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  2. Methyl group - Wikipedia

    en.wikipedia.org/wiki/Methyl_group

    [15] [16] The term "methyl" was derived in about 1840 by back-formation from "methylene", and was then applied to describe "methyl alcohol" (which since 1892 is called "methanol"). Methyl is the IUPAC nomenclature of organic chemistry term for an alkane (or alkyl) molecule, using the prefix "meth-" to indicate the presence of a single carbon.

  3. IUPAC nomenclature of organic chemistry - Wikipedia

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

    For example, ethyl comes before dihydroxy or dimethyl, as the "e" in "ethyl" precedes the "h" in "dihydroxy" and the "m" in "dimethyl" alphabetically. The "di" is not considered in either case). When both side chains and secondary functional groups are present, they should be written mixed together in one group rather than in two separate groups.

  4. Chemical nomenclature - Wikipedia

    en.wikipedia.org/wiki/Chemical_nomenclature

    The IUPAC system is often criticized for failing to distinguish relevant compounds (for example, for differing reactivity of sulfur allotropes, which IUPAC does not distinguish). While IUPAC has a human-readable advantage over CAS numbering, IUPAC names for some larger, relevant molecules (such as rapamycin ) are barely human-readable, so ...

  5. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    The methyl "substituent" or "group" is highlighted red. According to the usual rules of nomenclature, alkyl groups are included in the name of the molecule before the root, as in methylpentane. This name is, however, ambiguous, as the methyl branch could be on various carbon atoms.

  6. Ethyl sulfate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_sulfate

    Ethyl sulfate can be produced in a laboratory setting by reacting ethanol with sulfuric acid under a gentle boil, while keeping the reaction below 140 °C. The sulfuric acid must be added dropwise or the reaction must be actively cooled because the reaction itself is highly exothermic.

  7. Organosulfate - Wikipedia

    en.wikipedia.org/wiki/Organosulfate

    Alkyl sulfates consist of a hydrophobic hydrocarbon chain, a polar sulfate group (containing an anion) and either a cation or amine to neutralize the sulfate group. Examples include: sodium lauryl sulfate (also known as sulfuric acid mono dodecyl ester sodium salt) and related potassium and ammonium salts.

  8. Methylation - Wikipedia

    en.wikipedia.org/wiki/Methylation

    Methylation, in the chemical sciences, is the addition of a methyl group on a substrate, or the substitution of an atom (or group) by a methyl group. Methylation is a form of alkylation, with a methyl group replacing a hydrogen atom. These terms are commonly used in chemistry, biochemistry, soil science, and biology.

  9. Mercury methylation - Wikipedia

    en.wikipedia.org/wiki/Mercury_methylation

    The Acetyl-CoA pathway for mercury methylation is done by sulfate reducing bacteria and is catalyzed by a corrinoid dependent protein. Through this pathway, the methyl group is proposed to originate from C-3 serine. A transfer of the methyl group from CH3-Tetrahydrofolate to the corrinoid protein requires the genes hgcA and hgcB. [4]