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123-30-8

Basic Information
CAS No.: 123-30-8
Name: Phenol,4-amino-
Molecular Structure:
Molecular Structure of 123-30-8 (Phenol,4-amino-)
Formula: C6H7NO
Molecular Weight: 109.13 .
Synonyms: Phenol,p-amino- (8CI);1-Amino-4-hydroxybenzene;4-Amino-1-hydroxybenzene;4-Hydroxy-1-aminobenzene;4-Hydroxyaniline;4-Hydroxybenzenamine;4-Hydroxyphenylamine;Activol;Azol;BASF Ursol P Base;Benzofur P;C.I. 76550;C.I. Oxidation Base 6;Certinal;Citol;Durafur Brown RB;Fouramine P;Fourrine84;Fourrine P Base;Furro P base;NSC 1545;Nako Brown R;Paranol;PelagolGrey P Base;Pelagol P Base;Renal AC;Rodinal;Tertral P Base;Unal;Ursol P;Ursol P Base;Zoba Brown P Base;p-Aminophenol;p-Hydroxyaniline;p-Hydroxyphenylamine;p-Amino phenol;4-Aminophenol, para amino phenol;4-Aminophenol;
EINECS: 204-616-2
Density: 1.21 g/cm3
Melting Point: 188 °C
Boiling Point: 281.984 °C at 760 mmHg
Flash Point: 124.34 °C
Solubility: Water: 1.5 g/100 mL (20 °C)
Appearance: Off white granular powder
Hazard Symbols: HarmfulXn,DangerousN
Risk Codes: 20/22-50/53-68-40
Safety: 28-36/37-60-61-28A
Transport Information: UN 2512 6.1/PG 3
PSA: 46.25000
LogP: 1.55560
Synthetic route
100-02-7

4-nitro-phenol

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With copper(I) chloride; potassium borohydride In methanol for 0.166667h; Ambient temperature;100%
With palladium diacetate; carbon monoxide; triphenylphosphine In water; acetic acid at 56℃; under 532 Torr; for 14h;100%
With hydrazine hydrate In ethanol at 80℃;100%
62-53-3

aniline

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With dihydrogen peroxide In water at 20℃; for 1.66667h; Reagent/catalyst; UV-irradiation; Green chemistry; regioselective reaction;100%
With dihydrogen peroxide; polymer 1-A In methanol for 0.05h; Ambient temperature;4.9%
With dihydrogen peroxide; polymer 1-A In methanol for 0.05h; Product distribution; Kinetics; Ambient temperature; various catalysts were used;4.9%
103-90-2

4-acetaminophenol

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With ammonium bromide; ethylenediamine at 70℃; for 5h; Reagent/catalyst; Temperature; Microwave irradiation;100%
With ammonium bromide; ethylenediamine at 70℃; for 5h; Microwave irradiation; Inert atmosphere; neat (no solvent);99%
With ammonium iodide; hydrazine hydrate at 50℃; for 12h; Inert atmosphere; Sealed tube;97%
54840-09-4

carbamate de methyle et de N(hydroxy-4 phenyle)

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With 3-azapentane-1,5-diamine at 130℃; for 12h; Sealed tube;99%
24541-43-3

4-azidophenol

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With hydrazine hydrate In ethanol at 20℃; chemoselective reaction;98%
With aluminium(III) iodide In benzene for 0.166667h; Reduction; Heating;93%
With gallium(III) triflate; potassium iodide In acetonitrile at 60℃; for 1h; Inert atmosphere; Green chemistry; chemoselective reaction;93%
36309-42-9

4-(trimethylsilyloxy)aniline

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With methanol; 1,3-disulfonic acid imidazolium hydrogen sulfate at 20℃; for 0.0666667h; Green chemistry;98%
With nano magnetic sulfated zirconia (Fe3O4 at ZrO2/SO42-) In neat (no solvent) at 20℃; for 0.25h; Green chemistry;83%
With Kaolinitic clay; water for 0.0416667h; Irradiation; microwave;63%
54840-15-2

