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Both Jmol and JSmol render an interactive 3D representation of a molecule or other structure that may be used as a teaching tool, [5] or for research, in several fields, e.g. chemistry, biochemistry, materials science, crystallography, [6] symmetry or nanotechnology.
Sodium bicarbonate (IUPAC name: sodium hydrogencarbonate [9]), commonly known as baking soda or bicarbonate of soda, is a chemical compound with the formula NaHCO 3. It is a salt composed of a sodium cation (Na +) and a bicarbonate anion (HCO 3 −). Sodium bicarbonate is a white solid that is crystalline but often appears as a
Printable version; In other projects ... 3D model [3]: Interactive image ... Sodium bitartrate; References
Printable version; In other projects ... 3D model . Interactive image; ... Diethyl diethylmalonate or diethyl 2,2-diethylmalonate is a derivative of diethyl ...
Sodium nonanoyloxybenzenesulfonate (NOBS) is an important component of laundry detergents and bleaches. It is known as a bleach activator for active oxygen sources, allowing formulas containing hydrogen peroxide releasing chemicals (specifically sodium perborate , sodium percarbonate , sodium perphosphate , sodium persulfate , and urea peroxide ...
The dihydrate, Na 3 H(CO 3) 2 · 2H 2 O, occurs in nature as the evaporite mineral trona. [1] Due to concerns about the toxicity of borax which was withdrawn as a cleaning and laundry product, sodium sesquicarbonate is sold in the European Union (EU) as "Borax substitute". [2] It is also known as one of the E number food additives E500(iii).
This mixture is sometimes mistakenly made with vinegar and sodium bicarbonate (baking soda), which actually react to neutralize each other, creating carbon dioxide and a sodium acetate solution. Cream of tartar was often used in traditional dyeing where the complexing action of the tartrate ions was used to adjust the solubility and hydrolysis ...
2-Nitrobenzaldehyde is an intermediate in an early route to indigo, a water-insoluble dye commonly used to dye jeans and other fabrics.In the Baeyer-Drewson indigo synthesis, 2-nitrobenzaldehyde condenses with acetone in basic aqueous solution to yield indigo in a one-pot synthesis [9] [10] The method was abandoned in the early part of the 20th century, being replaced by routes from aniline.