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JSmol is also free and open source under the same license. Molecules can be displayed in different styles of rendering, like ball-and-stick models , space-filling models , ribbon diagrams , etc. [ 6 ] Jmol supports a wide range of chemical file formats , including Protein Data Bank (pdb), Crystallographic Information File (cif), MDL Molfile ...
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
The parameter standard bicarbonate concentration (SBC e) is the bicarbonate concentration in the blood at a P a CO 2 of 40 mmHg (5.33 kPa), full oxygen saturation and 36 °C. [13] Reference ranges for blood tests, comparing blood content of bicarbonate (shown in blue at right) with other constituents.
Allophanic acid is the organic compound with the formula H 2 NC(O)NHCO 2 H. It is a carbamic acid, the carboxylated derivative of urea. Biuret can be viewed as the amide of allophanic acid. The compound can be prepared by treating urea with sodium bicarbonate: [1] H 2 NC(O)NH 2 + NaHCO 3 → H 2 NC(O)NHCO 2 H + NaOH
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 [1] Due to concerns about the toxicity of borax which was withdrawn as a cleaning and laundry product, sodium sesquicarbonate is sold in the European Union (EU) as "Borax substitute".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).
Sodium bisulfite (or sodium bisulphite, sodium hydrogen sulfite) is a chemical mixture with the approximate chemical formula NaHSO 3. Sodium bisulfite is not a real compound, [ 2 ] but a mixture of salts that dissolve in water to give solutions composed of sodium and bisulfite ions.
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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.