4-N-tert-butoxycarbonylaminophenol

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With water at 100℃; for 2h; Inert atmosphere;97%
With water at 150℃; for 2h; Subcritical conditions;95%
HY-Zeolite In dichloromethane for 2h; Heating;92%
With 3-butyl-l-methyl-1H-imidazol-3-iumtrifloroacetate In 1,4-dioxane; water at 70 - 72℃; for 2h;82%
With H-β zeolite In dichloromethane for 10h; Heating;71%
106-41-2

4-bromo-phenol

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With ammonium hydroxide at 20℃; for 10h; Catalytic behavior;96%
With ammonia; triethylamine In water at 20℃; for 8h;95%
With ammonium hydroxide at 20℃; for 12h; Catalytic behavior;94%
2050-16-0

4,4'-dihydroxyazobenzene

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With zinc In methanol at 25℃; for 0.166667h; Inert atmosphere;96%
With magnesium In methanol at 25℃; for 0.2h; Inert atmosphere;95%
With sodium dithionite; water In dimethyl sulfoxide at 20℃; pH=7.4; Kinetics; phosphate buffer;
With hydrogenchloride; tin(ll) chloride
With sodium hydroxide; zinc
540-38-5

4-Iodophenol

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With ammonium hydroxide In water at 20℃; for 9h; Green chemistry;95%
With copper(l) iodide; 2-carboxyquinoline N-oxide; potassium carbonate; ammonium hydroxide In dimethyl sulfoxide at 50℃; for 23h; Inert atmosphere;90%
With copper(I) oxide; ammonium hydroxide; potassium carbonate at 140℃; for 13h; Inert atmosphere;80%
With copper(l) iodide; ascorbic acid In ammonia at 25℃; for 18h; liquid NH3;57%
89415-43-0

(4-aminophenyl)boronic acid

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With iron(III) oxide; oxygen In tetrahydrofuran Irradiation;95%
With iron(III) oxide; oxygen In tetrahydrofuran at 20℃; Irradiation;95%
With dihydrogen peroxide In water at 20℃; chemoselective reaction;95%
84253-23-6

4-(2,4-Dimethyl-benzyloxy)-phenylamine

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With hydrogen; palladium on activated charcoal In ethanol under 3040 Torr; for 15h;94%
104-91-6

p-nitrosophenol

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With titanium(III) chloride In 1,4-dioxane at 20℃; for 4h; Product distribution; var. substituted nitrosobenzenes;93%
With nickel; methyl cyclohexane at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation;
With hydrogenchloride; tin
117635-44-6

tert-butyldimethyl(4-nitrophenoxy)silane

A

123-30-8

4-amino-phenol

B

111359-74-1

4-[(tert-butyldimethylsilyl)oxy]aniline

Conditions
ConditionsYield
With potassium fluoride; polymethylhydrosiloxane; palladium diacetate In tetrahydrofuran; water at 20℃; for 0.5h;A 7%
B 92%
With potassium fluoride; polymethylhydrosiloxane; palladium diacetate In tetrahydrofuran at 20℃; for 0.5h;A 7%
B 92%
13871-68-6

p-aminophenyl acetate

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With amberlyst-15 In methanol at 20℃; for 3h;90%
103-14-0

4-(benzylamino)phenol

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With ammonium formate; zinc In ethylene glycol for 0.05h; microwave irradiation;90%
With ammonium formate; magnesium In ethylene glycol for 0.05h; microwave irradiation;90%
1016987-47-5

4-[[tris(propan-2-yl)silyl]oxy]aniline

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With potassium acetate In water; N,N-dimethyl-formamide at 70℃; for 22h;90%
1145-76-2

benzyl 4-nitrophenyl ether

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With formic acid; potassium hydroxide In ethanol at 70℃; for 1h; Catalytic behavior; Reagent/catalyst;89%
With Pd(0)EnCat; ammonium formate In N,N-dimethyl-formamide at 80℃; for 0.166667h; Irradiation; microwave;20%
13795-24-9

benzyl 4-nitrophenyl carbonate

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With methanol; sodium tetrahydroborate; nickel(II) chloride hexahydrate at 20℃; for 0.25h; chemoselective reaction;89%
1145-76-2

benzyl 4-nitrophenyl ether

A

6373-46-2

p-benzyloxyaniline

B

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With hydrogen; platinum(IV) oxide In various solvent(s) at 25℃; for 10h;A 88%
B 7%
631-61-8

ammonium acetate

123-31-9

hydroquinone

A

103-90-2

4-acetaminophenol

B

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With acetic acid at 160 - 230℃; for 15h; Temperature; Autoclave; Inert atmosphere;A 88%
B n/a
7107-59-7

