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O-Phenyl phenol (90-43-7)

Identification
Name:O-Phenyl phenol
Synonyms:Biphenyl-2-ol~2-Hydroxybiphenyl; 2-Hydroxybiphenyl; 2-Biphenylol; O-HYDROXIDIPHENYL; 1,1'-Biphenyl-2-ol; orthohydroxydipbenyl; 2-Phenylphenol; Orthoxenol; o-Xonal; Biphenylol; Dowicide 1; Hydroxdiphenyl; Hydroxy-2-phenylbenzene; Hydroxybiphenyl; OPP; Phenylphenol; Preventol O extra; Remol TRF; Torsite; Tumescal OPE; Xenol; BIPHENYL-2-OL; BIPHENYLOL-2; HYDROXY-(2-PHENYL)BENZENE; FEMA 3959; DOWICIDE 1(R); 2-DIPHENYLOL; 2-HYDROXYDIPHENYL; Ortho Phenylphenol
CAS:90-43-7
EINECS: 201-993-5
Molecular Formula: C12H10O
Molecular Weight: 170.21
InChI: InChI=1/C12H10O/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10/h1-9,13H
Molecular Structure: (C12H10O) Biphenyl-2-ol~2-Hydroxybiphenyl; 2-Hydroxybiphenyl; 2-Biphenylol; O-HYDROXIDIPHENYL; 1,1'-Biphenyl-2...
Properties
Transport:UN 3077
Density:1.213
Stability:Stable. Combustible. Incompatible with strong oxidizing agents, halogens.
Refractive index:1.604
Appearance:off-white powder
Specification:

?2-Phenylphenol (CAS NO.90-43-7) is also named as 'Dowicide A' ; (1,1'-Biphenyl)-2-ol ; 1-Hydroxy-2-phenylbenzene ; 2-Biphenylol ; 2-Fenylfenol ; 2-Fenylfenol [Czech] ; 2-Hydroxybifenyl ; 2-Hydroxybifenyl [Czech] ; 2-Hydroxybiphenyl ; 2-Hydroxydiphenyl ; 4-06-00-04579 (Beilstein Handbook Reference) ; AI3-00062 ; Anthrapole 73 ; BRN 0606907 ; Biphenyl, 2-hydroxy- ; Biphenyl-2-o1 ; CCRIS 1388 ; Caswell No. 623AA ; Dowicide 1 ; Dowicide 1 antimicrobial ;
EPA Pesticide Chemical Code 064103 ; HSDB 1753 ; Invalon OP ; Kiwi lustr 277 ; NCI-C50351 ; NSC 1548 ; Nectryl
OPP [pesticide] ; Orthohydroxydiphenyl ; Orthophenylphenol ; Orthoxenol ; Phenol, o-phenyl- ; Phenyl-2 phenol ; USAF EK-2219 ; o-Biphenylol ; o-Diphenylol ; o-Hydroxybiphenyl ; o-Hydroxydiphenyl ; o-Phenyl phenol ; o-Phenylphenol ; o-Phenylphenol, cosmetic grade ; o-Xenol?.?2-Phenylphenol (CAS NO.90-43-7) is?off-white powder. It?is insoluble in water.
2-Phenylphenol react as a weak organic acid. Exothermically neutralizes bases. It may react with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides to generate flammable gas (H2) and the heat of the reaction may ignite the gas. Is sulfonated very readily (for example, by concentrated sulfuric acid at room temperature) in exothermic reactions. May be nitrated very rapidly.?It can react with oxidizing agents. 2-Phenylphenol is combustible.

Report:

IARC Cancer Review: Group 3 IMEMDT?IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man 7 (1987),p. 56.(World Health Organization, Internation Agency for Research on Cancer,Lyon. France.:?) (single copies can be ordered from WHO Publications centre U.S.A., 49 Sheridan Avenue, Albany, NY 12210) ; Animal Inadequate Evidence IMEMDT ?? IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man 30 (1983),p. 329.(World Health Organization, Internation Agency for Research on Cancer,Lyon. France.:?) (single copies can be ordered from WHO Publications centre U.S.A., 49 Sheridan Avenue, Albany, NY 12210) ; NTP Carcinogenesis Studies (dermal); No Evidence: mouse NTPTR* ?? National Toxicology Program Technical Report Series. (Research Triangle Park, NC 27709) No. NTP-TR-301,86 . . Reported in EPA TSCA Inventory. On Community Right-To-Know List.

Packinggroup: III
HS Code: 29071900
Sensitive: Hygroscopic
Safety Data
Hazard Symbols Xi:Irritant
 

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