Diiodohydroxypropane

Last updated
Diiodohydroxypropane
1,3-diiodo-2-propanol.svg
Names
Preferred IUPAC name
1,3-Diiodopropan-2-ol [1]
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.007.807 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 208-586-1
MeSH 1,3-diiodo-2-propanol
PubChem CID
UNII
  • InChI=1S/C3H6I2O/c4-1-3(6)2-5/h3,6H,1-2H2 X mark.svgN
    Key: DNKPFCQEGBJJTE-UHFFFAOYSA-N X mark.svgN
  • OC(CI)CI
Properties
C3H6I2O
Molar mass 311.889 g·mol−1
Pharmacology
D08AG04 ( WHO )
Related compounds
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Diiodohydroxypropane is an antiseptic and disinfectant. It is also known as jothion [2] or iothion. [3]

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<span class="mw-page-title-main">Hexafluoro-2-propanol</span> Chemical compound

Hexafluoroisopropanol, commonly abbreviated HFIP, is the organic compound with the formula (CF3)2CHOH. This fluoroalcohol finds use as solvent and synthetic intermediate. It appears as a colorless, volatile liquid that is characterized by a strong, pungent odor. As a solvent hexafluoro-2-propanol is polar and exhibits strong hydrogen bonding properties enabling it to dissolve substances that serve as hydrogen-bond acceptors, such as amides and ethers. (CF3)2CHOH is classified as a hard Lewis acid and its acceptor properties are discussed in the ECW model. Its relative acceptor strength toward a series of bases, versus other Lewis acids, can be illustrated by C-B plots. Dual XH–π interaction of HFIP with arenes has been found (benzene/HFIP, 7.22 kcal/mol) even stronger than the hydrogen bond in a water dimer (5-6 kcal/mol). Hexafluoro-2-propanol is transparent to UV light with high density, low viscosity and low refractive index.

<span class="mw-page-title-main">Acetone</span> Organic compound ((CH3)2CO); simplest ketone

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<span class="mw-page-title-main">Isobutanol</span> Chemical compound

Isobutanol (IUPAC nomenclature: 2-methylpropan-1-ol) is an organic compound with the formula (CH3)2CHCH2OH (sometimes represented as i-BuOH). This colorless, flammable liquid with a characteristic smell is mainly used as a solvent either directly or as its esters. Its isomers are 1-butanol, 2-butanol, and tert-butanol, all of which are important industrially.

<span class="mw-page-title-main">Alaproclate</span> Chemical compound

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1-Naphthol, or α-naphthol, is a fluorescent organic compound with the formula C10H7OH. It is a white solid. It is an isomer of 2-naphthol differing by the location of the hydroxyl group on the naphthalene ring. The naphthols are naphthalene homologues of phenol, with the hydroxyl group being more reactive than in the phenols. Both isomers are soluble in simple alcohols, ethers, and chloroform. They are precursors to a variety of useful compounds. Naphthols are used as biomarkers for livestock and humans exposed to polycyclic aromatic hydrocarbons.

<span class="mw-page-title-main">BSPP (drug)</span> Chemical compound

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<span class="mw-page-title-main">Propionaldehyde</span> Chemical compound

Propionaldehyde or propanal is the organic compound with the formula CH3CH2CHO. It is the 3-carbon aldehyde. It is a colourless, flammable liquid with a slightly fruity odour. It is produced on a large scale industrially.

<span class="mw-page-title-main">G-130</span> Chemical compound

G-130 is a drug with stimulant and anorectic effects, related to phenmetrazine.

<span class="mw-page-title-main">Aminomethyl propanol</span> Chemical compound

Aminomethyl propanol is an organic compound with the formula H2NC(CH3)2CH2OH. It is colorless liquid that is classified as an alkanolamine. It is a useful buffer and a precursor to numerous other organic compounds.

Nonafluoro-<i>tert</i>-butyl alcohol Chemical compound

Nonafluoro-tert-butyl alcohol is a fluoroalcohol. It is the perfluorinated analog of tert-butyl alcohol. Notably, as a consequence of its electron withdrawing fluorine substituents, it is very acidic for an alcohol, with a pKa value of 5.4, similar to that of a carboxylic acid. As another consequence of being a perfluorinated compound, it is also one of the lowest boiling alcohols, with a boiling point lower than that of methanol.

References

  1. "1,3-diiodo-2-propanol - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 28 August 2005. Identification and Related Records. Retrieved 3 March 2012.
  2. Shinohara M, Ieiri M, Fukukei K, Okada S, Oura K (1983). "[Disinfecting mechanism of jothion (1,3-diiodo-2-hydroxypropane)]". Shikai Tenbo = Dental Outlook (in Japanese). 61 (3): 605–8. PMID   6573800.
  3. Mazzei M, Balbi A, Ermili A, Roma G (1985). "[Assay of 1,3-diiodo-2-propanol (Iothion) in various pharmaceutical preparations]". Il Farmaco; Edizione Pratica (in Italian). 40 (8): 266–72. PMID   4029372.