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95-86-3 Usage

Uses

Used in dye manufacture, in hair and fur dyeing, and in tests for formaldehyde and ammonia.

Check Digit Verification of cas no

The CAS Registry Mumber 95-86-3 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 95-86:
(4*9)+(3*5)+(2*8)+(1*6)=73
73 % 10 = 3
So 95-86-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H8N2O/c7-4-1-2-6(9)5(8)3-4/h1-3,9H,7-8H2

95-86-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-Diaminophenol

1.2 Other means of identification

Product number -
Other names 2,4-diaminophenol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:95-86-3 SDS

95-86-3Synthetic route

2,4-Dinitrophenol
51-28-5

2,4-Dinitrophenol

2,4-diaminophenol
95-86-3

2,4-diaminophenol

Conditions
ConditionsYield
With sodium tetrahydroborate; pyrographite In tetrahydrofuran; water at 50 - 60℃; for 5h;97%
With sodium tetrahydroborate In ethanol; water at 45℃; for 0.0833333h;96%
Stage #1: 2,4-Dinitrophenol With palladium on activated charcoal In methanol at 20℃; for 0.0833333h; Autoclave; Inert atmosphere;
Stage #2: With hydrogen In methanol at 65℃; under 3600.36 - 6375.64 Torr; for 1.5h; Pressure; Temperature; Autoclave;
96.16%
meta-dinitrobenzene
99-65-0

meta-dinitrobenzene

2,4-diaminophenol
95-86-3

2,4-diaminophenol

Conditions
ConditionsYield
With sulfuric acid; mercury(II) sulfate Electrolysis;
With cerium (IV)-sulfate; sulfuric acid at 90 - 95℃; Electrolysis;
With sulfuric acid bei der elektrolytischen Reduktion;
With sulfuric acid bei der elektrolytischen Reduktion;
2-nitro-4-(4'-sulfophenylazo)-phenol
67329-17-3

2-nitro-4-(4'-sulfophenylazo)-phenol

A

2,4-diaminophenol
95-86-3

2,4-diaminophenol

B

4-aminobenzene sulfonic acid
121-57-3

4-aminobenzene sulfonic acid

Conditions
ConditionsYield
bei der Reduktion;
bei der Reduktion;
3-nitro-aniline
99-09-2

3-nitro-aniline

2,4-diaminophenol
95-86-3

2,4-diaminophenol

Conditions
ConditionsYield
With sulfuric acid Electrolysis;
With sulfuric acid bei der elektrolytischen Reduktion;
With oxalic acid; aluminium
2.4-diamino-phenol hydrochloride

2.4-diamino-phenol hydrochloride

2,4-diaminophenol
95-86-3

2,4-diaminophenol

Conditions
ConditionsYield
With sodium sulfite
sulfuric acid
7664-93-9

sulfuric acid

3-nitro-aniline
99-09-2

3-nitro-aniline

aluminium

aluminium

2,4-diaminophenol
95-86-3

2,4-diaminophenol

2,4-Dinitrophenol
51-28-5

2,4-Dinitrophenol

sulfuric acid
7664-93-9

sulfuric acid

2,4-diaminophenol
95-86-3

2,4-diaminophenol

Conditions
ConditionsYield
at 85 - 90℃; Electrolysis;
2,4-Dinitrophenol
51-28-5

2,4-Dinitrophenol

water
7732-18-5

water

iodophosphorus

iodophosphorus

2,4-diaminophenol
95-86-3

2,4-diaminophenol

2,4-Dinitrophenol
51-28-5

2,4-Dinitrophenol

water
7732-18-5

water

hydrogen

hydrogen

nickel

nickel

2,4-diaminophenol
95-86-3

2,4-diaminophenol

Conditions
ConditionsYield
at 40 - 50℃; under 6080 - 7600 Torr;
meta-dinitrobenzene
99-65-0

meta-dinitrobenzene

sulfuric acid
7664-93-9

sulfuric acid

platinum cathode

platinum cathode

2,4-diaminophenol
95-86-3

2,4-diaminophenol

Conditions
ConditionsYield
durch elektrolytische Reduktion;
durch elektrolytische Reduktion;
hydrogenchloride
7647-01-0

