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Neostigmine iodide

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Identification
Molecular formula
C13H22N2O2 · I
CAS number
114-80-7
IUPAC name
trimethyl-[4-(methylcarbamoyloxy)phenyl]ammonium;iodide
State
State

At room temperature, neostigmine iodide is typically in a solid state.

Melting point (Celsius)
145.00
Melting point (Kelvin)
418.15
Boiling point (Celsius)
232.00
Boiling point (Kelvin)
505.15
General information
Molecular weight
446.32g/mol
Molar mass
446.3190g/mol
Density
1.2500g/cm3
Appearence

Neostigmine iodide appears as a crystalline white or off-white powder. It is odorless and hygroscopic in nature, which means it absorbs moisture from the environment.

Comment on solubility

Solubility of Trimethyl-[4-(methylcarbamoyloxy)phenyl]ammonium Iodide

Trimethyl-[4-(methylcarbamoyloxy)phenyl]ammonium iodide, with the chemical formula C12H17ClN2O2, demonstrates unique solubility characteristics that are essential for its applications in various chemical and biological processes.

Factors Influencing Solubility

  • Polar Nature: The presence of the ammonium group and the methylcarbamoyloxy functional group enhances the polarity of the compound, promoting solubility in polar solvents like water.
  • Ionic Nature: Being an iodide, the compound is likely to dissolve readily in solutions that can stabilize ions, further aiding its solubility profile.
  • Hydrogen Bonding: The capability for hydrogen bonding due to the -NH and -OH groups also plays a pivotal role in enhancing its interaction with solvent molecules.

Solubility Insights

Generally, compounds that are:

  • High in polarity tend to dissolve well in polar solvents.
  • Capable of ionization demonstrate better solubility in ionic contexts.
  • Potentially forming hydrogen bonds with the solvent increase dissolution rates significantly.

In summary, trimethyl-[4-(methylcarbamoyloxy)phenyl]ammonium iodide is expected to exhibit a good degree of solubility in various polar solvents, making it versatile for different chemical applications. As with many organic compounds, it is essential to consider the solvent environment, as solubility can vary significantly with changes in temperature and pH.

Interesting facts

Interesting Facts about Trimethyl-[4-(methylcarbamoyloxy)phenyl]ammonium Iodide

Trimethyl-[4-(methylcarbamoyloxy)phenyl]ammonium iodide, often simply referred to by its component names, is a fascinating compound that showcases the intricate nature of organic chemistry. Here are some compelling points to consider:

  • Quaternary Ammonium Compound: This compound belongs to a class of chemicals known as quaternary ammonium compounds, which are characterized by a positively charged nitrogen atom bonded to four organic groups. They play a key role in various applications, including surface-active agents and disinfectants.
  • Biological Relevance: The presence of the methylcarbamoyloxy group in this compound may suggest potential biological activity. Such functional groups are often involved in pharmacological processes and could provide avenues for drug development.
  • Solubility Properties: Being an iodide, this compound tends to be more soluble in polar solvents, which can make it advantageous in biochemical assays or reactions that require a dissolvable salt.
  • Synthesis of Complex Molecules: The synthesis of trimethyl-[4-(methylcarbamoyloxy)phenyl]ammonium iodide typically involves multi-step organic reactions, showcasing the synthetic methods chemists can employ to obtain complex structures from simpler precursors.
  • Versatile Applications: Compounds with ammonium functionalities are widely used in industries ranging from cosmetics to pharmaceuticals, contributing to the formulation of various products.

In summary, trimethyl-[4-(methylcarbamoyloxy)phenyl]ammonium iodide is not just another chemical compound; it is a gateway to understanding *diverse applications in both laboratory settings and industrial contexts*. As one delves deeper into its properties and potential uses, the complexities of its structure and behavior become increasingly intriguing!

Synonyms
AR-17
T-1088
TL-1097
3983-40-2
NSC 127880
AMMONIUM, (p-HYDROXYPHENYL)TRIMETHYL-, IODIDE, METHYLCARBAMATE
Methiodide of N-methylurethane of 4-dimethylaminophenol
Methylcarbamic ester of p-oxyphenyltrimethylammonium iodide
Ammonium, ((p-methylcarbamoyloxy)phenyl)trimethyl-, iodide
Ammonium, (4-(N-methylcarbamoyloxy)phenyl)trimethyl-, iodide
Carbamic acid, N-methyl-, 4-dimethylaminophenyl ester, methiodide
Carbamic acid, N-methyl-, p-(trimethylammonio)phenyl ester, iodide
NSC-127880
36ETW2N9V5
NSC127880
WLN: 1MVOR DK1&1&1 &Q &I
(p-Hydroxyphenyl)trimethylammonium iodide methylcarbamate
Carbamic acid, 4-(diethylamino)phenyl ester, methiodide
Carbamic acid, 4-(dimethylamino)phenyl ester, methiodide
Carbamic acid, p-(trimethylammonio)phenyl ester, iodide
N,N,N-Trimethyl-4-[[(methylamino)carbonyl]oxy]benzenaminium iodide
Benzenaminium, N,N,N-trimethyl-4-[[(methylamino)carbonyl]oxy]-, iodide (1:1)