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Neostigmine bromide

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Identification
Molecular formula
C12H19BrN2O2
CAS number
51-60-5
IUPAC name
trimethyl-[3-(methylcarbamoyloxy)phenyl]ammonium;iodide
State
State

At room temperature, neostigmine bromide is typically a solid.

Melting point (Celsius)
203.50
Melting point (Kelvin)
476.65
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
303.20g/mol
Molar mass
303.2300g/mol
Density
1.3600g/cm3
Appearence

Neostigmine bromide appears as a white, odorless, crystalline powder.

Comment on solubility

Solubility of Trimethyl-[3-(methylcarbamoyloxy)phenyl]ammonium Iodide

The solubility of trimethyl-[3-(methylcarbamoyloxy)phenyl]ammonium iodide is a key consideration for its applications in various chemical processes. This compound, being a quaternary ammonium salt, exhibits unique solubility characteristics due to its ionic nature and steric effects from the organic groups attached to the nitrogen atom.

Factors Influencing Solubility:

  • Ionic Nature: The presence of the iodide ion contributes to the compound's ability to dissolve in polar solvents such as water.
  • Hydrophilic Functional Groups: The methylcarbamoyloxy group enhances the interaction with water molecules, promoting solubility.
  • Temperature: Increased temperature typically enhances solubility for many salts, so consideration of thermal conditions is important.

In summary, while trimethyl-[3-(methylcarbamoyloxy)phenyl]ammonium iodide is likely to be soluble in polar solvents, the **extent of solubility can vary significantly** based on the conditions and the medium used. As a general guideline, compounds of this type tend to display good solubility, making them useful for a variety of chemical applications.

Interesting facts

Interesting Facts about Trimethyl-[3-(methylcarbamoyloxy)phenyl]ammonium Iodide

Trimethyl-[3-(methylcarbamoyloxy)phenyl]ammonium iodide is an intriguing compound that offers many valuable insights into the world of quaternary ammonium salts. Here are some fascinating points about this compound:

  • Quaternary Structure: The presence of the trimethyl group signifies that this compound belongs to a class of quaternary ammonium compounds, known for their diverse applications and unique properties.
  • Biological Relevance: Compounds like this one often play essential roles in biological systems. They can act as surfactants or facilitate drug delivery systems due to their ability to interact with both hydrophilic and hydrophobic environments.
  • Mechanism of Action: The methylcarbamoyloxy group in the compound serves as a functional moiety that can alter the binding properties, making this compound a subject of interest in medicinal chemistry, especially in drug design.
  • Innovative Applications: Research has shown that quaternary ammonium compounds can be utilized as antimicrobial agents, surface disinfectants, and even in the development of anti-cancer therapies!
  • Environmental Impact: It's crucial to approach the use of such compounds with caution, as their environmental effects and biodegradability are topics of ongoing research, particularly in the context of water pollution.

In summary, Trimethyl-[3-(methylcarbamoyloxy)phenyl]ammonium iodide represents a fascinating blend of organic chemistry and practical application, making it a subject of intense study and innovation. As researchers continue to unravel its potential, the emphasis on safety and environmental stewardship remains paramount.

Synonyms
Ammonium, (3-(methylcarbamoyloxy)phenyl)trimethyl-, iodide
T-1152
3983-39-9
Methiodide of N-methylurethane of 3-dimethylaminophenol
TL 1178
trimethyl-[3-(methylcarbamoyloxy)phenyl]azanium,iodide
T-1152 iodide
Carbamic acid, methyl-, (m-(trimethylammonio)phenyl) ester, iodide
AMMONIUM, (m-HYDROXYPHENYL)TRIMETHYL-, IODIDE, METHYLCARBAMATE
7KPX8SZ9L6
N,N,N-trimethyl-3-[(methylcarbamoyl)oxy]anilinium iodide
(m-HYDROXYPHENYL)TRIMETHYLAMMONIUM IODIDE, METHYLCARBAMATE
Benzenaminium, N,N,N-trimethyl-3-[[(methylamino)carbonyl]oxy]-, iodide (1:1)