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Thiol information


Thiol with a   blue highlighted sulfhydryl group.

In organic chemistry, a thiol (/ˈθɒl/;[1] from Ancient Greek θεῖον (theion) 'sulfur'[2]), or thiol derivative, is any organosulfur compound of the form R−SH, where R represents an alkyl or other organic substituent. The −SH functional group itself is referred to as either a thiol group or a sulfhydryl group, or a sulfanyl group. Thiols are the sulfur analogue of alcohols (that is, sulfur takes the place of oxygen in the hydroxyl (−OH) group of an alcohol), and the word is a blend of "thio-" with "alcohol".

Many thiols have strong odors resembling that of garlic or rotten eggs. Thiols are used as odorants to assist in the detection of natural gas (which in pure form is odorless), and the "smell of natural gas" is due to the smell of the thiol used as the odorant. Thiols are sometimes referred to as mercaptans (/mərˈkæptæn/)[3] or mercapto compounds,[4][5][6] a term introduced in 1832 by William Christopher Zeise and is derived from the Latin mercurio captāns ('capturing mercury')[7] because the thiolate group (RS) bonds very strongly with mercury compounds.[8]

  1. ^ Dictionary Reference: thiol Archived 2013-04-11 at the Wayback Machine
  2. ^ θεῖον Archived 2017-05-10 at the Wayback Machine, Henry George Liddell, Robert Scott, A Greek–English Lexicon
  3. ^ Dictionary Reference: mercaptan Archived 2012-11-13 at the Wayback Machine
  4. ^ Patai, Saul, ed. (1974). The Chemistry of the Thiol Group. Part 1. London: Wiley. doi:10.1002/9780470771310. ISBN 9780470771310.
  5. ^ Patai, Saul, ed. (1974). The Chemistry of the Thiol Group. Part 2. London: Wiley. doi:10.1002/9780470771327. ISBN 9780470771327.
  6. ^ R. J. Cremlyn (1996). An Introduction to Organosulfur Chemistry. Chichester: John Wiley and Sons. ISBN 978-0-471-95512-2.
  7. ^ Oxford American Dictionaries (Mac OS X Leopard).
  8. ^ See:
    • Zeise, William Christopher (1834). "Mercaptanet, med bemaerkninger over nogle andre nye producter af svovelvinsyresaltene, som og af den tunge vinolie, ved sulfureter" [Mercaptan, with remarks on some other new products of salts of ethyl hydrogen sulfate as well as of heavy oil of wine, by means of hydrogen sulfide]. Kongelige Danske Videnskabers Selskabs Skrifter. 4th series (in Danish). 6: 1–70. On p. 13 the word "mercaptan" is coined.
    • German translation: Zeise, W. C. (1834). "Das Mercaptan, nebst Bermerkungen über einige neue Producte aus der Einwirkung der Sulfurete auf weinschwefelsaure Salze und auf das Weinöl" [Mercaptan together with comments on some new products from the effect of hydrogen sulfide on salts of ethyl sulfate ((C2H5)HSO4) and heavy oil of wine (a mixture of diethyl sulfate, diethyl sulfite, and polymerized ethylene)]. Annalen der Physik und Chemie. 2nd series (in German). 31 (24): 369–431. From p. 378: " … nenne ich den vom Quecksilber aufgenommenen Stoff Mercaptum (von: Corpus mercurio captum) … " ( … I name the substance [that is] absorbed by mercury "mercaptum" (from: the body (substance) [that] has been absorbed by mercury) … )
    • German translation is reprinted in:Zeise, W. C. (1834). "Das Mercaptan, nebst Bemerkungen über einige andere neue Erzeugnisse der Wirkung schwefelweinsaurer Salze, wie auch des schweren Weinöls auf Sulphurete". Journal für Praktische Chemie. 1 (1): 257–268, 345–356, 396–413, 457–475. doi:10.1002/prac.18340010154.
    • Summarized in: Zeise, W. C. (1834). "Ueber das Mercaptan" [On mercaptan]. Annalen der Pharmacie. 11 (1): 1–10. doi:10.1002/jlac.18340110102. Archived from the original on 2015-03-20.
    • Zeise, William Christopher (1834). "Sur le mercaptan; avec des observations sur d'autres produits resultant de l'action des sulfovinates ainsi que de l'huile de vin, sur des sulfures metalliques" [On mercaptan; with observations on other products resulting from the action of sulfovinates [typically, ethyl hydrogen sulfate] as well as oil of wine [a mixture of diethylsulfate and ethylene polymers] on metal sulfides]. Annales de Chimie et de Physique. 56: 87–97. Archived from the original on 2015-03-20. "Mercaptan" (ethyl thiol) was discovered in 1834 by the Danish professor of chemistry William Christopher Zeise (1789–1847). He called it "mercaptan", a contraction of "corpus mercurio captans" (mercury-capturing substance) [p. 88], because it reacted violently with mercury(II) oxide ("deutoxide de mercure") [p. 92].
    • The article in Annales de Chimie et de Physique (1834) was translated from the German article: Zeise, W. C. (1834). "Das Mercaptan, nebst Bemerkungen über einige neue Producte aus der Einwirkung der Sulfurete auf weinschwefelsaure Salze und auf das Weinöl". Annalen der Physik und Chemie. 107 (27): 369–431. Bibcode:1834AnP...107..369Z. doi:10.1002/andp.18341072402. Archived from the original on 2015-03-20.