4-(N-Benzyloxycarbonylamino)phenol

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With methylmagnesium bromide; hydrogen; palladium diacetate; nickel diacetate In water at 45℃; for 19h;88%
With methanol; sodium tetrahydroborate; nickel(II) chloride hexahydrate at 20℃; for 0.25h; chemoselective reaction;86%
89415-43-0

(4-aminophenyl)boronic acid

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With triethanolamine In water at 20℃; for 18h; Sonication; Irradiation; Green chemistry;88%

3-(4-nitro-phenoxymethyl)-benzoic acid ethyl ester

A

120-33-2

ethyl 3-methylbenzoate

B

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With magnesium In methanol at 20℃; for 5h;A n/a
B 87%
111359-74-1

4-[(tert-butyldimethylsilyl)oxy]aniline

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With lithium acetate In water; N,N-dimethyl-formamide at 70℃; for 24h; Inert atmosphere;87%
With sodium cyanide In ethanol; water at 80℃; for 38h; chemoselective reaction;27.3%
100-02-7

4-nitro-phenol

108-24-7

acetic anhydride

A

103-90-2

4-acetaminophenol

B

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With sodium tetrahydroborate; chloro-trimethyl-silane In methanol; water for 0.25h; Reagent/catalyst; Irradiation;A 86%
B 13%
98-95-3

nitrobenzene

123-30-8

4-amino-phenol

Conditions
ConditionsYield
With palladium diacetate; carbon monoxide; triphenylphosphine In sulfuric acid; butan-1-ol at 56℃; under 532 Torr; for 30h;85%
With sulfuric acid; Pt/Al2O3; hydrogen; cetyltrimethylammonim bromide; zinc(II) sulfate In water at 120℃; under 7500.75 Torr; for 4h; Reagent/catalyst; Pressure;83%
With formic acid; sulfate-doped zirconia; cetyltrimethylammonim bromide at 150℃; for 6h; Reagent/catalyst; Temperature; Inert atmosphere; Sealed tube;51.3%
123-30-8

4-amino-phenol

104-88-1

4-chlorobenzaldehyde

1749-05-9

4-{[(4-chlorophenyl)methylidene]amino}phenol

Conditions
ConditionsYield
for 24h; Ambient temperature;100%
With piperidine In ethanol Condensation; Heating;85%
With dodecatungstosilic acid; phosphorus pentoxide In neat (no solvent, solid phase) at 20℃;82%
108-30-5

succinic acid anhydride

123-30-8

4-amino-phenol

62558-67-2

4-(4'-hydroxy-phenylamino)-4-oxo-butanoic acid

Conditions
ConditionsYield
With sodium dodecyl-sulfate In methanol; water at 20℃; for 0.583333h;100%
With sodium dodecyl-sulfate In water87%
In water at 50℃;86%
1118-02-1

trimethylsilyl isocyanate

123-30-8

4-amino-phenol

100238-66-2

(4-Trimethylsilanyloxy-phenyl)-urea

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 20 - 50℃; for 2h;100%
24424-99-5

di-tert-butyl dicarbonate

123-30-8

4-amino-phenol

54840-15-2

4-N-tert-butoxycarbonylaminophenol

Conditions
ConditionsYield
With triethylamine In methanol at 22℃; for 14h;100%
With guanidine hydrochloride In ethanol at 35 - 40℃; for 0.0166667h;100%
In tetrahydrofuran at 0℃; for 12h;100%
71105-17-4

phenylene-1,2-diisothiocyanate

123-30-8

4-amino-phenol

75644-26-7

1-(4-hydroxyanilino-thiocarbonyl)-benzimidazolidine-2-thione

Conditions
ConditionsYield
for 1h; Solid phase reaction; cyclization; addition;100%
In acetonitrile for 0.5h; Ambient temperature;81%
63673-58-5

