ChemicalBook--->CAS DataBase List--->92-88-6

92-88-6

92-88-6 Structure

92-88-6 Structure
IdentificationMore
[Name]

4,4'-Biphenol
[CAS]

92-88-6
[Synonyms]

4,4'-BIPHENOL
4,4'-BIPHENYLDIOL
4,4'-DIHYDROXYBIPHENYL
4,4'-DIHYDROXYDIPHENYL
4,4'-DIPHENOL
BIPHENOL
BIPHENYL-4,4'-DIOL
DHB
P,P'-BIPHENOL
P,P'-DIHYDROXYBIPHENYL
P,P'-DIPHENOL
PPDP
(1,1’-Biphenyl)-4,4’-diol
[1,1’-biphenyl]-4,4’-diol
[1,1'-Biphenyl]-4,4'-diol
4,4’-bisphenol
4,4'-Dihydroxy-1,1'-biphenyl
4,4'-Dioxydiphenyl
Antioxidant DOD
antioxidantdod
[EINECS(EC#)]

202-200-5
[Molecular Formula]

C12H10O2
[MDL Number]

MFCD00002348
[Molecular Weight]

186.21
[MOL File]

92-88-6.mol
Chemical PropertiesBack Directory
[Appearance]

Powder
[Melting point ]

280-282 °C(lit.)
[Boiling point ]

280.69°C (rough estimate)
[density ]

1.22
[vapor pressure ]

0Pa at 25℃
[refractive index ]

1.6010 (estimate)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

Powder
[pka]

9.74±0.26(Predicted)
[color ]

Off-white to light beige or light gray
[Water Solubility ]

sparingly soluble
[Usage]

Intermediates of Liquid Crystals
[Detection Methods]

HPLC,NMR
[BRN ]

1908886
[LogP]

2.7 at 20℃
[CAS DataBase Reference]

92-88-6(CAS DataBase Reference)
[NIST Chemistry Reference]

p,p'-Biphenol(92-88-6)
[EPA Substance Registry System]

92-88-6(EPA Substance)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

R21:Harmful in contact with skin.
R36/37/38:Irritating to eyes, respiratory system and skin .
R36:Irritating to the eyes.
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S24/25:Avoid contact with skin and eyes .
S36/37:Wear suitable protective clothing and gloves .
[RIDADR ]

3077
[WGK Germany ]

2
[RTECS ]

DV4725000
[TSCA ]

Yes
[HazardClass ]

9
[PackingGroup ]

III
[HS Code ]

29061900
[Toxicity]

LD50 orl-rat: 9850 mg/kg TXAPA9 28,313,74
Raw materials And Preparation ProductsBack Directory
[Raw materials]

4,4'-Bis(trimethylsilyloxy)biphenyl-->6,6'-DI-TERT.BUTYL-4,4'-BI-ORTHO-CRESOL-->4-HYDROXY-4'-METHOXYBIPHENYL-->4,4'-Dimethoxybiphenyl-->3,3',5,5'-TETRA(TERT-BUTYL)[1,1'-BIPHENYL]-4,4'-DIOL-->4-Hydroxy-4'-fluorobiphenyl-->4,4'-Difluorobiphenyl-->1-Chloro-4-fluorobenzene-->4-Bromophenol
[Preparation Products]

4'-Hydroxy-4-biphenylcarbonitrile-->6fapbp-->3,3',5,5'-tetraformyl-4,4'-biphenyldiol-->4,4'-BIPHENYLDICARBONITRILE-->Cyanic acid, [1,1'-biphenyl]-4,4'-diyl ester-->[1,1'-biphenyl]-4,4'-diyl bis(2-Methylacrylate)-->3,3',5,5'-tetrabromo-[1,1'-biphenyl]-4,4'-diol
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

Biphenyl-4,4'-diol(92-88-6).msds
Hazard InformationBack Directory
[Chemical Properties]

Powder
[Uses]

4,4'-biphenol be used intermediate liquid crystal polymers raw materials. Synthetic polymers, due to its excellent heat resistance, it is used as polyester, urethane modified monomer, polycarbonate, polysulfone, and epoxy resin, for the manufacture of an excellent engineering plastics and composite materials. Antioxidant antioxidants for rubber and plastics. Dye intermediates or petroleum products stabilizer.
[Uses]

Biphenol is an intermediate used in the manufacture of thermoplastics such as liquid crystalline polymers (LCP), polyesters, polycarbonates and polysulfones.
[Uses]

Intermediates of Liquid Crystals
[Definition]

ChEBI: A member of the class of hydroxybiphenyls that is biphenyl with hydroxy groups at positions 4 and 4'.
[Production Methods]

4,4'-Biphenol can be synthesized in excellent yields by debutylation of 3,3',5,5'-tetra-tert-butyl-4,4'-dihydroxybiphenyl. Other production processes are the alkaline fusion of 4,4'-biphenyldisulfonic acid, the boil down of benzidinebisdiazonium salts, and the decarboxylation of 4,4'-dihydroxybiphenyl-2-carboxylic acid. Symmetrically alkylated 4,4'-dihydroxybiphenyls such as 4,4'-dihydroxy-2,2',3,3',5,5',6,6'-hexamethylbiphenyl are preferably obtained by the oxidative coupling of the corresponding substituted monophenols. Here, diphenoquinones are generally formed in the first step which must be reduced. Phenol itself always gives isomeric mixtures of dihydroxybiphenyls on coupling with various oxidants. These mixtures are also formed by alkaline fusion of 4,4'-dihydroxybiphenylsulfone.
[Flammability and Explosibility]

Notclassified
[Safety Profile]

Poison by intraperitoneal route.Moderately toxic by skin contact. Mildly toxic byingestion. Human mutation data reported. When heated todecomposition it emits acrid smoke and irritating fumes.
[Purification Methods]

Recrystallise the biphenol from aqueous EtOH preferably under N2 to avoid oxidation to the extended qiunone. It is characterized as the dimethyl derivative (4,4’-dimethoxybiphenyl) from which it is prepared by demethylation. The dimethoxy derivative has m 176.5-177o (from AcOH, EtOH, hexane or *C6H6) and sublimes in vacuo. [Williamson & Rodebush J Am Chem Soc 63 3019 1941, Beilstein 6 I 485, 6 II 962, 6 III 6389, 6 IV 6651.]
Spectrum DetailBack Directory
[Spectrum Detail]

4,4'-Biphenol(92-88-6)1HNMR
4,4'-Biphenol(92-88-6)IR1
4,4'-Biphenol(92-88-6)IR2
4,4'-Biphenol(92-88-6)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

4,4'-Biphenol, 97%(92-88-6)
[Alfa Aesar]

4,4'-Dihydroxybiphenyl, 99%(92-88-6)
[Sigma Aldrich]

92-88-6(sigmaaldrich)
[TCI AMERICA]

4,4'-Biphenol,>99.0%(GC)(92-88-6)
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