2-Phenylphenol supplier | CasNO.90-43-7

Name
11 -Hydroxy-2-phenylbenzene
EINECS 201-993-5
CAS No. 90-43-7
Article Data265
CAS DataBase
Density 1.111 g/cm³
Solubility 0.7 g/L (20 °C) in water
Melting Point 57-59 °C(lit.)
Formula C₁₂H₁₀O
Boiling Point 282 °C at 760 mmHg
Molecular Weight 170.211
Flash Point 140.3 °C
Transport Information UN 3077 9/PG 3
Appearance Off-white powder
Safety 22-61
Risk Codes 36/37/38-50-37/38/50-36
Molecular Structure
Hazard Symbols Xi, N
Synonyms 1,1'-Biphenyl-2-ol;2-Biphenylol;2-Hydroxybiphenyl;2-hydroxydiphenyl;
PSA 20.23000
LogP 3.05920

Synthetic route

: 86-26-0
2-methoxy-1,1'-biphenyl

: 90-43-7
2-Phenylphenol

Conditions

Conditions	Yield
With boron tribromide In dichloromethane at 0 - 25℃;	100%
With boron tribromide In dichloromethane at -80℃;

: 1444-65-1
(RS)-2-phenylcyclohexanone

: 90-43-7
2-Phenylphenol

Conditions

Conditions	Yield
With palladium chloride*2MeCN; chloranil In 1,4-dioxane at 100℃; for 18h;	100%
Multi-step reaction with 2 steps 1: dimethyl sulfoxide; oxygen; palladium(II) trifluoroacetate / acetic acid / 12 h / 80 °C / Reflux; Sealed tube 2: dimethyl sulfoxide; iodine / nitromethane / 24 h / 100 °C / Sealed tube; Green chemistry View Scheme

: 533-58-4
2-Iodophenol

: 98-80-6
phenylboronic acid

: 90-43-7
2-Phenylphenol

Conditions

Conditions	Yield
With potassium phosphate; SBA-Si-PEG-Pd(PPh3)n In water at 50℃; for 10h; Suzuki coupling;	99%
With palladium 10% on activated carbon; potassium carbonate In water at 20 - 80℃; for 18.5h; Suzuki-Miyaura Coupling; Inert atmosphere;	97%
With bis(1,1'-ethylene-3,3'-divinylimidazole-2,2'-diylidene)nickel(II) dibromide dihydrate; potassium carbonate In water; N,N-dimethyl-formamide at 100℃; for 8h; Suzuki-Miyaura Coupling; Inert atmosphere; Schlenk technique;	96%

: 1178513-84-2
6-tert-butyl-6-phenyl-6H-dibenzo[c,e][1,2]oxasiline

: 90-43-7
2-Phenylphenol

Conditions

Conditions	Yield
With tetrabutyl ammonium fluoride In tetrahydrofuran at 70℃; for 5h;	99%

: 1022-21-5
trimethyl(biphenyl-2-yloxy)silane

: 90-43-7
2-Phenylphenol

Conditions

Conditions	Yield
With methanol; 1,3-disulfonic acid imidazolium hydrogen sulfate at 20℃; for 0.0666667h; Green chemistry;	99%

: 4688-76-0
2-Biphenylboronic acid

: 90-43-7
2-Phenylphenol

Conditions

Conditions	Yield
With oxygen; N-ethyl-N,N-diisopropylamine; [5,6]fullerene-C70 In chloroform; toluene at 20℃; for 12h; Irradiation;	98%
With N,N-dimethyl-p-toluidine N-oxide In dichloromethane at 20℃; for 0.0166667h;	95%
With tert.-butylhydroperoxide; potassium tert-butylate In water at 20 - 50℃; for 5h;	90%

: 132-64-9
dibenzofuran

: 90-43-7
2-Phenylphenol

Conditions

Conditions	Yield
With sodium hydride at 190 - 192℃; for 7h;	92.5%
With LiCrH42LiCl2THF In tetrahydrofuran at 25℃; for 12h;	84%
With lithium aluminium tetrahydride; cobalt acetylacetonate; sodium t-butanolate In toluene at 140℃; for 24h; Inert atmosphere; Sealed tube;	81%

