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Tropicamide

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Identification
Molecular formula
C17H24BrNO3
CAS number
1508-75-4
IUPAC name
4-methylbenzenesulfonate;triethyl-[2-(2,3,4-trimethoxybenzoyl)oxyethyl]ammonium
State
State

At room temperature, tropicamide is in a solid state, appearing as a crystalline powder.

Melting point (Celsius)
96.00
Melting point (Kelvin)
369.15
Boiling point (Celsius)
379.40
Boiling point (Kelvin)
652.50
General information
Molecular weight
289.40g/mol
Molar mass
289.3960g/mol
Density
1.2568g/cm3
Appearence

Tropicamide appears as a white or almost white crystalline powder. It is practically odorless and is commonly used in the form of an ophthalmic solution.

Comment on solubility

Solubility of 4-methylbenzenesulfonate; triethyl-[2-(2,3,4-trimethoxybenzoyl)oxyethyl]ammonium

The solubility of the compound 4-methylbenzenesulfonate; triethyl-[2-(2,3,4-trimethoxybenzoyl)oxyethyl]ammonium is influenced by several factors, given its complex structure. Here are some key points to consider:

  • Polar Character: The presence of multiple methoxy groups typically enhances solubility in polar solvents, particularly in alcohols and water, due to favorable hydrogen bonding interactions.
  • Ammonium Group: The triethylammonium moiety is highly polar, which often leads to increased solubility in aqueous solutions.
  • Hydrophobic Interactions: The benzene rings can demonstrate hydrophobic properties, potentially reducing solubility in purely aqueous environments.
  • Sulfonate Group: The sulfonate part of the compound is ionic and generally soluble in water, which can counterbalance the hydrophobic tendencies of the aromatic groups.

In summary, the solubility behavior of this compound can be described as:

  1. Moderately soluble in water due to the interplay of ionic and hydrophobic groups.
  2. Soluble in organic solvents such as methanol and ethanol owing to its molecular structure that promotes favorable interactions.
  3. Dependent on pH as changes in ionic form might influence solubility, especially in varying pH environments.

Ultimately, understanding these nuances is crucial for practical applications in synthesis and chemical analyses.

Interesting facts

Interesting Facts about 4-methylbenzenesulfonate; triethyl-[2-(2,3,4-trimethoxybenzoyl)oxyethyl]ammonium

This compound, with its intricate structure, represents a fascinating intersection of organic chemistry and materials science. Here are some noteworthy points:

  • Biological Relevance: The triethyl-[2-(2,3,4-trimethoxybenzoyl)oxyethyl]ammonium moiety may exhibit biological activity, making it a potential candidate for pharmaceutical development.
  • Solubility Properties: The presence of the 4-methylbenzenesulfonate group often enhances the solubility of compounds in polar solvents, which is crucial for biological and industrial applications.
  • Versatile Usage: Compounds of this nature are commonly utilized in the synthesis of complex molecules due to their ability to act as intermediates in various chemical reactions.
  • Synthetic Applications: The functional groups present within this compound allow it to serve as an effective surfactant, which is essential in the fields of detergents and personal care products.

As we continue to explore the properties and applications of this compound, it enhances our understanding of how chemical structure relates to function. Researchers often quote, "The combination of functionality and reactivity is what makes organics so captivating."

In summary, the study of 4-methylbenzenesulfonate; triethyl-[2-(2,3,4-trimethoxybenzoyl)oxyethyl]ammonium not only opens up avenues in drug discovery but also serves as an exemplar of how complex organic molecules can possess diverse attributes, paving the way for innovation across multiple scientific disciplines.

Synonyms
Troxonii tosilas
Tosilate de troxonium [INN-French]
Tosilato de troxonio
Troxonii tosilas [INN-Latin]
Tosilate de troxonium
FWH 429
Tosilato de troxonio [INN-Spanish]
NSC 96643
Troxonium tosilate [INN:BAN]
DTXSID30192346
02X87P827K
Triethyl-2-(3,4,5-trimethoxybenzoyloxy)ethylammonium tosylate
Triethyl-2-(3,4,5-trimethoxybenzoyloxy)ethylammonium p-toluenesulfate
Triethyl(2-hydroxyethyl)ammonium p-toluenesulfonate 3,4,5-trimethoxybenzoate
Ammonium, triethyl(2-hydroxyethyl)-, p-toluenesulfonate, 2,3,4-trimethoxybenzoate (ester)
Ammonium, triethyl(2-hydroxyethyl)-, p-toluenesulfonate, 3,4,5-trimethoxybenzoate
Ethanaminium, N,N,N-triethyl-2-((3,4,5-trimethoxybenzoyl)oxy)-, salt with 4-methylbenzenesulfonic acid (1:1)
N,N,N-Triethyl-2-((3,4,5-trimethoxybenzoyl)oxy)ethanaminium, salt with 4-methylbenzenesulfonic acid (1:1)
Troxonii tosilas (INN-Latin)
Tosilate de troxonium (INN-French)
Tosilato de troxonio (INN-Spanish)
UNII-02X87P827K
DTXCID40114837
AKOS026745442
NS00127010
Q27231554
N,N,N-triethyl-2-(3,4,5-trimethoxybenzyoyloxy)ethylammonium tosylate
Ammonium, triethyl(2-hydroxyethyl)-, p-toluenesulfonate, 3,4,5-trimethoxybenzoate (8CI)
654-958-5
Ethanaminium, N,N,N-triethyl-2-((3,4,5-trimethoxybenzoyl)oxy)-, salt with 4-methylbenzenesulfonic acid (1:1) (9CI)