• 1. Fatty acid eutectic mixtures and derivatives from non-edible animal fat as phase change materials?
  Pau Gallart-Sirvent,Marc Martín,Gemma Villorbina,Mercè Balcells,Aran Solé,Luisa F. Cabeza,Ramon Canela-Garayoa RSC Adv., 2017,7, 24133-24139
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  Olga Guselnikova,Gérard Audran,Jean-Patrick Joly,Andrii Trelin,Evgeny V. Tretyakov,Vaclav Svorcik,Oleksiy Lyutakov,Sylvain R. A. Marque Chem. Sci., 2021,12, 4154-4161
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  Hanie Hashtroudi,Ian D. R. Mackinnon J. Mater. Chem. C, 2020,8, 13108-13126
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Salicylic acids

Exploring the Versatile Applications and Properties of 2-Hydroxy-6-methylbenzoic Acid (CAS No. 567-61-3)

2-Hydroxy-6-methylbenzoic acid (CAS No. 567-61-3) is a specialized organic compound that has garnered significant attention in various industries due to its unique chemical properties and wide-ranging applications. This hydroxy-methylbenzoic acid derivative serves as a crucial intermediate in pharmaceutical synthesis, cosmetic formulations, and specialty chemical production. With the growing demand for benzoic acid derivatives in research and industrial applications, understanding this compound's characteristics and potential uses becomes increasingly important for chemists and product developers.

The molecular structure of 2-Hydroxy-6-methylbenzoic acid features both a carboxylic acid group and a hydroxyl group on the aromatic ring, along with a methyl substituent at the 6-position. This particular arrangement contributes to its unique solubility properties and reactivity patterns, making it valuable for creating more complex molecular architectures. Recent studies in green chemistry applications have highlighted how such functionalized benzoic acids can serve as eco-friendly building blocks for sustainable material development.

In the pharmaceutical sector, 567-61-3 has shown promise as a precursor for developing novel anti-inflammatory compounds and antimicrobial agents. Researchers are particularly interested in how the hydroxy-methyl substitution pattern influences biological activity, with several patent applications filed in recent years for derivatives of this compound. The cosmetic industry utilizes 2-Hydroxy-6-methylbenzoic acid in certain specialty formulations, where it functions as a pH adjuster and stabilizing agent in premium skincare products.

The compound's thermal stability and compatibility with various solvents make it valuable for industrial applications as well. Manufacturers of specialty chemicals often employ 2-Hydroxy-6-methylbenzoic acid as an intermediate in producing advanced materials, including liquid crystals and polymer additives. Recent advancements in catalyzed organic synthesis have opened new possibilities for using this compound in more efficient synthetic pathways, reducing waste and energy consumption in chemical production.

Analytical chemists frequently encounter questions about the spectroscopic characterization of 567-61-3, particularly regarding its distinctive NMR and IR spectral features. The compound exhibits characteristic peaks that help identify its purity and structural integrity, which is crucial for quality control in industrial settings. Many researchers searching for "methyl-substituted hydroxybenzoic acids" are particularly interested in comparative studies between different positional isomers and their respective properties.

From a market perspective, the demand for 2-Hydroxy-6-methylbenzoic acid has shown steady growth, driven by expanding applications in biodegradable materials and renewable energy technologies. Suppliers are increasingly focusing on developing more sustainable production methods to meet the needs of environmentally conscious manufacturers. The compound's role in developing bio-based alternatives to petroleum-derived chemicals has positioned it as an important player in the transition toward greener industrial processes.

Safety considerations for handling 2-Hydroxy-6-methylbenzoic acid follow standard laboratory protocols for carboxylic acid compounds. While not classified as hazardous under normal conditions, proper personal protective equipment should be used when working with the substance in powder form. Storage recommendations typically suggest keeping the compound in a cool, dry environment away from strong oxidizers to maintain its stability over extended periods.

Future research directions for 567-61-3 include exploring its potential in metal-organic frameworks (MOFs) and as a ligand in catalytic systems. The compound's ability to coordinate with metal ions while maintaining thermal stability makes it an interesting candidate for advanced material science applications. Additionally, its derivatives are being investigated for possible use in organic electronic devices, where the balance between electron-donating and withdrawing groups can be finely tuned.

For researchers and industry professionals seeking high-quality 2-Hydroxy-6-methylbenzoic acid, several technical parameters should be considered, including purity levels, crystalline form, and packaging options. The compound is typically available in laboratory-scale quantities from specialty chemical suppliers, with some manufacturers offering bulk quantities for industrial applications. Recent advancements in analytical techniques have improved the ability to characterize and verify the quality of this important chemical intermediate.

In conclusion, 2-Hydroxy-6-methylbenzoic acid (CAS No. 567-61-3) represents a versatile and valuable compound with growing importance across multiple scientific and industrial domains. Its unique structural features and reactivity profile continue to inspire new applications and research directions, particularly in fields emphasizing sustainable chemistry and green technology development. As our understanding of functionalized aromatic compounds deepens, this methyl-substituted hydroxybenzoic acid derivative is likely to play an increasingly significant role in advanced material and pharmaceutical innovation.

• 4961-03-9(5-hydroxybenzene-1,2,4-tricarboxylic acid)
• 3921-12-8(2-hydroxy-3,6-dimethylbenzoic acid)
• 71150-13-5(Benzenedicarboxylic acid, hydroxy-)
• 4821-91-4(2-Benzenedicarboxylic acid, 3-hydroxy-5-methyl-1)
• 4743-48-0(2-Formyl-6-hydroxybenzoic acid)
• 113665-35-3(6-hydroxybenzene-1,2,4-tricarboxylic acid)
• 6370-32-7(2-hydroxy-4,6-dimethylbenzoic acid)
• 4435-90-9(Benzoic acid, 3-formyl-4,6-dihydroxy-2-methyl-)
• 3786-46-7(3,6-Dihydroxyphthalic acid)
• 601-97-8(3-hydroxybenzene-1,2-dicarboxylic acid)