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Xylometazoline Hydrochloride

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Identification
Molecular formula
C16H25ClN2
CAS number
1218-35-5
IUPAC name
N-tetralin-1-yl-4,5-dihydro-1H-imidazol-3-ium-2-amine;chloride
State
State

At room temperature, Xylometazoline Hydrochloride is typically a solid.

Melting point (Celsius)
144.00
Melting point (Kelvin)
417.15
Boiling point (Celsius)
253.00
Boiling point (Kelvin)
526.15
General information
Molecular weight
265.80g/mol
Molar mass
265.7950g/mol
Density
1.0900g/cm3
Appearence

Xylometazoline Hydrochloride is typically a white or almost white, crystalline powder that is soluble in water.

Comment on solubility

Solubility Characteristics of N-tetralin-1-yl-4,5-dihydro-1H-imidazol-3-ium-2-amine;chloride

N-tetralin-1-yl-4,5-dihydro-1H-imidazol-3-ium-2-amine;chloride exhibits interesting solubility properties that can be summarized as follows:

  • Polar Nature: The presence of the imidazolium cation and chloride anion contributes to a relatively high degree of polarity, suggesting good solubility in polar solvents.
  • Solvent Interaction: It is expected to be soluble in water due to the ionic nature of the chloride component, which aids in its dissolution by interacting with water molecules.
  • Organic Solvents: This compound may also show solubility in various organic solvents, particularly those that have polar characteristics.
  • pH Dependence: The solubility may vary with changes in pH due to the potential for protonation and deprotonation of the imidazole ring, which can further affect its solubility behavior.

Overall, the solubility of N-tetralin-1-yl-4,5-dihydro-1H-imidazol-3-ium-2-amine;chloride is influenced by its ionic structure, interactions with solvents, and the surrounding pH conditions, making it a compound of interest for various applications.

Interesting facts

Discovering N-tetralin-1-yl-4,5-dihydro-1H-imidazol-3-ium-2-amine;chloride

N-tetralin-1-yl-4,5-dihydro-1H-imidazol-3-ium-2-amine;chloride is a fascinating compound that presents a rich blend of structural complexity and potential applications. Here are some intriguing facts about this compound:

  • Structural Interest: This compound features an imidazolium cation, which is characterized by its five-membered ring containing two nitrogen atoms. These types of structures are prominent in various biochemical processes, especially in the study of ionic liquids.
  • Biological Implications: Compounds with imidazolium moieties have been researched as potential candidates in medicinal chemistry, including their roles as anti-cancer and anti-inflammatory agents.
  • Solvent and Electrolyte Uses: N-tetralin-1-yl-4,5-dihydro-1H-imidazol-3-ium-2-amine;chloride may exhibit properties beneficial for application in electrolytes for batteries or fuel cells, thanks to its ionic nature.
  • Exchangeable Cation: The chloride anion can often be exchanged for other anions, paving the way for innovative syntheses and the development of new materials.
  • Research Adventure: The multidimensional uses of this compound in synthetic chemistry open doors to interdisciplinary research, enhancing our understanding of nucleophiles and electrophiles in chemical reactions.

As with many complex organic compounds, further investigation into N-tetralin-1-yl-4,5-dihydro-1H-imidazol-3-ium-2-amine;chloride could yield important discoveries, highlighting the synergy between chemical structure and functionality.

"The beauty of chemistry lies in the connections it uncovers within the molecular world."

Synonyms
KB-227
2-(1,2,3,4-Tetrahydro-1-naphthylamino)-2-imidazoline hydrochloride
5254-29-5
2-IMIDAZOLINE, 2-(1,2,3,4-TETRAHYDRO-1-NAPHTHYLAMINO)-, HYDROCHLORIDE
4MJZ3RG16P
UNII-4MJZ3RG16P