoethyl)carbodiimide metho-p-toluenesulfonate, >=97% (CHN)
N-Cyclohexyl-N'-(2-morpholinoethyl)carbodiimide metho-p-toluenesulfonate, >=99.0% (CHN)
N-Cyclohexyl-N'-(2-morpholinoethyl)carbodiimide methyl-p-toluenesulfonate, 95%
N-Cyclohexyl-N'-.beta.-(methylmorpholinium)ethylcarbodiimide p-toluenesulfonate
4-(2-{[(Cyclohexylimino)methylidene]amino}ethyl)-4-methylmorpholin-4-ium 4-methylbenzene-1-sulfonate
CHM
N-cyclohexyl-N'-(2-(4-methyl-1,45-oxazinan-4-yl)ethyl)carbodiimide 4-methylbenzenesulfonate