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  2. IUPAC numerical multiplier - Wikipedia

    en.wikipedia.org/wiki/IUPAC_numerical_multiplier

    The IUPAC numerical multiplier is a system of prefixes used in chemistry to indicate the number of atoms or groups in a molecule.

  3. Chemical nomenclature - Wikipedia

    en.wikipedia.org/wiki/Chemical_nomenclature

    The IUPAC's rules for naming organic and inorganic compounds are contained in two publications, known as the Blue Book [1] [2] and the Red Book, [3] respectively. A third publication, known as the Green Book , [ 4 ] recommends the use of symbols for physical quantities (in association with the IUPAP ), while a fourth, the Gold Book , [ 5 ...

  4. Hexane - Wikipedia

    en.wikipedia.org/wiki/Hexane

    Hexane and other volatile hydrocarbons (petroleum ether) present an aspiration risk. [26] n-Hexane is sometimes used as a denaturant for alcohol, and as a cleaning agent in the textile, furniture, and leather industries. It is slowly being replaced with other solvents. [27] Like gasoline, hexane is highly volatile and is an explosion risk.

  5. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    [4] To avoid long and tedious names in normal communication, the official IUPAC naming recommendations are not always followed in practice, except when it is necessary to give an unambiguous and absolute definition to a compound. IUPAC names can sometimes be simpler than older names, as with ethanol, instead of ethyl alcohol. For relatively ...

  6. IUPAC nomenclature of inorganic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    The names "caffeine" and "3,7-dihydro-1,3,7-trimethyl-1H-purine-2,6-dione" both signify the same chemical compound.The systematic name encodes the structure and composition of the caffeine molecule in some detail, and provides an unambiguous reference to this compound, whereas the name "caffeine" simply names it.

  7. IUPAC polymer nomenclature - Wikipedia

    en.wikipedia.org/wiki/IUPAC_polymer_nomenclature

    An example is The preferred CRU is an acyclic subunit of 4 carbon atoms with 4 free valences, one at each atom, as shown. It is oriented so that the lower left atom has the lowest number. The free-valence locants are written before the suffix, and they are cited clockwise from the lower left position as: lower-left, upper-left:upper-right ...

  8. Naming of chemical elements - Wikipedia

    en.wikipedia.org/wiki/Naming_of_chemical_elements

    The naming rules promulgated by IUPAC in 2002 declared that all newly discovered elements should have names ending in -ium, for linguistic consistency. [40] In 2016, this was amended so that elements in the halogen and noble gas groups would receive the traditional -ine and -on suffixes. This amendment was put into practice for tennessine ...

  9. 2-Methylpentane - Wikipedia

    en.wikipedia.org/wiki/2-Methylpentane

    As of early 1990s, it was present in American [4] and European [5] gasoline in small amounts, and by 2011 its share in US gas varied between 2 and 8%. [6] Using a quantitative structure-activity relationship (QSAR) prediction model, 2-Methylpentane has a research octane number (RON) of 75, motor octane number (MON) of 77, and cetane number (CN ...