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Cyclamic acid

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Identification
Molecular formula
C6H11NO3S
CAS number
139-05-9
IUPAC name
N-cyclohexylsulfamate;2-furylmethyl-methyl-[1-methyl-2-[3-(trifluoromethyl)phenyl]ethyl]ammonium
State
State

Cyclamic acid, as a sodium or calcium salt, is typically a solid at room temperature. The salts are highly soluble in water, making them valuable as sweeteners in various applications.

Melting point (Celsius)
170.00
Melting point (Kelvin)
443.15
Boiling point (Celsius)
433.00
Boiling point (Kelvin)
706.15
General information
Molecular weight
201.24g/mol
Molar mass
201.2440g/mol
Density
1.5800g/cm3
Appearence

N-cyclohexylsulfamate, commonly known as cyclamic acid or its salts, is a fine white crystalline powder. It is often used in its sodium or calcium salt form and appears as a colorless saline solution in commercial products.

Comment on solubility

Solubility of N-cyclohexylsulfamate; 2-furylmethyl-methyl-[1-methyl-2-[3-(trifluoromethyl)phenyl]ethyl]ammonium

The solubility characteristics of the compound N-cyclohexylsulfamate; 2-furylmethyl-methyl-[1-methyl-2-[3-(trifluoromethyl)phenyl]ethyl]ammonium can be quite complex due to its unique structure. Generally speaking, solubility is influenced by various factors including polarity, molecular size, and the presence of functional groups.

Some key points to consider regarding solubility include:

  • Polarity: The presence of polar functional groups can enhance solubility in polar solvents such as water.
  • Molecular Size: Larger molecules tend to have lower solubility due to steric hindrance affecting interactions with solvent molecules.
  • Hydrogen Bonding: Compounds capable of forming hydrogen bonds often exhibit increased solubility in water.

For this specific compound, the combination of the -N-cyclohexyl, -2-furylmethyl, and -trifluoromethyl moieties suggests a diverse range of intermolecular interactions. This may lead to solubility in:

  • Organic Solvents: Given the hydrophobic cyclohexyl and trifluoromethyl groups.
  • Aqueous Solutions: Although slightly less predictable, the sulfamate functional group could offer increased affinity for water.

In conclusion, while definitive solubility data would require empirical investigation, it can be anticipated that the compound may exhibit variable solubility depending on the solvent choice, primarily leaning towards enhanced solubility in organic solvents. Therefore, a careful assessment using various solvents is recommended to elucidate its solubility profile.

Interesting facts

N-cyclohexylsulfamate; 2-furylmethyl-methyl-[1-methyl-2-[3-(trifluoromethyl)phenyl]ethyl]ammonium

This remarkable compound can be considered a unique blend of organic structures that showcases both functional versatility and potential applications across various scientific fields. Here are several intriguing aspects of this compound:

  • Structural Diversity: The combination of a furyl group and a trifluoromethyl-phenyl moiety contributes to its unique characteristics, enhancing its potential as a bioactive compound.
  • Biochemical Applications: N-cyclohexylsulfamate moiety has been investigated for its role in pharmaceuticals, particularly in antidiabetic agents, showcasing its therapeutic potential.
  • Fluorinated Compounds: The presence of trifluoromethyl group often improves lipid solubility and metabolic stability, allowing for enhanced interactions within biological systems.
  • Sulfamate Group: Sulfamates have been recognized as excellent candidates in the development of insecticides and herbicides, reflecting their significance in agricultural science.

As a scientist or student exploring this compound, it’s essential to appreciate the synergy between its structural elements and the resultant properties that each contribute. Understanding these relationships lays a foundation for potential innovations in both medicinal chemistry and agricultural applications.

In summary, N-cyclohexylsulfamate; 2-furylmethyl-methyl-[1-methyl-2-[3-(trifluoromethyl)phenyl]ethyl]ammonium exemplifies the cutting-edge innovations at the intersection of chemistry, biology, and environmental science. Delving into its specific functions and interactions can lead to exciting discoveries!

Synonyms
Furfurylamine, N-methyl-N-(alpha-methyl-m-(trifluoromethyl)phenethyl)-, cyclohexanesulfamate (+-)-
5843-58-3
N-Methyl-N-(alpha-methyl-m-(trifluoromethyl)phenethyl)furfurylamine cyclohexanesulfamate