The new guidelines set by the United States Pharmacopeia (USP) have pushed the pharmaceutical and nutraceutical industries to provide accurate, quantifiable results for metal analysis in drugs, pharmaceutical substances and raw materials.
USP <232> outlines new limits in pharmaceutical products for arsenic, cadmium, lead, and mercury. ICP-MS instrumentation, along with accurate ICP-MS standards, allow for increased efficiency and accuracy of the analysis necessary to comply with the new regulations.
Use these standards can be used as a calibration or check standard to verify Oral Daily Dose PDE, Parenteral Component Limit or Parenteral Daily Dose PDE as well as Inhalation Component Limit or Daily Dose.
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This multi-component standard contains 7 components.
• USP <232> Revision 40, Parenteral 2B Mix 2 elemental impurities standard is a 125 mL bottle which contains 100 mg/kg (100 ppm) Gold and 10 mg/kg (10 ppm) Iridium, Osmium, Palladium, Platinum, Rhodium, Ruthenium in 10% HCl.
Hazardous material shipping fees may apply.
Specifications
ConcentrationMultiple
Matrix10% HCl
Element/IonMultiple
FormLiquid
Volume (mL)125
DOT InformationHazardous; Hydrochloric acid; Class 8, Packing Group II