: 2052-07-5
2-Bromobiphenyl

: 90-43-7
2-Phenylphenol

Conditions

Conditions	Yield
With oxygen; triethylamine; sodium iodide In acetonitrile at 32℃; for 24h; Schlenk technique; UV-irradiation;	91%

: 2051-60-7
2-chloro-1,1'-biphenyl

: 90-43-7
2-Phenylphenol

Conditions

Conditions	Yield
With 5-(di-tert-butylphosphino)-1′, 3′, 5′-triphenyl-1′H-[1,4′]bipyrazole; tris-(dibenzylideneacetone)dipalladium(0); cesiumhydroxide monohydrate In 1,4-dioxane at 110℃; Inert atmosphere; Glovebox; Sealed tube;	90%
With water; silica gel; copper(II) oxide at 525 - 600℃;
With water; sodium carbonate at 300 - 360℃;

: 863418-13-7
(Z)-4-phenylocta-1,4,7-trien-3-one

: 90-43-7
2-Phenylphenol

Conditions

Conditions	Yield
tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride In dichloromethane at 20℃; for 2h;	90%

: (1,1'-biphenyl)-2-yl formate

: 90-43-7
2-Phenylphenol

Conditions

Conditions	Yield
With copper; Selectfluor In acetonitrile at 80℃;	90%

: potassium (2-hydroxyphenyl)trifluoroborate

: 591-50-4
iodobenzene

: 90-43-7
2-Phenylphenol

Conditions

Conditions	Yield
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In ethanol; water; toluene at 80℃; Suzuki Coupling; Inert atmosphere; Sonication; Reflux;	89%

: 132939-03-8
Diethylcarbamic acid, <1,1'-biphenyl>-2-yl ester

: 90-43-7
2-Phenylphenol

Conditions

Conditions	Yield
With zirconocene dichloride In tetrahydrofuran at 20℃; Inert atmosphere;	87%
With water; sodium hydroxide In ethanol for 8h; Reflux;	85%

: 1016-05-3
dibenzothiophene sulfone

: 90-43-7
2-Phenylphenol

Conditions

Conditions	Yield
Stage #1: dibenzothiophene sulfone With sodium hydroxide In water at 300℃; for 1.5h; Autoclave; Stage #2: With hydrogenchloride In water pH=7; Product distribution / selectivity;	86.5%

: 95-56-7
2-hydroxybromobenzene

: 100-58-3
phenylmagnesium bromide

: 90-43-7
2-Phenylphenol

Conditions

Conditions	Yield
Stage #1: 2-hydroxybromobenzene; phenylmagnesium bromide With tris-(dibenzylideneacetone)dipalladium(0); 4-bromo-phenol; C30H23O2P In tetrahydrofuran at -78 - 25℃; for 2.16667h; Stage #2: With hydrogenchloride In tetrahydrofuran; water	86%
With tris-(dibenzylideneacetone)dipalladium(0); 1-bromo-4-methoxy-benzene; C30H23O2P In tetrahydrofuran at -78 - 25℃; Inert atmosphere;	96 %Spectr.

: 188646-07-3
([1,1′-biphenyl]-2-yloxy)(tert-butyl)dimethylsilane

: 90-43-7
2-Phenylphenol

Conditions

Conditions	Yield
With acetyl chloride In methanol	86%

: 33948-36-6
2-iodocyclohex-2-en-1-one

: 98-80-6
phenylboronic acid

A: 4556-09-6
2-phenylcyclohex-2-enone

B: 90-43-7
2-Phenylphenol

Conditions

Conditions	Yield
With palladium 10% on activated carbon; sodium carbonate In 1,4-dioxane; water at 20℃; for 24h; Suzuki-Miyaura Coupling;	A 86% B 4%

...Expand

: 65109-75-3
N-(phenoxy)-4-methylbenzenesulfonamide

: 71-43-2
benzene

A: 92-69-3
4-Phenylphenol

B: 65109-81-1
2-hydroxyphenyl p-toluenesulfonimidate

C: 70-55-3
toluene-4-sulfonamide

D: 90-43-7
2-Phenylphenol

Conditions

Conditions	Yield
With trifluorormethanesulfonic acid; trifluoroacetic acid for 1h; Ambient temperature; Further byproducts given;	A 14% B 13% C 85% D 29%

