length × I.D. 30 m × 0.53 mm, df 3.00 μmTemp. Limits: • -20°C to 260°C General description For USP Analysis of residual solvents - This column is specially prepared and tested to meet the requirements of United States Pharmacopoeia (USP) Method 467 and the European Pharmacopoeia general method for determining residual solvents in pharmaceutical preparations. Use this column to separate residual solvents for research purposes or qualitative analysis. The USP and European Pharmacopoeia methods als... Read more
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OVI-G43
length × I.D. 30 m × 0.53 mm, df 3.00 μm
Temp. Limits:
• -20°C to 260°C
General description
For USP Analysis of residual solvents - This column is specially prepared and tested to meet the requirements of United States Pharmacopoeia (USP) Method 467 and the European Pharmacopoeia general method for determining residual solvents in pharmaceutical preparations. Use this column to separate residual solvents for research purposes or qualitative analysis. The USP and European Pharmacopoeia methods also specify using a deactivated 5-meter guard column.
In order to ensure analysis under optimum conditions, we strongly suggest the use of a deactivated guard column (Cat. No. 25339) with the OVI-G43 column.
This column meets USP G43 requirements.
Temp. Limits:
• -20°C to 260°C
General description
For USP Analysis of residual solvents - This column is specially prepared and tested to meet the requirements of United States Pharmacopoeia (USP) Method 467 and the European Pharmacopoeia general method for determining residual solvents in pharmaceutical preparations. Use this column to separate residual solvents for research purposes or qualitative analysis. The USP and European Pharmacopoeia methods also specify using a deactivated 5-meter guard column.
In order to ensure analysis under optimum conditions, we strongly suggest the use of a deactivated guard column (Cat. No. 25339) with the OVI-G43 column.
This column meets USP G43 requirements.
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