Skip to main content

Etofenprox

ADVERTISEMENT
Identification
Molecular formula
C10H14ClNO3P
CAS number
80844-07-1
IUPAC name
[3-amino-2-(4-chlorophenyl)propyl]phosphonic acid
State
State

At room temperature, this compound is typically in a solid state, though it can appear as a viscous liquid above its melting point. The state may vary slightly depending on the purity and specific conditions such as temperature.

Melting point (Celsius)
53.00
Melting point (Kelvin)
326.00
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.00
General information
Molecular weight
221.65g/mol
Molar mass
221.6500g/mol
Density
1.0830g/cm3
Appearence

Etofenprox appears as a viscous, pale yellow liquid or solid crystalline material. It is characterized by a faint odor, which is typical for many phosphonic acid derivatives. The compound is usually handled in solution due to its viscous nature, which facilitates its application in its primary uses.

Comment on solubility

Solubility of [3-amino-2-(4-chlorophenyl)propyl]phosphonic acid

The solubility of [3-amino-2-(4-chlorophenyl)propyl]phosphonic acid (C10H14ClNO3P) is influenced by various factors owing to its unique chemical structure. Understanding its solubility properties is essential for applications in biological and industrial contexts.

Key Factors Affecting Solubility:

  • Polarity: The presence of the amino group and phosphonic acid group enhances the polarity of the molecule, which tends to increase solubility in polar solvents such as water.
  • Hydrogen Bonding: The ability to form hydrogen bonds, particularly with water molecules, significantly contributes to improved solubility. This characteristic may lead to higher solubility in aqueous solutions.
  • Ionization: At physiological pH, the phosphonic acid group can ionize, leading to better solubility of the compound in biological fluids, making it potentially bioavailable.
  • Temperature Effects: Generally, an increase in temperature can enhance solubility; however, this relationship may vary depending on the specific traits of the compound.

In conclusion, while [3-amino-2-(4-chlorophenyl)propyl]phosphonic acid exhibits a favorable profile for solubility, the precise solubility values can vary depending on the solvent, temperature, and ionic strength conditions. As a result, further empirical studies are recommended to establish quantitative solubility data tailored for specific applications.

Interesting facts

Interesting Facts about [3-amino-2-(4-chlorophenyl)propyl]phosphonic acid

[3-amino-2-(4-chlorophenyl)propyl]phosphonic acid is a fascinating compound that straddles the fascinating worlds of organic chemistry and medicinal applications. Here are some key points worth noting:

  • Phosphonic Acid Derivative: This compound is a derivative of phosphonic acid, a class of compounds known for their diverse biological activities and applications in agrochemicals and pharmaceuticals.
  • Structural Diversity: The presence of both an amino group and a chlorophenyl moiety contributes significantly to the compound's potential reactivity and biological activity, making it an interesting subject for drug design and synthesis.
  • Biological Significance: Compounds similar to [3-amino-2-(4-chlorophenyl)propyl]phosphonic acid have been investigated for their roles in various biological systems, including as inhibitors or substrates in metabolic pathways.
  • Pharmacological Potential: The unique structure of this compound raises the possibility of its activity as a pharmaceutical agent. It can potentially interact with various biological targets, making it of interest for developing new drugs.
  • Environmental Impact: Phosphonic acids are also studied for their environmental impact, particularly in terms of their degradation and persistence in various ecosystems.

As you delve into the study of [3-amino-2-(4-chlorophenyl)propyl]phosphonic acid, consider how its distinct characteristics may unlock new avenues in both synthetic chemistry and medicinal development. The intricate balance of structure and function is at the heart of this compound's appeal, making it a valuable topic for ongoing research and exploration.

Synonyms
Phaclofen
114012-12-3
[3-amino-2-(4-chlorophenyl)propyl]phosphonic acid
108351-35-5
Phosphonic acid, (3-amino-2-(4-chlorophenyl)propyl)-
Phosphonic acid, P-[3-amino-2-(4-chlorophenyl)propyl]-
(3-Amino-2-(4-chlorophenyl)propyl)phosphonic acid
beta-(4-Chlorophenyl)-3-aminopropylphosphonic acid
3-Amino-2-(4-chlorophenyl)propylphosphonic acid
Phosphonic acid, (3-amino-2-(4-chlorophenyl)propyl)-, (+-)-
SR-01000075640
Phosphonic acid, P-(3-amino-2-(4-chlorophenyl)propyl)-
Phaclofen, solid
Phosphonic acid,P-[3-amino-2-(4-chlorophenyl)propyl]-
Biomol-NT_000256
3-Amino-2-(4-chlorophenyl)propanephosphonic acid
Lopac0_000967
SCHEMBL339995
BPBio1_000970
GTPL1091
CHEMBL1255941
DTXSID80871598
HMS3263A15
Tox21_500967
MFCD00069328
AKOS024418761
CCG-205047
LP00967
SDCCGSBI-0050940.P002
NCGC00015781-03
NCGC00015781-04
NCGC00015781-05
NCGC00015781-06
NCGC00015781-08
NCGC00024483-02
NCGC00024483-03
NCGC00024483-04
NCGC00261652-01
DB-041194
HY-100798
CS-0020445
EU-0100967
P-118
L000482
Q7179950
SR-01000075640-1
SR-01000075640-3
(+/-)-3-Amino-2-(4-chlorophenyl)-propylphosphomic acid
P-a[3-aAmino-a2-a(4-achlorophenyl)apropyl]a-Phosphonic acid