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Agilent liquid chromatography/mass spectrometry (LC/MS) brings powerful analytical capability to a wide range of applications. Complete LC/MS workflows feature sample preparation, InfinityLab chromatography, and Agilent mass spectrometry, as well as software to acquire high-quality data and turn it into definitive answers.
The Agilent family of liquid chromatography/mass spectrometry instruments provides the versatility and performance to solve virtually any analytical challenge. A broad selection of ion sources enables the most flexible detection for the variety of compound classes amenable to HPLC separation and beyond. Powerful software along with curated compound databases and libraries allow you to quickly set up an LC/MS or LC/MS/MS method for your specific application.
- Multiple versatile and easy-to-configure ion sources including AJS, ESI, APCI, and MMI allow you to tackle any type of LC/MS analysis
- Wide mass range allows the analysis of ions of various classes and sizes, from small molecules to multiply charged peptides
- VacShield allows you to do front-end ion injector maintenance without breaking vacuum, drastically reducing routine maintenance from at least 6 hours to 30 minutes
- Early maintenance feedback (EMF) provides instrument health and status reports by reporting actively monitored metrics so you can anticipate downtime or address an immediate issue
- Intelligent Reflex ensures that results are within operational limits through active monitoring of sample carryover and samples above calibration range, adding additional blanks or reducing sample volume if one of these conditions is met
- Fast screening workflow with Intelligent Reflex dramatically improves sample throughput with a shortened LC method for screening and a standard method for quantitation; if a target is detected during screening, the sample is reinjected using a standard quantitation method.
- Built-in technical controls combined with procedural controls ensure the security of your data, control access, and facilitate compliance as defined by US FDA 21 CFR Part 11, EU Annex 11, and similar national electronic record regulation
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