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E-mail
nanowetech@163.com
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Phone
13928824355
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Address
No. 579 Jingang Avenue, Nansha District, Guangzhou City
Nano Micro (Guangzhou) Instrument Technology Co., Ltd
nanowetech@163.com
13928824355
No. 579 Jingang Avenue, Nansha District, Guangzhou City
Flow chemistry synthesis system
Flow chemistry (sometimes referring to intermittent flow, microchemistry, or continuous flow chemistry) innovatively integrates traditional independent and separate operational processes, accelerating the speed of research and development. Flow chemistry has emerged as a new production technology in the field of drug development. Flow chemistry reaction systems can quickly optimize reaction processes and synthesize large amounts of organic compounds, especially under high-risk and difficult to achieve reaction conditions, greatly promoting the development of green chemistry and laboratory automation. The flow chemistry reaction system is suitable for screening, optimizing, scaling up, and establishing chemical libraries in pharmaceutical chemistry, as well as organic chemistry research such as the synthesis of metal nanoparticles.

Flow chemistry synthesis systemTechnical Specifications:
Reaction temperature: -100 ℃~+250 ℃
Liquid phase reactor volume: 62.5 μ l, 250 μ l, 1ml, 4ml, 16ml
Solid phase reactor volumes: 0.7ml, 2.4ml, 5.6ml, 12ml
Pressure: 0-20bar (300psi)
流速: 1μl/min –10ml/min
Duration of stay: 1 second to several hours
Wetting component materials: Glass, PTFE, and PCTFE (both stainless steel and nickel alloy are acceptable)
Mixing: Rapid diffusion mixing
Production: micrograms to kilograms
Leakage automatic detection: automatic leakage diagnosis before operation
Automatic blockage detection: equipped with pressure sensor
Application of Flow Chemistry Synthesis:
Suzuki reaction: Faster reaction and improved selectivity, with negligible Pd content in the product
Hantzash pyrrole synthesis: improving reaction rate and yield, one-step process
Synthesis of metal nanoparticles: narrow particle size distribution, safe handling of corrosive reagents
N-alkylation to primary amines: faster reaction and significant monoalkylation selectivity