...Expand

: 65109-75-3
N-(phenoxy)-4-methylbenzenesulfonamide

: 71-43-2
benzene

A: 92-69-3
4-Phenylphenol

B: 65109-81-1
2-hydroxyphenyl p-toluenesulfonimidate

C: 70-55-3
toluene-4-sulfonamide

D: 65109-80-0
4-hydroxyphenyl trifluoromethanesulfonate

E: 90-43-7
2-Phenylphenol

Conditions

Conditions	Yield
With trifluorormethanesulfonic acid; trifluoroacetic acid for 1h; Mechanism; Product distribution; Ambient temperature; other N-acyl- and N-sulfonyl-O-arylhydroxylamines under various reaction conditions, different nucleophiles;	A 14% B 13% C 85% D 3% E 29%

...Expand

: 35616-01-4
toluene-4-sulfonic acid,2-hydroxyphenyl ester

: 100-58-3
phenylmagnesium bromide

: 90-43-7
2-Phenylphenol

Conditions

Conditions	Yield
Stage #1: phenylmagnesium bromide With C24H52Cl2O12P4Pd2 In tetrahydrofuran; 1,4-dioxane at 20℃; for 0.0833333h; Kumada-Corriu cross-coupling reaction; Inert atmosphere; Stage #2: toluene-4-sulfonic acid,2-hydroxyphenyl ester In tetrahydrofuran; 1,4-dioxane at 110℃; for 24h; Kumada-Corriu cross-coupling reaction; Inert atmosphere; chemoselective reaction;	84%

: 75-36-5
acetyl chloride

: 90-43-7
2-Phenylphenol

: 3271-80-5
2-acetoxybiphenyl

Conditions

Conditions	Yield
With pyridine In dichloromethane for 3h;	100%
With dmap; triethylamine In dichloromethane at 0 - 20℃; for 6h; Schlenk technique; Inert atmosphere;	98%

: 106-95-6
allyl bromide

: 90-43-7
2-Phenylphenol

: 20281-39-4
2-(allyloxy)-1,1'-biphenyl

Conditions

Conditions	Yield
With potassium carbonate In acetone at 60℃; for 20h;	100%
With cesium fluoride In acetonitrile at 82℃;	62%
With cesium fluoride In acetonitrile at 82℃;	62%

: 50-00-0
formaldehyd

: 90-43-7
2-Phenylphenol

: 14562-10-8
2-hydroxy-3-phenylbenzaldehyde

Conditions

Conditions	Yield
With triethylamine; magnesium chloride In tetrahydrofuran for 3h; Heating;	100%
Stage #1: formaldehyd; 2-Phenylphenol With triethylamine; magnesium chloride In tetrahydrofuran for 1.7h; Heating / reflux; Stage #2: With hydrogenchloride In water at 0℃; pH=5;	92%
With triethylamine; magnesium chloride In tetrahydrofuran at 70℃; for 16h;	90%

: 106-96-7
propargyl bromide

: 90-43-7
2-Phenylphenol

: 26627-30-5
1-phenyl-2-(2-propynyloxy)benzene

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 2h;	100%
With potassium carbonate In acetone; toluene at 65℃; for 14h;	95%
With potassium carbonate In acetone; toluene	95%

: 358-23-6
trifluoromethylsulfonic anhydride

: 90-43-7
2-Phenylphenol

: 17763-65-4
biphenyl-2-yl trifluoromethanesulfonate

Conditions

Conditions	Yield
With pyridine In dichloromethane at 0℃; for 2h;	100%
With 2,6-dimethylpyridine In dichloromethane at 0 - 20℃; for 2h; Inert atmosphere;	98%
With pyridine In dichloromethane at 20℃; for 2h; Inert atmosphere;	95%

: 90-43-7
2-Phenylphenol

: 22749-43-5
p-chlorodibenzo[c.e][1,2]oxaphosphorine

Conditions

Conditions	Yield
With zinc(II) chloride; phosphorus trichloride at 20 - 180℃; for 7h;	100%
With anhydrous phosphorus trichloride; phosphorus trichloride; Zinc chloride In 5,5-dimethyl-1,3-cyclohexadiene	95%
Stage #1: 2-Phenylphenol With phosphorus trichloride at 140℃; for 5h; Inert atmosphere; Neat (no solvent); Stage #2: With zinc(II) chloride at 210℃; for 3h; Inert atmosphere; Neat (no solvent);	90%