2,6-dimethyl-4-oxo-5-phenyl-1,3-oxazinium perchlorate

123-30-8

4-amino-phenol

122664-34-0

perchlorate 2,6-dimethyl-5-phenyl-1-(4'-hydroxyphenyl)-4-oxopyrimidinium

Conditions
ConditionsYield
In acetic acid for 48h; Ambient temperature;100%
In acetic acid for 0.5h; Heating;94%
13154-24-0

triisopropylsilyl chloride

123-30-8

4-amino-phenol

1016987-47-5

4-[[tris(propan-2-yl)silyl]oxy]aniline

Conditions
ConditionsYield
With 1H-imidazole In dichloromethane at 20℃; for 26h; Inert atmosphere;100%
With 1H-imidazole for 26h; Inert atmosphere;85%
With 1H-imidazole In dichloromethane at 15℃; for 12h;73.9%
123-30-8

4-amino-phenol

70237-44-4

4-amino(2H4)phenol

Conditions
ConditionsYield
Stage #1: 4-amino-phenol With diclazuril; water-d2 at 175℃; for 0.333333h; microwave irradiation;
Stage #2: With water
100%
With hydrogen chloride In water-d2 at 28 - 180℃; for 42h; Inert atmosphere; Sealed tube; Microwave irradiation;50%
With hydrogenchloride; water-d2 In water-d2 at 180℃; for 7h; Microwave irradiation;
123-30-8

4-amino-phenol

4-hydroxybenzenediazonium tetrafluoroborate

Conditions
ConditionsYield
With acetic acid; isopentyl nitrite In ethanol; water at -10℃; for 1.5h;100%
With sodium tetrafluoroborate; perchloric acid; sodium nitrite In water at -10℃; for 24h;
With tetrafluoroboric acid; isopentyl nitrite In ethanol at 0℃; for 1h;
123-30-8

4-amino-phenol

350-46-9

4-Fluoronitrobenzene

6149-33-3

4-(4-nitrophenoxy)aniline

Conditions
ConditionsYield
With sodium hydride In N,N-dimethyl-formamide at 90℃;100%
With potassium carbonate In DMF (N,N-dimethyl-formamide) at 20℃; for 12h;71%
With potassium carbonate In dimethyl sulfoxide at 70℃;67%
123-30-8

4-amino-phenol

162364-72-9

7-benzyloxy-4-chloro-6-methoxyquinazoline

516526-37-7

4-((7-(benzyloxy )-6-methoxyquinazolin-4-yl)oxy)aniline

Conditions
ConditionsYield
With sodium hydroxide; tetrabutyl-ammonium chloride In water; butanone for 2h; Heating / reflux;100%
With sodium hydroxide; tetrabutyl-ammonium chloride In water; butanone for 2h; Heating / reflux;100%
Stage #1: 4-amino-phenol With sodium hydride In dimethyl sulfoxide; mineral oil at 17 - 25℃; for 0.166667h; Inert atmosphere;
Stage #2: 7-benzyloxy-4-chloro-6-methoxyquinazoline In dimethyl sulfoxide; mineral oil at 22 - 90℃; for 1h; Inert atmosphere;
91%
871024-38-3

4-chloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidine

123-30-8

4-amino-phenol

919278-08-3

4-[(5-methyl-5H-pyrrolo[3,2-d]pyrimidin-4-yl)oxy]aniline

Conditions
ConditionsYield
With caesium carbonate In 1-methyl-pyrrolidin-2-one at 120℃; for 16h; Product distribution / selectivity;100%
With potassium carbonate In 1-methyl-pyrrolidin-2-one at 110℃; for 3h; Product distribution / selectivity;60%
With potassium carbonate In 1-methyl-pyrrolidin-2-one at 110℃; for 2h;60%
924909-13-7

1-benzyloxymethyl-4-chloro-1H-pyrazolo[3,4-b]pyridine

123-30-8

4-amino-phenol

924909-14-8

4-(1-benzyloxymethyl-1H-pyrazolo[3,4-b]pyridin-4-yloxy)aniline

Conditions
ConditionsYield
Stage #1: 4-amino-phenol With potassium tert-butylate; potassium carbonate In 1-methyl-pyrrolidin-2-one at 20℃; for 1h;
Stage #2: 1-benzyloxymethyl-4-chloro-1H-pyrazolo[3,4-b]pyridine In 1-methyl-pyrrolidin-2-one at 80℃; for 0.5h;
100%
123-30-8

