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 4 components.
• USP <232> Revision 40 Oral 3 Mix 1 Elemental Impurities standard is a 125 mL bottle which contains 110,000 mg/kg (110,000 ppm) Chromium; 3,000 mg/kg (3,000 ppm) Copper; 1,400 mg/kg (1,400 ppm) Barium; and 550 mg/kg (550 ppm) Lithium in 10% HNO3.
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Specifications
ConcentrationMultiple
Matrix10% HNO3
Element/IonMultiple
FormLiquid
Volume (mL)125
DOT InformationHazardous; Nitric acid solution; Class 8, Packing Group II
Storage SymbolAmbient
Hazard SymbolCorrosion
UN NumberUN2031
Shelf Life (months)12
DescriptionUSP <232> Revision 40, Oral 3 Mix 1 Elemental Impurities in 10% HNO3; 125 mL