Synple Chem – Automated Chemical Synthesis Platform by Synple | Speed, Safety and Reproducibility for Advanced Chemistry

Streamline your laboratory workflow with the Synple Chem automated chemical synthesis platform.
Why Choose Synple Chem Automated Chemical Synthesis Platform
- Reduced hands-on time: Cuts user time to about 5 to 10 minutes, compared with manual synthesis that can take several hours.
- Higher laboratory efficiency: Increases speed and overall efficiency while freeing time to focus on other important experiments.
- Improved reproducibility: Delivers optimized reactions with better reproducibility for routine synthesis and optimization work.
- Lower risk of human error: Reduces operator error through automated processing and optimized reaction execution.
- Enhanced safety: Minimizes user exposure to chemicals through a fully enclosed reaction process that complies with the latest safety standards.
- Reduced contamination risk: Lowers cross-contamination risk through automated washing between runs.
- Cost savings: Offers a more economical alternative to manual chemical synthesis through lower personnel and reagent costs.
- Less chemical waste: Uses minimum reagents and solvents in an optimized reaction sequence, greatly reducing waste.
- Convenient operation: Requires no special training or detailed chemistry knowledge for routine use.
- Flexible experiment planning: Enables unattended overnight and multi-step synthesis planning for routine optimization.
Platform Features and System Components
- Platform architecture: Benchtop synthesizer combined with pre-filled reagent cartridges for automated organic chemical synthesis.
- Programmable handling scope: End-to-end programmable operation covering reaction setup, execution, workup, isolation, and purification.
- Reaction configuration: Fully enclosed reaction format with synthesis occurring in the cartridge itself or in the reaction vial.
- System format: Modular system configured for a range of reactions through cartridge-based operation.
- Fluidic components: Synple 2 incorporates two syringe pumps and two rotary valves.
- Integrated hardware: Synple 2 includes a sample holder, cartridge holder, RFID chip scanner, and touchscreen.
- Cartridge design: Each pre-filled cartridge contains the reagents required to generate, isolate, and purify the product.
- Method recognition: Cartridge RFID chip encoded with the reaction method for automated method loading after scanning.
- Experiment modes: Platform supports parallel or sequential experiments and routine optimization.
- Cleaning function: Automated wash sequence prepares the instrument for subsequent runs.
Technical Specifications
- Dimensions: W 26 cm, H 36 cm, D 49 cm
- Setup time: 5 minutes
- User time: 5 to 10 minutes
- Internal fluid handling components: Two syringe pumps and two rotary valves
- Reaction classes available: 8 (including N-heterocycle formation, reductive amination, protein degrader formation, biotin tagging, Mitsunobu reaction, Boc protection, Boc deprotection, and fluorination)
- Reagents across cartridge range: More than 40
Application and Basic Operation
- Primary use: Synple Chem automated chemical synthesis platform is used for fully automated organic chemical synthesis with pre-filled reagent cartridges that generate, isolate, and purify research products.
- Workflow scope: The platform handles the synthesis process end to end, including reaction setup, execution, workup, isolation, and purification through programmable operation.
- Reaction coverage: Synple cartridges are offered for a variety of reactions, including N-heterocycle formation, reductive amination, protein degrader formation, biotin tagging, Mitsunobu reaction, Boc protection, Boc deprotection, and fluorination.
- Run initiation: The user scans or selects the pre-filled reagent cartridge, inserts it into the synthesizer, adds the starting material, and presses START.
- Method loading: Scanning the cartridge automatically loads the appropriate reaction method encoded on the cartridge RFID chip.
- Process execution: After initiation, the instrument prepares the starting material and carries out the programmed reaction sequence through the required cartridge compartments or in the reaction vial, depending on the method.
- Product handling: During the run, the platform generates the product and performs the associated isolation and purification steps automatically.
- Preparation for next run: After product collection, the synthesizer performs an automated washing sequence to prepare the instrument for the next synthesis.
- Experiment planning: The platform supports parallel or sequential experiments and routine optimization workflows.
Synple Chem Product and Cartridge Lineup
| Reaction Type | Reagent Cartridge | Cartridge Contents |
|---|---|---|
| N-Heterocycle Formation Conversion of aldehydes into N-heterocycles. | Morpholine |
|
| Oxazepane | ||
| 2-Methylmorpholine | ||
| Piperazine | ||
| Diazepane | ||
| 3-Methylmorpholine | ||
| Morpholine-2-spiro-(2-Pyr) | ||
| Morpholine-2-spiro-(4-Pip) | ||
| 9-OMe-Benzoxazepane | ||
| 7-Br-9-OMe-Benzoxazepane | ||
| Reductive Amination Transformation of aldehydes/ketones and amines into complex amines. | Reductive Amination |
|
| Protein Degrader Formation PROTAC® synthesis using VHL or CRBN ligands and various PEG linker lengths. | CRBN-PEG1, -PEG2, -PEG3, -PEG4, -PEG5 |
|
| VHL-PEG1, -PEG2, -PEG3, -PEG4, -PEG5 | ||
| Biotin Tags Attachment to aldehydes, ketones, or amines via reductive amination or acylation. | Biotin tag-PEG2/3/4-NH2 Biotin tag-PEG2/3/4-O-4-P-NH | Amine Linker:
|
| Biotin tag-PEG2/3/4-a-COOTfp Biotin tag-PEG2/3/4-COOTfp | Amide Linker:
| |
| Mitsunobu Dehydrative coupling of alcohols with pronucleophiles. | Mitsunobu (Standard) |
|
| Boc Protection N-Boc protection of primary and secondary amines. | Boc Protection (0.5 mmol) Boc Protection (1.2 mmol) |
|
| Boc Deprotection Transformation of Boc-protected amines into free amine salts without using volatile acids. | Boc Deprotection (0.5 mmol) |
|
| Fluorination Transformation of primary/secondary alcohols into fluorinated products (Deoxyfluorination). | Deoxyfluorination |
|
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