  | ChEMBL = 14060 | StdInChI_Ref =  | StdInChI = 1S/C6H6O/c7-6-4-2-1-3-5-6/h1-5,7H | StdInChIKey_Ref =  | StdInChIKey = ISWSIDIOOBJBQZ-UHFFFAOYSA-N | CASNo_Ref =  | CASNo = 108-95-2 |   ChemSpiderID_Ref =  | ChemSpiderID = 971 |   RTECS = SJ3325000 |   UNII_Ref =  | UNII = 339NCG44TV | KEGG_Ref =  | KEGG = D06536 | InChI=1/C6H6O/c7-6-4-2-1-3-5-6/h1-5,7H   }} | Section2 =  | Section7 = //--///- | SPhrases = -/---//-   }} | Section8 =  }}  '''Phenol''', also known as '''carbolic acid''', is an organic compound with the chemical formula C6H5OH. It is a white crystalline solid. The molecule consists of a phenyl (-C6H5), bonded to a hydroxyl (-OH) group. It is produced on a large scale (about 7 billion kg/year) as a precursor to many materials and useful compounds.Manfred Weber, Markus Weber, Michael Kleine-Boymann &quot;Phenol&quot; in Ullmann's Encyclopedia of Industrial Chemistry 2004, Wiley-VCH. .  It is only mildly acidic but requires careful handling due to its propensity to cause burns.  ==Phenols==  The word ''phenol'' is also used to refer to any compound that contains a six-membered aromatic ring, bonded directly to a hydroxyl group (-OH). Thus, phenols are a class of organic compounds of which the phenol discussed in this article is the simplest member.  ==Properties== Phenol is appreciably soluble in water, with about 8.3&amp;nbsp;g dissolving in 100&amp;nbsp;mL (0.88 M). The sodium salt of phenol, sodium phenoxide, is far more water soluble.   ===Acidity=== It is slightly acidic: the phenol molecule has weak tendencies to lose the H+ ion from the hydroxyl group, resulting in the highly water-soluble '''phenolate''' anion C6H5O&amp;minus; (also called '''phenoxide'''). Compared to aliphatic alcohols, phenol about 1 million times more acidic, although it is still considered a weak acid. It reacts completely with aqueous NaOH to lose H+, whereas most alcohols react only partially.  Phenols are less acidic than carboxylic acids, and even the carbonic acid.  One explanation for the increased acidity over alcohols is resonance stabilization of the phenoxide anion by the aromatic ring. In this way, the negative charge on oxygen is shared by the ortho and para carbon atoms.''Organic Chemistry'' 2nd Ed. John McMurry ISBN 0534079687 In another explanation, increased acidity is the result of orbital overlap between the oxygen's lone pairs and the aromatic system. In a third, the dominant effect is the induction from the sp2 hybridised carbons; the comparatively more powerful inductive withdrawal of electron density that is provided by the sp2 system compared to an sp3 system allows for great stabilization of the oxyanion.  In making this conclusion, one can examine the pKa of the enol of acetone, which is 19.0 in comparison to phenol with a pKa of 10.0.For further reading on the fine points of this topic, see [  David A. Evans]'s explanation. However, this similarity of acidities of phenol and acetone enol is not observed in the gas phase, and is because the difference of solvation energies of the deprotonated acetone enol and phenoxide almost exactly offsets the experimentally observed gas phase acidity difference. It has recently been shown that only about 1/3 of the increased acidity of phenol is due to inductive effects, with resonance accounting for the rest.(Solvation effects on the relative acidities of acetaldehyde enol and phenol described in the Supporting Information)  ====Phenoxide anion==== Phenol can be deprotonated with moderate base such as triethylamine, forming the nucleophilic ''phenoxide anion'' or ''phenolate anion'', which is highly water-soluble. [[Resonance structures of the phenoxide anion]] The phenoxide anion has a similar nucleophilicity to free amines, with the further advantage that its conjugate acid (neutral phenol) does not become entirely deactivated as a nucleophile even in moderately acidic conditions. Phenols are sometimes used in peptide synthesis to &quot;activate&quot; carboxylic acids or esters to form activated esters. Phenolate esters are far more stable than acid anhydrides or acyl halides but are sufficiently reactive under mild conditions to facilitate the formation of amide bonds.  