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Ipratropium Bromide

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Identification
Molecular formula
C20H30BrNO3
CAS number
60205-81-4
IUPAC name
4-[(3-chlorophenyl)carbamoyloxy]but-2-ynyl-trimethyl-ammonium;chloride
State
State

At room temperature, Ipratropium Bromide is typically in a solid crystalline form.

Melting point (Celsius)
230.00
Melting point (Kelvin)
503.15
Boiling point (Celsius)
215.00
Boiling point (Kelvin)
488.15
General information
Molecular weight
430.38g/mol
Molar mass
430.3750g/mol
Density
1.3400g/cm3
Appearence

Ipratropium Bromide typically appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of 4-[(3-chlorophenyl)carbamoyloxy]but-2-ynyl-trimethyl-ammonium;chloride

The solubility of 4-[(3-chlorophenyl)carbamoyloxy]but-2-ynyl-trimethyl-ammonium;chloride (C20H30BrNO3) is influenced by several factors, making it a compound of interest in various chemical applications.

Key Factors Affecting Solubility:

  • Polarity: The presence of polar functional groups, such as ammonium and carbamoyloxy, typically enhances solubility in polar solvents, especially water.
  • Temperature: As with many compounds, an increase in temperature can significantly increase solubility, allowing for higher concentrations in solution.
  • Form of the Compound: The chloride salt form tends to be more soluble in water compared to its non-salt counterpart.
  • Interactions with Solvent: Hydrogen bonding and ionic interactions can play a crucial role in how well this compound dissolves in various solvents.

In general, one might expect that due to the combination of hydrophilic and hydrophobic characteristics, this compound demonstrates good solubility in polar solvents. However, detailed empirical testing would provide insight into its precise solubility parameters. As chemists often quote, "solubility is the gateway to reactivity," emphasizing its critical role in chemical behavior and reactivity in solutions.

Interesting facts

Interesting Facts about 4-[(3-chlorophenyl)carbamoyloxy]but-2-ynyl-trimethyl-ammonium;chloride

4-[(3-chlorophenyl)carbamoyloxy]but-2-ynyl-trimethyl-ammonium;chloride is a fascinating chemical compound that showcases the intricate world of organic chemistry. Here are some intriguing aspects of this compound:

  • Complex Structure: This compound belongs to the class of quaternary ammonium salts, which are often characterized by their unique properties and potential applications in various fields.
  • Functional Groups: It features a variety of functional groups, including a carbamoyloxy group and a chlorophenyl moiety. Such diverse functionalities can contribute to its biological activity and potential applications in medicinal chemistry.
  • Biological Relevance: Compounds of this nature have been studied for their potential as pharmacological agents. The presence of nitrogen and chlorine atoms may enhance the compound's interactions with biological targets.
  • Versatile Applications: Quaternary ammonium compounds are known for their surfactant, antibacterial, and antifungal properties, making them useful in a variety of applications ranging from personal care products to agricultural chemicals.

In the words of renowned chemist Linus Pauling, "Chemistry is about the structure of matter and how it behaves." Understanding compounds like this one not only helps in grasping the complexities of molecular interactions but also opens doors for innovative solutions in science and industry.

Overall, the study of 4-[(3-chlorophenyl)carbamoyloxy]but-2-ynyl-trimethyl-ammonium;chloride reveals how intricate the design of chemical compounds can be, with each component playing a critical role in the compound's properties and potential applications.

Synonyms
McN-A-343
55-45-8
McN-A 343
MCN A-343 chloride
(4-(m-Chlorophenylcarbamoyloxy)-2-butynyl)trimethylammonium chloride
A 343
4-(N-[3-CHLOROPHENYL]-CARBAMOYLOXY)-2-BUTYNYLTRIMETHYLAMMONIUM CHLORIDE
CW55R761RE
4-(m-Chlorophenylcarbamoyloxy)-2-butynyl)trimethylammonium Chloride
DTXSID80203532
MCN-343
4-[(3-chlorophenyl)carbamoyloxy]but-2-ynyl-trimethylazanium;chloride
MCN-A-343-11
2-Butyn-1-aminium, 4-((((3-chlorophenyl)amino)carbonyl)oxy)-N,N,N-trimethyl-, chloride
Butyl-1-aminium, 4-((((3-chlorophenyl)amino)carbonyl)oxy)-N,N,N-trimethyl-, chloride
Carbanilic acid, m-chloro-, ester with (4-hydroxy-2-butynyl)trimethylammonium chloride
A-343
4-[(3-chlorophenyl)carbamoyloxy]but-2-ynyl-trimethylazanium chloride
Ammonium, (4-hydroxy-2-butynyl)trimethyl-, chloride, m-chlorocarbanilate
MCN A-343
CHEMBL74300
(4-HYDROXY-2-BUTYNYL)TRIMETHYLAMMONIUM CHLORIDE, M-CHLOROCARBANILATE
4-(M-CHLOROPHENYLCARBAMOYLOXY)-2-BUTYNYLTRIMETHYLAMMONIUM CHLORI
2-BUTYN-1-AMINIUM, 4-((((3-CHLOROPHENYL)AMINO)CARBONYL)OXY)-N,N,N-TRIMETHYL-, CHLORIDE (1:1)
UNII-CW55R761RE
4-((3-chlorophenyl)carbamoyloxy)but-2-ynyl-trimethylazanium chloride
GTPL290
MLS000859939
SCHEMBL2977744
DTXCID10126023
HMS2235M19
HMS3260H16
HMS3372P11
Tox21_500277
MFCD00055068
AKOS024456563
CCG-221581
LP00277
NCGC00093733-01
NCGC00260962-01
MS-24679
SMR000058673
HY-107648
CS-0029051
EU-0100277
C 7041
G77705
SR-01000075310
SR-01000075310-1
Q27083728
(4-Hydroxy-2-butynyl)-1-trimethyl-ammonium-3-chloro-carbanilate chloride
(4-Hydroxy-2-butynyl)-1-trimethylammonium-3-chlorocarbanilate chloride
(4-Hydroxy-2-butynyl)-1-trimethylammonium-m-chlorocarbanilate chloride
4-[N-(3-Chlorophenyl)carbamoyloxy]-2--butynyl-trimethyl-ammonium chloride
4-(((3-Chlorophenyl)carbamoyl)oxy)-N,N,N-trimethylbut-2-yn-1-aminium chloride
4-(((3-Chlorophenyl)carbamoyl)oxy)-N,N,N-trimethylbut-2-yn-1-aminiumchloride