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Suxamethonium chloride

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Identification
Molecular formula
C12H19ClN2O2
CAS number
71-27-2
IUPAC name
(2-chlorophenyl)methyl-[2-[[2-[2-[(2-chlorophenyl)methyl-diethyl-ammonio]ethylamino]-2-oxo-acetyl]amino]ethyl]-diethyl-ammonium
State
State

At room temperature, suxamethonium chloride is a solid.

Melting point (Celsius)
160.00
Melting point (Kelvin)
433.15
Boiling point (Celsius)
230.80
Boiling point (Kelvin)
503.95
General information
Molecular weight
183.10g/mol
Molar mass
183.1000g/mol
Density
1.1290g/cm3
Appearence

Suxamethonium chloride appears as a white or off-white crystalline powder.

Comment on solubility

Solubility of (2-chlorophenyl)methyl-[2-[[2-[2-[(2-chlorophenyl)methyl-diethyl-ammonio]ethylamino]-2-oxo-acetyl]amino]ethyl]-diethyl-ammonium

The solubility of the compound C12H19ClN2O2, also known as (2-chlorophenyl)methyl-[2-[[2-[2-[(2-chlorophenyl)methyl-diethyl-ammonio]ethylamino]-2-oxo-acetyl]amino]ethyl]-diethyl-ammonium, can be influenced by various factors, including its chemical structure and the presence of functional groups.

Key Factors Influencing Solubility:

  • Polarity: The presence of the ammonium group increases polarity, suggesting potential solubility in polar solvents such as water.
  • Hydrophobic Regions: The chlorophenyl groups contribute hydrophobic characteristics, potentially reducing solubility in non-polar solvents.
  • pH Sensitivity: The soluble form may vary with pH, as ammonium salts tend to be more soluble in acidic conditions.
  • Intermolecular Interactions: Hydrogen bonding can enhance solubility in polar solvents, which may be a significant factor here.

In conclusion, while the exact solubility of this complex compound can vary based on experimental conditions, it is expected to exhibit moderate solubility in water due to its ionic character, while hydrophobic interactions may limit solubility in organic solvents. It is always advisable to conduct solubility tests under specific conditions to determine the most accurate solubility profile.

Interesting facts

Interesting Facts about (2-chlorophenyl)methyl-[2-[[2-[2-[(2-chlorophenyl)methyl-diethyl-ammonio]ethylamino]-2-oxo-acetyl]amino]ethyl]-diethyl-ammonium

This complex compound, often involving intricate molecular structures, has several notable characteristics that interest both chemists and those studying pharmaceuticals:

  • Antimicrobial Potential: Many related compounds in this class are studied for their potential as antimicrobial agents. This compound's unique structure may allow it to interact effectively with bacterial membranes.
  • Chlorophenyl Substitution: The presence of chlorophenyl groups is significant. Chlorine atoms can enhance lipophilicity, allowing the compound to penetrate biological membranes more easily, possibly affecting its bioactivity.
  • Ammonium Functionality: The ammonium moieties in the structure contribute to the compound's hydrogen-bonding capabilities, which may play a role in its interaction with biological targets.
  • Pharmacophore Model: This compound may serve as a model for developing new drugs. The combination of amino and oxo groups provides a versatile platform for modifications aimed at optimizing therapeutic effects.
  • Structure-Activity Relationships: Studying how variations in this compound's structure affect its biological activity can lead to valuable insights in medicinal chemistry, particularly in designing more effective agents.

In conclusion, this compound exemplifies the complexity that can arise in organic synthesis and the exciting possibilities it holds in medicinal applications. The intertwining of various functional groups in its structure presents a profound area of research that can lead to innovations in drug development.

Synonyms
ambenonium
Ambenonum
Ambenonium Base
7648-98-8
Ambenonium kation
Ambenonium ion
Ambenonium cation
Ambenonium [USAN]
CHEBI:2627
L16PUN799N
2,2'-[(1,2-dioxoethane-1,2-diyl)diimino]bis[n-(2-chlorobenzyl)-n,n-diethylethanaminium]
(2-chlorophenyl)methyl-[2-[[2-[2-[(2-chlorophenyl)methyl-diethylazaniumyl]ethylamino]-2-oxoacetyl]amino]ethyl]-diethylazanium
AMBENONIUM [VANDF]
AMBENONIUM [WHO-DD]
DTXSID5048396
OXALYLBIS(IMINOETHYLENE))BIS((O-CHLOROBENZYL)DIETHYLAMMONIUM
BENZENEMETHANAMINIUM, N,N'-((1,2-DIOXO-1,2-ETHANEDIYL)BIS(IMINO-2,1-ETHANEDIYL))BIS(2-CHLORO-N',N'-DIETHYL-
Benzenemethanaminium, N,N'-((1,2-dioxo-1,2-ethanediyl)bis(imino-2,1-ethanediyl))bis(2-chloro-N,N-diethyl-
NCGC00163221-01
UNII-L16PUN799N
2,2'-((1,2-dioxoethane-1,2-diyl)diimino)bis(N-(2-chlorobenzyl)-N,N-diethylethanaminium)
((2-chlorophenyl)methyl)(2-(((2-(((2-chlorophenyl)methyl)diethylazaniumyl)ethyl)carbamoyl)formamido)ethyl)diethylazanium
[(2-chlorophenyl)methyl](2-{[(2-{[(2-chlorophenyl)methyl]diethylazaniumyl}ethyl)carbamoyl]formamido}ethyl)diethylazanium
Tocris-0388
CHEMBL1652
SCHEMBL284678
DTXCID6028369
BDBM50262988
STL430453
AKOS037479279
DB01122
NCGC00024567-01
NCGC00024567-02
(2-chlorophenyl)methyl-[2-[[2-[(2-chlorophenyl)methyl-diethyl-ammonio]ethylcarbamoylformyl]amino]ethyl]-diethyl-azanium
NS00069747
C07773
Q4064027
BRD-K11292736-300-02-8
Benzenemethanaminium, N,N'-((1,2-dioxo-1,2-ethanediyl)bis(imino-2,1-ethanediyl))bis(2-chloro-N,N-diethyl)-
N-(2-chlorobenzyl)-2-(2-(2-((2-chlorobenzyl)diethylammonio)ethylamino)-2-oxoacetamido)-N,N-diethylethanaminium