22385-96-2

Basic information

• Product Name: 5,5'-di-tert-butyl-2,2'-dihydroxybiphenyl
• Synonyms: 5,5'-di-tert-butyl-2,2'-dihydroxybiphenyl
• CAS NO: 22385-96-2
• Molecular Weight: 298.425
• Mol File: 22385-96-2.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 5,5'-di-tert-butyl-2,2'-dihydroxybiphenyl(CAS DataBase Reference)
• NIST Chemistry Reference: 5,5'-di-tert-butyl-2,2'-dihydroxybiphenyl(22385-96-2)
• EPA Substance Registry System: 5,5'-di-tert-butyl-2,2'-dihydroxybiphenyl(22385-96-2)

Safety Data

• Hazardous Substances Data: 22385-96-2(Hazardous Substances Data)

Upstream product

• 98-54-4 para-tert-butylphenol 
• 6390-69-8 3,3',5,5'-tetra(tert-butyl)biphenyl-2,2'-diol 

Downstream Products

• 132-64-9 dibenzofuran 
• 7397-06-0 4-t-butyl-o-xylene 
• 133373-14-5 2,8-di-tert-butyldibenzofuran 
• 87586-50-3 5,5',5',5''',5'''',5'''''-hexa-tert-butyl-2,2',2'',2''',2'''',2'''''-hexahydroxy-1,1':3',1'':3'',1''':3''',1'''':3'''',1'''''-sexiphenyl 
• 87586-49-0 2,2',2,2'''-Tetrahydroxy-5,5',5,5'''-tetra-tert-butyl-1,1':3',1:3,1'''-quaterphenyl 
• 1622074-15-0 C₃₈H₄₆N₄O₂S₂ 
• 1622074-14-9 C₃₈H₄₄N₆O₆S₂ 
• 1379680-60-0 C₄₄H₄₄P₂ 
• 1379680-59-7 C₄₄H₄₄O₂P₂ 
• 117110-87-9 4-(3-bromo-2-hydroxy-5-t-butylphenyl)-6-t-butyl-2,1,3-benzothiadiazole 
• 117110-92-6 4-(2,3-diamino-5-t-butylphenyl)-6-t-butyl-2,1,3-benzothiadiazole 
• 117110-85-7 1,8-diamino-9H-carbazole 
• 100-39-0 benzyl bromide 

Relevant articles and documents

Interaction between biphenols and anions: Selective receptor for dihydrogenphosphate

Biphenol was shown to bind dihydrogenphosphate (H2PO 4-) selectively over various other anions (MeCO 2-, Cl-, Br-, I-, NO 3-, HSO4-). The highly selectivity of biphenol toward dihydrogenphosphate is explained in terms of the basicity and shape of the guest anion.

THERMOCHROMIC COMPOSITIONS FROM TRISUBSTITUTED PYRIDINE LEUCO DYES

A thermochromic leuco dye composition contains a leuco dye moiety including one or more tri-aryl substituted pyridines, a UVA developer moiety including at least one UVA developer selected from the group consisting of salicylic acid and derivatives thereof, and biphenyls and derivatives thereof, and a carrier selected from the group consisting of a fatty ester, fatty alcohol, fatty amide, and combinations thereof.

Enzymatic oxidative polymerization of p-t-butylphenol and characterization of the product polymer

For structural control and analysis of an enzymatically synthesized polyphenol, peroxidase-catalyzed polymerization of p-t-butylphenol in a mixture of polar organic solvent and phosphate buffer has been examined in detail. The resulting products were subjected to preparative HPLC. Two dimers and one trimer were isolated and their structures were determined by 1H and 13C NMR. ESI-TOF mass analysis showed the formation of two kinds of dimer and of at least four kinds of trimer. These data clearly showed that the polymer was composed of a mixture of phenylene and oxyphenylene units. The ratio of phenylene and oxyphenylene units in the product could be controlled by changing the solvent composition. The phenylene unit linearly increased as a function of the water content in the mixed solvent.