

Soxhlet Extraction System
索氏萃取系统
- SKU EXT-0001
- Extractors
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Extraction positions | 2–6 |
|---|---|
| Sample thimble | Cellulose or glass fibre |
| Solvent volume | 50–150 mL per position |
| Cycle time | About 10–20 min |
| Extraction time | 1–6 h typical |
| Heating | Electrical mantle or block |
By Lab Manufacturers China Technical TeamLast reviewed Standards: EPA 3540C, EPA 3545A, EPA 3546
What is the Soxhlet Extraction System?
A Soxhlet extraction system cycles condensed solvent through a sample to extract fats, oils and other analytes. It is the classical reference method and is used for gravimetric fat and oil determination.
What is the Soxhlet Extraction System?
A Soxhlet extraction system cycles condensed solvent through a sample to extract fats, oils and other analytes. It is the classical reference method and is used for gravimetric fat and oil determination.
Overview
A Soxhlet extraction system heats a solvent, condenses its vapour and drips it onto the sample held in a thimble, then siphons the extract back to the boiling flask. This cycle repeats, so fresh solvent continually contacts the sample and extraction proceeds to completion over several hours. The system can be manual, with individual glassware, or automated, with multiple positions, controlled heating and solvent recovery. It is the reference method for fat and oil content in food and feed, and for other analytes where thorough extraction is required. Solvent volume, cycle rate and extraction time determine the result, and the fat is usually determined gravimetrically after drying.
How does it work?
Extraction transfers analytes from a solid or semi-solid matrix into a solvent that can be analyzed or further cleaned. Soxhlet extraction repeatedly cycles condensed solvent through the sample, giving thorough extraction over time. Accelerated solvent extraction uses elevated temperature and pressure to keep the solvent liquid and speed transfer. Supercritical fluid extraction uses carbon dioxide above its critical point, whose low viscosity and high diffusivity penetrate the matrix rapidly and leave little residue. Microwave extraction heats the solvent and sample together, while ultrasonic extraction uses cavitation to disrupt the matrix and improve mass transfer. Temperature, pressure, solvent choice and time determine recovery.
What are the key features?
- Solvent cycling with condensation and siphoning
- Automated multi-position versions available
- Solvent recovery to reduce consumption
- Reference method for fat and oil determination
- Controlled heating for reproducible cycles
What are the technical specifications?
A typical soxhlet extraction system configuration offers extraction positions of 2–6, sample thimble of Cellulose or glass fibre, solvent volume of 50–150 mL per position, cycle time of About 10–20 min, extraction time of 1–6 h typical and heating of Electrical mantle or block. Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
Which applications is it used for?
The Soxhlet Extraction System is used in fat and oil determination in food, feed and grain analysis, environmental solid extraction and polymer additive extraction. Across the wider Extractors class, laboratories also deploy it for fat and oil determination in food, environmental organic pollutant extraction and pharmaceutical and natural product isolation.
Which standards and certifications apply?
Relevant standards and methods include EPA 3540C, EPA 3545A, EPA 3546, ISO 659 and IEC 61010-1. Certification candidates for this model are CE and ISO 9001 manufacturing; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Handle solvents in a fume hood and use the protective equipment specified for the solvent and the extraction conditions. Dry and grind the sample consistently, because moisture and particle size affect penetration and recovery. Optimise and validate temperature, pressure, solvent and time for each matrix, and verify recovery with a certified reference material or a spiked sample. Clean and check seals, vessels and tubing, since leaks waste solvent and can be hazardous at high pressure. Recover or dispose of solvents according to regulations, and record all parameters for traceability.
How do I select the right Soxhlet Extraction System?
Choose a Soxhlet extraction system when the reference method requires it or when exhaustive extraction is needed. Confirm the number of positions matches the workload, the solvent recovery reduces consumption, and the temperature control suits the solvent. In an RFQ state the sample type, analyte, solvent and throughput.
How does it compare with other Extractors variants?
Choose an extraction technique according to the analyte, the matrix and the required throughput. Soxhlet extraction is the classical reference method and suits fat and oil determination, but it is slow and uses more solvent. Accelerated solvent extraction is faster and uses less solvent, and suits many environmental and food methods. Supercritical fluid extraction is efficient and nearly solvent-free, and suits non-polar and moderately polar analytes. Microwave and ultrasonic extraction are rapid and suit samples where the matrix is easily penetrated. Confirm the achievable recovery, the solvent consumption, the temperature and pressure limits, and whether the system can handle the sample number required.
Full specifications
| Extraction positions | 2–6 |
|---|---|
| Sample thimble | Cellulose or glass fibre |
| Solvent volume | 50–150 mL per position |
| Cycle time | About 10–20 min |
| Extraction time | 1–6 h typical |
| Heating | Electrical mantle or block |
| Temperature range | Up to 150 °C |
| Solvent recovery | Automatic option |
| Water bath | Optional for volatile solvents |
| Power supply | 220–240 V AC |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Fat and oil determination in food
- Feed and grain analysis
- Environmental solid extraction
- Polymer additive extraction
Key features
- Solvent cycling with condensation and siphoning
- Automated multi-position versions available
- Solvent recovery to reduce consumption
- Reference method for fat and oil determination
- Controlled heating for reproducible cycles
Frequently asked questions about Soxhlet Extraction System
Extraction typically takes one to six hours, depending on the matrix, solvent and required completeness. The cycle rate and number of cycles determine how often fresh solvent contacts the sample. Faster alternatives exist, but Soxhlet remains the reference method where the procedure specifies it.
The thimble holds the sample and allows solvent to pass while retaining solids, so the extract stays free of particles and the sample is fully exposed to fresh solvent. Cellulose thimbles are common, and glass or quartz fibre thimbles suit higher temperatures or trace work.
For fat and oil determination, the solvent is evaporated and the residue weighed to give the extractable matter, often reported as a percentage of the sample. The dried extract mass, sample mass and any correction for co-extracted material are recorded in the method.
Soxhlet extraction cycles solvent through the sample at atmospheric pressure and takes hours, but it is the classical reference method. Accelerated solvent extraction uses high temperature and pressure to extract in minutes with less solvent. Both are accepted, and the choice depends on throughput and the method specified.
Smaller particles shorten the distance the solvent must travel to reach the analyte and increase the surface area, so extraction is faster and more complete. However, very fine powder can compact and restrict flow, so a consistent, moderate particle size is preferred and should be reproducible.
Recovery is verified by extracting a certified reference material or a blank sample spiked with a known amount of the analyte and comparing the measured amount with the added amount. Acceptable recovery ranges depend on the method and analyte concentration, and regular checks confirm method performance.
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