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Thiol

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In organic chemistry, a thiol (/ˈθaɪɒl/; from Ancient Greek θεῖον (theion) 'sulfur'), or thiol derivative, is any organosulfur compound of the form R−SH...

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Disulfide

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an SS-bond or sometimes a disulfide bridge and usually derived from two thiol groups. In inorganic chemistry, the anion appears in a few rare minerals...

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Propanethiol

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organic compound with the molecular formula C3H8S. It belongs to the group of thiols. It is a colorless liquid with a strong, offensive odor. It is moderately...

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Thiol sulfotransferase

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enzymology, a thiol sulfotransferase (EC 2.8.2.16) is an enzyme that catalyzes the chemical reaction 3'-phosphoadenylyl sulfate + a thiol ⇌ {\displaystyle...

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Thioester

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the product of esterification of a carboxylic acid (R−C(=O)−O−H) with a thiol (R'−S−H). In biochemistry, the best-known thioesters are derivatives of...

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Methanethiol

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responsible for bad breath and the smell of flatus. Methanethiol is the simplest thiol and is sometimes abbreviated as MeSH. It is very flammable. The molecule...

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Prenylthiol

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Prenylthiol or 3-methyl-2-butene-1-thiol is a chemical compound. It is one of a group of chemicals that give cannabis its characteristic "skunk-like"...

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Thiobenzoic acid

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Names Preferred IUPAC name Benzenecarbothioic S-acid Other names Benzoyl thiol Monothiobenzoic acid Identifiers CAS Number 98-91-9 Y 3D model (JSmol) Interactive...

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Thiol oxidoreductase

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Thiol oxidoreductases are proteins that redox control by utilizing catalytic cysteine (Cys) residues for oxidation or reduction of their substrates. Examples...

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Ethanethiol

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Abbreviated EtSH, it consists of an ethyl group (Et), CH3CH2, attached to a thiol group, SH. Its structure parallels that of ethanol, but with sulfur in place...

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Cysteine protease

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Cysteine proteases, also known as thiol proteases, are hydrolase enzymes that degrade proteins. These proteases share a common catalytic mechanism that...

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Peroxiredoxin

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the sulfenic acid back to a thiol is what distinguishes the three enzyme classes. 2-Cys peroxiredoxins are reduced by thiols such as thioredoxins, thioredoxin-like...

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Thiol oxidase

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In enzymology, a thiol oxidase (EC 1.8.3.2) is an enzyme that catalyzes the chemical reaction 4 R'C(R)SH + O2 ⇌{\displaystyle \rightleftharpoons } 2 R'C(R)S-S(R)CR'...

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Maleimide

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molecule often containing a maleimide group, which conjugates the drug through thiols or dienes to the antibody. Maleimides linked to polyethylene glycol chains...

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Skunk

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sulfur-containing chemicals such as thiols (traditionally called mercaptans), which have an offensive odor. The thiols also make their spray highly flammable...

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Glutathione

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reactive oxidants, glutathione participates in thiol protection and redox regulation of cellular thiol proteins under oxidative stress by protein S-glutathionylation...

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Mercaptobenzothiazole

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measurements by NMR spectroscopy could not measure the presence of the thiol tautomer that the name implies, instead it exists as a thione/dithiocarbamate...

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Dithiothreitol

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charged thiolate form -S− is reactive (the protonated thiol form -SH is not); the pKa of the thiol groups is 9.2 and 10.1. DTT is used as a reducing or...

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Sulfanyl

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Sulfanyl (HS•), also known as the mercapto radical, hydrosulfide radical, or hydridosulfur, is a simple radical molecule consisting of one hydrogen and...

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Thiolysis

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Thiolysis is a reaction with a thiol (R-SH) that cleaves one compound into two. Thiolysis involves the addition of coenzyme A to one of the products....

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Allyl mercaptan

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mercaptan Names Preferred IUPAC name Prop-2-ene-1-thiol Other names 2-Propene-1-thiol Allyl thiol 3-Mercaptopropene Identifiers CAS Number 870-23-5 3D...

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Cat pheromone

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3-Mercapto-3-methylbutan-1-ol 4-Methoxy-2-methylbutane-2-thiol 4-Mercapto-4-methylpentan-2-one...

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