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(3-Aminophenyl)-trimethyl-arsonium chloride

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Identification
Molecular formula
C9H14AsClN
CAS number
7506-11-4
IUPAC name
(3-aminophenyl)-trimethyl-arsonium;chloride
State
State

At room temperature, (3-Aminophenyl)-trimethyl-arsonium chloride is a solid compound.

Melting point (Celsius)
230.00
Melting point (Kelvin)
503.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
233.57g/mol
Molar mass
233.5700g/mol
Density
1.4500g/cm3
Appearence

(3-Aminophenyl)-trimethyl-arsonium chloride typically appears as a crystalline, colorless to pale yellow solid. The exact color can differ slightly based on purity and crystalline structure.

Comment on solubility

Solubility of (3-aminophenyl)-trimethyl-arsonium;chloride

The solubility of (3-aminophenyl)-trimethyl-arsonium;chloride, often referred to as a quaternary ammonium salt, is influenced by several factors inherent to its structure and ionic nature.

Key Solubility Characteristics

  • High Solubility in Polar Solvents: This compound typically shows good solubility in polar solvents such as water and alcohols due to its ionic character, which enhances interactions with solvent molecules.
  • Limited Solubility in Non-Polar Solvents: Conversely, its solubility in non-polar solvents is negligible. This is primarily due to the ionic nature of the compound, which cannot effectively interact with non-polar molecules.
  • Temperature Dependence: Like many salts, the solubility of (3-aminophenyl)-trimethyl-arsonium;chloride may increase with temperature, making it more soluble in warm solvents.

In conclusion, the solubility profile of (3-aminophenyl)-trimethyl-arsonium;chloride underscores the importance of understanding ionic compounds and their interactions with varying solvent types. As a general rule, ionic compounds tend to be soluble in polar solvents while remaining insoluble or poorly soluble in non-polar environments.

Interesting facts

Interesting Facts about (3-aminophenyl)-trimethyl-arsonium Chloride

(3-aminophenyl)-trimethyl-arsonium chloride is a fascinating compound that showcases the diverse chemistry of organoarsenic compounds. Here are some intriguing aspects:

  • Functional Groups: The presence of the aminophenyl group gives this compound interesting properties, allowing it to participate in various chemical reactions typical of amines.
  • Organometallic Chemistry: As a trimethyl arsonium salt, it is part of a larger family of organometallic compounds, which are crucial for understanding the behavior of metals in organic environments.
  • Biological Activity: Compounds containing arsenic have been studied for their potential medicinal properties. This specific arsonium compound might have applications in pharmaceuticals, particularly in antiparasitic or anticancer research.
  • Environmental Impact: The chemistry of arsenic compounds is significant in environmental science, as understanding their behavior can help assess risks and develop remediation strategies.
  • Carrier Systems: (3-aminophenyl)-trimethyl-arsonium chloride has potential applications in organic electronics and as a *carrier system* for the delivery of drugs or genes due to its ability to form complexes.

As a chemistry student, one should appreciate how compounds like this illustrate the interplay between organic and inorganic chemistry, and the importance of functional groups in determining reactivity and application. As stated by chemist Linus Pauling, “The best way to have a good idea is to have a lot of ideas.” Compounds like (3-aminophenyl)-trimethyl-arsonium chloride provide vast opportunities for exploration and innovation in the chemical sciences.

Synonyms
Trimethyl-3-aminophenylarsonium chloride
Arsonium, (m-aminophenyl)trimethyl-, chloride
7145-92-8
ARSONIUM, 3-AMINOPHENYL-, TRIMETHYL-, CHLORIDE
NSC-16406
NSC 16406
Arsonium, chloride
Arsonium, trimethyl-, chloride
79HS764ZGL
DTXSID10991854
NSC16406
WLN: ZR C-AS-1&1&1 &Q &G
(3-Aminophenyl)(trimethyl)arsanium chloride
Arsonium, (3-aminophenyl)trimethyl-, chloride
(M-AMINOPHENYL)TRIMETHYLARSONIUM CHLORIDE
Arsonium, (3-aminophenyl)trimethyl-, chloride (1:1)