• 1. Esterase-responsive polymeric prodrug-based tumor targeting nanoparticles for improved anti-tumor performance against colon cancer?
  Gang Pan,Yi-jie Bao,Jie Xu,Tao Liu,Cheng Liu,Yan-yan Qiu,Xiao-jing Shi,Hui Yu,Ting-ting Jia,Xia Yuan,Ze-ting Yuan,Yi-jun Cao RSC Adv., 2016,6, 42109-42119
• 2. Ester-mediated peptide formation promoted by deep eutectic solvents: a facile pathway to proto-peptides?
  Chen-Yu Chien,Sheng-Sheng Yu Chem. Commun., 2020,56, 11949-11952
• 3. Fatty acid positional distribution in colostrum and mature milk of women living in Inner Mongolia, North Jiangsu and Guangxi of China?
  Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
• 4. Emerging investigators
  Polym. Chem., 2015,6, 5501-5502
• 5. Excellent lithium ion storage property of porous MnCo2O4 nanorods?
  Peiyuan Zeng,Xiaoxiao Wang,Ming Ye,Qiuyang Ma,Jianwen Li,Wanwan Wang,Baoyou Geng,Zhen Fang RSC Adv., 2016,6, 23074-23084

• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Hydroxybenzoic acid derivatives
• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzoic acids and derivatives Hydroxybenzoic acid derivatives

3,4-Dihydroxy-2-methylbenzoic Acid (CAS No. 168899-47-6): A Comprehensive Overview of Its Properties and Applications

3,4-Dihydroxy-2-methylbenzoic acid (CAS No. 168899-47-6) is a naturally occurring phenolic compound with significant interest in pharmaceutical, cosmetic, and biochemical research. This methylbenzoic acid derivative is characterized by its two hydroxyl groups at the 3 and 4 positions, which contribute to its antioxidant and chelating properties. As researchers and industries increasingly focus on sustainable and bioactive compounds, this molecule has garnered attention for its potential in skin care formulations, nutraceuticals, and biodegradable materials.

The chemical structure of 3,4-dihydroxy-2-methylbenzoic acid includes a carboxylic acid functional group, making it a versatile intermediate in organic synthesis. Its CAS number 168899-47-6 is frequently searched in scientific databases, reflecting its relevance in studies related to polyphenol chemistry and plant-derived antioxidants. Recent trends in green chemistry have further highlighted its role as a building block for eco-friendly polymers and natural preservatives.

In the context of health and wellness, this compound is often compared to other dihydroxybenzoic acids, such as protocatechuic acid, due to its potential anti-inflammatory and anti-aging effects. Users searching for "natural alternatives to synthetic antioxidants" or "plant-based active ingredients" will find this molecule particularly relevant. Its applications extend to functional foods, where it may enhance shelf life and nutritional value.

From a technical perspective, 3,4-Dihydroxy-2-methylbenzoic acid exhibits stability under moderate pH conditions, making it suitable for cosmetic formulations. Its solubility profile (soluble in polar solvents like ethanol and water) is a key factor in its industrial adoption. Researchers investigating "stable phenolic compounds for topical use" or "non-toxic chelating agents" frequently explore this compound’s properties.

The synthesis and extraction methods for CAS 168899-47-6 are also topics of interest. Modern techniques emphasize enzymatic catalysis and low-waste processes, aligning with the global push toward sustainable manufacturing. Questions like "How to isolate dihydroxybenzoic acids from natural sources?" or "Scalable production of methylbenzoic acid derivatives" are common in academic and industrial forums.

In summary, 3,4-Dihydroxy-2-methylbenzoic acid (CAS No. 168899-47-6) bridges multiple disciplines, from material science to dermatology. Its dual functionality as an antioxidant and synthetic intermediate positions it as a compound of growing importance in both research and commercial applications. As demand for bio-based chemicals rises, this molecule’s versatility ensures its continued relevance in scientific literature and industrial innovation.

• 1020719-51-0(3-HYDROXY-2-METHYL-D3-BENZOIC ACID)
• 111342-37-1(1,2-Benzenedicarboxylic acid, 3,4-dihydroxy-6-methyl-)
• 6021-31-4(4-Hydroxy-2,3-dimethylbenzoic acid)
• 82784-82-5(1,2-Benzenedicarboxylicacid, 3,4-dihydroxy-)
• 603-80-5(3-Hydroxy-2-methylbenzoic Acid)
• 27023-06-9(3-Hydroxy-2,5-dimethylbenzoic acid)
• 50790-68-6(Benzoic acid, 5-hydroxy-2,4-dimethyl-)
• 4780-63-6
• 147214-67-3(Benzoic acid, 3,5-dihydroxy-2,6-dimethyl-)
• 27021-04-1(4-Hydroxy-2,5-dimethylbenzoic acid)