I tested 1 or 2 drops of diluted acidic Lugol's iodine (1 drop in 10 ml seawater) and 0.5 % formalin solution on 500 ul of Akashiwo sanguinea on slides. The cells sometime fixed, sometime not. Cell also burst frequently after staining.

So I'm trying to prepare a basic version of Lugol's iodine using sodium acetate CH3COONa. However, my lab does not has the anhydrous version but only CH3COONa.3H2O.

I attempted to dry it using oven at 80' c for 1 hour, however, the drying was incomplete, powder still appear moist and tend to stick together. I extended the drying time for another 12 hours at the same temperature.

Do you think this will completely remove the water (.3H2O) from it?

Plus, as part of the preparation work, I weighted KI and Iodine resublimed on Aluminum foil. Of course, a small portion of I2 reacted with the Al foil and change to liquid. I transferred the remaining solid to a crucible and placed it in a desiccator. Do you think I can still re-use the I2 later?

Thanks.

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