If you work in cli­ni­cal dia­gno­stics, en­vi­ron­men­tal or food safe­ty, fo­ren­sics, or run a mass spec core fa­ci­li­ty, you know the drill. The goal is to run your ana­lytes smooth­ly, wrap up on time, and catch the Bru­ins, Red Sox, or Cel­tics. But in­s­tead:

01 Coffee

You start your day not with a cof­fee, but with de­ri­va­tiza­ti­on or an­o­ther sam­ple prep step.

It’s time-con­sum­ing, not ever­yo­ne can do it, and the­re’s ple­nty of room for er­ror that can ruin ever­y­thing. Still, the­re’s no way around it if you want to io­ni­ze your ana­ly­te.

02 HPLC

You fire up your HPLC and the pres­su­re is all over the place.

Tra­di­tio­nal­ly, you can’t run LC-MS wi­t­hout an LC, so you start trou­ble­shoo­ting. Bubbles in the mo­bi­le pha­se? Pump seals? Need­le seal? One by one. It ta­kes fo­re­ver, and the sam­ple queue just keeps gro­wing.

03 Switch

You switch from ESI to APCI or APPI.

The more ion sources, the bet­ter, right? APCI is gre­at for mid-po­lar com­pounds, but once in­stal­led, you need to op­ti­mi­ze ga­ses, tweak vol­ta­ge, and make sure ever­y­thing is re­pro­du­ci­b­le. Sure, the­re’s an au­to­ma­ted set­up in the soft­ware, but if that fails, you’re stuck in the trou­ble­shoo­ting loop again, with zero samples me­a­su­red.

04 No Peak

Or there’s no mole­cu­lar peak in your TIC.

May­be just a few frag­ments, and that’s it. You start ques­tio­ning: Is the ana­ly­te de­gra­ded? Was the sam­ple even cor­rect? Should you dive into de­con­vo­lu­ti­on or start brow­sing frag­ment li­bra­ri­es? Eit­her way, it’s ever­y­thing but straight­for­ward.

05 Service

And fi­nal­ly, your MS va­cu­um pump or a PCB gave up yes­ter­day and ser­vice won’t ar­ri­ve for two weeks. Lucki­ly, there’s an­o­ther in­stru­ment from a dif­fe­rent ven­dor.

But now you need to trans­fer your me­thod. That me­ans new source geo­me­try, new set­tings, and li­kely a dif­fe­rent io­niza­ti­on re­spon­se. It should be a pie­ce of cake, but it’s not.

That’s exact­ly what this mee­ting is about.

Jan is a sea­so­ned mass spec ex­pert. Du­ring his stu­dies and aca­de­mic care­er, he lear­ned first­hand that mass spec­tro­me­try is one of the most powerful ana­ly­ti­cal tools out the­re. La­ter, in in­dus­try, working with ven­dor-agno­stic so­lu­ti­on, he gai­ned deep in­sights across do­zens of ap­pli­ca­ti­ons and ven­dor eco­sys­tems.

Why talk to Jan?

Be­cau­se every time Jan talks to labs, one thing stands out: work­flows haven’t ch­an­ged much in the last 20 ye­ars. There’s a lot of room to rethink how things are done, and to ta­ck­le some of the key chal­lenges head-on.

De­tect what you’­re miss­ing

Un­co­ver why key com­pounds aren’t show­ing up and how to fix it.

Save hours on prep

Cut down hours of in­stal­la­ti­on, ca­li­bra­ti­on or sam­ple prep.

Skip chro­ma­to­gra­phy

Learn how others are get­ting re­lia­ble data wi­t­hout LC or GC.

Con­nect pre­vious un­linkable

Use the be­ne­fits of GC’s high se­pa­ra­ti­on power in com­bi­na­ti­on with LC-MS high re­so­lu­ti­on.

All of this, wi­t­hout sacri­fi­ci­ng what mat­ters most to you as a sci­en­tist: data qua­li­ty.

You’ve got not­hing to lose. A quick 15-mi­nu­te vi­deo chat has al­re­a­dy hel­ped many labs save hours th­rough smar­ter work­flows. Why not be one of them?