Cas no 82001-52-3 (2-sulfanylpentanoic acid)

2-sulfanylpentanoic acid structure
2-sulfanylpentanoic acid structure
Product Name:2-sulfanylpentanoic acid
CAS No:82001-52-3
MF:C5H10O2S
MW:134.196700572968
CID:3482792
PubChem ID:14181808
Update Time:2025-05-26

2-sulfanylpentanoic acid Chemical and Physical Properties

Names and Identifiers

    • PENTANOIC ACID, 2-MERCAPTO-
    • 2-sulfanylpentanoic acid
    • n-propylthioglycolic acid
    • 2-sulfanylpentanoicacid
    • 2-mercaptopentanoic acid
    • SCHEMBL204061
    • AKOS006375846
    • 82001-52-3
    • 2-mercaptovaleric acid
    • EN300-1267943
    • DTXSID601313183
    • Inchi: 1S/C5H10O2S/c1-2-3-4(8)5(6)7/h4,8H,2-3H2,1H3,(H,6,7)
    • InChI Key: IMGGANUNCHXAQF-UHFFFAOYSA-N
    • SMILES: SC(C(=O)O)CCC

Computed Properties

  • Exact Mass: 134.04015073g/mol
  • Monoisotopic Mass: 134.04015073g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 8
  • Rotatable Bond Count: 3
  • Complexity: 82.5
  • 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: 1.4
  • Topological Polar Surface Area: 38.3?2

2-sulfanylpentanoic acid Pricemore >>

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2-sulfanylpentanoic acid Related Literature

Additional information on 2-sulfanylpentanoic acid

2-Sulfanylpentanoic Acid: A Comprehensive Overview

2-Sulfanylpentanoic acid, also known by its CAS number 82001-52-3, is a sulfur-containing organic compound that has garnered significant attention in recent years due to its unique chemical properties and potential applications in various fields. This compound, which belongs to the class of thiocarboxylic acids, is characterized by its pentanoic acid backbone with a sulfur atom attached to the second carbon. The presence of the sulfur group introduces interesting reactivity and functional properties, making it a valuable molecule for both academic research and industrial applications.

The structure of 2-sulfanylpentanoic acid consists of a five-carbon chain with a carboxylic acid group at one end and a thiol group (-SH) on the second carbon. This arrangement allows for versatile chemical transformations, including oxidation, reduction, and condensation reactions. Recent studies have explored the use of this compound in the synthesis of bioactive molecules, where its sulfur moiety plays a critical role in modulating biological activity. For instance, researchers have demonstrated that derivatives of 2-sulfanylpentanoic acid can exhibit antioxidant properties, making them potential candidates for use in pharmaceuticals and nutraceuticals.

In terms of synthesis, 2-sulfanylpentanoic acid can be prepared through various methods, including the oxidation of 2-mercaptoacetic acid or through the hydrolysis of corresponding thioesters. These methods have been optimized in recent years to improve yield and purity, making large-scale production more feasible. The compound's stability under different conditions has also been a topic of interest, with studies showing that it is relatively stable under neutral and mildly acidic conditions but can undergo decomposition under strong alkaline or oxidative environments.

The application of 2-sulfanylpentanoic acid extends beyond traditional chemistry. In materials science, it has been investigated as a precursor for the synthesis of novel polymers and coatings. Its sulfur content provides these materials with enhanced mechanical properties and thermal stability, which are desirable in high-performance applications such as aerospace and electronics. Additionally, recent advancements in green chemistry have highlighted the potential of this compound as a sustainable alternative to traditional reagents in organic synthesis.

In the field of biotechnology, 2-sulfanylpentanoic acid has shown promise as a building block for peptide synthesis. Its thiol group facilitates the formation of disulfide bonds, which are crucial for maintaining the tertiary structure of proteins. Researchers have also explored its role in enzyme catalysis, where it serves as a cofactor or substrate analog in enzymatic reactions. These findings underscore its importance in both fundamental biochemical studies and applied biotechnological processes.

The environmental impact of 2-sulfanylpentanoic acid has also been a subject of recent research. Studies have shown that it is biodegradable under aerobic conditions, making it an eco-friendly choice for industrial applications. Furthermore, its low toxicity profile has been confirmed in various toxicity assays, which adds to its suitability for use in consumer products and medical devices.

In conclusion, 2-sulfanylpentanoic acid, with its unique chemical structure and versatile properties, continues to be a focal point in scientific research and industrial development. Its applications span across multiple disciplines, from pharmaceuticals to materials science, and its eco-friendly nature makes it an attractive option for sustainable technologies. As research into this compound progresses, it is likely that new discoveries will further expand its utility and impact across various industries.

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