Phenoxides are enolates stabilised by aromaticity. Under normal circumstances, phenoxide is more reactive at the oxygen position, but the oxygen position is a &quot;hard&quot; nucleophile whereas the alpha-carbon positions tend to be &quot;soft&quot;.  ==== Tautomerism ==== Phenol exhibits keto-enol tautomerism with its unstable keto tautomer cyclohexadienone, but only a tiny fraction of phenol exists as the keto form. The equilibrium constant for enolisation is approximately 10−13, meaning that only one in every ten trillion molecules is in the keto form at any moment. The small amount of stabilisation gained by exchanging a C=C bond for a C=O bond is more than offset by the large destabilisation resulting from the loss of aromaticity. Phenol therefore exists entirely in the enol form. Phenol-cyclohexadienone tautomerism  ===Reactions=== Neutral phenol substructure &quot;shape&quot;. An image of a computed electrostatic surface of neutral phenol, showing neutral regions in green, electronegative areas in orange-red, and the electropositive phenolic proton in blue. Phenol is highly reactive toward electrophilic aromatic substitution as the oxygen atom's pi electrons donate electron density into the ring.  By this general approach, many groups can be appended to the ring, via halogenation, acylation, sulfonation, and other processes. However, phenol's ring is so strongly activated - second only to aniline - that bromination or chlorination of phenol leads to substitution on all carbons ortho and para to the hydroxy group, not only on one carbon.  ==Production== Because of phenol's commercial importance, many methods have been developed for its production.  The main route being practiced presently involves the partial oxidation of cumene (isopropylbenzene) via the Hock rearrangement: :C6H5CH(CH3)2  +  O2   →    C6H5OH  +  (CH3)2CO The first commercial route begins with the reaction of strong base with benzenesulfonate: :C6H5SO3H  +  2 NaOH   →   C6H5OH  +  Na2SO3  +  H2O Other methods involve conversions of chlorobenzene using base or steam (Raschig-Hooker process). It is a recoverable byproduct of coal pyrolysis.  ==Uses== The major uses of phenol involve its conversion to plastics or related materials.  Condensation with acetone gives bisphenol-A, a key building block for polycarbonates. Condensation with formaldehyde gives phenolic resins, the most famous of which is Bakelite. Hydrogenation of phenol gives cyclohexanone, an intermediate en route to nylon. Nonionic detergents are produced by alkylation of phenol to give the alkylphenols, which are then subjected to ethoxylation.  Phenol is also a versatile precursor to a large collection of drugs, most notably aspirin but also many herbicides and pharmaceuticals. Phenol is also used as an oral anesthetic/analgesic, commonly used to temporarily treat pharyngitis.  Phenol was widely used as an antiseptic, especially as Carbolic soap, from the early 1900s through the 1970s.  ===Niche uses=== Phenol is one of the chemicals for embalming bodies for study because of its ability to preserve tissues for extended periods of time. However, formaldehyde is usually preferred over phenol for embalming with intent of public viewing because of phenol's tendency to turn tissues an unpleasant bleach-white color.  Phenol is also used in the preparation of cosmetics including sunscreens, hair dyes, and skin lightening preparations.DeSelms, R. H.; ''[ UV-Active Phenol Ester Compounds]'';  Enigen Science Publishing: Washington, DC, 2008.  In cosmetic surgery, phenol serves as an exfoliant.  It is also used in phenolization, a surgical procedure used to treat an ingrown nail, in which it is applied to the nail bed to prevent regrowth of nails. 5% phenol is sometimes injected near a sensory nerve in order to temporarily (up to a year) stop it from transmitting impulses in some intractable cases of chronic neuropathic pain.  In molecular biology, phenol is used to denature and remove proteins when purifying nucleic acids.  In clinical medicine, phenol is used in the management of spasticity and refractory cancer pain.  When injected in 6-8% concentrations in water, phenol can be markedly toxic to peripheral nerve cell structures.  