The International Union of Pure and Applied Chemistry is an international federation of National Adhering Organizations working for the advancement of the chemical sciences, especially by developing nomenclature and terminology. It is a member of the International Science Council (ISC). IUPAC is registered in Zürich, Switzerland, and the administrative office, known as the "IUPAC Secretariat", is in Research Triangle Park, North Carolina, United States. IUPAC's executive director heads this administrative office, currently Greta Heydenrych.
In chemistry, a trivial name is a non-systematic name for a chemical substance. That is, the name is not recognized according to the rules of any formal system of chemical nomenclature such as IUPAC inorganic or IUPAC organic nomenclature. A trivial name is not a formal name and is usually a common name.
Peroxymonosulfuric acid, also known as persulfuric acid, peroxysulfuric acid is the inorganic compound with the formula H2SO5. It is a white solid. It is a component of Caro's acid, which is a solution of peroxymonosulfuric acid in sulfuric acid containing small amounts of water. Peroxymonosulfuric acid is a very strong oxidant.
Chemical nomenclature is a set of rules to generate systematic names for chemical compounds. The nomenclature used most frequently worldwide is the one created and developed by the International Union of Pure and Applied Chemistry (IUPAC).
In chemical nomenclature, the IUPAC nomenclature of inorganic chemistry is a systematic method of naming inorganic chemical compounds, as recommended by the International Union of Pure and Applied Chemistry (IUPAC). It is published in Nomenclature of Inorganic Chemistry. Ideally, every inorganic compound should have a name from which an unambiguous formula can be determined. There is also an IUPAC nomenclature of organic chemistry.
In coordination chemistry, a bridging ligand is a ligand that connects two or more atoms, usually metal ions. The ligand may be atomic or polyatomic. Virtually all complex organic compounds can serve as bridging ligands, so the term is usually restricted to small ligands such as pseudohalides or to ligands that are specifically designed to link two metals.
Quantities, Units and Symbols in Physical Chemistry, also known as the Green Book, is a compilation of terms and symbols widely used in the field of physical chemistry. It also includes a table of physical constants, tables listing the properties of elementary particles, chemical elements, and nuclides, and information about conversion factors that are commonly used in physical chemistry. The Green Book is published by the International Union of Pure and Applied Chemistry (IUPAC) and is based on published, citeable sources. Information in the Green Book is synthesized from recommendations made by IUPAC, the International Union of Pure and Applied Physics (IUPAP) and the International Organization for Standardization (ISO), including recommendations listed in the IUPAP Red Book Symbols, Units, Nomenclature and Fundamental Constants in Physics and in the ISO 31 standards.
The peroxomonosulfate ion, SO2−
5, is a sulfur oxoanion. It is sometimes referred to as the persulfate ion, but this term also refers to the peroxydisulfate ion, S
2O2−
8.
Dithionic acid, H2S2O6, is the inorganic compound with the formula H2S2O6. It is the doubly protonated derivative of dithionate, a well-characterized dianion. Dithionic acid is mainly observed and characterized as an aqueous solution.
In chemical nomenclature, a preferred IUPAC name (PIN) is a unique name, assigned to a chemical substance and preferred among all possible names generated by IUPAC nomenclature. The "preferred IUPAC nomenclature" provides a set of rules for choosing between multiple possibilities in situations where it is important to decide on a unique name. It is intended for use in legal and regulatory situations.
Propadiene or allene is the organic compound with the formula H2C=C=CH2. It is the simplest allene, i.e. a compound with two adjacent carbon double bonds. As a constituent of MAPP gas, it has been used as a fuel for specialized welding.
An Interpenetrating polymer network (IPN) is a polymer comprising two or more networks which are at least partially interlaced on a polymer scale but not covalently bonded to each other. The network cannot be separated unless chemical bonds are broken. The two or more networks can be envisioned to be entangled in such a way that they are concatenated and cannot be pulled apart, but not bonded to each other by any chemical bond.
Nomenclature of Organic Chemistry, commonly referred to by chemists as the Blue Book, is a collection of recommendations on organic chemical nomenclature published at irregular intervals by the International Union of Pure and Applied Chemistry (IUPAC). A full edition was published in 1979, an abridged and updated version of which was published in 1993 as A Guide to IUPAC Nomenclature of Organic Compounds. Both of these are now out-of-print in their paper versions, but are available free of charge in electronic versions. After the release of a draft version for public comment in 2004 and the publication of several revised sections in the journal Pure and Applied Chemistry, a fully revised edition was published in print in 2013 and its online version is also available.
The Compendium of Analytical Nomenclature is an IUPAC nomenclature book published by the International Union of Pure and Applied Chemistry (IUPAC) containing internationally accepted definitions for terms in analytical chemistry. It has traditionally been published in an orange cover, hence its informal name, the Orange Book.
In chemistry, a ring is an ambiguous term referring either to a simple cycle of atoms and bonds in a molecule or to a connected set of atoms and bonds in which every atom and bond is a member of a cycle. A ring system that is a simple cycle is called a monocycle or simple ring, and one that is not a simple cycle is called a polycycle or polycyclic ring system. A simple ring contains the same number of sigma bonds as atoms, and a polycyclic ring system contains more sigma bonds than atoms.
Disulfurous acid, metabisulfurous acid or pyrosulfurous acid is an oxoacid of sulfur with the formula H2S2O5. Its structure is HO−S(=O)2−S(=O)−OH. The salts of disulfurous acid are called disulfites or metabisulfites. Disulfurous acid is, like sulfurous acid, a phantom acid, which does not exist in the free state. In contrast to disulfate, disulfite has two directly connected sulfur atoms. The oxidation state of the sulfur atom bonded to three oxygen atoms is +5 and its valence is 6, while that of the other sulfur is +3 and 4 respectively.
The Compendium of Macromolecular Nomenclature, by the International Union of Pure and Applied Chemistry (IUPAC), provides definition of polymer related terms and rules of nomenclature of polymers. It is referred to as the Purple Book. It was published in 1991 (ISBN 0-63202-8475) by Blackwell Science. The author of this book is W.V. Metanomski.
The Inorganic Chemistry Division of the International Union of Pure and Applied Chemistry (IUPAC), also known as Division II, deals with all aspects of inorganic chemistry, including materials and bioinorganic chemistry, and also with isotopes, atomic weights and the periodic table. It furthermore advises the Chemical Nomenclature and Structure Representation Division on issues dealing with inorganic compounds and materials. For the general public, the most visible result of the division's work is that it evaluates and advises the IUPAC on names and symbols proposed for new elements that have been approved for addition to the periodic table. For the scientific end educational community the work on isotopic abundances and atomic weights is of fundamental importance as these numbers are continuously checked and updated.
The International Union of Pure and Applied Chemistry (IUPAC) has published four sets of rules to standardize chemical nomenclature.
In chemical nomenclature, a descriptor is a notational prefix placed before the systematic substance name, which describes the configuration or the stereochemistry of the molecule. Some of the listed descriptors should not be used in publications, as they no longer accurately correspond with the recommendations of the IUPAC. Stereodescriptors are often used in combination with locants to clearly identify a chemical structure unambiguously.
