• 1. Evidence of pre-micellar aggregates in aqueous solution of amphiphilic PDMS–PEO block copolymer?
  Domenico Lombardo,Gianmarco Munaò,Pietro Calandra,Luigi Pasqua,Maria Teresa Caccamo Phys. Chem. Chem. Phys., 2019,21, 11983-11991
• 2. Evidence that the availability of an allylic hydrogen governs the regioselectivity of the Wacker oxidation
  Matthew J. Gaunt,Jinquan Yu,Jonathan B. Spencer Chem. Commun., 2001, 1844-1845
• 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. Empowering microfluidics by micro-3D printing and solution-based mineral coating?
  Hongxia Li,Aikifa Raza,Qiaoyu Ge,Jin-You Lu,TieJun Zhang Soft Matter, 2020,16, 6841-6849
• 5. Evolution of shape, size, and areal density of a single plane of Si nanocrystals embedded in SiO2 matrix studied by atom probe tomography
  Bin Han,Yasuo Shimizu,Gabriele Seguini,Celia Castro,Gérard Ben Assayag,Koji Inoue,Yasuyoshi Nagai,Sylvie Schamm-Chardon,Michele Perego RSC Adv., 2016,6, 3617-3622

• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Diphenylmethanes

3,4-Dimethoxybenzhydrol (CAS No. 56139-08-3): Properties, Applications, and Market Insights

3,4-Dimethoxybenzhydrol (CAS No. 56139-08-3) is a versatile organic compound with significant applications in pharmaceuticals, fragrances, and specialty chemicals. This aromatic alcohol, characterized by its two methoxy groups attached to the benzene ring, has garnered attention for its unique chemical properties and broad utility. As researchers and industries increasingly seek sustainable and efficient chemical solutions, 3,4-dimethoxybenzhydrol stands out as a valuable intermediate in synthetic chemistry.

The molecular structure of 3,4-dimethoxybenzhydrol features a benzhydrol core with methoxy substituents at the 3 and 4 positions. This configuration imparts distinct solubility and reactivity characteristics, making it a preferred choice for various chemical transformations. Its CAS number 56139-08-3 is frequently searched in scientific databases, reflecting its relevance in academic and industrial research. Recent trends indicate a growing interest in green chemistry applications of such compounds, aligning with global sustainability goals.

One of the primary uses of 3,4-dimethoxybenzhydrol is in the pharmaceutical industry, where it serves as a key intermediate in the synthesis of active pharmaceutical ingredients (APIs). Its role in the production of central nervous system (CNS) drugs has been particularly noteworthy. Additionally, the compound's aromatic properties make it suitable for use in flavor and fragrance formulations, where it contributes to complex scent profiles. The demand for high-purity 3,4-dimethoxybenzhydrol has risen in recent years, driven by advancements in drug discovery and specialty chemicals.

From a market perspective, 3,4-dimethoxybenzhydrol (56139-08-3) is witnessing steady growth, particularly in regions with robust pharmaceutical and chemical manufacturing sectors. Suppliers and distributors emphasize the importance of quality control and regulatory compliance, as these factors significantly impact the compound's usability in sensitive applications. Furthermore, the rise of custom synthesis services has enabled smaller enterprises to access this compound for niche applications, fostering innovation across industries.

In the context of synthetic methodology, researchers have explored various routes to produce 3,4-dimethoxybenzhydrol efficiently. Catalytic hydrogenation and Grignard reactions are among the commonly employed techniques. Recent studies have also investigated biocatalytic approaches to enhance the sustainability of its production. These developments align with the broader shift toward environmentally friendly chemical processes, a topic of significant interest in both academic and industrial circles.

The analytical characterization of 3,4-dimethoxybenzhydrol typically involves techniques such as nuclear magnetic resonance (NMR) spectroscopy, high-performance liquid chromatography (HPLC), and mass spectrometry. These methods ensure the compound's purity and identity, which are critical for its intended applications. As analytical technologies advance, the ability to detect and quantify trace impurities in CAS 56139-08-3 has improved, further enhancing its reliability in high-stakes industries.

Looking ahead, the future of 3,4-dimethoxybenzhydrol appears promising, with potential expansions into material science and advanced polymer chemistry. Its structural features make it a candidate for designing novel functional materials, an area gaining traction due to the demand for smart and responsive systems. Additionally, the compound's compatibility with green solvents and renewable feedstocks positions it well for sustainable innovation.

For researchers and industry professionals seeking detailed information on 3,4-dimethoxybenzhydrol (56139-08-3), reliable sources include chemical databases, supplier catalogs, and peer-reviewed journals. The compound's Safety Data Sheet (SDS) provides essential handling and storage guidelines, ensuring safe laboratory and industrial practices. As the chemical landscape evolves, 3,4-dimethoxybenzhydrol is poised to remain a relevant and valuable component in the toolkit of modern chemistry.

• 510-13-4(Solvent Green 1)
• 1063170-85-3((4-(Naphthalen-2-ylamino)phenyl)(phenyl)methanol)
• 149302-71-6(1-4-(dimethylamino)phenylethane-1,2-diol)
• 561-41-1(a,a-Bis4-(dimethylamino)phenyl-4-(methylamino)-benzenemethanol (Technical Grade))
• 5339-01-5(1-(3-Dimethylaminophenyl)ethanol)
• 123333-61-9(MALACHITE GREEN CARBINOL HYDROCHLORIDE)
• 119-58-4(4,4'-Bis(dimethylamino)diphenylcarbinol)
• 7494-77-1(4-(Dimethylamino)benzhydrol)
• 467-63-0(Solvent Violet 9 (Technical Grade))
• 1063170-79-5(Phenyl(4-(phenylamino)phenyl)methanol)