In patients with severe spasticity, phenol injected into the locations where the nerves connect to muscle can result in a flaccid state, making a contracted limb less painful and more functional.  In end of life pain management in advanced cancer, phenol can be injected into the spinal fluid or onto major nerves supplying organs (such as the pancreas) to relieve pain otherwise unresponsive to medications.  ==History== Phenol was discovered in 1834, when it was extracted from coal tar, which remained the primary source until the development of the petrochemical industry.  The antiseptic properties of phenol were used by Sir Joseph Lister (1827–1912) in his pioneering technique of antiseptic surgery, although the skin irritation caused by continual exposure to phenol eventually led to the substitution of aseptic (germ-free) techniques in surgery. Lister decided that the wounds themselves had to be thoroughly cleaned. He then covered the wounds with a piece of rag or lint covered in carbolic acid. It is also the active ingredient in some oral analgesics such as Chloraseptic spray as well as Carmex. Phenol was also the main ingredient of the Carbolic Smoke Ball, an ineffective device marketed in London in the 19th century as protecting the user against influenza and other ailments, and the subject of a famous law case.  ===Second World War=== Injections of phenol have occasionally been used as a means of rapid execution. In particular, phenol was used as a means of execution by the Nazis during the Second World War. Originally used by the Nazis in 1939 as part of Action T4, phenol, inexpensive, easy to make and quickly lethal, became the injectable toxin of choice through the last days of the war. Although Zyklon-B pellets, invented by Gerhard Lenz, were used in the gas chambers to exterminate large groups of people, the Nazis learned that extermination of smaller groups was more economical via injection of each victim, one at a time, with phenol. Phenol injections were given to thousands of people in concentration camps, especially at Auschwitz-Birkenau. Approximately one gram is enough to cause death. Injections were administered by medical doctors, their assistants, or sometimes prisoner doctors; such injections were originally given intravenously, more commonly in the arm, but injection directly into the heart, so as to induce nearly instant death, was later adopted. One of the best known inmates to be executed with a phenol injection in Auschwitz was St. Maximilian Kolbe, a Catholic priest who volunteered to undergo three weeks of starvation and dehydration in the place of another inmate.  ==Occurrence== Phenol is a measurable component in the aroma and taste of the distinctive Islay scotch whisky, generally ~30, but up to 100 ppm.  ==Toxicity== Phenol and its vapors are corrosive to the eyes, the skin, and the respiratory tract. Repeated or prolonged skin contact with phenol may cause dermatitis, or even second and third-degree burns due to phenol's caustic and defatting properties.  Inhalation of phenol vapor may cause lung edema. The substance may cause harmful effects on the central nervous system and heart, resulting in dysrhythmia, seizures, and coma. The kidneys may be affected as well. Exposure may result in death and the effects may be delayed. Long-term or repeated exposure of the substance may have harmful effects on the liver and kidneys.&quot;World Health Organization/International Labour Organization: International Chemical Safety Cards,  There is no evidence to believe that phenol causes cancer in humans. Besides its hydrophobic effects, another mechanism for the toxicity of phenol may be the formation of phenoxyl radicals.  Chemical burns from skin exposures can be decontaminated by washing with polyethylene glycol, isopropyl alcohol, or perhaps even copious amounts of water. Removal of contaminated clothing is required, as well as immediate hospital treatment for large splashes.  This is particularly important if the phenol is mixed with chloroform (a commonly-used mixture in molecular biology for DNA &amp; RNA purification from proteins).  