• Product Name2-Amino-4-chlorophenol
  • CasNo. 95-85-2
  • MFC6H6ClNO
  • MW143.573
  • Purity
  • Appearancebrown crystalline solid
  • Packing
  • Contact usInquiry

Product Details

CasNo: 95-85-2

MF: C6H6ClNO

Appearance: brown crystalline solid

Reputable Factory Supply Best Quality 95-85-2 In Stock

  • Molecular Formula:C6H6ClNO
  • Molecular Weight:143.573
  • Appearance/Colour:brown crystalline solid 
  • Melting Point:136-141 °C(lit.) 
  • Refractive Index:1.5618 (estimate) 
  • Boiling Point:276.8 °C at 760 mmHg 
  • PKA:9.31±0.18(Predicted) 
  • Flash Point:121.2 °C 
  • PSA:46.25000 
  • Density:1.406 g/cm3 
  • LogP:2.20900 

2-Amino-4-chlorophenol(Cas 95-85-2) Usage

Air & Water Reactions

5-Chloro-2-hydroxyaniline may be sensitive to prolonged exposure to air and/or light. Insoluble in water.

Reactivity Profile

5-Chloro-2-hydroxyaniline may react with strong oxidizing agents.

Health Hazard

Highly toxic, may be fatal if inhaled, swallowed or absorbed through skin. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.

Fire Hazard

Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Containers may explode when heated. Runoff may pollute waterways.

Safety Profile

A poison. Moderately toxic by ingestion. Mutation data reported. When heated to decomposition it emits very toxic fumes of Cland NOx. See also AROMATIC MINES and CHLORIDES.

Potential Exposure

Used as a chemical raw material, especially in dye manufacture

Shipping

UN2673 2-Amino-4-chlorophenol, Hazard Class: 6.1; Labels: 6.1-Poisonous materials

Incompatibilities

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides, iron, moisture and temperatures .43 C.

General Description

5-Chloro-2-hydroxyaniline is a light brown colored crystalline solid. 5-Chloro-2-hydroxyaniline may be toxic by ingestion. 5-Chloro-2-hydroxyaniline is insoluble in water. 5-Chloro-2-hydroxyaniline is used to make other chemicals.

InChI:InChI=1/C6H6ClNO/c7-4-1-2-6(9)5(8)3-4/h1-3,9H,8H2

95-85-2 Relevant articles

Kinetics of liquid-phase catalytic hydrogenation of 4-chioro-2-nitrophenol

Mukhopadhyay, Sudip,Gandi, Ganesh K.,Chandalia, Sampatraj B.

, p. 201 - 205 (1999)

Process parameters were studied to incre...

Kinetic study of alkaline induced hydrolysis of the skeletal muscle relaxant chlorzoxazone using ratio spectra first derivative spectrophotometry

Ellaithy,El-Ragehy,El-Ghobashy

, p. 337 - 342 (2003)

2-Amino-4-chlorophenol was found to be t...

Highly porous copper-supported magnetic nanocatalysts: made of volcanic pumice textured by cellulose and applied for the reduction of nitrobenzene derivatives

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Herein, a novel designed heterogeneous c...

Convenient conversion of hazardous nitrobenzene derivatives to aniline analogues by Ag nanoparticles, stabilized on a naturally magnetic pumice/chitosan substrate

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, p. 43670 - 43681 (2020/12/25)

Herein, silver nanoparticles (Ag NPs), a...

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Rahimi, Jamal,Taheri-Ledari, Reza,Niksefat, Maryam,Maleki, Ali

, (2019/11/02)

Herein, we present an organic–inorganic ...

Synthesis, docking, 3-D-qsar, and biological assays of novel indole derivatives targeting serotonin transporter, dopamine D2 receptor, and mao-a enzyme: In the pursuit for potential multitarget directed ligands

Alarcón-Espósito, Jazmín,Araya-Maturana, Ramiro,Cabezas, David,Cerda-Cavieres, Christopher,Chung, Hery,Iturriaga-Vásquez, Patricio,Mella-Raipán, Jaime,Ojeda-Gómez, Claudia,Pessoa-Mahana, Carlos D.,Pessoa-Mahana, Hernán,Quiroz, Gabriel,Reyes-Parada, Miguel,Rodríguez-Lavado, Julio,Saitz, Claudio

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A series of 27 compounds of general stru...

