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Palladium on CaCO3 (5 wt % Pd, 0.05 equiv) was added to a stirred solution of acetate (1.0 equiv) and quinoline (0.2 equiv) in toluene (0.1 m).
Briefly, the stock solution of acetate buffer; (300 mM, pH 3.6), 2,4,6-tris 2-pyridyl -S-triazinee (TPTZ) solution, (10 mM TPTZ in 40 mM/L HCl) and aqueos ferric chloride (2-pyridyl -S-triazinerepared.
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Buffer solutions of acetate and phosphate (0.5 mol L−1) were prepared by dissolving the appropriate amount of sodium acetate (Merck) or NaH2PO4·2H2O (Merck) in double distilled water, respectively.
The tissue samples were homogenised in a 4 : 1 solution of ethyl acetate : glacial acetic acid mixture.
The tumour samples were homogenised in a 4 : 1 solution of ethyl acetate : glacial acetic acid mixture according to Batlle (1997).
The tissue samples were homogenised in a 4 : 1 solution of ethyl acetate : glacial acetic acid mixture according to Batlle (1997).
The oxidation of 2-methylnaphthalene in the solution of lithium acetate in glacial acetic acid has been investigated.
Amendments were made by mixing acetate and a 200 μM stock solution of uranyl acetate in groundwater at a 1 10 dilution to the influent groundwater.
A buffered solution containing various concentrations of acetic acid and acetate ion, for example, can be prepared by mixing solutions of acetic acid and sodium acetate, by partially neutralizing a solution of acetic acid with sodium hydroxide, or by adding less than one equivalent of a strong acid to a solution of sodium acetate.
The other route of sol preparation was to prepare 10% solution of zinc acetate [Zn(CH3COO 2 · 2H2O] by dissolving 10 g of zinc acetate in 100 mL of boiling isopropyl alcohol at 84 °C.
After ALA or He ALA exposure, explants of 50 mg were homogenised in a 4 : 1 solution of ethyl acetate-glacial acetic acid mixture.
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