Euflavine | Solubility of Things

Identification

Molecular formula

C₂₄H₄₂N₃O₂(I₃)

CAS number

518-82-1

IUPAC name

2-[2,3-bis[2-(triethylammonio)ethoxy]phenoxy]ethyl-triethyl-ammonium;triiodide

State

At room temperature, Euflavine triiodide is primarily a solid compound. It remains in a stable crystalline form under normal atmospheric conditions. Its solid-state is due to the ionic nature of the triiodide ion interactions within the compound's structure, which facilitates the formation of a stable lattice.

Melting point (Celsius)

190.00

Melting point (Kelvin)

463.15

Boiling point (Celsius)

305.00

Boiling point (Kelvin)

578.15

General information

Molecular weight

879.09g/mol

Molar mass

879.0920g/mol

Density

1.6575g/cm³

Appearence

Euflavine, in its triiodide form, typically appears as a deep yellow to orange crystalline solid. The compound is known for its vivid color, which is often a characteristic of iodine-based salts. The crystalline form can appear as a crystalline powder or small granules, depending on the specific processing and handling it has undergone. Its appearance can be further characterized by a glossy surface, reflecting its ordered internal structure typical of crystalline substances.

Comment on solubility

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

The compound 2-[2,3-bis[2-(triethylammonio)ethoxy]phenoxy]ethyl-triethyl-ammonium;triiodide, with the chemical formula C₂₄H₄₂N₃O₂(I₃), exhibits interesting solubility characteristics, largely influenced by its unique molecular structure. Its solubility behavior can be summarized through the following points:

Polar Nature: The presence of multiple triethylammonio groups suggests that this compound is polar, which is likely to enhance its solubility in polar solvents.
Solvent Compatibility: This compound may show good solubility in solvents such as water and alcohols due to its ionic nature, particularly because of the triiodide counterion.
Ionic Interactions: The triiodide ion (I₃^-) may facilitate increased solubility in organic solvents that can stabilize ionic species, like methanol or dimethyl sulfoxide (DMSO).
Temperature Dependency: Like many ionic compounds, its solubility may increase with temperature, allowing for better dissolution in solution.

In summary, while the 2-[2,3-bis[2-(triethylammonio)ethoxy]phenoxy]ethyl-triethyl-ammonium;triiodide displays promising solubility in polar environments, the exact solubility profile can significantly depend on both the solvent used and external conditions such as temperature. Further experimental investigations are typically warranted to determine quantitative solubility data in various solvents.

Interesting facts

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

The compound known as 2-[2,3-bis[2-(triethylammonio)ethoxy]phenoxy]ethyl-triethyl-ammonium;triiodide is a fascinating example of a complex ionic compound that finds utility in various fields, particularly in medicinal chemistry and materials science. Here are some intriguing insights regarding this compound:

Ionic Form: This compound exists as a triiodide salt, where the presence of iodide ions enhances its ability to interact with biological systems, potentially increasing its efficacy as a drug carrier or contrast agent.
Ammonium Cation: The triethylammonio groups impart cationic characteristics, which facilitate interactions with negatively charged biological membranes, making it a candidate for studies in drug delivery.
Versatile Structure: The unique architecture of this molecule, featuring multiple ethoxy groups, significantly influences its solubility and reactivity, enabling varied applications in synthesis and formulation.
Potential Applications: Research suggests potential uses in antibacterial agents, and targeted therapeutic delivery mechanisms thanks to its precise ionic character and biological compatibility.

For scientists, understanding the interplay of this compound's structure and properties is key to unlocking its full potential in various applications. As highlighted in research literature, "the modulation of biocompatibility via structural modifications offers exciting pathways in drug development." As such, this compound presents exciting opportunities for future innovations in therapeutic methods and drug formulations.

Synonyms

GALLAMINE TRIETHIODIDE

65-29-2

Flaxedil

Benzcurine iodide

Remyolan

Syncurarine

Pirolakson

Sincurarine

Gallaflex

Parexyl

Pyrolaxon

Relaxan

Retensin

Tricuran

Gallamin triethiodide

Gallamone triethiodide

Gallamoni jodidum

Miowas G

Gallaminii iodidum

Gallamine-3ETI

Benzkurin

Fourneau 2559

Gallamine iodide

Gallamini triethiodidum

Gallaminum triaethjodidum

Triethiodure de gallamine

Gallaminum triaethoiodatum

Gallamina triodoetilato

Gallamine triiodoethylate

Triethioduro de galamina

HL 8583

RP 3697

HSDB 3229

Triiodoethylate de gallamine

EINECS 200-605-1

Gallamini triethiodidum [INN-Latin]

F 2559

NSC 102690

Triethiodure de gallamine [INN-French]

Triethioduro de galamina [INN-Spanish]

1,2,3-Tris(diethylaminoethoxy)benzene triethiodide

DTXSID5023089

UNII-Q3254X40X2

1,2,3-Tris(2-diethylaminoethoxy)benzene triethiodide

Trietioduro de galamina

1,2,3-Tri(beta-diethylaminoethoxy)benzene triethiodide

(v-Phenenyltris(oxyethylene))tris(triethylammoniumiodide)

1,2,3-Tris(2-triethylammonium ethoxy)benzene triiodide

(v-Phenenyltris(oxyethylene))tris(triethylammonium iodide)

1,2,3-Tris(2-diethylaminoethoxy)benzene tris(ethyliodide)

