Cas no 101568-19-8 (2,2,3-trimethylpentanoic acid)

2,2,3-Trimethylpentanoic acid is a branched-chain carboxylic acid with the molecular formula C8H16O2. Its unique sterically hindered structure contributes to enhanced stability and resistance to degradation under harsh conditions. The compound exhibits low volatility and good solubility in organic solvents, making it suitable for applications in specialty chemical synthesis, lubricant additives, and polymer modification. The presence of multiple methyl groups adjacent to the carboxyl group influences its reactivity, allowing selective derivatization for fine chemical production. Its hydrophobic nature also lends utility in surface modification and corrosion inhibition formulations. The acid's defined branching pattern ensures consistent performance in high-precision industrial processes.
2,2,3-trimethylpentanoic acid structure
2,2,3-trimethylpentanoic acid structure
Product Name:2,2,3-trimethylpentanoic acid
CAS No:101568-19-8
MF:C8H16O2
MW:144.211442947388
CID:5941030
PubChem ID:17810189
Update Time:2025-06-09

2,2,3-trimethylpentanoic acid Chemical and Physical Properties

Names and Identifiers

    • 2,2,3-trimethylpentanoic acid
    • 101568-19-8
    • AKOS006375461
    • EN300-1245300
    • SCHEMBL1572815
    • Inchi: 1S/C8H16O2/c1-5-6(2)8(3,4)7(9)10/h6H,5H2,1-4H3,(H,9,10)
    • InChI Key: JAUKQUVPYOBDNP-UHFFFAOYSA-N
    • SMILES: OC(C(C)(C)C(C)CC)=O

Computed Properties

  • Exact Mass: 144.115029749g/mol
  • Monoisotopic Mass: 144.115029749g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 3
  • Complexity: 127
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.5
  • Topological Polar Surface Area: 37.3?2

2,2,3-trimethylpentanoic acid Pricemore >>

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Additional information on 2,2,3-trimethylpentanoic acid

2,2,3-Trimethylpentanoic Acid (CAS No. 101568-19-8): An Overview of Its Properties, Applications, and Recent Research

2,2,3-Trimethylpentanoic acid (CAS No. 101568-19-8) is a branched-chain fatty acid that has garnered significant attention in recent years due to its unique chemical structure and potential applications in various fields. This compound is characterized by its molecular formula C8H16O2 and a molecular weight of 144.21 g/mol. The presence of three methyl groups and a carboxylic acid functional group endows it with distinct physical and chemical properties, making it a valuable compound in both academic research and industrial applications.

The physical properties of 2,2,3-trimethylpentanoic acid are well-documented. It is a colorless to light yellow liquid with a characteristic odor. The compound has a melting point of -5°C and a boiling point of 170°C at 760 mmHg. Its solubility in water is limited, but it is highly soluble in organic solvents such as ethanol, acetone, and ethyl acetate. These properties make it suitable for use in various chemical reactions and formulations.

In terms of chemical properties, 2,2,3-trimethylpentanoic acid exhibits typical behavior of carboxylic acids. It can undergo esterification reactions to form esters, which are widely used in the fragrance and flavor industries. Additionally, it can participate in condensation reactions to form amides and other derivatives. The presence of multiple methyl groups also influences its reactivity, making it an interesting substrate for synthetic chemists exploring novel reaction pathways.

One of the key areas where 2,2,3-trimethylpentanoic acid has found significant application is in the pharmaceutical industry. Recent studies have shown that branched-chain fatty acids like 2,2,3-trimethylpentanoic acid can play a role in modulating metabolic pathways and have potential therapeutic effects. For instance, research published in the Journal of Medicinal Chemistry has demonstrated that certain derivatives of 2,2,3-trimethylpentanoic acid exhibit anti-inflammatory properties and may be useful in the treatment of inflammatory diseases such as arthritis.

Beyond its pharmaceutical applications, 2,2,3-trimethylpentanoic acid is also used in the food industry as a flavoring agent. Its unique chemical structure contributes to its distinctive aroma and taste profile, making it a valuable component in the development of food flavors. Additionally, it has been explored for its potential as a preservative due to its antimicrobial properties.

In the cosmetics industry, 2,2,3-trimethylpentanoic acid is utilized for its emollient properties and ability to enhance the texture and stability of cosmetic formulations. Its low toxicity and good skin compatibility make it a safe and effective ingredient for use in skincare products.

Recent advancements in analytical techniques have facilitated a deeper understanding of the behavior of 2,2,3-trimethylpentanoic acid in various environments. High-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS) are commonly employed methods for the detection and quantification of this compound in complex matrices. These techniques have been instrumental in ensuring the quality control of products containing 2,2,3-trimethylpentanoic acid.

The environmental impact of 2,2,3-trimethylpentanoic acid has also been a subject of interest. Studies have shown that it biodegrades readily under aerobic conditions and does not pose significant environmental risks when used responsibly. However, proper disposal practices are essential to minimize any potential adverse effects on ecosystems.

In conclusion, 2,2,3-trimethylpentanoic acid (CAS No. 101568-19-8) is a versatile compound with a wide range of applications across multiple industries. Its unique chemical structure and favorable physical properties make it an attractive candidate for further research and development. As new studies continue to uncover its potential benefits and applications, 2,2,3-trimethylpentanoic acid is likely to play an increasingly important role in various scientific and industrial fields.

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