

Pulsed NMR Food Fat Analyzer
脉冲核磁共振食品脂肪分析仪
- SKU FAN-0004
- 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
| Measurement principle | Pulsed proton NMR |
|---|---|
| Magnet field | 0.2–0.5 T permanent magnet |
| Analysis time | 2–5 min per sample |
| Fat range | 0.1–100 percent |
| Moisture range | 0.1–60 percent |
| Sample volume | 20–40 mL tube |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 1443, ISO 1735, ISO 3433
What is the Pulsed NMR Food Fat Analyzer?
A pulsed NMR food analyzer measures fat and moisture directly from the hydrogen signal of the sample, with no solvent and no weighing of extracts. It gives results in two to five minutes for oilseeds, chocolate, snack foods and dairy powders.
What is the Pulsed NMR Food Fat Analyzer?
A pulsed NMR food analyzer measures fat and moisture directly from the hydrogen signal of the sample, with no solvent and no weighing of extracts. It gives results in two to five minutes for oilseeds, chocolate, snack foods and dairy powders.
Overview
The sample is placed in a strong permanent magnet, where a radio-frequency pulse excites hydrogen nuclei. The amplitude of the resulting signal, measured after a defined delay, is proportional to the amount of liquid hydrogen-bearing material, mainly oil and water. Because the signal from solids decays quickly, a longer echo delay isolates the liquid fraction so that fat and moisture can be distinguished. Calibration against a reference extraction method is required, and results are expressed as oil or fat percentage on the sample mass. Whole seeds can be measured without grinding in some instruments, and solids such as chocolate must be melted or tempered first. Analysis takes two to five minutes, requires no solvent and leaves the sample intact for other tests.
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?
- Permanent magnet NMR with no solvent use
- Fat and moisture determined in 2–5 minutes
- Non-destructive measurement leaves sample intact
- Temperature-stabilised magnet for stable signals
- Calibration against Soxhlet or hydrolysis reference
- Interface for LIMS and result records
What are the technical specifications?
A typical pulsed nmr food fat analyzer configuration offers measurement principle of Pulsed proton NMR, magnet field of 0.2–0.5 T permanent magnet, analysis time of 2–5 min per sample, fat range of 0.1–100 percent, moisture range of 0.1–60 percent and sample volume of 20–40 mL tube. 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 Pulsed NMR Food Fat Analyzer is used in oilseed and nut oil content testing, chocolate and confectionery fat control, snack food oil and moisture monitoring and dairy powder fat screening. 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 Pulsed NMR Food Fat Analyzer?
Choose a pulsed NMR analyser when you need fast, solvent-free fat and moisture data and can invest in product-specific calibrations against a reference method. Confirm that sample tubes and melting accessories suit your products, and verify that calibration transfers between instruments if you operate more than one.
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
| Measurement principle | Pulsed proton NMR |
|---|---|
| Magnet field | 0.2–0.5 T permanent magnet |
| Analysis time | 2–5 min per sample |
| Fat range | 0.1–100 percent |
| Moisture range | 0.1–60 percent |
| Sample volume | 20–40 mL tube |
| Temperature stability | ±0.1 °C magnet control |
| Sample type | Liquid, powdered, whole seeds, melted solids |
| Calibrations | Product-specific, against reference method |
| Data output | USB, LIMS export |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Oilseed and nut oil content testing
- Chocolate and confectionery fat control
- Snack food oil and moisture monitoring
- Dairy powder fat screening
Key features
- Permanent magnet NMR with no solvent use
- Fat and moisture determined in 2–5 minutes
- Non-destructive measurement leaves sample intact
- Temperature-stabilised magnet for stable signals
- Calibration against Soxhlet or hydrolysis reference
- Interface for LIMS and result records
Frequently asked questions about Pulsed NMR Food Fat Analyzer
The signal corresponds to liquid hydrogen-bearing material, which for most foods is the oil or extractable fat plus moisture. Bound or solid fat is not detected unless the sample is melted, so results are calibrated and reported against a defined reference method.
Yes, many benchtop instruments accept whole seeds in a tube, which saves preparation time and avoids losses during grinding. Calibration curves must be built for each seed type, and moisture content influences the reading.
NMR gives a relative physical signal rather than a chemically isolated fat fraction. Regressions against Soxhlet, acid hydrolysis or Roese-Gottlieb results convert the signal into an equivalent fat percentage, which must be maintained over time.
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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