Fully automatic TLC/HPTLC development with high reproducibility Automated Chromatogram Development under Standard Conditions The ADC 2 (Automatic Developing Chamber) is designed to automate all manual operations necessary during chromatogram development, thereby offering convenience, safety and high reproducibility for isocratic developments of TLC/HPTLC plates and foils in 20 x 10 cm and 10 x 10 cm formats. It provides automatic development,
A varied range of heads and pipettes for dispensing a wide selection of fluids Microdrop Dispenser Heads Microdrop dispenser heads – except for the Nanojet – use the same piezo-driven technology as an inkjet printer for contactless dispensing, generating a micro-fine droplet of liquid at the nozzle tip which departs from the dispenser head at high speed (approximately 2 m/s).
Advanced platform for high precision inkjet printing in the μm-range Versatile High-Precision Inkjet Printing Platform The microdrop Autodrop system provides a versatile platform for inkjet printing and material deposition on a broad range of substrates. The most advanced model, the Autodrop Professional Positioning System MD-P-802 is a versatile printing platform designed for high precision in the μm-range. Using the same
Manual Disintegration Tester Manual tablet disintegration tester with two stations The DT2 is a very easy-to-use and flexible disintegration tester with reliable temperature control. It records and reports disintegration times individually per sample or as a completed set. Two stations can be controlled, started, and stopped individually and allow performing 2 tests independently. Two independent testing stations with automated lift-in
Enjoy the full benefits of high-throughput crystallization experimentation ml-scale parallel crystallizer with novel non-intrusive turbidity probe Combining powerful performance with ease of use, the Crystal16 multiple reactor station is designed for automated crystallization screening research, enabling users to greatly accelerate their research – for example, solubility curves can be determined within 4 hours using only 100mg. Originally developed for medium
Parallel crystallization made visible Parallel Crystallizer with Particle Viewer In addition to providing all the benefits of Technobis’s Crystalline SE (Standard Edition), the Crystalline PV (Particle Viewer) enables automatic determination of particle-size distribution and visualization of all crystallization processes, making it perfect for crystallization process development and optimization. Like other models in the Crystalline range, the PV allows parallel crystallization
Real-time Raman capability in a sophisticated parallel crystallizer Parallel Crystallizer with Raman Probe In addition to providing all the benefits of Technobis’s Crystalline SE (Standard Edition), the advanced Crystalline RR (Raman Ready) incorporates the real-time Raman function. It monitors chemical and morphological changes, providing powerful capabilities in developing and optimizing crystallization processes. Like other models in the Crystalline range, the
Parallel crystallization experimentation made flexible and easy Compact Yet Sophisticated Parallel Crystallizer Technobis’s compact yet sophisticated Crystalline SE (Standard Edition) allows parallel crystallization processes in various modes suitable for crystallization process development and optimization. Its intuitive control and analysis software gives unparalleled access to real-time information on experiments. The Crystalline series meets the needs of a broad range of industries.
Automated Solutions This section presents a selection of solutions to fit common needs – but every case is unique. Put yourself in the hands of our experts, and you can be confident that your process will be automated in a way that is efficient, practical, based on world-class equipment, seamlessly integrated with your existing systems, and can save you time
Application Crystallization With increasing economic demands, it is becoming progressively more important to gain additional information on drug candidates early in the development cycle. Better informed decision can be made during the selection of candidates if further solid state information is available – saving time and money later on in the development process. But early stage drug candidates are difficult