1.0 2010-04-08 22:15:35 UTC 2015-07-21 06:51:42 UTC FDB021262 5-Chloro-2-(3,5-di-tert-butyl-2-hydroxyphenyl)-2H-benzotriazole FDA approved for use in food-contact polymers 2-(5-Chloro-2H-benzotriazol-2-yl)-4,6-bis(1,1-dimethylethyl)phenol, 9CI 2-(5-Chloro-2H-benzotriazol-2-yl)-4,6-di-tert-butylphenol 2,4-di-tert-butyl-6-(5-chloro-2H-benzotriazol-2-yl)phenol 2,4-Di-tert-butyl-6-(5-chloro-2H-benzotriazol-2-yl)phenol, 8CI 2,4-Di-tert-butyl-6-(5-chlorobenzotriazol-2-yl)phenol C20H24ClN3O 357.877 357.160790112 2,4-di-tert-butyl-6-(5-chloro-2H-1,2,3-benzotriazol-2-yl)phenol 2,4-di-tert-butyl-6-(5-chloro-1,2,3-benzotriazol-2-yl)phenol 3864-99-1 CC(C)(C)C1=CC(=C(O)C(=C1)N1N=C2C=CC(Cl)=CC2=N1)C(C)(C)C InChI=1S/C20H24ClN3O/c1-19(2,3)12-9-14(20(4,5)6)18(25)17(10-12)24-22-15-8-7-13(21)11-16(15)23-24/h7-11,25H,1-6H3 UWSMKYBKUPAEJQ-UHFFFAOYSA-N belongs to the class of organic compounds known as phenyl-1,2,3-triazoles. These are organic compounds containing a 1,2,3-triazole substituted by a phenyl group. Phenyl-1,2,3-triazoles Organic compounds Organoheterocyclic compounds Azoles Triazoles Aromatic heteropolycyclic compounds Aryl chlorides Azacyclic compounds Benzotriazoles Heteroaromatic compounds Hydrocarbon derivatives Organochlorides Organonitrogen compounds Organooxygen compounds Organopnictogen compounds Phenols Phenylpropanes Aromatic heteropolycyclic compound Aryl chloride Aryl halide Azacycle Benzenoid Benzotriazole Heteroaromatic compound Hydrocarbon derivative Monocyclic benzene moiety Organic nitrogen compound Organic oxygen compound Organochloride Organohalogen compound Organonitrogen compound Organooxygen compound Organopnictogen compound Phenol Phenyl-1,2,3-triazole Phenylpropane logp 6.27 ALOGPS logs -5.09 ALOGPS solubility 2.93e-03 g/l ALOGPS melting_point Mp 153-154° logp 6.49 ChemAxon pka_strongest_acidic 10.2 ChemAxon pka_strongest_basic -1 ChemAxon iupac 2,4-di-tert-butyl-6-(5-chloro-2H-1,2,3-benzotriazol-2-yl)phenol ChemAxon average_mass 357.877 ChemAxon mono_mass 357.160790112 ChemAxon smiles CC(C)(C)C1=CC(=C(O)C(=C1)N1N=C2C=CC(Cl)=CC2=N1)C(C)(C)C ChemAxon formula C20H24ClN3O ChemAxon inchi InChI=1S/C20H24ClN3O/c1-19(2,3)12-9-14(20(4,5)6)18(25)17(10-12)24-22-15-8-7-13(21)11-16(15)23-24/h7-11,25H,1-6H3 ChemAxon inchikey UWSMKYBKUPAEJQ-UHFFFAOYSA-N ChemAxon polar_surface_area 50.94 ChemAxon refractivity 113.49 ChemAxon polarizability 40.4 ChemAxon rotatable_bond_count 3 ChemAxon acceptor_count 3 ChemAxon donor_count 1 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 287473 Specdb::MsMs 287474 Specdb::MsMs 287475 Specdb::MsMs 326338 Specdb::MsMs 326339 Specdb::MsMs 326340 Specdb::MsMs 2455983 Specdb::MsMs 2455984 Specdb::MsMs 2455985 Specdb::MsMs 2478817 Specdb::MsMs 2478818 Specdb::MsMs 2478819 Specdb::CMs 9729 Specdb::CMs 27557 Specdb::CMs 47266 Specdb::CMs 102202 Specdb::CMs 133856 Specdb::CMs 141590 HMDB41339 #<Reference:0x000055ce30330de8>