Pyrogallol 1,2,3-(diethylaminoethyl ether) trisethyl iodide

Tri(beta-diethylaminoethoxy)-1,2,3-benzene tri-iodoethylate

Triiodoethylate of tri(diethylaminoethyloxy)-1,2,3-benzene

(v-Phenenyltris(oxyethylene))tris(triethylammonium) triiodide

Pyrogallol 1,2,3-(diethylaminoethyl ether) tris(ethyliodide)

Ammonium, (v-phenenyltris(oxyethylene))tris(triethyl-, triiodide

NSC-102690

Q3254X40X2

2,2',2''-(1,2,3-Benzenetriyltris(oxy))tris(N,N,N-triethylethanaminium) triiodide

3697 R.P.

Ethanaminium, 2,2',2''-(1,2,3-benzenetriyltris(oxy))tris(N,N,N-triethyl)-, triiodide

Ethanaminium, 2,2',2''-(1,2,3-benzenetriyltris(oxy))tris(N,N,N-triethyl-, triiodide

DTXCID303089

Triiodure de tri(beta-triethylammoniumethoxy)-1,2,3 benzene

3.697 R.P.

Ammonium, (v-phenenyltris(oxyethylene)tris(triethyl-, triiodide

Tri(iodoethylate) de tri (beta diethylaminoethoxy)-1,2,3 benzene

Gallamine triethiodide [USP:INN]

Flacedil

Gallamin

2-[2,3-bis[2-(triethylazaniumyl)ethoxy]phenoxy]ethyl-triethylazanium;triiodide

Gallamonium Iodide

2,2',2''-(Benzene-1,2,3-triyltris(oxy))tris(N,N,N-triethylethanaminium) iodide

Gallamine triethiodide [INN]

Gallamine triethiodide (USP:INN)

Gallamina triodoetilato [DCIT]

Gallamini triethiodidum (INN-Latin)

Gallamine Triethyl Iodide

GALLAMINE TRIETHIODIDE (MART.)

GALLAMINE TRIETHIODIDE [MART.]

Triethiodure de gallamine (INN-French)

Triethioduro de galamina (INN-Spanish)

Flaxedil (TN)

Triiodoethylate de gallamine [French]

ETHANAMINIUM, 2,2',2''-(BENZENE-1,2,3-TRIYLTRIS(OXY))TRIS(N,N,N-TRIETHYL-, TRIIODIDE

Iodide, Gallamonium

GALLAMINE TRIETHIODIDE (USP IMPURITY)

GALLAMINE TRIETHIODIDE [USP IMPURITY]

Triethiodide, Gallamine

CAS-65-29-2

SR-01000075317

NCGC00163245-01

Iodide, Gallamine Triethyl

Triethyl Iodide, Gallamine

[v-Phenenyltris(oxyethylene)]tris[triethylammonium] triiodide

Gallamine triethiodide (USP)

gallamine (base)

Triiodure de tri(beta-triethylammoniumethoxy)-1,2,3 benzene [French]

Gallamin triethiodid

Tri(iodoethylate) de tri (beta diethylaminoethoxy)-1,2,3 benzene [French]

Prestwick_237

gallaminum triethoidatum

G 8134

triiodoAthylate de gallamine

Ethanaminium, 2,2',2'-(1,2,3-benzenetriyltris(oxy))tris(N,N,N-triethyl)-, triiodide

CHEMBL1200993

HMS502A12

HY-B0416R

Gallamine triethiodide (Flaxedil)

M03AC02

Gallamine Triethiodide (Standard)

REEUVFCVXKWOFE-UHFFFAOYSA-K

HMS1568O16

HMS2091H09

HMS2095O16

HMS3261N21

HMS3656G04

HMS3712O16

HMS3884B21

GALLAMINE TRIETHIODIDE [MI]

HY-B0416

Tox21_112040

Tox21_500550

CCG-40105

GALLAMINE TRIETHIODIDE [HSDB]

MFCD00011832

s2471

GALLAMINE TRIETHIODIDE [VANDF]

AKOS026749935

Tox21_112040_1

DB00483

GALLAMINE TRIETHIODIDE [WHO-DD]

GALLAMINE TRIETHIODIDE [WHO-IP]

LP00550

2,2',2''-(benzene-1,2,3-triyltris(oxy))tris(N,N,N-triethylethan-1-aminium) iodide

2,2',2''-[benzene-1,2,3-triyltris(oxy)]tris(N,N,N-triethylethanaminium) triiodide

NCGC00015482-07

NCGC00093937-01

NCGC00261235-01

AS-57694

DA-63677

GALLAMINE TRIETHIODIDE [ORANGE BOOK]

EU-0100550

G0554

NS00041180

SW196544-3

GALLAMINI TRIETHIODIDUM [WHO-IP LATIN]

C76041

D02292

Q3094785

SR-01000075317-1

SR-01000075317-3

SR-01000075317-6

Z1546616201

(V-PHENENYLTRIS(OXYETHYLENE))TRIS(TRIETHYLAMMONIUM TRIIODIDE)

(V-PHENENYLTRIS(OXYETHYLENE))TRIS(TRIETHYLAMMONIUM)IODIDE

(2-{2,3-bis[2-(triethylazaniumyl)ethoxy]phenoxy}ethyl)triethylazanium triiodide

(2-{2,6-bis[2-(triethylammonio)ethoxy]phenoxy}ethyl)triethylazanium triiodide

Gallamine triethiodide, >=98% (TLC), powder, muscarinic receptor antagonist

200-605-1