: 7550-45-0
titanium tetrachloride

: 90-43-7
2-Phenylphenol

: 263547-03-1
trichloro mono(2-phenylphenoxide) titanium(IV)

Conditions

Conditions	Yield
In dichloromethane byproducts: HCl; under N2; 2-phenylphenol in CH2Cl2 added to TiCl4 (molar ratio 1:1) in CH2Cl2; refluxed for 12.5 h; filtered; solvent removed; dried under vac. for 4 h; elem. anal.;	100%

: 7550-45-0
titanium tetrachloride

: 90-43-7
2-Phenylphenol

: 864720-65-0
[dichlorobis(2-phenylphenolate)titanium(IV)]

Conditions

Conditions	Yield
In toluene byproducts: HCl; N2, vigorously refluxed for 12 h; cooled, filtered, solvent removed;	100%

: 20452-67-9
phenylethylketene

: 90-43-7
2-Phenylphenol

: 2-phenylphenyl 2-phenylbutanoate

Conditions

Conditions	Yield
With potassium hexamethylsilazane In toluene	100%

: 1565-71-5
3-phenylpentan-3-ol

: 90-43-7
2-Phenylphenol

: 1186337-44-9
C23H24O

Conditions

Conditions	Yield
With sulfuric acid In water for 1h; Reflux;	100%

: 90-43-7
2-Phenylphenol

: 1493-27-2
ortho-nitrofluorobenzene

: 2688-91-7
2-(2-nitrophenoxy)biphenyl

Conditions

Conditions	Yield
With potassium carbonate In dimethyl sulfoxide at 95℃; for 24h;	100%
Stage #1: 2-Phenylphenol With sodium hydride In N,N-dimethyl-formamide at 20℃; for 1h; Inert atmosphere; Stage #2: ortho-nitrofluorobenzene In N,N-dimethyl-formamide at 20 - 50℃; for 13h; Inert atmosphere;	83%

: 19009-39-3
N,N-diisopropylcarbamoyl chloride

: 90-43-7
2-Phenylphenol

: [1,1'-biphenyl]-2-yl diisopropylcarbamate

Conditions

Conditions	Yield
With sodium hydride In tetrahydrofuran at 20℃; for 12h; Sealed tube;	100%

: 96-49-1
[1,3]-dioxolan-2-one

: 90-43-7
2-Phenylphenol

: 7501-02-2
2-(<1,1'-biphenyl>2-yloxy)ethanol

Conditions

Conditions	Yield
With potassium carbonate at 160℃; for 1h; Temperature; Reagent/catalyst;	99.2%

: 88-10-8
N,N-diethylcarbamyl chloride

: 90-43-7
2-Phenylphenol

: 132939-03-8
Diethylcarbamic acid, <1,1'-biphenyl>-2-yl ester

Conditions

Conditions	Yield
With potassium carbonate In acetonitrile for 3h; Inert atmosphere; Reflux;	99%
With potassium carbonate In acetonitrile for 7h; Heating;	95%
With potassium carbonate In acetonitrile for 8h; Reflux;

: 90-43-7
2-Phenylphenol

: 67-64-1
acetone

: 24038-68-4
2,2-bis-(3-phenyl-4-hydroxyphenyl)-propane

Conditions

Conditions	Yield
With hydrogenchloride; 3-mercaptopropionic acid In water at 80℃; Reagent/catalyst; Inert atmosphere;	99%
With hydrogenchloride for 18h; Heating;	42%
With methanol; sulfuric acid; 1-dodecylthiol In toluene at 40℃; for 2.5h; Inert atmosphere;	9 %Chromat.

: 90-43-7
2-Phenylphenol

: 1795-48-8
Isopropyl isocyanate

: 417698-00-1
O-2-biphenylyl N-isopropylcarbamate

Conditions

Conditions	Yield
With dmap In tetrahydrofuran at 60℃; for 24h;	99%

: 90-43-7
2-Phenylphenol

: 14205-96-0
dibenzo[c,e][1,2]oxaborinin-6-ol

Conditions

Conditions	Yield
With boron trichloride; aluminium trichloride In hexane at 70 - 75℃; for 6h;	99%
Multi-step reaction with 2 steps 1: (i) BCl3, CH2Cl2, (ii) AlCl3, PE 2: Et2O / light petroleum View Scheme
With boron trichloride

