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Heptadecafluorooctylsulfonyl ethylaminoacetate

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Identification
Molecular formula
C10H5F17NO4S
CAS number
55846-78-5
IUPAC name
2-[ethyl(1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctylsulfonyl)amino]acetic acid
State
State

At room temperature, the compound is typically found in a solid state. It can exist as a crystalline substance due to the presence of various functional groups that provide structural rigidity.

Melting point (Celsius)
154.00
Melting point (Kelvin)
427.15
Boiling point (Celsius)
217.00
Boiling point (Kelvin)
490.15
General information
Molecular weight
615.26g/mol
Molar mass
615.2580g/mol
Density
1.8000g/cm3
Appearence

The compound typically appears as a colorless to light yellow solid. It can often be seen as a crystalline powder under ambient conditions. Due to the presence of perfluorinated groups, this compound can exhibit unique wetting and non-stick characteristics.

Comment on solubility

Solubility of 2-[ethyl(1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctylsulfonyl)amino]acetic acid

This compound, known as a highly fluorinated amino acid derivative, exhibits some unique solubility characteristics that can be outlined as follows:

  • Fluorocarbon Influence: The presence of a long hydrophobic fluorocarbon chain tends to decrease solubility in polar solvents while increasing it in non-polar organic solvents.
  • Acidic Functional Group: The carboxylic acid group in the structure enhances solubility in water and other polar solvents due to its ability to ionize. This allows for hydrogen bonding with water.
  • Overall Solubility: The compound is likely to be:
    • Partially soluble in aqueous solutions at certain pH levels due to the acidic nature of the amino acid.
    • Slightly soluble or insoluble in most non-polar solvents due to conflicting polarities from the chemical structure.

In summary, while the compound demonstrates some aqueous solubility due to its acidic functional group, its extensive fluorocarbon chain limits its compatibility in many common solvents. This makes solubility exploration of this compound particularly intriguing for applications needing specific solvent interactions.

Interesting facts

Interesting Facts about 2-[Ethyl(1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctylsulfonyl)amino]acetic Acid

2-[Ethyl(1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctylsulfonyl)amino]acetic acid is a remarkable compound in the realm of organic chemistry. This unique compound stands out due to its complex structure and diverse applications. Here are some fascinating aspects:

  • Fluorinated Properties: The presence of the heptadecafluorooctyl group makes this compound exceptionally hydrophobic. This fluorinated moiety can significantly impact the compound's behavior in various chemical environments.
  • Potential Applications: Due to its unique properties, this compound can find applications in areas including:
    • Surfactants
    • Biological activities – potential for use in pharmaceuticals
    • Environmental science – studying interactions with organic and inorganic substrates
  • Designing Interfaces: The compound can be essential in formulating materials with specific interface properties, altering adhesion, and surface tension behavior.
  • Synthetic Pathways: The synthesis of this compound involves intricate organic reactions, which can serve as an educational point for students studying organic synthesis methodologies.
  • Eco-Friendly Research: In recent studies, compounds like this are significant in the quest for greener alternatives, as scientists seek to develop materials that have a lesser environmental impact.

Overall, 2-[Ethyl(1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctylsulfonyl)amino]acetic acid exemplifies the exciting possibilities present in the world of chemistry, serving as a bridge between fundamental science and practical applications.

Synonyms
2991-50-6
N-ETHYL-N-[(HEPTADECAFLUOROOCTYL)SULPHONYL]GLYCINE
2-(N-Ethylperfluorooctanesulfonamido)acetic acid
EINECS 221-061-1
DTXSID5062760
Glycine, N-ethyl-N-((heptadecafluorooctyl)sulfonyl)-
Glycine, N-ethyl-N-((1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctyl)sulfonyl)-
N-Ethyl-N-((heptadecafluorooctyl)sulphonyl)glycine
N-ETHYL-N-((1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-HEPTADECAFLUOROOCTYL)SULFONYL)GLYCINE
EtFOSAA
Glycine, N-ethyl-N-[(1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctyl)sulfonyl]-
DTXCID0038097
NEtFOSAA
N-ethylperfluorooctane sulfonamidoacetic acid
2-[ethyl(1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctylsulfonyl)amino]acetic acid
IT4R503EPH
N-Ethyl-N-(perfluoro-1-octanesulfonyl) Glycine
2-(N-Ethylperfluorooctanesulfonamido)acetic acid 100 microg/mL in Acetonitrile
2-(N-Ethylperfluorooctanesulfonamido)acetic acid 50 microg/mL in Methanol:Water
N-EtFOSAA
MFCD32200806
N-Ethyl perfluorooctanesulfonamidoacetic acid
UNII-IT4R503EPH
1336-61-4
2-(N-ethyl-perfluorooctane sulfonamido) acetic acid
SCHEMBL2892539
CHEBI:83507
FE91897
Ethylperfluorooctane sulfonamidoacetic acid
PD192533
N-ethyl-N-((perfluorooctyl)sulfonyl)glycine
NS00000428
N-Ethyl perfluorooctane sulfonamidoacetic acid
N-ethylperfluorooctane sulfonamido acetic acid
D93420
N-ethylperfluoro-1-octanesulfonamideoacetic acid
2-N-Ethyl(perfluorooctanesulfonamido)acetic acid
2-(N-ethyl-perfluorooctanesulfonamido) acetic acid
n-(ethyl)n-(perfluorooctylsulfonyl)-aminoacetic acid
N-ethyl perfluorooctane sulfonamido acetic acid, n=8
N-(ethyl)-N-(perfluorooctylsulfonyl)-aminoacetic acid
Q27156890