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Chloramine-T

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Identification
Molecular formula
C7H7Cl2NO2S
CAS number
127-65-1
IUPAC name
trimethyl-[2-(4,5,6,7-tetrachloro-2-methyl-isoindolin-2-ium-2-yl)ethyl]ammonium;dichloride
State
State

At room temperature, Chloramine-T is typically in a solid state, appearing as a crystalline powder. It is stable under normal conditions but should be stored in a cool, dry place to maintain its integrity.

Melting point (Celsius)
153.00
Melting point (Kelvin)
426.15
Boiling point (Celsius)
235.00
Boiling point (Kelvin)
508.15
General information
Molecular weight
227.64g/mol
Molar mass
227.6400g/mol
Density
2.0400g/cm3
Appearence

Chloramine-T is typically a white crystalline powder. It may appear slightly colored if impurities are present. The compound is noted for its solubility in water and its mild bleaching and disinfectant properties. When dissolved, it can form a clear, colorless solution.

Comment on solubility

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

The solubility of trimethyl-[2-(4,5,6,7-tetrachloro-2-methyl-isoindolin-2-ium-2-yl)ethyl]ammonium dichloride (C7H7Cl2NO2S) can be quite interesting, considering its structural characteristics. This compound exhibits notable behavior in different solvents:

  • Water solubility: Generally, quaternary ammonium compounds like this one tend to have good solubility in water due to the presence of positively charged ammonium ions.
  • Organic solvents: It may show varying degrees of solubility in organic solvents, which can depend heavily on the solvent's polarity.
  • Temperature effects: Solubility can also be temperature-dependent, with increased temperatures often leading to increased solubility.
  • pH influence: The ionization state of the compound can change with pH, affecting solubility; lower pH might favor ionization and, hence, increased solubility in aqueous solutions.

As a result, the overall solubility of this compound can be summarized as:

  1. Good solubility in polar solvents, particularly water.
  2. Variable solubility in non-polar organic solvents.

It is important to *experiment* and *characterize* under various conditions to get a complete profile of its solubility traits. Understanding these factors can be crucial for applications in formulations and chemical processes.

Interesting facts

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

This fascinating compound, known as trimethyl-[2-(4,5,6,7-tetrachloro-2-methyl-isoindolin-2-ium-2-yl)ethyl]ammonium dichloride, reveals intriguing characteristics that make it a significant subject of study within the realm of chemistry. Here are some interesting facts about this compound:

  • Unique Composition: The presence of chlorine, particularly in the tetrachloro substituents, enhances the compound's reactivity and stability, making it a valuable player in various chemical reactions.
  • Application Potential: Due to its quaternary ammonium structure, this compound may exhibit interesting properties such as antimicrobial activity, making it possible to explore its applications in disinfectants and antiseptics.
  • Structural Complexity: The isoindoline moiety contributes to the compound's structural diversity, which is essential for developing novel materials and pharmaceuticals.
  • Chirality Consideration: The configuration of substituents around the isoindoline structure introduces potential chirality, which can be critical in drug design and synthesis.
  • Research Opportunities: Because of its complexity and unique properties, researchers often find it an intriguing candidate for further studies in organic synthesis and materials science.

As with many compounds containing halogens, understanding the behavior and interactions of trimethyl-[2-(4,5,6,7-tetrachloro-2-methyl-isoindolin-2-ium-2-yl)ethyl]ammonium dichloride could pave the way for advancements in chemical applications across various fields, including pharmaceuticals, agrochemicals, and materials science. Exploring such compounds opens avenues for innovative discoveries.

Synonyms
Chlorisondamine chloride
69-27-2
Ecolid chloride
Hisindamone A
Ecolid R
Cloruro de clorisondamina
Chlorure de chlorisondamine
Chlorisondamine dimethochloride
CHLORISONDAMONE CHLORIDE
DTXSID7046332
Chlorisondamini chloridum
Chlorisondamine chloride [INN:BAN]
Chlorisondamini chloridum [INN-Latin]
7B58W7756G
SU 3088
Cloruro de clorisondamina [INN-Spanish]
Chlorure de chlorisondamine [INN-French]
Chloride, Chlorisondamine
1H-Isoindolium, 4,5,6,7-tetrachloro-2,3-dihydro-2-methyl-2-(2-(trimethylammonio)ethyl)-, dichloride
DTXCID5026332
UNII-7B58W7756G
CHLORISONDAMINE CHLORIDE [MI]
4,5,6,7-Tetrachloro-2-(2-dimethylaminoethyl)-2-methylisoindolinum chloride methochloride
CHLORISONDAMINE CHLORIDE [INN]
Isoindolinium, 4,5,6,7-tetrachloro-2-methyl-2-(2-(trimethylammonio)ethyl)-, dichloride
Ecolid
4,5,6,7-Tetrachlor-2-(2-trimethylammonioethyl)-2-methylisoindolinium chlorid
4,5,6,7-Tetrachloro-2-(2-dimethylaminoethyl)-isoindoline dimethochloride
Isoindoline, 2-(2-dimethylaminoethyl)-4,5,6,7-tetrachlorodimetho chloride
N-((2-Dimethylammonium)ethyl)-4,5,6,7-tetrachloroisoindolinium dimethochloride
Ammonium, (2-(2-methyl-4,5,6,7-tetrachloroisoindolinyl)ethyl)trimethyl-, dichloride
trimethyl-[2-(4,5,6,7-tetrachloro-2-methyl-1,3-dihydroisoindol-2-ium-2-yl)ethyl]azanium;dichloride
Chlorisondamini chloridum (INN-Latin)
CAS-69-27-2
Cloruro de clorisondamina (INN-Spanish)
Chlorure de chlorisondamine (INN-French)
NCGC00163230-01
Chlorisondamine Dichloride
Dichloride, Chlorisondamine
SCHEMBL309177
CHEMBL2104531
Tox21_112032
Tox21_112032_1
NCGC00024930-03
Q27268005
1H-Isoindolium, 4,5,6,7-tetrachloro-2,3-dihydro-2-methyl-2-[2-(trimethylammonio)ethyl]-, chloride (1:2)