

LC-Q-TOF High-Resolution MS System
液相色谱四极杆飞行时间高分辨质谱仪(LC-Q-TOF)
- SKU LCM-0003
- LC-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 50–20000 (MS mode) |
|---|---|
| Mass resolution | 30000–60000 FWHM (m/z 922) |
| Mass accuracy | < 2 ppm RMS (internal calibration) |
| Acquisition rate | up to 100 spectra/s |
| In-spectrum dynamic range | ~10^4–10^5 |
| Sensitivity (reserpine, 1 pg on column, ESI+ MS) | S/N ≥ 1000:1 (typical) |
By Lab Manufacturers China Technical TeamLast reviewed Standards: EPA Method 1633, EPA Method 537.1, EPA Method 533
What is the LC-Q-TOF High-Resolution MS System?
An LC-Q-TOF combines a quadrupole precursor filter with a time-of-flight analyzer to deliver accurate-mass MS and MS/MS spectra. It is used for identifying unknowns, impurities and metabolites, non-targeted screening and retrospective data mining where quantitation and identification must share one platform.
What is the LC-Q-TOF High-Resolution MS System?
An LC-Q-TOF combines a quadrupole precursor filter with a time-of-flight analyzer to deliver accurate-mass MS and MS/MS spectra. It is used for identifying unknowns, impurities and metabolites, non-targeted screening and retrospective data mining where quantitation and identification must share one platform.
Overview
An LC-Q-TOF places a quadrupole, collision cell and orthogonal-acceleration TOF tube in series. In MS mode the quadrupole acts as an ion guide, and the TOF records accurate-mass spectra with resolving power of 30000 to 60000 FWHM and mass accuracy typically below 2 ppm with internal or frequent external calibration. In MS/MS mode the quadrupole selects a precursor, and the TOF records accurate-mass product ions. Data-dependent acquisition triggers MS/MS on detected peaks, while data-independent acquisition fragments all ions across mass windows, enabling retrospective interrogation. Acquisition rates of 10 to 100 spectra per second are compatible with UHPLC. Compared with triple quadrupole systems, targeted sensitivity is somewhat lower and linear dynamic range narrower, but the platform reveals unexpected compounds and supports elemental composition assignment.
How does it work?
In LC-MS, a high-pressure pump delivers a mobile phase through a column, typically C18, where analytes separate by their affinity for the stationary phase. The eluent, usually at 0.2 to 1 mL per minute, enters an atmospheric-pressure ion source. Electrospray ionization applies 3 to 5 kV to a nebulized stream so that charged droplets shrink and release gas-phase ions, while atmospheric-pressure chemical ionization uses a corona discharge for less polar compounds. Ions pass through a skimmer or capillary and ion guides into progressively lower-pressure regions, then into the mass analyzer. Quadrupole, ion trap, time-of-flight or hybrid analyzers then measure m/z. Mobile phases must be volatile, such as formic acid, acetic acid or ammonium formate, because non-volatile buffers foul the source.
What are the key features?
- Resolving power of 30000 to 60000 FWHM for separating isobaric interferences
- Mass accuracy below 2 ppm with automated lock-mass or calibrant delivery system
- Data-dependent and data-independent acquisition modes for MS/MS of unknowns
- Acquisition rate up to 100 spectra per second compatible with UHPLC peaks
- Ion-source options including ESI, APCI and dual-spray reference mass infusion
- Software for formula prediction, isotope pattern matching and library searching
What are the technical specifications?
A typical lc-q-tof high-resolution ms system configuration offers mass range of m/z 50–20000 (MS mode), mass resolution of 30000–60000 FWHM (m/z 922), mass accuracy of < 2 ppm RMS (internal calibration), acquisition rate of up to 100 spectra/s, in-spectrum dynamic range of ~10^4–10^5 and sensitivity (reserpine, 1 pg on column, ESI+ MS) of S/N ≥ 1000:1 (typical). 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 LC-Q-TOF High-Resolution MS System is used in impurity and degradation product identification, drug metabolite identification, non-targeted food and environmental screening, forensic and doping screening and peptide mapping and intact protein analysis. Across the wider LC-MS class, laboratories also deploy it for drug impurity profiling and metabolite identification, bioanalysis of drugs in plasma and urine and pesticide and veterinary drug residue testing.
Which standards and certifications apply?
Relevant standards and methods include EPA Method 1633, EPA Method 537.1, EPA Method 533, USP <621> Chromatography, FDA Bioanalytical Method Validation Guidance, ICH M10 Bioanalytical Method Validation, EN 15662, CLSI C62-A, 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.