4-amino-phenol

24801-88-5

3-(triethoxypropyl) isocyanate

1028843-30-2

1-(3-(triethoxysilyl)propyl)-3-(4-hydroxyphenyl)urea

Conditions
ConditionsYield
In chloroform at 80℃; for 5h;100%
In chloroform at 80℃; for 5h;95%
128615-83-8

1-chloro-4-(4-methoxyphenyl)phthalazine

123-30-8

4-amino-phenol

1071584-40-1

4-(4-(4-methoxyphenyl)phthalazin-1-ylamino)phenol hydrochloride

Conditions
ConditionsYield
In iso-butanol at 100℃;100%
In iso-butanol at 100℃;
123-30-8

4-amino-phenol

95-01-2

2,4-Dihydroxybenzaldehyde

111279-02-8

4-((4-hydroxyphenylimino)methyl)benzene-1,3-diol

Conditions
ConditionsYield
With acetic acid In ethanol for 2h; Reflux; Inert atmosphere;100%
26153-38-8

3,5-dihydroxybenzaldehyde

123-30-8

4-amino-phenol

(E)-5{(4-hydroxyphenylimino)methyl}benzene-1,3-diol

Conditions
ConditionsYield
With magnesium sulfate In dichloromethane at 20℃; for 3h;100%
In water at 25℃; for 2h;92%
In water at 20℃; for 2h;
123-30-8

4-amino-phenol

68-12-2, 33513-42-7

N,N-dimethyl-formamide

2350-69-8

C9H13N2O(1+)*Cl(1-)

Conditions
ConditionsYield
With trichlorophosphate at 20℃; Cooling with ice;100%
26153-38-8

3,5-dihydroxybenzaldehyde

123-30-8

4-amino-phenol

1365617-17-9

5-[(4-hydroxy-phenylimino)-methyl]-benzene-1,3-diol

Conditions
ConditionsYield
With sodium sulfate In dichloromethane at 20℃; for 1h;100%
With sodium sulfate In dichloromethane at 20℃; for 3h; Solvent; Reagent/catalyst; Inert atmosphere;93%
123-30-8

4-amino-phenol

127099-85-8, 780722-26-1

N-Cyanoguanidine

116604-04-7

1-carbamimidamido-N-(4-hydroxyphenyl)methanimidamide hydrochloride

Conditions
ConditionsYield
In acetonitrile at 150℃; for 4.5h; Inert atmosphere;100%
1118-02-1

trimethylsilyl isocyanate

123-30-8

4-amino-phenol

1566-41-2

1-(4-hydroxyphenyl)urea

Conditions
ConditionsYield
In tetrahydrofuran at 65℃; for 6h;100%
73583-41-2

bromo-4 chloro-3 pyridine

123-30-8

4-amino-phenol

4-((3-chloropyridin-4-yl)oxy)aniline

Conditions
ConditionsYield
Stage #1: 4-amino-phenol With potassium tert-butylate In N,N-dimethyl acetamide at 20℃; for 0.5h;
Stage #2: bromo-4 chloro-3 pyridine In N,N-dimethyl acetamide at 85℃; for 4h;
100%

2-((4-chlorobenzyl)oxy)-5-fluorobenzaldehyde

123-30-8

4-amino-phenol

4-((2-((4-chlorobenzyl)oxy)-5-fluorobenzyl)amino)phenol

Conditions
ConditionsYield
Stage #1: 2-((4-chlorobenzyl)oxy)-5-fluorobenzaldehyde; 4-amino-phenol With acetic acid In methanol at 20℃; Inert atmosphere;
Stage #2: With sodium cyanoborohydride In methanol Inert atmosphere;
99.8%
51779-32-9

iminodicarboxylic acid di-tert-butyl ester

123-30-8

4-amino-phenol

54840-15-2

4-N-tert-butoxycarbonylaminophenol

Conditions
ConditionsYield
In tetrahydrofuran for 12h; Inert atmosphere;99.46%
108-24-7

