

GC-TOF MS System
气相色谱飞行时间质谱仪(GC-TOF MS)
- SKU GCM-0003
- GC-MS
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
- IEC 61010-1 safety (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Mass range | m/z 10–1500 |
|---|---|
| Acquisition rate | up to 500 spectra/s |
| Mass resolution | 1000 (unit) to 25000 FWHM, model dependent |
| Mass accuracy | ≤ 5 ppm (high-resolution models, internal lock) |
| Instrument detection limit (OFN, 1 pg/µL) | ≤ 20 fg (typical) |
| Linear dynamic range | 10^4–10^5 |
By Lab Manufacturers China Technical TeamLast reviewed Standards: EPA Method 8270, EPA Method 524.2, EPA Method 8260
What is the GC-TOF MS System?
A GC-TOF MS pairs a gas chromatograph with a time-of-flight analyzer that records full spectra at very high acquisition rates. It is chosen for fast GC, comprehensive two-dimensional GC, deconvolution of co-eluting peaks and non-targeted screening of complex volatile mixtures.
What is the GC-TOF MS System?
A GC-TOF MS pairs a gas chromatograph with a time-of-flight analyzer that records full spectra at very high acquisition rates. It is chosen for fast GC, comprehensive two-dimensional GC, deconvolution of co-eluting peaks and non-targeted screening of complex volatile mixtures.
Overview
In a GC-TOF MS, ions are accelerated into a field-free drift tube and arrive at the detector in order of mass. Because all ions are pulsed and recorded together, full spectra are acquired at rates of 50 to 500 spectra per second without the sensitivity loss that scanning instruments suffer at high speed. This makes the platform the usual detector for comprehensive two-dimensional GC, where second-dimension peaks are only tens of milliseconds wide, and for fast GC methods. Mass resolution ranges from unit resolution in routine models to 25000 or more in high-resolution versions with reflectron or multi-pass geometries. Spectral deconvolution software separates overlapping compounds mathematically. Dynamic range is narrower than in quadrupole systems, so very high-concentration analytes may saturate the detector. The configuration suits metabolomics, flavor, petroleum and environmental screening.
How does it work?
In GC-MS, a liquid or gas sample is vaporized in a heated inlet and carried by helium or hydrogen through a capillary column, typically 15 to 60 m long with a 0.25 mm internal diameter. Compounds separate according to boiling point and interaction with the stationary phase and elute at characteristic retention times. The column exit feeds an ion source, most often electron ionization at 70 eV, which produces reproducible fragmentation patterns that can be matched against libraries such as NIST. Ions are filtered by a mass analyzer, commonly a quadrupole, and counted by an electron multiplier. Acquisition can run in full scan for identification or selected ion monitoring for higher sensitivity. A turbomolecular pump maintains the high vacuum required in the analyzer.
What are the key features?
- Full-spectrum acquisition at 50 to 500 spectra per second with no scanning skew
- Orthogonal-acceleration TOF analyzer with reflectron for improved resolving power
- Automated peak deconvolution for overlapping compounds in complex chromatograms
- Compatible with comprehensive two-dimensional GC modulators and fast temperature programs
- Accurate-mass option for elemental formula assignment of unknown compounds
- Electron ionization with library-searchable spectra plus optional chemical ionization
What are the technical specifications?
A typical gc-tof ms system configuration offers mass range of m/z 10–1500, acquisition rate of up to 500 spectra/s, mass resolution of 1000 (unit) to 25000 FWHM, model dependent, mass accuracy of ≤ 5 ppm (high-resolution models, internal lock), instrument detection limit (OFN, 1 pg/µL) of ≤ 20 fg (typical) and linear dynamic range of 10^4–10^5. 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 GC-TOF MS System is used in comprehensive two-dimensional GC (GC×GC) profiling, metabolomics of volatile and derivatized metabolites, petroleum and fuel composition analysis, non-targeted environmental screening and flavor, aroma and off-odor investigation. Across the wider GC-MS class, laboratories also deploy it for environmental VOC and semi-volatile analysis, pesticide residue testing in food and forensic toxicology and drug screening.
Which standards and certifications apply?