Provide a nitrogen supply of at least 99.5 percent purity, either from a generator delivering about 20 to 35 L per minute or from liquid supply, plus a fume extraction line for source exhaust. Use LC-MS grade solvents and additives, since impurities raise background and suppress ionization. Calibrate the mass scale regularly with the manufacturer's calibrant solution, and run system suitability injections before each batch. Clean the spray shield, capillary and ion transfer optics when sensitivity drops, and replace rotary pump oil on schedule. Monitor for ion suppression through post-column infusion during method development. Regulated laboratories need software with audit trails and electronic signatures compatible with 21 CFR Part 11, and instrument qualification to IQ, OQ and PQ protocols.
How do I select the right LC-Q-TOF High-Resolution MS System?
Select LC-Q-TOF when identification of unknowns or retrospective screening matters as much as quantitation. Choose triple quadrupole for maximum targeted sensitivity. In an RFQ, specify resolving power at a stated m/z, mass accuracy conditions, acquisition rate, DIA capability, calibration approach and the compound databases required.
How does it compare with other LC-MS variants?
The decisive choice is the mass analyzer. Single quadrupole LC-MS confirms molecular weight and performs simple quantitation at a modest cost. Triple quadrupole instruments deliver the best sensitivity for targeted quantitation in bioanalysis, residues and clinical assays. Q-TOF systems provide accurate mass and MS/MS of unknowns, suited to impurity profiling, metabolite identification and screening. Ion traps offer multi-stage fragmentation for structural work. Mass-directed purification systems add fraction collection. Then check the ion source options such as ESI, APCI and APPI, scan speed for UHPLC peaks below 3 seconds wide, polarity switching speed, and the robustness of the source with dirty matrices. Confirm compatibility with your LC pumps, available software for regulated work, and nitrogen consumption for sheath and drying gases.
Full specifications
| Mass range | m/z 50–20000 (MS mode) |
|---|---|
| Mass resolution | 30000–60000 FWHM (m/z 922) |
| Mass accuracy | < 2 ppm RMS (internal calibration) |
| Acquisition rate | up to 100 spectra/s |
| In-spectrum dynamic range | ~10^4–10^5 |
| Sensitivity (reserpine, 1 pg on column, ESI+ MS) | S/N ≥ 1000:1 (typical) |
| Precursor isolation width | 0.4–4 u (adjustable) |
| Collision energy range | 0–200 eV (lab frame) |
| Ion sources | ESI, APCI, dual-spray reference |
| Polarity switching | ≤ 50 ms |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Impurity and degradation product identification
- Drug metabolite identification
- Non-targeted food and environmental screening
- Forensic and doping screening
- Peptide mapping and intact protein analysis
Key features
- Resolving power of 30000 to 60000 FWHM for separating isobaric interferences
- Mass accuracy below 2 ppm with automated lock-mass or calibrant delivery system
- Data-dependent and data-independent acquisition modes for MS/MS of unknowns
- Acquisition rate up to 100 spectra per second compatible with UHPLC peaks
- Ion-source options including ESI, APCI and dual-spray reference mass infusion
- Software for formula prediction, isotope pattern matching and library searching
Frequently asked questions about LC-Q-TOF High-Resolution MS System
Accuracy of 2 to 5 ppm combined with isotope pattern matching narrows candidate formulas for small molecules below about 400 Da. For larger molecules, accurate mass alone becomes ambiguous and MS/MS fragments, retention time and standards are needed for confident identification.
Data-independent acquisition fragments all ions within defined m/z windows or alternates low and high collision energy, recording MS and MS/MS data for every detectable compound. Because data are comprehensive, samples can be interrogated later for new targets without re-injection.
For many applications at moderate sensitivity, yes, using extracted ion chromatograms from accurate-mass data. For trace-level regulated assays, triple quadrupole MRM usually provides lower limits, wider linear range and established regulatory acceptance, so many laboratories keep both.
Electrospray ionization is the most common and suits polar and ionizable compounds from small molecules to proteins. APCI suits less polar, thermally stable analytes below about 1500 Da. APPI handles nonpolar compounds such as PAHs. Many sources allow switching or dual-mode operation.
Ion suppression is a reduction in analyte signal caused by co-eluting matrix components that compete for charge or disrupt droplet formation. It affects accuracy and sensitivity. It is managed with better sample cleanup, chromatographic separation, dilution and isotopically labeled internal standards.
Use volatile additives such as formic acid, acetic acid, ammonium formate, ammonium acetate and ammonium hydroxide, generally at 0.1 percent or 2 to 10 mM. Avoid non-volatile phosphate, borate and high concentrations of ion-pairing reagents, which contaminate the source and suppress ionization.
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