95-85-2 Process route

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Conditions
Conditions Yield
With trifluoroacetic acid; at 30 ℃; for 5.5h; Product distribution; Rate constant; Kinetics; ΔH(excit.), ΔG(excit.), ΔS(excit.);
 
p-chloro-o-nitrophenol
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Conditions
Conditions Yield
With hydrazine hydrate; In water; at 110 ℃; Sealed tube; Green chemistry;
99%
With hydrazine hydrate; In ethanol; at 70 ℃; for 0.133333h;
96%
With sodium tetrahydroborate; water; potassium carbonate; at 70 ℃; for 7h; pH=Ca. 8; Green chemistry;
96%
With hydrazine hydrate; In isopropyl alcohol; at 110 ℃; for 0.2h; chemoselective reaction; Catalytic behavior; Sealed tube;
94%
With hydrazine hydrate; In ethanol; at 70 ℃; for 0.116667h;
92%
With (phthalocyaninato)iron(II); diphenylsilane; In ethanol; at 100 ℃; for 24h; Reagent/catalyst;
86%
With tin(IV) chloride; pyrographite; hydrazine hydrate; In methanol; at 70 ℃; for 14h; Temperature; Reagent/catalyst; Large scale;
86.3%
With ethanol; palladium on activated charcoal; sodium hydroxide; silicon; at 20 ℃; for 72h; Schlenk technique;
86%
With copper(II) phthalocyanine; hydrazine hydrate; In ethylene glycol; at 120 ℃; for 2h; chemoselective reaction;
80%
With sulfur; aluminum oxide; sodium hydroxide; at 80 ℃; for 3h;
69%
p-chloro-o-nitrophenol; With sulfuric acid; In water; at 100 ℃; for 4.25h; pH=4.5;
With sodium carbonate; In water; at 100 ℃; for 1.25h; pH=7 - 12;
61%
With ammonium chloride; zinc; In ethanol; water; for 0.416667h;
48%
With sodium dithionite;
 
With nickel; Hydrogenation;
 
With sulfuric acid; at 70 ℃; durch elektrolytische Reduktion an einer Bleikathode;
 
With hydrogenchloride; iron;
 
With hydrogenchloride; tin;
 
With hydrazine hydrate; nickel; In ethanol;
 
With hydrogen; palladium on activated charcoal; In ethanol;
 
With hydrogen; platinum; 3-(2-hydroxyethyl)-1-methyl-1H-imidazol-3-ium tetrafluoroborate; at 89.84 ℃; for 2h; under 7500.75 Torr; Autoclave;
 
With C32H16FeN8*Fe(2+)*7H2O*O4S(2-); hydrazine hydrate; In ethanol; water; at 120 ℃; chemoselective reaction;
99 %Chromat.
With hydrogen; platinum on carbon; In methanol; for 1h; under 2844.39 Torr;
 
p-chloro-o-nitrophenol; With sulfuric acid; In water; at 100 ℃; for 2h; pH=4.5;
With sodium carbonate; In water; at 100 ℃; for 0.5h; pH=12;
 
With 5%-palladium/activated carbon; hydrogen; In methanol; at 100 ℃; for 5h; under 19001.3 Torr; Concentration; Pressure; Reagent/catalyst; Solvent; Temperature; Kinetics; Autoclave;
 
With iron; acetic acid; In water; for 0.75h; Reflux;
 
With hydrogen; In methanol; at 20 ℃; under 750.075 - 1500.15 Torr; Autoclave;
7.4 g
With iron; acetic acid; In ethanol; water;
 
With sodium tetrahydroborate; In water; at 20 ℃; for 0.0666667h; chemoselective reaction;
 
With hydrazine hydrate; In water; at 110 ℃; for 1h; Sealed tube;
 

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