# Selenol
A **selenol** is an organoselenium compound having the structure \( \mathrm{RSeH} \), where R is an organic group and R is not hydrogen; it is the selenium analog of a thiol (RSH) and of an alcohol (ROH)[1](https://goldbook.iupac.org/terms/view/S05574). Simple examples are methaneselenol (CH\(_3\)SeH) and benzeneselenol, also called selenophenol (C\(_6\)H\(_5\)SeH)[5](https://www.benchchem.com/product/b7769099).
| Key fact | Detail |
|---|---|
| Definition | Compounds of structure \( \mathrm{RSeH} \) with \( \mathrm{R} \neq \mathrm{H} \); IUPAC class name, NOC Rule C-701[1](https://goldbook.iupac.org/terms/view/S05574) • [2](https://publications.iupac.org/pac/1995/pdf/6708x1307.pdf) |
| Suffix | –SeH is expressed by the preselected suffix 'selenol'; the prefixes 'hydroseleno' and 'selenyl' are no longer recommended[3](https://iupac.qmul.ac.uk/BlueBook/P6.html) |
| Acidity | Selenols are stronger acids than thiols; selenophenol has pK\(_a\) ≈ 5.9 against ≈ 6.5–6.6 for thiophenol[4](https://www.sciencedirect.com/science/article/pii/S0272059083800177) • [5](https://www.benchchem.com/product/b7769099) |
| Ionization state | At physiological pH selenols exist mainly as the anion \( \mathrm{R\!-\!Se^{-}} \), whereas sulfhydryl groups remain mainly protonated[4](https://www.sciencedirect.com/science/article/pii/S0272059083800177) |
| Bond strengths | Se–H ≈ 326 kJ/mol versus S–H ≈ 366 kJ/mol; C–Se 234 kJ/mol versus C–S 272 kJ/mol[5](https://www.benchchem.com/product/b7769099) |
| Air sensitivity | Selenophenol is notably air-sensitive, readily oxidizing to diphenyl diselenide (PhSeSePh)[5](https://www.benchchem.com/product/b7769099) |
| Biological occurrence | Endogenous selenols include selenocysteine, glutathione selenopersulfide (GSSeH), and methylselenol[6](https://www.sciencedirect.com/topics/biochemistry-genetics-and-molecular-biology/selenol) |
## Nomenclature
The IUPAC Compendium of Chemical Terminology defines selenols as compounds of structure \( \mathrm{RSeH} \) with \( \mathrm{R} \neq \mathrm{H} \), under NOC Rule C-701[1](https://goldbook.iupac.org/terms/view/S05574) • [2](https://publications.iupac.org/pac/1995/pdf/6708x1307.pdf). In current substitutive nomenclature, sulfur, selenium, and tellurium analogs of hydroxy compounds are named with the suffixes 'thiol', 'selenol', and 'tellurol' and the prefixes 'sulfanyl', 'selanyl', and 'tellanyl' respectively; the older prefixes 'mercapto' (–SH) and 'hydroseleno' or selenyl (–SeH) are no longer recommended[3](https://iupac.qmul.ac.uk/BlueBook/P6.html). The –SeH group is a preselected suffix, and the presence of several such groups on one parent is denoted by multiplying prefixes such as 'di' and 'tri'[3](https://iupac.qmul.ac.uk/BlueBook/P6.html). Related selenium classes defined alongside selenols include seleninic acids (RSe(=O)OH), selenoxides (R\(_2\)Se=O), and selenones (R\(_2\)Se(=O)\(_2\))[2](https://publications.iupac.org/pac/1995/pdf/6708x1307.pdf).
## Acidity and reactivity
The defining chemical feature of the SeH group is its acidity. Selenium is larger and more polarizable than sulfur, and the Se–H bond is weaker (about 326 kJ/mol against about 366 kJ/mol for S–H), so the proton is lost more readily[5](https://www.benchchem.com/product/b7769099). Selenols are stronger acids than mercaptans (thiols), and at physiological pH they exist mainly in the anionic form \( \mathrm{R\!-\!Se^{-}} \), while the sulfhydryl group of a thiol remains mainly protonated[4](https://www.sciencedirect.com/science/article/pii/S0272059083800177). This matters in biology because the reactive species of a selenol at neutral pH is the selenolate anion rather than the neutral molecule.
