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Complete ICP-MS standards range at 10 mg/l 68 single elements ICP-MS standards for metal trace analysis calibration Large ICP-MS single element standards range at 10 mg/l delivered with an extensive Certificate of Analysis (NIST traceability contr...

Merck As the world leader in chemical analysis Merck offers a complete range of high quality products to meet rigorous analytical needs. Merck helps its clients improve the health and lives of people all over the world. The brand offers a wide ran...

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Kjeldahl Kjeldahl nitrogen determinations are performed on a variety of food substances. The Kjeldahl method may be broken down into three main steps: digestion distillation and titration. 1. Digestion: is accomplished by boiling a homogeneous sam...

Gehaltsbestimmung von Ca und Mg in Mineralwässern Application date: 07.11.2013 page 1 from 10 Determination of bases with Perchloric acid titration Application date: 07.11.2013 page 2 from 10 Use This application note describes the non-aqueous tit...

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(Microsoft PowerPoint - Pr\344sentation VWR ChromJournal_Chromolith WP Epoxy-Immobilization_062018-vs2_BP \(005\).PPTX [Read-Only]) Benjamin Peters Tom Kupfer Gisela Jung Peter Knoell Egidijus Machtejevas Petra Lewits Juni 2018 via immobilization ...

Kjeldahl Analysis Kjeldahl nitrogen determinations are performed on a variety of food substances. The Kjeldahl method may be broken down into three main steps: digestion distillation and titration. 1. Digestion: is accomplished by boiling a homoge...

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HPLC The right choice of chemical is crucial for your chromatography process. Below an overview of our chemical range for chromatography. Are you looking for columns instruments or other consumables as well? Promotions Chemical Innovations Contact...

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Final fill for mAbs Progressing from the drug substance to the final injectable drug product requires final packaging vials and stoppers that meet a number of quality requirements. To meet these requirements products must be prepared in an ISO Cla...

Final fill for vaccines Progressing from the drug substance to the final injectable drug product requires final packaging vials and stoppers that meet a number of quality requirements. To meet these requirements products must be prepared in an ISO...