

Randall Extraction System for Fat Analysis
Randall 脂肪提取系统
- SKU FAN-0002
- Fat Analyzers
- 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 | 6 simultaneous |
|---|---|
| Method | Immersion (Randall) with rinsing |
| Immersion time | 10–60 min programmable |
| Rinse time | 10–60 min programmable |
| Total time | 30–60 min typical |
| Solvent volume | 25–80 mL per position |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 1443, ISO 1735, ISO 3433
What is the Randall Extraction System for Fat Analysis?
A Randall extraction system immerses the sample in boiling solvent before a short rinsing step, cutting extraction time substantially. It measures crude fat in food and feed with lower solvent use than conventional Soxhlet.
What is the Randall Extraction System for Fat Analysis?
A Randall extraction system immerses the sample in boiling solvent before a short rinsing step, cutting extraction time substantially. It measures crude fat in food and feed with lower solvent use than conventional Soxhlet.
Overview
In the Randall method the thimble sits partly immersed in boiling solvent in the extraction cup, so lipid dissolves rapidly by hot immersion rather than by repeated condensation. After the immersion stage, the thimble is raised and the sample is rinsed with condensed solvent for a shorter period, then the solvent is recovered and the cup weighed. Overall time is typically 30 to 60 minutes against several hours for conventional Soxhlet, and solvent consumption drops because recovery is integrated. The equipment usually follows the same six-position format as Soxhlet systems, so laboratories can standardise glassware and workflows. Recovery values are equivalent to Soxhlet for most matrices, provided the immersion time and rinse time are validated for each product.
How does it work?
Fat is not a single compound but a mixture of triglycerides, phospholipids and other lipids, so methods recover an operationally defined fraction. Soxhlet extraction repeatedly cycles a solvent such as petroleum ether or hexane through the sample, dissolving lipids that are then weighed after solvent evaporation. The Randall method shortens this by immersing the sample in boiling solvent before the rinsing step. Acid hydrolysis with hydrochloric acid releases fat bound in proteins and cell walls before extraction, which raises recovery for dairy, meat and baked products. The Roese-Gottlieb and Mojonnier procedures use ammonia, alcohol and a mixed solvent for dairy products. Pulsed NMR measures the hydrogen signal of liquid fat directly, without solvent, after calibration against a reference method.
What are the key features?
- Boiling immersion followed by short solvent rinse
- Extraction time of 30–60 minutes
- Six-position format compatible with Soxhlet glassware
- Integrated solvent recovery to reduce consumption
- Programmable immersion and rinse times
- Sealed design with fume exhaust
What are the technical specifications?
A typical randall extraction system for fat analysis configuration offers extraction positions of 6 simultaneous, method of Immersion (Randall) with rinsing, immersion time of 10–60 min programmable, rinse time of 10–60 min programmable, total time of 30–60 min typical and solvent volume of 25–80 mL per position. 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 Randall Extraction System for Fat Analysis is used in high-throughput crude fat testing, feed, pet food and premix fat control, snack and baked product fat monitoring and replacing slow Soxhlet runs in production QC. Across the wider Fat Analyzers class, laboratories also deploy it for total fat determination for nutrition labelling, feed and pet food crude fat control and dairy product fat standardisation and pricing.
Which standards and certifications apply?
Relevant standards and methods include ISO 1443, ISO 1735, ISO 3433, AOAC 920.39, AOAC 989.05 and ISO/IEC 17025. 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.
Solvent extraction requires ventilation, fume extraction and solvent recovery, and laboratories must follow local rules for flammable and chlorinated solvents. Extraction thimbles, boiling stones and drying ovens must be clean and the drying step controlled, because residual solvent and moisture bias the weighed fat. Acid hydrolysis needs careful handling of hot hydrochloric acid and adequate rinsing to remove acid before extraction. NMR analysers must be calibrated and temperature-stabilised, and calibration transfer between instruments should be demonstrated. Reference standards, duplicate determinations and participation in proficiency testing are expected for accredited laboratories.
How do I select the right Randall Extraction System for Fat Analysis?
Choose a Randall system when reference-grade extraction is needed but turnaround time is a constraint, as in production QC with many daily samples. Confirm that your method permits the immersion approach and that rinse and immersion times have been validated for your matrices. Check solvent recovery and exhaust requirements.
How does it compare with other Fat Analyzers variants?
Choose the method from the product and the fat fraction you must report. Soxhlet and Randall systems are the classic reference methods for free fat in feed, cereals and snack products, with Randall offering faster runs and lower solvent use. Acid hydrolysis extraction is required when fat is bound within the matrix, as in dairy powders, meat products and bakery goods. Roese-Gottlieb or Mojonnier procedures are standard for milk and dairy products. Pulsed NMR gives solvent-free results in minutes and suits routine control of oilseeds, chocolate and snack products once calibrated against a reference method. For milk fat specifically, butyrometer centrifugation remains a rapid, low-cost screening method on the intake platform.
Full specifications
| Extraction positions | 6 simultaneous |
|---|---|
| Method | Immersion (Randall) with rinsing |
| Immersion time | 10–60 min programmable |
| Rinse time | 10–60 min programmable |
| Total time | 30–60 min typical |
| Solvent volume | 25–80 mL per position |
| Temperature range | Ambient to 150 °C |
| Solvent recovery | ≥ 85 percent |
| Thimble size | 26 × 60 mm or 33 × 80 mm |
| Safety | Sealed vessels, exhaust port, cut-out |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- High-throughput crude fat testing
- Feed, pet food and premix fat control
- Snack and baked product fat monitoring
- Replacing slow Soxhlet runs in production QC
Key features
- Boiling immersion followed by short solvent rinse
- Extraction time of 30–60 minutes
- Six-position format compatible with Soxhlet glassware
- Integrated solvent recovery to reduce consumption
- Programmable immersion and rinse times
- Sealed design with fume exhaust
Frequently asked questions about Randall Extraction System for Fat Analysis
Randall immerses the sample partly in boiling solvent so fat dissolves quickly, then rinses briefly with condensed solvent. Soxhlet relies entirely on repeated condensation and dripping, which takes hours. Results are equivalent when the method is validated.
Yes, it is recognised in official methods such as AOAC 2003.05 and ISO 11085 for certain matrices, and it is accepted once the laboratory demonstrates equivalence with Soxhlet for its own products and validates the time programme.
No, provided extraction is complete. Immersion at boiling point accelerates dissolution, and a subsequent rinse removes residual fat. Completeness is confirmed by additional extraction cycles or by comparison with reference results during validation.
Crude fat is the fraction extracted by a solvent such as petroleum ether and includes triglycerides and some other lipids but not fat bound in cell structures. Total fat is measured after acid hydrolysis and includes bound fat, so it is higher for many foods.
In dairy powders, meat products and baked goods, fat is trapped inside proteins and cell structures that solvent cannot reach. Hydrochloric acid breaks these bonds and releases the fat, so recovery is markedly higher and results represent total rather than free fat.
Pulsed nuclear magnetic resonance excites hydrogen nuclei in liquid fat and measures their signal, which is proportional to fat content after calibration. The method needs no solvent and takes only a few minutes, but solids such as cocoa butter require a melting or tempering step.
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