3D model (JSmol)
|Molar mass||193.922 g/mol|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
In inorganic chemistry, bicarbonate (IUPAC-recommended nomenclature: hydrogencarbonate) is an intermediate form in the deprotonation of carbonic acid. It is a polyatomic anion with the chemical formula HCO−3.
Bicarbonate serves a crucial biochemical role in the physiological pH buffering system.The term "bicarbonate" was coined in 1814 by the English chemist William Hyde Wollaston. The prefix "bi" in "bicarbonate" comes from an outdated naming system and is based on the observation that there is twice as much carbonate (CO2−3) per sodium ion in sodium bicarbonate (NaHCO3) and other bicarbonates than in sodium carbonate (Na2CO3) and other carbonates. The name lives on as a trivial name.
According to the Wikipedia article IUPAC nomenclature of inorganic chemistry, the prefix bi– is a deprecated way of indicating the presence of a single hydrogen ion. The recommended nomenclature today mandates explicit referencing of the presence of the single hydrogen ion: sodium hydrogen carbonate or sodium hydrogencarbonate. A parallel example is sodium bisulfite (NaHSO3).Caesium carbonate
Caesium carbonate or cesium carbonate is a white crystalline solid compound. Caesium carbonate has a high solubility in polar solvents such as water, alcohol and DMF. Its solubility is higher in organic solvents compared to other carbonates like potassium and sodium carbonates, although it remains quite insoluble in other organic solvents such as toluene, p-xylene, and chlorobenzene. This compound is used in organic synthesis as a base. It also appears to have applications in energy conversion.Caesium chloride
Caesium chloride or cesium chloride is the inorganic compound with the formula CsCl. This colorless solid is an important source of caesium ions in a variety of niche applications. Its crystal structure forms a major structural type where each caesium ion is coordinated by 8 chlorine ions. Caesium chloride dissolves in water. CsCl changes to NaCl structure on heating. Caesium chloride occurs naturally as impurities in carnallite (up to 0.002%), sylvite and kainite. Less than 20 tonnes of CsCl is produced annually worldwide, mostly from a caesium-bearing mineral pollucite.Caesium chloride is widely used medicine structure in isopycnic centrifugation for separating various types of DNA. It is a reagent in analytical chemistry, where it is used to identify ions by the color and morphology of the precipitate. When enriched in radioisotopes, such as 137CsCl or 131CsCl, caesium chloride is used in nuclear medicine applications such as treatment of cancer and diagnosis of myocardial infarction. Another form of cancer treatment was studied using conventional non-radioactive CsCl. Whereas conventional caesium chloride has a rather low toxicity to humans and animals, the radioactive form easily contaminates the environment due to the high solubility of CsCl in water. Spread of 137CsCl powder from a 93-gram container in 1987 in Goiânia, Brazil, resulted in one of the worst-ever radiation spill accidents killing four and directly affecting more than 100,000 people.Glossary of chemical formulas
This is a list of common chemical compounds with chemical formulas and CAS numbers, indexed by formula. This complements alternative listing at inorganic compounds by element. There is no complete list of chemical compounds since by nature the list would be infinite.
Note: There are elements for which spellings may differ, such as aluminum/ aluminium, sulfur/ sulphur, and caesium/ cesium.List of inorganic compounds
Although most compounds are referred to by their IUPAC systematic names (following IUPAC nomenclature), "traditional" names have also been kept where they are in wide use or of significant historical interests.