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It is the sodium salt of oxalic acid. It contains sodium cations Na + and oxalate anions C 2 O 2− 4. It is a white, crystalline, odorless solid, that decomposes above 290 °C. [2] Sodium oxalate can act as a reducing agent, and it may be used as a primary standard for standardizing potassium permanganate (KMnO 4) solutions.
Honeybee coated with oxalate crystals. Oxalic acid is used by some beekeepers as a miticide against the parasitic varroa mite. [52] Dilute solutions (0.05–0.15 M) of oxalic acid can be used to remove iron from clays such as kaolinite to produce light-colored ceramics. [53] Oxalic acid can be used to clean minerals like many other acids.
It is an ammonium salt of oxalic acid. It consists of ammonium cations ([NH 4] +) and oxalate anions (C 2 O 2− 4). The structure of ammonium oxalate is ([NH 4] +) 2 [C 2 O 4] 2−. Ammonium oxalate sometimes comes as a monohydrate ([NH 4] 2 C 2 O 4 ·H 2 O). It is a colorless or white salt under standard conditions and is odorless and non ...
Oxalic acid binds with calcium to form calcium oxalate crystals which may deposit and cause damage to many areas of the body including the brain, heart, kidneys, and lungs. [7] The most significant effect is accumulation of calcium oxalate crystals in the kidneys which causes kidney damage leading to oliguric or anuric acute kidney failure. [7]
Oxalate (systematic IUPAC name: ethanedioate) is an anion with the chemical formula C 2 O 2− 4.This dianion is colorless. It occurs naturally, including in some foods. It forms a variety of salts, for example sodium oxalate (Na 2 C 2 O 4), and several esters such as dimethyl oxalate ((CH 3) 2 C 2 O 4).
Calcium oxalate crystals are commonly found in lichens, where they occur in two mineral forms: weddellite (CaC 2 O 4 ·(2+x)H 2 O) and whewellite (CaC 2 O 4 ·H 2 O). These crystals can form both on the surface of the lichen as a powdery coating called pruina and within the internal structures of the lichen thallus. The type and distribution of ...
It can also be prepared by treating oxalic acid with phosphorus pentachloride. [6] [7] Oxalyl chloride is produced commercially from ethylene carbonate. Photochlorination gives the perchloroethylene carbonate C 2 Cl 4 O 2 CO and hydrogen chloride HCl, which is subsequently degraded to oxalyl chloride and phosgene COCl 2: [8] C 2 H 4 O 2 CO + 4 ...
This chemical is the double ester of phenol with oxalic acid. Upon reaction with hydrogen peroxide , 1,2-dioxetanedione is formed, along with release of the two phenols. [ 2 ] The dioxetanedione then reacts with a dye molecule, decomposing to form carbon dioxide and leaving the dye in an excited state .
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