Relevant standards and methods include EPA Method 8270, EPA Method 524.2, EPA Method 8260, ASTM D5769, USP <467> Residual Solvents, ISO 11423, EN 15662, ISO/IEC 17025 and IEC 61010-1. Certification candidates for this model are CE, ISO 9001 manufacturing and IEC 61010-1 safety; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Install the GC-MS on a level bench with a dedicated power outlet, a vented exhaust for the rotary pump, and stable room temperature. Use high-purity carrier gas of at least 99.999 percent with moisture and oxygen traps, since contamination shortens column and filament life. Perform an autotune with perfluorotributylamine before each batch and verify mass accuracy and isotope ratios. Routine maintenance includes replacing inlet liners, septa and gold seals, trimming the column, cleaning the ion source and changing pump oil. Keep leak checks in the daily routine, as air peaks at m/z 28 and 32 indicate a leak. Regulated laboratories should require audit trails, electronic signatures and access control that support 21 CFR Part 11.
How do I select the right GC-TOF MS System?
Select GC-TOF MS for GC×GC, fast GC below 10 minutes, or untargeted work where spectra must be recorded across the whole peak without skew. Choose a quadrupole if linear dynamic range and low-cost targeted quantitation matter more. In an RFQ, specify acquisition rate, resolution, mass accuracy, GC×GC compatibility and deconvolution software.
How does it compare with other GC-MS variants?
Select a GC-MS by matching the detector to the task. A single quadrupole is the economical choice for routine identification and quantitation of residues, volatiles and unknowns using library matching. A triple quadrupole configuration is needed when matrix interference limits sensitivity, as in pesticide multi-residue or dioxin-related work. Time-of-flight offers fast acquisition and accurate mass for non-targeted screening. Headspace and pyrolysis configurations suit specific sample types without solvent extraction. Check the scan speed, mass range, source cleanliness tolerance, and whether the ion source can be changed without venting. Verify support for helium alternatives such as hydrogen, autosampler capacity, and library and data-integrity software. Ask vendors for detection-limit data, such as octafluoronaphthalene instrument detection limit, measured on the exact configuration quoted.
Full specifications
| Mass range | m/z 10–1500 |
|---|---|
| Acquisition rate | up to 500 spectra/s |
| Mass resolution | 1000 (unit) to 25000 FWHM, model dependent |
| Mass accuracy | ≤ 5 ppm (high-resolution models, internal lock) |
| Instrument detection limit (OFN, 1 pg/µL) | ≤ 20 fg (typical) |
| Linear dynamic range | 10^4–10^5 |
| Ionization modes | EI; optional CI |
| Ion source temperature | 150–350 °C |
| Drift tube length | ~0.5–1.3 m (model dependent) |
| Vacuum pumping | Turbomolecular, 2 or 3 stages |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Comprehensive two-dimensional GC (GC×GC) profiling
- Metabolomics of volatile and derivatized metabolites
- Petroleum and fuel composition analysis
- Non-targeted environmental screening
- Flavor, aroma and off-odor investigation
Key features
- Full-spectrum acquisition at 50 to 500 spectra per second with no scanning skew
- Orthogonal-acceleration TOF analyzer with reflectron for improved resolving power
- Automated peak deconvolution for overlapping compounds in complex chromatograms
- Compatible with comprehensive two-dimensional GC modulators and fast temperature programs
- Accurate-mass option for elemental formula assignment of unknown compounds
- Electron ionization with library-searchable spectra plus optional chemical ionization
Frequently asked questions about GC-TOF MS System
Second-dimension peaks in comprehensive GC often last only 50 to 200 ms. A scanning quadrupole cannot record enough full spectra across such a peak, while a TOF captures hundreds of spectra per second, preserving peak shape and spectral quality.
Generally yes. TOF detectors use time-to-digital or fast digitizer electronics, and saturation limits intra-spectrum dynamic range to about four to five orders of magnitude, often less than a quadrupole. Sample dilution or split injection is used for high-concentration analytes.
Deconvolution is a mathematical process that separates overlapping chromatographic peaks using small differences in ion profiles across the peak. It extracts a clean spectrum for each component, allowing library matching even when compounds are not chromatographically resolved.
GC-MS analyzes compounds that can be vaporized without decomposition, generally with molecular weights below about 500 Da. Examples are solvents, pesticides, hydrocarbons, fatty acid methyl esters, flavors and many drugs. Polar or non-volatile analytes can be made suitable by derivatization, for example silylation.
Full scan records the whole mass range, for example m/z 35 to 550, and gives spectra for library identification of unknowns. Selected ion monitoring records only chosen ions, which increases dwell time per ion and typically improves sensitivity by ten to one hundred times, but it loses information about unexpected compounds.
Yes, with conditions. Hydrogen gives faster separations and lower cost, but it can react with some analytes, change spectra in electron ionization sources, and requires safety measures. Many systems need a hydrogen-compatible ion source and method revalidation before replacing helium in regulated work.




