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Sevoflurane

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Identification
Molecular formula
C4H3F7O
CAS number
28523-86-6
IUPAC name
1,1,1,3,3,3-hexafluoro-2-(fluoromethoxy)propane
State
State

Sevoflurane is in a liquid state at room temperature. It easily vaporizes due to its relatively low boiling point, which makes it suitable for use as an inhalation anesthetic.

Melting point (Celsius)
-115.60
Melting point (Kelvin)
157.55
Boiling point (Celsius)
58.60
Boiling point (Kelvin)
331.75
General information
Molecular weight
200.06g/mol
Molar mass
200.0550g/mol
Density
1.5200g/cm3
Appearence

Sevoflurane is a volatile, colorless liquid with a characteristic mild, sweet odor. It is non-corrosive, stable with strong alkanes and inert perfluorinated alkanes, and does not require any additives to remain chemically stable.

Comment on solubility

Solubility of 1,1,1,3,3,3-Hexafluoro-2-(fluoromethoxy)propane (C4H3F7O)

1,1,1,3,3,3-Hexafluoro-2-(fluoromethoxy)propane (C4H3F7O) exhibits unique solubility characteristics primarily influenced by its highly fluorinated structure. The presence of multiple fluorine atoms imbues this compound with interesting interactions with solvents:

  • Polar Solvents: This compound demonstrates moderate solubility in polar solvents such as water due to dipolar interactions, yet the extensive fluorination limits its overall solubility.
  • Non-polar Solvents: It shows better solubility in non-polar organic solvents, where the van der Waals forces are more prominent.
  • Versatility: A potential application lies in its compatibility with various solvents, suggesting that it can be formulated into different mixtures for specialized purposes.

Given these factors, it is essential to consider the solvent's nature when evaluating the solubility of C4H3F7O. As with many fluorinated compounds, their high electronegativity and unique molecular geometry contribute to the complexities surrounding their solubility profiles.

In conclusion, while some solubility can be expected, a thorough understanding of the specific solvent system is crucial. "Fluorinated compounds require a meticulous approach in solubility assessment," making **empirical testing** a valuable method to ascertain the practical solubility in applications.

Interesting facts

Interesting Facts About 1,1,1,3,3,3-Hexafluoro-2-(fluoromethoxy)propane

1,1,1,3,3,3-Hexafluoro-2-(fluoromethoxy)propane, often referred to as a unique fluorinated compound, exhibits distinctive properties that make it a subject of interest in various fields, including materials science and chemical engineering. Here are some key points to consider:

  • Fluorination Mastery: The presence of multiple fluorine atoms significantly enhances the chemical stability and hydrophobicity of this molecule, making it resistant to oxidation and decomposition.
  • Applications in Industry: Due to its unique properties, this compound can be utilized in specialized applications, such as in the production of refrigerants or in advanced coatings where resistance to temperature and chemical corrosion is crucial.
  • Environmental Considerations: Understanding the environmental impact of fluorinated compounds is increasingly important. Research is ongoing to assess their effects on global warming and atmospheric chemistry.
  • Structure & Reactivity: The molecular structure reveals interesting steric effects and electron-withdrawing capabilities due to the fluorine substituents, which affect its reactivity and interactions with other substances.

In summary, the exploration of 1,1,1,3,3,3-hexafluoro-2-(fluoromethoxy)propane opens doors to both practical applications and theoretical insights. As quoted in scientific literature, "the unique characteristics of fluorinated compounds are reshaping our approach to chemical engineering and environmental science."

The study of such compounds is vital for the continued development of innovative technologies, underlining the importance of chemistry in addressing global challenges.

Synonyms
sevoflurane
28523-86-6
1,1,1,3,3,3-Hexafluoro-2-(fluoromethoxy)propane
Sevofluran
Ultane
Sevorane
Sevoflurano
Sojourn
MR6S4
sevoflo
Sevofluranum
Fluoromethyl 1,1,1,3,3,3-Hexafluoroisopropyl Ether
Sevofluranum [INN-Latin]
Sevoflurano [INN-Spanish]
Propane, 1,1,1,3,3,3-hexafluoro-2-(fluoromethoxy)-
Sevocalm
Petrem
fluoromethyl hexafluoroisopropyl ether
MR-6S4
NSC-760367
Fluoromethyl 2,2,2-trifluoro-1-(trifluoromethyl)ethyl ether
38LVP0K73A
CHEBI:9130
DTXSID8046614
1H,1H,3H-Perfluoro(3-methyl-2-oxabutane)
DTXCID6026614
1173021-96-9
MFCD00153189
NCGC00167421-01
Sevofrane
Fluoromethyl 2H-hexafluoroprop-2-yl ether
ETHER, FLUOROMETHYL 2,2,2-TRIFLUORO-1-(TRIFLUOROMETHYL)ETHYL-
Bax 3084
SEVOFLURANE (MART.)
SEVOFLURANE [MART.]
SEVOFLURANE (USP-RS)
SEVOFLURANE [USP-RS]
SEVOFLURANE (EP IMPURITY)
SEVOFLURANE [EP IMPURITY]
SEVOFLURANE (EP MONOGRAPH)
SEVOFLURANE (USP IMPURITY)
SEVOFLURANE [EP MONOGRAPH]
SEVOFLURANE [USP IMPURITY]
SEVOFLURANE (USP MONOGRAPH)
SEVOFLURANE [USP MONOGRAPH]
SEVOFLURANE (EMA EPAR VETERINARY)
SEVOFLURANE [EMA EPAR VETERINARY]
Sevoflurane-d3, Fluoromethyl 1,1,1,3,3,3-hexafluoro-2-propyl ether-d3, Fluoromethyl 2,2,2-trifluoro-1-(trifluoromethyl)ethyl ether-d3
Ultane (TN)
BRN 2041023
UNII-38LVP0K73A
Sevospire
FlurovessTM
fluoromethyl-2,2,2-trifluoro-1-(trifluoromethyl)ethyl ether
HSDB 8059
Sevoflurane Bostonbio
Propane,1,1,1,3,3,3-hexafluoro-2-(fluoromethoxy)-
Sevoflurane [USAN:USP:INN:BAN:JAN]
SEVOFLURANE [MI]
SEVOFLURANE [INN]
SEVOFLURANE [JAN]
F0691
SEVOFLURANE [USAN]
SEVOFLURANE [VANDF]
(CF3)2CHOCH2F
SCHEMBL61918
SEVOFLURANE [WHO-DD]
GTPL7296
CHEMBL1200694
SEVOFLURANE [GREEN BOOK]
Sevoflurane (JP18/USAN/INN)
N01AB08
SEVOFLURANE [ORANGE BOOK]
HMS3264N21
Pharmakon1600-01503680
Tox21_112425
NSC760367
AKOS007930500
CCG-213707
DB01236
FS29164
NSC 760367
NCGC00167421-02
AC-15484
AS-13261
CAS-28523-86-6
DB-047409
NS00014360
S2464
C07520
D00547
D78401
EN300-123016
SBI-0653442.0001
AB01563174_01
Q419394
SR-01000944968
SR-01000944968-1
BRD-K05638300-001-01-2
Fluoromethyl 1,1,1,3,3,3-hexafluoro-2-propyl ether
Z1269113624