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Bis-Tris propane

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Identification
Molecular formula
C11H24N2O6Si
CAS number
64431-96-5
IUPAC name
2-[2,3-bis[2-(triethylammonio)ethoxy]phenoxy]ethyl-triethyl-ammonium
State
State

At room temperature, Bis-Tris propane is a stable solid substance.

Melting point (Celsius)
160.00
Melting point (Kelvin)
433.15
Boiling point (Celsius)
197.00
Boiling point (Kelvin)
470.00
General information
Molecular weight
324.50g/mol
Molar mass
324.5030g/mol
Density
1.0881g/cm3
Appearence

Bis-Tris propane appears as a white crystalline solid. It is commonly used in biochemical applications as a buffering agent.

Comment on solubility

Solubility of 2-[2,3-bis[2-(triethylammonio)ethoxy]phenoxy]ethyl-triethyl-ammonium (C11H24N2O6Si)

The solubility of 2-[2,3-bis[2-(triethylammonio)ethoxy]phenoxy]ethyl-triethyl-ammonium is influenced by its complex structure and the presence of multiple functional groups. Here are some key points regarding its solubility characteristics:

  • Ammonium Groups: The presence of triethylammonio groups typically enhances water solubility due to their positive charge, which interacts favorably with polar solvents.
  • Ether Linkages: The ethoxy groups contribute to the hydrophilicity of the compound, promoting better solubility in aqueous environments.
  • Hydrophobic Phenyl Ring: The phenoxy group introduces some hydrophobic character, which may limit solubility in purely aqueous systems, but in mixed solvents, this effect can be mitigated.
  • Temperature Dependency: Solubility may vary with temperature; generally, increasing temperature can enhance the solubility of many compounds.

Overall, it is anticipated that 2-[2,3-bis[2-(triethylammonio)ethoxy]phenoxy]ethyl-triethyl-ammonium would exhibit good solubility in polar solvents, especially in water, due to the presence of ionic and polar functional groups. However, the exact solubility can be highly dependent on the specific conditions, including pH and the presence of other solutes.

Interesting facts

Interesting Facts about 2-[2,3-bis[2-(triethylammonio)ethoxy]phenoxy]ethyl-triethyl-ammonium

This fascinating compound is a member of the quaternary ammonium class, which is well-known for its significant biological activity. Some interesting aspects of this compound include:

  • Quaternary Ammonium Compounds: These compounds are particularly useful in various applications, including as surfactants, antiseptics, and disinfectants. Due to their ability to interact with biological membranes, they often display antimicrobial properties.
  • Ion Exchange Properties: The presence of triethylammonium groups allows this compound to participate in ion exchange reactions. Such characteristics can be incredibly valuable in fields like environmental chemistry and water treatment.
  • Potential Biological Applications: Research indicates potential applications in drug delivery systems, where the ammonium moiety can enhance cellular uptake and improve the bioavailability of therapeutic agents.
  • Structure-Activity Relationship (SAR): Understanding how structural variations influence the activity of this compound can lead to innovations in developing new pharmaceuticals with improved efficacy and reduced toxicity.

As a chemistry student or scientist, studying compounds like this opens doors to various interdisciplinary collaborations, from medicinal chemistry to materials science. It illustrates the connection between molecular structure and function. In the words of renowned chemist Linus Pauling, "The best way to get a good idea is to have a lot of ideas." Exploring numerous compounds can inspire novel applications and hypotheses in the scientific community!

Synonyms
Triethylgallamine
7006-17-9
Lopac G-8134
UNII-VYJ027LZ05
Flaxedil
VYJ027LZ05
Gallamine triiodoethylate
CHEMBL360055
Benzkurin
Ethanaminium, 2,2',2''-(benzene-1,2,3-triyltris(oxy))tris(N,N,N-triethyl-
Gallamine iodide
2,2',2''-(1,2,3-Benzenetriyltrisoxy)tris(N,N,N-triethylethanaminium)
2-[2,3-bis[2-(triethylazaniumyl)ethoxy]phenoxy]ethyl-triethylazanium
Triiodoethylate de gallamine
2,2',2''-(benzene-1,2,3-triyltris(oxy))tris(N,N,N-triethylethan-1-aminium)
CAS-65-29-2
NCGC00163245-01
gallamine-triethiodide
Gallamine Triethiiodide
Spectrum_000823
Prestwick0_000157
Prestwick1_000157
Prestwick2_000157
Prestwick3_000157
Spectrum2_001078
Spectrum3_000439
Spectrum4_000561
Spectrum5_000748
Lopac G 8134
Lopac-G-8134
Lopac0_000550
BSPBio_000294
BSPBio_002058
GTPL356
KBioGR_000962
KBioSS_001303
DivK1c_000650
SPBio_001096
SPBio_002233
BPBio1_000324
DTXSID5048392
SCHEMBL12638600
CHEBI:94609
KBio1_000650
KBio2_001303
KBio2_003871
KBio2_006439
KBio3_001278
NINDS_000650
HMS2089F21
BDBM50149891
CCG-204640
IDI1_000650
NCGC00015482-01
NCGC00015482-02
NCGC00015482-03
NCGC00015482-04
NCGC00015482-05
NCGC00015482-16
NCGC00162183-01
SBI-0050533.P004
AB00053799
NS00069351
AB00053799-08
AB00053799-09
AB00053799_10
AB00053799_11
L001056
BRD-K43106192-320-09-2
BRD-K43106192-320-10-0
BRD-K43106192-320-11-8
Q27077765
2-[2,3-bis[2-(triethylammonio)ethoxy]phenoxy]ethyl-triethylammonium
2,2',2''-[benzene-1,2,3-triyltris(oxy)]tris(N,N,N-triethylethanaminium)
2,2'',2''''-[1,2,3-BENZENE-TRIYLTRIS(OXY)]TRIS[N,N,N-TRIETHYLETHANAMINIUM]