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Succinylcholine chloride

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Identification
Molecular formula
C14H30Cl2N2O4
CAS number
71-27-2
IUPAC name
diethyl-[2-(2-hydroxy-2,2-diphenyl-acetyl)oxyethyl]-methyl-ammonium;bromide
State
State

At room temperature, succinylcholine chloride is typically found as a solid. It is usually handled in its salt form, which is ideal for its use in pharmaceutical applications.

Melting point (Celsius)
158.40
Melting point (Kelvin)
431.60
Boiling point (Celsius)
404.90
Boiling point (Kelvin)
678.10
General information
Molecular weight
290.74g/mol
Molar mass
290.7430g/mol
Density
1.3673g/cm3
Appearence

Succinylcholine chloride appears as a white, crystalline powder that is commonly used in medical settings. It is highly soluble in water and has a slightly saline taste. The powder is stable under normal conditions of use and storage.

Comment on solubility

Solubility of Diethyl-[2-(2-hydroxy-2,2-diphenyl-acetyl)oxyethyl]-methyl-ammonium Bromide

The solubility of diethyl-[2-(2-hydroxy-2,2-diphenyl-acetyl)oxyethyl]-methyl-ammonium bromide can be quite intriguing due to its complex molecular structure. Here are some key points to consider:

  • Polar vs. Non-Polar: The presence of functional groups, such as the hydroxyl group and the quaternary ammonium structure, suggests that this compound may be relatively soluble in polar solvents, particularly water.
  • Solvent Compatibility: It is expected to demonstrate good solubility in organic solvents such as ethanol and methanol due to its hydrophobic phenyl groups combined with hydrophilic functional groups.
  • Electrolytic Properties: As a bromide salt, it may dissociate in solution, enhancing its ionic conductivity, which can influence solubility dynamics.

In general, the solubility of such compounds can be described by the rule of thumb: “like dissolves like.” Therefore, observance of this principle is crucial when selecting solvents for dissolution.

In summary, while specific solubility data may not be readily available, it stands to reason that diethyl-[2-(2-hydroxy-2,2-diphenyl-acetyl)oxyethyl]-methyl-ammonium bromide will show favorable solubility characteristics in both polar and non-polar environments, contingent upon the interactions facilitated by its molecular structure.

Interesting facts

Interesting Facts about Diethyl-[2-(2-hydroxy-2,2-diphenyl-acetyl)oxyethyl]-methyl-ammonium Bromide

Diethyl-[2-(2-hydroxy-2,2-diphenyl-acetyl)oxyethyl]-methyl-ammonium bromide is a fascinating compound, often studied for its unique properties and applications in various fields. Here are some noteworthy aspects of this chemical:

  • Quaternary Ammonium Compound: This compound belongs to a class of quaternary ammonium compounds, which are known for their effectiveness as surfactants and disinfectants. These features make them essential in both pharmaceuticals and industrial applications.
  • Biological Relevance: The presence of a hydroxy group (–OH) in its structure suggests potential interactions with biological macromolecules, opening doors for research in drug delivery systems and therapeutic applications.
  • Structure-Activity Relationship (SAR): The complex structure of this compound allows for the exploration of its pharmacokinetics. The diphenylacetyl moiety could enhance lipophilicity, influencing how the compound interacts within biological environments.
  • Research Potential: Due to its intricate molecular design, this compound serves as a valuable subject for studies in organic synthesis and medicinal chemistry. Its ability to incorporate different functional groups can lead to novel derivatives with varied properties.
  • Applications in Industry: Beyond pharmaceuticals, the structural characteristics of this compound may allow its use in emulsifiers, stabilizers, and as an ingredient in personal care products, leveraging its surfactant properties.

As a compound with myriad applications, Diethyl-[2-(2-hydroxy-2,2-diphenyl-acetyl)oxyethyl]-methyl-ammonium bromide exemplifies the importance of chemical diversity in advancing both scientific research and technological innovation. It challenges chemists to unlock its full potential, making it a compelling subject for ongoing study.

Synonyms
methylbenactyzium bromide
3166-62-9
Gastrimade
Igsain
Benzactyzine methobromide
Noinarin
Paragone
Semulgin
Alsain
Apulcin
Finalin
Sanrine
Final
Neo-aspamin
N,N-Diethyl-2-(2-hydroxy-2,2-diphenylacetoxy)-N-methylethanaminium bromide
BENACTYZINE METHOBROMIDE
Benzactyzine methylbromide
Benactyzine methyl bromide
Spatomac
Bromuro de metilbenacticio
Bromure de methylbenactyzium
Diethylaminoethyl diphenylglycolate methobromide
NSC-11525
diethyl-[2-(2-hydroxy-2,2-diphenylacetyl)oxyethyl]-methylazanium;bromide
Ethanaminium, N,N-diethyl-2-[(hydroxydiphenylacetyl)oxy]-N-methyl-,bromide
Diethyl(2-hydroxyethyl)methylammonium bromide benzilate
DTXSID2046832
M35Q3X4F69
Methyl benactyzium bromide
FWH-101
Methylbenactyzii bromidum
NCGC00181082-01
EINECS 221-628-3
ENT 26656
Methylbenactyzium bromide [INN:JAN]
NSC 11525
Methylbenactyzii bromidum [INN-Latin]
Bromuro de metilbenacticio [INN-Spanish]
Bromure de methylbenactyzium [INN-French]
UNII-M35Q3X4F69
AI3-26656
Ammonium, diethyl(2-hydroxyethyl)methyl-, bromide, benzilate
ammonium,diethyl(2-hydroxyethyl)methyl-,bromide,benzilate(ester)
Diethyl(2-hydroxyethyl)methylammonium bromide, benzilate (ester)
Ammonium, bromide, benzilate
SCHEMBL60901
CHEMBL2106570
DTXCID9032371
CHEBI:31834
DKMVJQCQTCLYIF-UHFFFAOYSA-M
HMS3885P10
HY-B2070
NSC11525
Tox21_112701
Ammonium, diethyl(2-hydroxyethyl)methyl-, bromide, benzilate (ester)
BDBM50491133
BENACTYZINE METHOBROMIDE [MI]
ENT-26656
MFCD00210328
s4624
AKOS015915023
diethyl-[2-(2-hydroxy-2,2-diphenylacetyl)oxyethyl]-methylazanium,bromide
Ethanaminium, N,N-diethyl-2-((hydroxydiphenylacetyl)oxy)-N-methyl-, bromide
Methylbenactyzium bromide (JP17/INN)
CCG-268910
CS-7909
METHYLBENACTYZIUM BROMIDE [INN]
METHYLBENACTYZIUM BROMIDE [JAN]
METHYLBENACTYZIUM BROMIDE [MART.]
AS-50336
DA-75492
METHYLBENACTYZIUM BROMIDE [WHO-DD]
CAS-3166-62-9
NS00081233
D01315
O12004
Q27283425
Benzilic acid, ester with diethyl(2-hydroxyethyl)methylammonium bromide
Ethanaminium,N-diethyl-2-[(hydroxydiphenylacetyl)oxy]-N-methyl-, bromide
N,N-Diethyl-2-(2-hydroxy-2,2-diphenylacetoxy)-N-methylethanaminiumbromide