Cas no 62071-09-4 (2,4-Dihydroxy-6-tridecylbenzoic Acid)

2,4-Dihydroxy-6-tridecylbenzoic acid is a substituted benzoic acid derivative featuring a long hydrophobic tridecyl chain and two hydroxyl groups at the 2- and 4-positions. This structure imparts amphiphilic properties, making it useful in applications requiring surfactant or chelating behavior. The compound’s phenolic hydroxyl groups enhance its ability to form stable complexes with metal ions, while the alkyl chain improves solubility in organic matrices. It is commonly employed as an intermediate in organic synthesis, particularly for designing specialty chemicals with tailored hydrophobicity and coordination capabilities. Its balanced polarity and functional group reactivity make it suitable for use in coatings, adhesives, and metal-chelating formulations.
2,4-Dihydroxy-6-tridecylbenzoic Acid structure
62071-09-4 structure
Product Name:2,4-Dihydroxy-6-tridecylbenzoic Acid
CAS No:62071-09-4
MF:C20H32O4
MW:336.465686798096
CID:956099
PubChem ID:162958
Update Time:2025-11-02

2,4-Dihydroxy-6-tridecylbenzoic Acid Chemical and Physical Properties

Names and Identifiers

    • 6-tridecylresorcylic acid
    • Benzoic acid, 2,4-dihydroxy-6-tridecyl-
    • 2,4-dihydroxy-6-tridecylbenzoic acid
    • Benzoic acid, 2,4-dihydroxy-6-tridecyl-, (S)-
    • 62071-09-4
    • DTXSID70211121
    • 6-Tdra
    • 6-Tridecylresorcyclic Acid
    • 2,4-Dihydroxy-6-tridecylbenzoic Acid
    • Inchi: 1S/C20H32O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-16-14-17(21)15-18(22)19(16)20(23)24/h14-15,21-22H,2-13H2,1H3,(H,23,24)
    • InChI Key: SGSYRRSNJWAOJZ-UHFFFAOYSA-N
    • SMILES: OC1=CC(=CC(=C1C(=O)O)CCCCCCCCCCCCC)O

Computed Properties

  • Exact Mass: 336.23016
  • Monoisotopic Mass: 336.23005950g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 24
  • Rotatable Bond Count: 13
  • Complexity: 332
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 8
  • Topological Polar Surface Area: 77.8?2

Experimental Properties

  • PSA: 77.76

2,4-Dihydroxy-6-tridecylbenzoic Acid Pricemore >>

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Additional information on 2,4-Dihydroxy-6-tridecylbenzoic Acid

2,4-Dihydroxy-6-tridecylbenzoic Acid (CAS No. 62071-09-4): Properties, Applications, and Market Insights

2,4-Dihydroxy-6-tridecylbenzoic Acid (CAS No. 62071-09-4) is a specialized organic compound that has garnered significant attention in both industrial and research applications. This hydroxybenzoic acid derivative is characterized by its unique molecular structure, featuring a tridecyl side chain and two hydroxyl groups at the 2 and 4 positions. Its chemical formula is C20H32O4, and it is often utilized as an intermediate in the synthesis of more complex molecules.

The physical and chemical properties of 2,4-Dihydroxy-6-tridecylbenzoic Acid make it a versatile compound. It typically appears as a white to off-white crystalline powder with a melting point ranging between 120-125°C. The presence of the hydroxyl groups enhances its solubility in polar organic solvents, such as ethanol and methanol, while the long alkyl chain (tridecyl) contributes to its lipophilic character. This dual nature allows it to function effectively in both aqueous and non-aqueous systems.

One of the most prominent applications of 2,4-Dihydroxy-6-tridecylbenzoic Acid is in the field of material science. Researchers have explored its use as a building block for polymeric materials, particularly in the development of high-performance coatings and adhesives. The compound's ability to form stable hydrogen bonds and its compatibility with various polymers make it an attractive candidate for enhancing material properties such as durability and thermal stability.

In the pharmaceutical industry, 2,4-Dihydroxy-6-tridecylbenzoic Acid has been investigated for its potential as a bioactive intermediate. While not a drug itself, its structural features are valuable in the design of novel therapeutic agents. For instance, its hydroxybenzoic acid core is a common motif in molecules with antioxidant and anti-inflammatory properties. This has led to its use in the synthesis of compounds targeting oxidative stress-related diseases.

The cosmetics and personal care industry has also shown interest in 2,4-Dihydroxy-6-tridecylbenzoic Acid, particularly in the formulation of skin care products. Its potential as a mild preservative and stabilizer is under exploration, given the growing consumer demand for natural and sustainable ingredients. The compound's ability to chelate metal ions and its mild acidity make it suitable for use in pH-balanced formulations.

From an environmental perspective, 2,4-Dihydroxy-6-tridecylbenzoic Acid has been studied for its biodegradability and eco-toxicity profile. Recent trends in green chemistry have spurred research into its potential as a sustainable alternative to more persistent organic compounds. Its degradation pathways and environmental fate are areas of active investigation, particularly in the context of industrial wastewater treatment.

The global market for 2,4-Dihydroxy-6-tridecylbenzoic Acid has seen steady growth, driven by its diverse applications. Key players in the fine chemicals sector have been scaling up production to meet increasing demand from Asia-Pacific and North American markets. The compound's pricing trends reflect its status as a specialty chemical, with purity grades ranging from technical (90-95%) to research-grade (≥98%).

Recent advancements in synthetic methodologies for 2,4-Dihydroxy-6-tridecylbenzoic Acid have focused on improving yield and selectivity. Modern catalytic processes and green synthesis routes are being developed to reduce energy consumption and minimize waste generation. These innovations align with the broader industry shift toward sustainable chemical production.

Quality control of 2,4-Dihydroxy-6-tridecylbenzoic Acid typically involves HPLC analysis and spectroscopic characterization (FTIR, NMR). The compound's stability under various storage conditions has been well-documented, with recommendations for cool, dry environments away from strong oxidizers. Proper handling procedures emphasize the use of standard laboratory PPE to ensure safety during research and industrial use.

Looking ahead, the future of 2,4-Dihydroxy-6-tridecylbenzoic Acid appears promising, with potential expansions into emerging technologies such as organic electronics and advanced material composites. Its unique combination of aromatic and aliphatic properties continues to inspire novel applications across multiple scientific disciplines.

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