: 90-43-7
2-Phenylphenol

: 23197-48-0
3-bromo[1,1’-biphenyl]-2-ol

Conditions

Conditions	Yield
With N-bromo-tert-butylamine In chloroform at 0℃; Inert atmosphere;	99%
With N-Bromosuccinimide; diisopropylamine In dichloromethane for 16h; Reflux; Inert atmosphere;	96%
With N-Bromosuccinimide; diisopropylamine In dichloromethane for 16h; Inert atmosphere; Reflux;	95%

: 42075-32-1
(2R,4R)-pentanediol

: 90-43-7
2-Phenylphenol

: 1373521-55-1
C17H20O2

Conditions

Conditions	Yield
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 20℃; for 96h; Mitsunobu reaction;	99%

: diphenyliodonium tetrafluoroborate

: 90-43-7
2-Phenylphenol

: 1655-68-1
1-methoxy-3-phenoxybenzene

Conditions

Conditions	Yield
Stage #1: 2-Phenylphenol With potassium tert-butylate In tetrahydrofuran at 0℃; for 0.25h; Stage #2: diphenyliodonium tetrafluoroborate In tetrahydrofuran at 20℃; for 3h;	99%

: bis(2-methylphenyl)iodonium tetrafluoroborate

: 90-43-7
2-Phenylphenol

: 23951-29-3
1-(3-methoxyphenoxy)-2-methylbenzene

Conditions

Conditions	Yield
Stage #1: 2-Phenylphenol With potassium tert-butylate In tetrahydrofuran at 0℃; for 0.25h; Stage #2: bis(2-methylphenyl)iodonium tetrafluoroborate In tetrahydrofuran at 40℃; for 0.5h;	99%

: 90-43-7
2-Phenylphenol

: 7189-69-7
N,N`-sulfuryldiimidazole

: (1,1'-biphenyl)-2-yl 1H-imidazole-1-sulfonate

Conditions

Conditions	Yield
With caesium carbonate In tetrahydrofuran	99%
With caesium carbonate In tetrahydrofuran at 20℃; for 12h;	98%

: 98-29-3
4-tert-Butylcatechol

: 4-(4-chlorophenoxy)-3,5,6-trifluorophthalonitrile

: 90-43-7
2-Phenylphenol

: C36H25ClN2O4

Conditions

Conditions	Yield
Stage #1: 4-tert-Butylcatechol; 4-(4-chlorophenoxy)-3,5,6-trifluorophthalonitrile With potassium carbonate In acetonitrile at 80℃; for 2h; Stage #2: 2-Phenylphenol With potassium carbonate In acetonitrile at 80℃; for 10h;	99%

...Expand

: 542-69-8
1-iodo-butane

: 201230-82-2
carbon monoxide

: 90-43-7
2-Phenylphenol

: 854880-18-5
valeric acid biphenyl-2-yl ester

Conditions

Conditions	Yield
With rhodium(III) chloride; 1,3-bis-(diphenylphosphino)propane; sodium carbonate; sodium bromide In 1,4-dioxane at 120℃; under 750.075 Torr; for 24h; Inert atmosphere; chemoselective reaction;	99%

...Expand

: 873-55-2
sodium benzenesulfonate

: 90-43-7
2-Phenylphenol

: 21419-72-7
[1,1’-biphenyl]-2-yl benzenesulfonate

Conditions

Conditions	Yield
In water; acetonitrile at 20℃; for 2h; Electrochemical reaction;	99%

2-Phenylphenol Chemical Properties

Molecule structure of 2-Phenylphenol (CAS NO.90-43-7):

IUPAC Name: 2-Phenylphenol
Molecular Weight: 170.2072 g/mol
Molecular Formula: C₁₂H₁₀O
Density: 1.111 g/cm³
Melting Point: 57-59 °C(lit.)
Boiling Point: 282 °C at 760 mmHg
Flash Point: 140.3 °C
Index of Refraction: 1.604
Molar Refractivity: 52.72 cm³
Molar Volume: 153.1 cm³
Surface Tension: 44.5 dyne/cm
Enthalpy of Vaporization: 54.18 kJ/mol
Vapour Pressure: 0.00202 mmHg at 25 °C
Storage Temp.: 0-6 °C
Water Solubility: 0.7 g/L (20 °C)
Sensitive: hygroscopic
XLogP3: 3.1
H-Bond Donor: 1
H-Bond Acceptor: 1
Rotatable Bond Count: 1
Tautomer Count: 3
Exact Mass: 170.073165
MonoIsotopic Mass: 170.073165
Topological Polar Surface Area: 20.2
Heavy Atom Count: 13
Canonical SMILES: C1=CC=C(C=C1)C2=CC=CC=C2O
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
EINECS: 201-993-5
Product Categories: Industrial/Fine Chemicals; Aromatic Compounds; Biphenyl & Diphenyl ether

