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IBUPROFEN USP (30-1192)



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Features

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  • 15687-27-1
  • C13H18O2
  • 206.28
  • Not a DOT controlled material (United States). This material is not classified dangerous good according to international transportation regulations (ADR/RID-IMDG-ICAO/IATA).

Caution: For Prescription Compounding/Rx Only

Warning: Must be subjected to further processing during the preparation of injectable dosage forms to ensure acceptable levels of bacterial endotoxins.

Test Specification
DESCRIPTION WHITE TO OFF WHITE POWDER OR CRYSTALLINE POWDER HAVING A SLIGHT CHARACTERISTIC ODOR
MELTING POINT 75-78 °C
SOLUBILITY VERY SOLUBLE IN ALCOHOL AND IN ACETONE PRACTICALLY INSOLUBLE IN WATER