• 1. Alternative mixtures to R-600a. Theoretical assessment and experimental energy evaluation of binary mixtures in a commercial cooler: Mélanges alternatifs au R-600a. évaluation théorique et évaluation énergétique expérimentale de mélanges binaires dans un refroidisseur commercial.
  DanielCalleja-Anta,DanielSánchez,LauraNebot-Andres,RamónCabello,RodrigoLlopis
• 2. Acenaphthenic hopanoids, a novel series of aromatised
  Teresita Carrillo-Hernández,Philippe Schaeffer,Pierre Albrecht Chem. Commun., 2001, 1976-1977
• 3. Aggregation-induced emission of luminol: a novel strategy for fluorescence ratiometric detection of ALP and As(v) with high sensitivity and selectivity?
  Yuan-Jun Tong,Lu-Dan Yu,Lu-Lu Wu,Shu-Ping Cao,Ru-Ping Liang,Li Zhang,Xing-Hua Xia,Jian-Ding Qiu Chem. Commun., 2018,54, 7487-7490
• 4. An antioxidative galactomannan extracted from Chinese Sesbania cannabina enhances immune activation of macrophage cells?
  Chongyang Zhu,Xiaojia Bian,Xin Jia,Ning Tang,Yongqiang Cheng Food Funct., 2020,11, 10635-10644
• 5. Aggregated-fluorescent detection of PFAS with a simple chip
  Cheng Fang,Jinjian Wu,Zahra Sobhani,Md. Al Amin,Youhong Tang Anal. Methods, 2019,11, 163-170

• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenols Methoxyphenols

3-Hydroxy-4-methoxybenzylamine (CAS No. 89702-89-6): Properties, Applications, and Market Insights

3-Hydroxy-4-methoxybenzylamine (CAS No. 89702-89-6) is a versatile organic compound with a wide range of applications in pharmaceuticals, agrochemicals, and specialty chemicals. This aromatic amine, also known as 4-methoxy-3-hydroxybenzylamine, has gained significant attention due to its unique structural properties and reactivity. Researchers and industry professionals often search for terms like "3-Hydroxy-4-methoxybenzylamine synthesis", "CAS 89702-89-6 applications", and "4-methoxy-3-hydroxybenzylamine price", reflecting the growing interest in this compound.

The molecular structure of 3-Hydroxy-4-methoxybenzylamine features both hydroxyl and methoxy functional groups attached to a benzylamine core, making it a valuable intermediate in organic synthesis. Its chemical formula is C₈H₁₁NO₂, with a molecular weight of 153.18 g/mol. The presence of these functional groups allows for diverse chemical modifications, which is why queries like "3-Hydroxy-4-methoxybenzylamine derivatives" and "functionalization of 89702-89-6" are common in scientific literature and patent searches.

In pharmaceutical applications, 3-Hydroxy-4-methoxybenzylamine serves as a key building block for drug development. Recent studies have explored its potential in creating novel therapeutic agents, particularly in neurological and cardiovascular research. The compound's structural similarity to certain neurotransmitters has sparked interest in its use for "neuroprotective drug development" and "CNS-active compounds", which are trending topics in medicinal chemistry.

The agrochemical industry utilizes 3-Hydroxy-4-methoxybenzylamine as an intermediate for producing crop protection agents. Its derivatives have shown promise in developing new generation pesticides with improved environmental profiles. This aligns with current market demands for "green chemistry solutions" and "sustainable agrochemicals", making the compound particularly relevant in today's environmentally conscious landscape.

From a commercial perspective, the global market for 3-Hydroxy-4-methoxybenzylamine has shown steady growth, driven by increasing R&D activities in life sciences and specialty chemicals. Manufacturers and suppliers frequently search for information on "89702-89-6 suppliers", "3-Hydroxy-4-methoxybenzylamine market trends", and "bulk pricing for CAS 89702-89-6", indicating robust industrial interest.

Quality control is crucial when working with 3-Hydroxy-4-methoxybenzylamine, as purity levels significantly impact its performance in various applications. Analytical methods such as HPLC, GC-MS, and NMR are commonly employed to verify the compound's quality, addressing common queries about "89702-89-6 purity testing" and "analytical methods for 4-methoxy-3-hydroxybenzylamine".

The synthesis of 3-Hydroxy-4-methoxybenzylamine typically involves multi-step organic transformations starting from vanillin or related phenolic compounds. Recent advancements in catalytic processes have improved yields and reduced environmental impact, responding to industry needs for "green synthesis of 89702-89-6" and "cost-effective production methods".

Storage and handling of 3-Hydroxy-4-methoxybenzylamine require standard precautions for aromatic amines. While not classified as hazardous under normal conditions, proper storage in cool, dry conditions away from strong oxidizers is recommended. These practical considerations generate searches for "89702-89-6 storage guidelines" and "handling 4-methoxy-3-hydroxybenzylamine".

Looking ahead, the future of 3-Hydroxy-4-methoxybenzylamine appears promising, with potential applications emerging in material science and nanotechnology. Researchers are investigating its use in polymer modification and as a ligand in catalytic systems, aligning with trends in "advanced material development" and "nanoscale engineering".

For those seeking technical specifications, 3-Hydroxy-4-methoxybenzylamine typically appears as a white to off-white crystalline powder with a melting point range of 105-110°C. Its solubility profile includes good solubility in polar organic solvents and limited solubility in water, information frequently searched as "89702-89-6 solubility data" and "physical properties of 3-Hydroxy-4-methoxybenzylamine".

The compound's stability under various conditions is another area of interest, with researchers often looking for "3-Hydroxy-4-methoxybenzylamine stability studies" and "degradation pathways of CAS 89702-89-6". Understanding these aspects is crucial for formulation development and process optimization in industrial applications.

In conclusion, 3-Hydroxy-4-methoxybenzylamine (CAS No. 89702-89-6) represents an important chemical intermediate with diverse applications across multiple industries. Its unique structural features, combined with growing market demand and research interest, ensure its continued relevance in chemical innovation. As new applications emerge and synthesis methods improve, this compound will likely maintain its position as a valuable tool in chemical research and industrial production.

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