acetic anhydride

123-30-8

4-amino-phenol

103-90-2

4-acetaminophenol

Conditions
ConditionsYield
With sodium dodecyl-sulfate In water99%
With silica gel for 0.5h; Time; Milling;99%
With sulfuric acid supported on poly(4-vinylpyridine) (P4VP) In dichloromethane at 20℃; for 1.25h;98%
108-24-7

acetic anhydride

123-30-8

4-amino-phenol

2623-33-8

4-acetoxyacetanilide

Conditions
ConditionsYield
With silver trifluoromethanesulfonate at 60℃; for 0.05h; neat (no solvent);99%
With 2,3-dihydro-5,7-bismethyl-1,4-diazepine monohydroperchlorate In neat (no solvent) at 40℃; for 1h;99%
With pyridine at 100℃;90%
123-30-8

4-amino-phenol

532-55-8

Benzoyl isothiocyanate

5461-34-7

N1-Benzoyl-N2-<4-hydroxyphenyl>thiourea

Conditions
ConditionsYield
In acetone for 0.5h; Heating;99%
In acetone at 20℃; for 1h; Sonication;91%
In acetone Ambient temperature;71%
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  • P-Aminophenol(PAP) CAS#123-30-8

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    123-30-8

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  • High purity 123-30-8 4-Aminophenol

  • Casno:

    123-30-8

    High purity 123-30-8 4-Aminophenol

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    Items Standard Result Assay (Ursolic acid) 98%min 98.22% ----------------------------------------------------------------

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    Chemical Name: 4-Aminophenol Synonyms: C.I. 76550; C.I. Oxidation Base 6; P-Aminophenol; 1-amino-4-hydroxybenzene; p-hydroxy-aniline CAS No.: 123-30-8 Molecular Formula: NH2C6H4OH Properties: White or Creamy-White crystal , soluble in alcoh

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    Aminophenol, also known hydroxy-aniline, amino hydroxy benzene, have three kind of isomers, namely o-aminophenol, m-aminophenol, and p-aminophenol (4-amino-phenol). In1874, Baeyer et al had first successfully obtained aminophenol. Owing to the

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    Min.Order: 0 Metric Ton

    FOB Price:  USD $ 0.0-0.0/Metric Ton

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  • 4-Aminophenol

  • Casno:

    123-30-8

    4-Aminophenol

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Consensus Reports

Related aminophenols  2-Aminophenol 3-Aminophenol
Related compounds     Aniline Phenol

Specification

The 4-Aminophenol, with the CAS registry number 123-30-8, is also known as 4-Amino-1-hydroxybenzene; 4-Hydroxyaniline.It belongs to the product categories of Metabolites & Impurities;Building Blocks;C6 to C8;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds;Phenols. This chemical's molecular formula is C6H7NO and molecular weight is 109.13. Its EINECS number is 204-616-2. What's more,Its systematic name is 4-Aminophenol. 4-Aminophenol may discolor on exposure to air and light.. It is not compatible with strong oxidizing agents, acids, bases, acid chlorides, acid anhydrides, chloroformates, and you must not take it with incompatible materials, light, exposure to a. And also prevent it to broken down into hazardous decomposition products: Nitrogen oxides, carbon monoxide, carbon dioxide.

Physical properties about 4-Aminophenol are: (1)ACD/LogP: 0.013; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -0.20; (4)ACD/LogD (pH 7.4): 0.01; (5)ACD/BCF (pH 5.5): 1.00; (6)ACD/BCF (pH 7.4): 1.00; (7)ACD/KOC (pH 5.5): 14.99; (8)ACD/KOC (pH 7.4): 23.99; (9)#H bond acceptors: 2; (10)#H bond donors: 3; (11)#Freely Rotating Bonds: 2; (12)Index of Refraction: 1.637; (13)Molar Refractivity: 32.371 cm3; (14)Molar Volume: 90.144 cm3; (15)Polarizability: 12.833 10-24cm3 ; (16)Surface Tension: 57.4010009765625 dyne/cm; (17)Density: 1.211 g/cm3; (18)Flash Point: 124.34 °C; (19)Enthalpy of Vaporization: 54.173 kJ/mol; (20)Boiling Point: 281.984 °C at 760 mmHg; (21)Vapour Pressure: 0.0020000000949949 mmHg at 25°C.

