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Identification of phenolic compounds was estimated on the basis of retention time.
The solubility of the compounds was estimated via the turbidimetric method using standard test buffers (pH 2.0 and pH 6.5) as previously described [23].
The relative amount of identified compounds was estimated by comparison with a 4-bromofluorobenzene internal standard calibration curve delivered in methanol over the concentration range of 2 to 75 μg/mL.
Potential for oncogenic transformation of each of the compounds was estimated from short-term bioassays.
The ability to solubilise insoluble phosphate compounds was estimated according to Ahmad et al. [ 30].
Exposure to both volatile and nonvolatile organochlorine compounds was estimated at the department level using an exposure matrix.
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The detection limits of the compounds are estimated to be 3 × 10-7 mol · l-1.
Finally, the standard Gibbs free energies of formation for the DyNi intermetallic compounds were estimated.
Furthermore, the partial molar volumes of those compounds were estimated following the theory developed by Kumar and Johnston.
Additionally, the partial molar volumes of those compounds were estimated following the theory developed by Kumar and Johnston.
The in vitro aldose reductase inhibitory activity of the prepared 1 7 compounds were estimated and compared with that of the initial compound (I).
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