Skip to main content

Tetrachlorosalicylanilide

ADVERTISEMENT
Identification
Molecular formula
C16H24Cl4N1
CAS number
84-49-5
IUPAC name
trimethyl-[2-(4,5,6,7-tetrachloro-2-methyl-isoindolin-2-ium-2-yl)ethyl]ammonium
State
State

At room temperature, this compound is typically solid.

Melting point (Celsius)
146.50
Melting point (Kelvin)
419.65
Boiling point (Celsius)
333.29
Boiling point (Kelvin)
606.44
General information
Molecular weight
487.02g/mol
Molar mass
487.0020g/mol
Density
0.9650g/cm3
Appearence

Trimethyl-[2-(4,5,6,7-tetrachloro-2-methyl-isoindolin-2-ium-2-yl)ethyl]ammonium typically appears as a crystalline solid. The presence of multiple chlorine atoms often imparts a pale yellowish to off-white color, although this can vary depending on the impurities and crystal structure.

Comment on solubility

Solubility of Trimethyl-[2-(4,5,6,7-tetrachloro-2-methyl-isoindolin-2-ium-2-yl)ethyl]ammonium

Trimethyl-[2-(4,5,6,7-tetrachloro-2-methyl-isoindolin-2-ium-2-yl)ethyl]ammonium (C16H24Cl4N1) presents a unique case in terms of solubility due to its complex molecular structure and the presence of multiple chlorine substituents. Here are some key points regarding its solubility:

  • Solvent Polarity: Generally, compounds with high halogen content, like this one, are more likely to be soluble in polar solvents. Therefore, you might find it soluble in solvents such as water or alcohols, but the presence of the bulky isoindoline moiety could hinder full solubility.
  • Electrolytic Properties: The ammonium group contributes to its ionic character, making it more favorable to dissolve in polar environments where ion-dipole interactions are favorable.
  • Temperature Influence: Increased temperature often enhances solubility for compounds with larger molecular sizes, so heating the solvent may improve the dissolution of this compound.
  • Potential Applications: Depending on its solubility behavior, this compound could be useful in various applications where solubility in specific solvents might be required, especially in chemical synthesis or pharmaceuticals.

In summary, while the interaction of this compound with different solvents can be predicted, the exact solubility will depend on specific environmental conditions. As a noteworthy characteristic, its ionic nature typically favors increased solubility in polar solvents.

Interesting facts

Interesting Facts about Trimethyl-[2-(4,5,6,7-tetrachloro-2-methyl-isoindolin-2-ium-2-yl)ethyl]ammonium

The compound known as trimethyl-[2-(4,5,6,7-tetrachloro-2-methyl-isoindolin-2-ium-2-yl)ethyl]ammonium is a fascinating example of a quaternary ammonium salt, which possesses a variety of unique properties and potential applications.

Key Features

  • Ion Exchange Properties: Due to its quaternary ammonium structure, this compound exhibits strong ion exchange capabilities, making it useful in various separation processes.
  • Antimicrobial Activity: Research has suggested that compounds with quaternary ammonium groups can demonstrate significant antimicrobial effects, highlighting their potential in medical and industrial applications.
  • Electrochemical Applications: The nature of its structure allows for interesting electrochemical properties, which can be harnessed in sensors or batteries.

Furthermore, the embedding of a tetrachloroisoindoline moiety provides additional intriguing characteristics. The chlorine substituents can enhance the compound's stability and potentially facilitate complexation with other chemical species.

Applications

  • Pesticides and Herbicides: The stability provided by the chlorinated structure may enable use in agricultural chemicals.
  • Disinfectants: Its antimicrobial properties make it a candidate for usage in sanitizing agents.
  • Corrosion Inhibitors: The compound could also find footing in formulations designed to prevent the corrosion of metals.

Overall, the study of trimethyl-[2-(4,5,6,7-tetrachloro-2-methyl-isoindolin-2-ium-2-yl)ethyl]ammonium demonstrates how intricate modifications of chemical structures can yield compounds with diverse functionalities and applications. As we continue to explore the world of quaternary ammonium compounds, the potential they hold in advancing technology and health sectors becomes increasingly evident.

Synonyms
Chlorisondamine
Chlorisondamine ion
Chlorisondamine cation
7701-62-4
JD3M24F66I
CHLORISONDAMINE [WHO-DD]
DTXSID0048395
4,5,6,7-Tetrachloro-2-methyl-2-(2-(trimethylammonio)ethyl)isoindolinium
Isoindolinium, 4,5,6,7-tetrachloro-2-methyl-2-(2-(trimethylammonio)ethyl)-
Chloride, Chlorisondamine
NCGC00163230-01
UNII-JD3M24F66I
chlorisondamine-diiodide
Tocris-1001
CHEMBL1398654
DTXCID1028368
SCHEMBL14340042
BDBM84948
CHEBI:135514
CAS_6243
NSC_6243
PDSP1_000172
PDSP2_000171
trimethyl-[2-(4,5,6,7-tetrachloro-2-methyl-1,3-dihydroisoindol-2-ium-2-yl)ethyl]azanium
NCGC00024930-01
NCGC00024930-02
NS00005654
Q5102966
BRD-K18030938-302-02-7
ISOINDOLINIUM, 4,5,6,7-TETRACHLORO-2-METHYL-2-(2- (TRIMETHYLAMMONIO)ETHYL)-
1H-ISOINDOLIUM, 4,5,6,7-TETRACHLORO-2,3-DIHYDRO-2-METHYL-2-(2- (TRIMETHYLAMMONIO)ETHYL)-
1H-ISOINDOLIUM, 4,5,6,7-TETRACHLORO-2,3-DIHYDRO-2-METHYL-2-(2-(TRIMETHYLAMMONIO)ETHYL)-