The 4-Aminophenol is Limited evidence of a carcinogenic effect ,harmful by inhalation and if swallowed and Possible risk of irreversible effects.When you use it,wear suitable protective clothing and gloves.After contact with skin, wash immediately with plenty of water (to be specified by the manufacturer) .The 4-Aminophenol is very Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment.Avoid release to the environment. Refer to special instructions safety data sheet,And this material and/or its container must be disposed of as hazardous waste.

You can still convert the following datas into molecular structure:
(1)SMILES:c1cc(ccc1N)O;
(2)Std. InChI:InChI=1S/C6H7NO/c7-5-1-3-6(8)4-2-5/h1-4,8H,7H2;
(3)Std. InChIKey:PLIKAWJENQZMHA-UHFFFAOYSA-N.

The toxicity data of 4-Aminophenol as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
bird - wild LD50 oral 56200ug/kg (56.2mg/kg)   Archives of Environmental Contamination and Toxicology. Vol. 12, Pg. 355, 1983.
cat LDLo subcutaneous 37mg/kg (37mg/kg)   Archiv fuer Experimentelle Pathologie und Pharmakologie. Vol. 72, Pg. 241, 1913.
cat LDLo subcutaneous 37mg/kg (37mg/kg) BLOOD: METHEMOGLOBINEMIA-CARBOXYHEMOGLOBIN

LUNGS, THORAX, OR RESPIRATION: CYANOSIS
Archiv fuer Experimentelle Pathologie und Pharmakologie. Vol. 72, Pg. 241, 1913.
guinea pig LDLo subcutaneous 1500mg/kg (1500mg/kg)   Archiv fuer Experimentelle Pathologie und Pharmakologie. Vol. 35, Pg. 401, 1895.
mammal (species unspecified) LD50 oral 1530mg/kg (1530mg/kg)   Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 45(10), Pg. 16, 1980.
mammal (species unspecified) LD50 skin 6400mg/kg (6400mg/kg)   Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 45(10), Pg. 16, 1980.
mammal (species unspecified) LD50 unreported 563mg/kg (563mg/kg)   Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 48(9), Pg. 19, 1983.
mouse LD50 unreported 750mg/kg (750mg/kg)   Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 50(3), Pg. 4, 1985.
mouse LDLo intraperitoneal 100mg/kg (100mg/kg)   Revue Belge de Pathologie et de Medecine Experimentale. Vol. 22, Pg. 1, 1952.
mouse LDLo subcutaneous 470mg/kg (470mg/kg)   Naunyn-Schmiedeberg's Archiv fuer Experimentelle Pathologie und Pharmakologie. Vol. 188, Pg. 130, 1938.
rabbit LD50 oral 10gm/kg (10000mg/kg)   Nippon Yakurigaku Zasshi. Japanese Journal of Pharmacology. Vol. 52, Pg. 215, 1956.
rabbit LD50 skin > 10gm/kg (10000mg/kg)   BIOFAX Industrial Bio-Test Laboratories, Inc., Data Sheets. Vol. 29-4/1973,
rat LC50 inhalation > 5mg/m3/1H (5mg/m3)   BIOFAX Industrial Bio-Test Laboratories, Inc., Data Sheets. Vol. 29-4/1973,
rat LD50 intraperitoneal 465mg/kg (465mg/kg) BLOOD: METHEMOGLOBINEMIA-CARBOXYHEMOGLOBIN Journal of Pharmacology and Experimental Therapeutics. Vol. 80, Pg. 31, 1944.
rat LD50 oral 375mg/kg (375mg/kg)   BIOFAX Industrial Bio-Test Laboratories, Inc., Data Sheets. Vol. 29-4/1973,
rat LD50 oral 375mg/kg (375mg/kg) LUNGS, THORAX, OR RESPIRATION: CYANOSIS

BEHAVIORAL: MUSCLE WEAKNESS
BIOFAX Industrial Bio-Test Laboratories, Inc., Data Sheets. Vol. 29-4/1973,
rat LD50 unreported 675mg/kg (675mg/kg)   Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 50(3), Pg. 4, 1985.