Skip to main content

Loxoprofen

ADVERTISEMENT
Identification
Molecular formula
C15H22O4
CAS number
68767-14-6
IUPAC name
6-(2-ethylhexoxy)-6-oxo-hexanoic acid
State
State

At room temperature, Loxoprofen is in a solid state.

Melting point (Celsius)
99.00
Melting point (Kelvin)
372.15
Boiling point (Celsius)
333.20
Boiling point (Kelvin)
606.35
General information
Molecular weight
246.32g/mol
Molar mass
246.3160g/mol
Density
1.0349g/cm3
Appearence

Loxoprofen appears as a white crystalline powder.

Comment on solubility

Solubility of 6-(2-ethylhexoxy)-6-oxo-hexanoic acid

The solubility of the compound 6-(2-ethylhexoxy)-6-oxo-hexanoic acid, notable for its unique branching structure, can be characterized by several important aspects:

  • Polarity: The presence of both a hydrophobic hydrocarbon chain (2-ethylhexoxy) and a more polar functional group (carboxylic acid) makes this compound amphiphilic. This dual nature often enhances solubility in varying environments.
  • Solvent Compatibility: It is typically more soluble in organic solvents such as ethanol or acetone than in water, primarily due to its large hydrocarbon moiety providing substantial non-polar surface area.
  • Hydrogen Bonding: The carboxylic acid group can form hydrogen bonds with polar solvents, potentially increasing solubility in certain conditions, particularly when the solvent is capable of hydrogen bonding.
  • Temperature Influence: Like many organic compounds, solubility can also depend on temperature—generally increasing with higher temperatures, which promotes the dissolution process.

In summary, the solubility profile of 6-(2-ethylhexoxy)-6-oxo-hexanoic acid highlights the exquisite balance of its amphiphilic character, making it a candidate for various applications where solubility in organic solvents is advantageous.

Interesting facts

Interesting Facts about 6-(2-ethylhexoxy)-6-oxo-hexanoic acid

6-(2-ethylhexoxy)-6-oxo-hexanoic acid, often referred to in scientific literature for its complex structure and unique properties, presents several fascinating characteristics:

  • Versatile Applications: This compound is utilized in various fields, particularly in the production of esters, which serve as important intermediates in the synthesis of pharmaceuticals, agrochemicals, and polymer materials.
  • Functional Groups: The presence of both a carboxylic acid and a ketone group allows for interesting reactivity, making the compound a valuable building block for organic synthesis.
  • Synthetic Pathways: Researchers have developed several synthetic routes to create this compound, often focusing on optimizing yields and minimizing environmental impact. 
  • Biological Activity: Compounds with similar structures are known to exhibit biological activity, leading to ongoing studies exploring potential applications in medicinal chemistry.
  • Research Opportunities: As a relatively less-explored compound, 6-(2-ethylhexoxy)-6-oxo-hexanoic acid offers significant opportunities for academic and industrial research, particularly in developing new materials or therapeutic agents.

In the words of a budding chemist: "Every compound tells a story, and the journey of discovering its potential is where the excitement lies!"

Understanding such compounds can lead to advancements in multi-disciplinary fields, bridging chemistry with technology and biology. The exploration of 6-(2-ethylhexoxy)-6-oxo-hexanoic acid is just one of the many pathways that illustrate the intricate tapestry of chemical science.

Synonyms
4337-65-9
2-Ethylhexyl hydrogen adipate
Mono(2-ethylhexyl) adipate
2-ethylhexyl adipate
Mono-2-ethylhexyl adipate
6-((2-Ethylhexyl)oxy)-6-oxohexanoic acid
CCRIS 4296
Hexanedioic acid, mono(2-ethylhexyl) ester
EINECS 224-386-7
6-[(2-Ethylhexyl)oxy]-6-oxohexanoic acid
D01X12CH07
DTXSID3025679
ADIPIC ACID, 2-ETHYLHEXYL ESTER
ADIPIC ACID, MONO(2-ETHYLHEXYL) ESTER
HEXANEDIOIC ACID, 1-(2-ETHYLHEXYL) ESTER
Mono2ethylhexyl adipate
2Ethylhexyl hydrogen adipate
Mono(2ethylhexyl) hexanedioate
Adipic acid, 2ethylhexyl ester
DTXCID405679
Adipic acid, mono(2ethylhexyl) ester
MONO(2-ETHYLHEXYL) HEXANEDIOATE
Hexanedioic acid, mono(2ethylhexyl) ester
224-386-7
6-(2-ethylhexoxy)-6-oxohexanoic acid
Hexanedioic acid, mono(2-ethylhexyl)ester
MEHA
Mono(2-ethylhexyl)adipate
SCHEMBL433435
UNII-D01X12CH07
AKOS032961420
AS-59653
hexanedioic acid mono(2-ethylhexyl) ester
NS00022190
NS00076527
6-[(2-Ethylhexyl)oxy]-6-oxohexanoic acid #
A12524
Q27893579