The selenolate anion is also the more nucleophilic form. Proton transfer from the selenol leads to a high-energy zwitterionic form in which the nucleophilicity of the selenolate is enhanced relative to the neutral selenol[7](https://www.sciencedirect.com/org/science/article/pii/S1615415022059696). The C–Se bond is weaker than C–S (234 kJ/mol against 272 kJ/mol), which contributes to the distinctive reactivity of organoselenium compounds compared with their sulfur analogs[5](https://www.benchchem.com/product/b7769099).
**Oxidation behavior.** Selenols are readily oxidized. Selenophenol is described as notably air-sensitive, oxidizing to diphenyl diselenide (PhSeSePh), the Se–Se coupled dimer[5](https://www.benchchem.com/product/b7769099). This tendency to form diselenides parallels the disulfide chemistry of thiols but proceeds more easily.
## Occurrence and applications
In biological systems, selenium is most likely present either as the selenol form (R–SeH) or as the selenium ether analogous to the sulfur in methionine[4](https://www.sciencedirect.com/science/article/pii/S0272059083800177). Endogenous low-molecular-weight selenols include selenocysteine, in which selenium replaces the sulfur of cysteine; the labile glutathione selenopersulfide (GSSeH); and methylselenol, which occurs in the intermediary metabolism of selenium. Selenols also occur in selenospecific proteins[6](https://www.sciencedirect.com/topics/biochemistry-genetics-and-molecular-biology/selenol).
Beyond biology, selenol chemistry has applications across organic synthesis, materials chemistry, and chemical biology, a range attributed to the unique properties of the SeH group[7](https://www.sciencedirect.com/org/science/article/pii/S1615415022059696). One materials use is the selenolation of metal nanoclusters: because selenium differs from sulfur in both electronic and steric features, selenolated nanoclusters have chemical and physical properties distinct from their thiolated analogs[7](https://www.sciencedirect.com/org/science/article/pii/S1615415022059696). Selenophenol itself serves as an organoselenium reagent for introducing the phenylseleno (PhSe) group into other molecules[5](https://www.benchchem.com/product/b7769099).
## References
1. [Selenols, IUPAC Compendium of Chemical Terminology (Gold Book), entry S05574](https://goldbook.iupac.org/terms/view/S05574)
2. [Glossary of class names of organic compounds and reactivity intermediates based on structure, Pure and Applied Chemistry 67, 1307–1375 (1995), p. 1365](https://publications.iupac.org/pac/1995/pdf/6708x1307.pdf)
3. [Nomenclature of Organic Chemistry (IUPAC Blue Book), Chapter P-6, Section P-63.1.5](https://iupac.qmul.ac.uk/BlueBook/P6.html)
4. [Biochemistry of selenium: a brief overview, ScienceDirect](https://www.sciencedirect.com/science/article/pii/S0272059083800177)
5. [Selenophenol (57880-10-1), BenchChem product summary](https://www.benchchem.com/product/b7769099)
6. [Selenol: an overview, ScienceDirect Topics](https://www.sciencedirect.com/topics/biochemistry-genetics-and-molecular-biology/selenol)
7. [Synthesis and Applications of Organic Selenols, ScienceDirect](https://www.sciencedirect.com/org/science/article/pii/S1615415022059696)
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*Topic: Encyclopedia › Physical world and mathematics › Chemistry › Organic substances › Alcohols, ethers, and organooxygen groups › Organosulfur, selenium, and heavier main-group organo derivatives › Organosulfur, selenium, and tellurium analogues › Organoselenium and organotellurium compounds › Selenols and tellurols*
*Initially written Sep 17, 2026 · Reviewed: Oct 15, 2026 · Edited: Oct 15, 2026 · Last review: Oct 15, 2026*
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