The phrase "acetate trihydrate" is correct and usable in written English.
It can be used in scientific or technical contexts, particularly in chemistry or materials science, to refer to a specific chemical compound that includes acetate and water molecules.
Example: "The experiment required the use of acetate trihydrate to achieve the desired reaction conditions."
Alternatives: "tri-hydrated acetate" or "acetate with three water molecules".
Boric acid, sodium acetate trihydrate, acetic acid 96%%, acetone, dimethyl formamide (DMF), methyl cellulose (MC), tween-80, sodium hydroxide, hydrogen peroxide (30 %) and hydrochloric acid (32%%) were all obtained from El-Nasr Pharmaceutical Chemicals Company (ADWIC) (Abu Zaabal, Egypt).
AlCl3.6H2O, sodium acetate trihydrate and acetic acid were all metal free.
Acetate buffer (pH 5.5) (J.T.-Baker, USA) was prepared by dissolving acetic acid sodium acetate trihydrate in Milli-Q water.
NaCl, Sodium acetate trihydrate, glacial acetic acid and acetone were purchased from Fisher Scientific and were AR grade.
Methanol ROTISOLV® HPLC Gradient Grade (MeOH), peptone from casein, K2HPO4, KH2PO4, Na2HPO4 × 2 H2O, NaH2PO4 × 2 H2O, sodium acetate trihydrate, TRIS, EDTA, 99% acetic acid, NaOH, ampicillin sodium salt, l-rhamnose monohydrate, agarose NEEO Ultra and ethidium bromide were supplied by Carl Roth Corporation (Karlsruhe, Germany).
The chloramine T solution and aldehyde-perchloric acid solution used for the assay were prepared as follows: Chloramine T (sodium N-chloro-p-toluenesulfonamide) 0.3535 g was dissolved in 5.175 mL of water, and then 6.5 mL of n-propanol and 13.325 mL of pH 6 buffer (citric acid monohydrate 25 g, acetic acid 6 mL, sodium acetate trihydrate 60 g, sodium hydroxide 17 g to 500 mL) were added.
After 1-hr in fixation solution, slices were rinsed in phosphate buffer for 2 min, and then submerged for 60 75 s in staining solution containing 1% thionin acetate, 0.1 M sodium acetate trihydrate, and 0.1 M acetic acid.
Samples (50 μL) were combined with 100 μL freshly prepared oxidizing solution (0.178 g chloramines-T in 15 mL n-propanol/10 mL ddH2O/25 mL citrate buffer (50 g citric acid monohydrate, 12 mL glacial acetic acid, 120 g sodium acetate trihydrate, 34 g NaOH to pH 6.0 in 1 L)) and incubated for 5 min at room temperature.
The FRAP reagent constituents were 300 mM acetate buffer (3.1 g sodium acetate trihydrate and 16 mL glacial acetic acid, pH 3.6), 10 mM TPTZ (2,4,6-tripyridyl s-triazine) solution in 40 mM HCl, and 20 mM ferric chloride hexahydrate solution.
Using the sol-gel method, BFO and PZT with excess Pb-acetate 10 mol% precursor solutions were prepared from the starting materials Bi-nitrate pentahydrate [Bi(NO3 3·5H2O], Fe-nitrate nonahydrate [Fe(NO3 3·9H2O], Pb-acetate trihydrate [Pb(CH3CO2 2·3H2O], Zr n-propoxide [Zr OCH2CH2CH3 4], and Ti iso-propoxide {Ti[OCH(CH3 2]4}, and the solvent 2-methoxyethanol.
The apo-Bbp273−598 crystals were grown in 0.2 mol/L calcium acetate hydrate, 0.1 mol/L sodium cacodylate trihydrate pH 6.5, 18% PEG8000.
