{"ATC Code":"D08AE06","Abbreviation":"","Aliases":["2-Hydroxybiphenyl","O-phenylphenol","Biphenyl-2-ol","2-Biphenylol","o-Hydroxybiphenyl","2-Hydroxydiphenyl","o-Hydroxydiphenyl","o-Phenyl phenol","Phenylphenol","Orthophenylphenol"],"Boiling Point":"527 °","CAS":"90-43-7","ChEBI":"CHEBI:17043","ChEMBL":"CHEMBL108829","ChemicalClasses":["phenol"],"Chirality":"achiral","Classes":null,"Color/Form":"Needles from petroleum ether","Decomposition":"When heated to decomposition it emits acrid smoke and irritating fumes.","Density":"1.213 at 77 °F (NTP, 1992) - Denser than water; will sink g/cm\u003csup\u003e3\u003c/sup\u003e","Dosing Info":[],"DrugClasses":[],"EINECS":"201-993-5","European Community (EC) Number":"201-993-5","Flash Point":"255 °F (NTP, 1992)","HMDB ID":"HMDB0032582","HeavyAtomCount":13,"IUPACName":"2-phenylphenol","InChI":"InChI=1S/C12H10O/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10/h1-9,13H","InChIKey":"LLEMOWNGBBNAJR-UHFFFAOYSA-N","MeSH Pharmacological Classification":"Substances that increase the risk of NEOPLASMS in humans or animals. Both genotoxic chemicals, which affect DNA directly, and nongenotoxic chemicals, which induce neoplasms by other mechanism, are included. (See all compounds classified as Carcinogens.)","Melting Point":"131.9 to 135.5 °F (NTP, 1992)","MolecularFormula":"C\u003csub\u003e12\u003c/sub\u003eH\u003csub\u003e10\u003c/sub\u003eO","MolecularWeight":"170.21 g/mol","Odor":"Mild characteristic odor","Physical Description":"2-phenylphenol appears as light lavender crystals or solid. (NTP, 1992)","PrevSalts":[],"PubChemId":7017,"Record Description":["o-Phenylphenol can cause cancer according to The Environmental Protection Agency (EPA).","2-phenylphenol appears as light lavender crystals or solid. (NTP, 1992)","Biphenyl-2-ol is a member of the class of hydroxybiphenyls that is biphenyl substituted by a hydroxy group at position 2. It is generally used as a post-harvest fungicide for citrus fruits. It has a role as an environmental food contaminant and an antifungal agrochemical. It derives from a hydride of a biphenyl.","2-Phenylphenol has been reported in Gossypium hirsutum, Vaccinium macrocarpon, and other organisms with data available.","2-Biphenylol is found in lemon. It is an antifungal agent and preservative. 2-Biphenylol is used for post-harvest control of storage disease in apples, citrus fruit, stone fruit, tomatoes, cucumber and peppers through the use of impregnated wrapping materials or by direct application in a wax. 2-Biphenylol is used in food seasonings. Inhibitory to a wider range of moulds than Biphenyl \u003cht\u003eHMJ12-A\u003c/ht\u003e. The practical way of treatment is to immerse citrus fruit in an alkaline aqueous solution of the parent compound or its Na salt. 2-Biphenylol belongs to the family of Biphenyls and Derivatives. These are organic compounds containing to benzene rings linked together by a C-C bond.","o-Phenylphenol can cause cancer according to The Environmental Protection Agency (EPA).","Biphenyl-2-ol is a member of the class of hydroxybiphenyls that is biphenyl substituted by a hydroxy group at position 2. It is generally used as a post-harvest fungicide for citrus fruits. It has a role as an environmental food contaminant and an antifungal agrochemical. It derives from a hydride of a biphenyl."],"References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/2-Phenylphenol","Name":"2-Phenylphenol","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q209467","Name":"2-Phenylphenol","Sub":false}]},{"Name":"DrugBank","Urls":[{"Link":"https://go.drugbank.com/drugs/DB13734","Name":"2-Phenylphenol","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/7017","Name":"2-Phenylphenol","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL108829","Name":"2-Phenylphenol","Sub":false}]},{"Name":"ChEBI","Urls":[{"Link":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:17043","Name":"2-Phenylphenol","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=90-43-7","Name":"2-Phenylphenol","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0032582","Name":"2-Phenylphenol","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/C02499","Name":"2-Phenylphenol","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/D343Z75HT8","Name":"2-Phenylphenol","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID2021151","Name":"2-Phenylphenol","Sub":false}]}],"Reported Fatal Dose":"Based on animal studies, 5 oz would be lethal to a 150 lb healthy adult.","SMILES":"C1=CC=C(C=C1)C2=CC=CC=C2O","Solubility":"less than 0.1 mg/mL at 68.9 °F (NTP, 1992)","Stability/Shelf Life":"Stable at normal conditions.","StoreUNII":["D343Z75HT8"],"StructureBase64":"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= 6.1 in aqueous solution at 22.7 °C"}