2-Phenylphenol Uses

2-Phenylphenol (CAS NO.90-43-7) is commonly used as a carrier for hydrophobic synthetic polyvinyl chloride fiber, polyester when using carrier dyeing methos.It also can be used as surface-active agent, sterilizing preservatives, dyes intermediates. The primary use of 2-phenylphenol is as an agricultural fungicide. It is also used for disinfection of seed boxes. It is used to disinfect hospital and veterinary equipment. It is a general surface disinfectant, used in households, hospitals, nursing homes, farms, laundries, barber shops, and food processing plants. It can be used on fibers and other materials. Other uses are in rubber industry and as a laboratory reagent. It is also used in the manufacture of other fungicides, dye stuffs, resins and rubber chemicals.

2-Phenylphenol Toxicity Data With Reference

1.	skn-rbt 250 mg	MccSB# Personal Communication from Susan B. McCollister, Dow Chemical U.S.A., Midland, MI 48640, to NIOSH, Cincinnati, OH 45226, June 15, 1984 15JUN84
2.	skn-rbt 20 mg/24H MOD	85JCAE Prehled Prumyslove Toxikologie; Organicke Latky Marhold, J.,Prague, Czechoslovakia.: Avicenum,1986,228.
3.	eye-rbt 50 µg/24H SEV	85JCAE Prehled Prumyslove Toxikologie; Organicke Latky Marhold, J.,Prague, Czechoslovakia.: Avicenum,1986,228.
4.	mmo-sat 60 µg/plate	ENMUDM Environmental Mutagenesis. 5 (Suppl 1)(1983),3.
5.	cyt-hmn:fbr 200 µg/L	MUREAV Mutation Research. 54 (1978),255.
6.	msc-hmn:emb 20 mg/L	MUREAV Mutation Research. 156 (1985),123.
7.	msc-hmn:oth 15 mg/L	TRENAF Kenkyu Nenpo-Tokyo-toritsu Eisei Kenkyusho. 35 (1984),399.
8.	cyt-ham:ovr 100 mg/L	MUREAV Mutation Research. 141 (1984),95.
9.	orl-rat LD₅₀:2000 mg/kg	NNGADV Nippon Noyaku Gakkaishi. 3 (1978),365.
10.	unr-rat LD₅₀:2700 mg/kg	TRENAF Kenkyu Ne

2-Phenylphenol Consensus Reports

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.

2-Phenylphenol Safety Profile

Hazard Codes: Irritant Xi, Dangerous N
Risk Statements: 36/37/38-50-37/38/50-36
R36/37/38:Irritating to eyes, respiratory system and skin.
R50:Very toxic to aquatic organisms.
R37/38:Irritating to respiratory system and skin.
R36:Irritating to eyes.
Safety Statements: 22-61
S22:Do not breathe dust.
S61:Avoid release to the environment. Refer to special instructions / safety data sheets.
RIDADR: UN 3077 9/PG 3
WGK Germany: 2
RTECS: DV5775000
HazardClass: 9
PackingGroup: III
HS Code: 29071900
A poison by intraperitoneal route. Moderately toxic by ingestion and possibly other routes. An experimental teratogen. Other experimental reproductive effects. Human mutation data reported. Severe eye and moderate skin irritant. Questionable carcinogen with experimental carcinogenic data. When heated to decomposition it emits acrid smoke and irritating fumes.

2-Phenylphenol 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.

Product Name

11 -Hydroxy-2-phenylbenzene

Synthetic route

2-Phenylphenol Chemical Properties

2-Phenylphenol Uses

2-Phenylphenol Toxicity Data With Reference

2-Phenylphenol Consensus Reports

2-Phenylphenol Safety Profile

2-Phenylphenol Specification

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