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Lithium acetate is used in the laboratory as buffer for gel electrophoresis of DNA and RNA. It has a lower electrical conductivity and can be run at higher speeds than can gels made from TAE buffer (5-30V/cm as compared to 5-10V/cm). At a given voltage, the heat generation and thus the gel temperature is much lower than with TAE buffers ...
Substance Formula 0 °C 10 °C 20 °C 30 °C 40 °C 50 °C 60 °C 70 °C 80 °C 90 °C 100 °C Barium acetate: Ba(C 2 H 3 O 2) 2: 58.8: 62: 72: 75: 78.5: 77: 75
The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.
Lithium hydroxide is an inorganic compound with the formula LiOH. It can exist as anhydrous or hydrated, and both forms are white hygroscopic solids. They are soluble in water and slightly soluble in ethanol. Both are available commercially. While classified as a strong base, lithium hydroxide is the weakest known alkali metal hydroxide.
lithium tetrahydridoaluminate: 16853–85–3 LiAlO 2: lithium aluminate: 12003–67–7 LiBF 4: lithium tetrafluoroborate: 14283–07–9 LiBH 4: lithium borohydride: 16949–15–8 LiBO 2: lithium metaborate: 13453–69–5 LiBr: lithium bromide: 7550–35–8 LiCHO 2: lithium formate: 556–63–8 LiCH 3 O: lithium methoxide: 865–34–9 ...
Lithium sulfate is used to treat bipolar disorder (see lithium pharmacology).. Lithium sulfate is researched as a potential component of ion conducting glasses. Transparent conducting film is a highly investigated topic as they are used in applications such as solar panels and the potential for a new class of battery.
It also reacts with carbon dioxide to give Lithium acetate: CH 3 Li + CO 2 → CH 3 CO 2 − Li + Transition metal methyl compounds can be prepared by reaction of MeLi with metal halides. Especially important are the formation of organocopper compounds (Gilman reagents), of which the most useful is lithium dimethylcuprate.
Dilithium acetylide is an organometallic compound with the formula Li 2 C 2.It is typically derived by double deprotonation of acetylene. X-ray crystallography confirms the presence of C≡C subunits attached to lithium, resulting in a polymeric structure. [3]
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