hydrogenchloride

2,4-Dinitrophenol
51-28-5

2,4-Dinitrophenol

tin

tin

2,4-diaminophenol
95-86-3

2,4-diaminophenol

meta-dinitrobenzene
99-65-0

meta-dinitrobenzene

sulfuric acid
7664-93-9

sulfuric acid

copper-cathodes

copper-cathodes

A

m-phenylenediamine
108-45-2

m-phenylenediamine

B

2,4-diaminophenol
95-86-3

2,4-diaminophenol

Conditions
ConditionsYield
Electrolysis;
meta-dinitrobenzene
99-65-0

meta-dinitrobenzene

sulfuric acid
7664-93-9

sulfuric acid

monel metal-cathodes

monel metal-cathodes

A

m-phenylenediamine
108-45-2

m-phenylenediamine

B

2,4-diaminophenol
95-86-3

2,4-diaminophenol

Conditions
ConditionsYield
Electrolysis;
hydrogenchloride
7647-01-0

hydrogenchloride

2-(4-bromo-phenylazo)-4-nitro-phenol
138507-63-8

2-(4-bromo-phenylazo)-4-nitro-phenol

tin dichloride

tin dichloride

A

2,4-diaminophenol
95-86-3

2,4-diaminophenol

B

4-bromo-aniline
106-40-1

4-bromo-aniline

hydrogenchloride
7647-01-0

hydrogenchloride

(3,5-bis-acetylamino-2-hydroxy-phenyl)-arsonic acid
861080-67-3

(3,5-bis-acetylamino-2-hydroxy-phenyl)-arsonic acid

2,4-diaminophenol
95-86-3

2,4-diaminophenol

hydrogenchloride
7647-01-0

hydrogenchloride

[4-Nitro-benzol-(1 azo 2)-(4-amino-phenol)

[4-Nitro-benzol-(1 azo 2)-(4-amino-phenol)

tin chloride

tin chloride

2,4-diaminophenol
95-86-3

2,4-diaminophenol

sulfuric acid
7664-93-9

sulfuric acid

acetic acid-(2,4-bis-phenylazo-phenyl ester)

acetic acid-(2,4-bis-phenylazo-phenyl ester)

zinc

zinc

A

2,4-diaminophenol
95-86-3

2,4-diaminophenol

B

aniline
62-53-3

aniline

C

Acetanilid
103-84-4

Acetanilid

hydrogenchloride
7647-01-0

hydrogenchloride

2-(4-bromo-phenylazo)-4-(phenyl-ONN-azoxy)-phenol

2-(4-bromo-phenylazo)-4-(phenyl-ONN-azoxy)-phenol

tin

tin

A

2,4-diaminophenol
95-86-3

2,4-diaminophenol

B

aniline
62-53-3

aniline

C

4-bromo-aniline
106-40-1

4-bromo-aniline

2,4-dinitrotoluene
121-14-2

2,4-dinitrotoluene

A

4-methylbenzene-1,3-diamine
95-80-7

4-methylbenzene-1,3-diamine

B

2,4-diaminophenol
95-86-3

2,4-diaminophenol

C

4-Methyl-3-nitroanilin
119-32-4

4-Methyl-3-nitroanilin

D

2-methyl-5-nitroaniline
99-55-8

2-methyl-5-nitroaniline

Conditions
ConditionsYield
With sodium hydroxide; sodium tetrahydroborate; cetyltrimethylammonim bromide; sodium chloride In water for 0.333333h; Kinetics; Further Variations:; Reagents; time; UV-irradiation;
4-amino-2-nitrophenol
119-34-6

4-amino-2-nitrophenol

2,4-diaminophenol
95-86-3

2,4-diaminophenol

Conditions
ConditionsYield
With hydrogen In ethanol at 20℃; under 750.075 Torr; for 4h; Schlenk technique;98 %Chromat.
2-hydroxy-5-nitroaniline
99-57-0

2-hydroxy-5-nitroaniline

2,4-diaminophenol
95-86-3

2,4-diaminophenol

Conditions
ConditionsYield
With sodium tetrahydroborate Kinetics;
With hydrogen In ethanol at 30℃; for 1.66667h; Autoclave;
With sodium tetrahydroborate In water at 20℃; for 0.05h;
With sodium tetrahydroborate In water at 20℃; for 0.00138889h; Kinetics;
With sodium tetrahydroborate In water Catalytic behavior;
4-chlorophenylacetic Acid
1878-66-6

4-chlorophenylacetic Acid

2,4-diaminophenol
95-86-3

2,4-diaminophenol

2-(4-chlorobenzyl)-5-aminobenzoxazole
381200-35-7

2-(4-chlorobenzyl)-5-aminobenzoxazole

Conditions
ConditionsYield
With PPA at 195 - 198℃; for 1.5h;100%
2,4 dichlorobenzoic acid
50-84-0

2,4 dichlorobenzoic acid

2,4-diaminophenol
95-86-3

2,4-diaminophenol

2-(2,4-dichlorophenyl)benzo[d]oxazol-5-amine
293737-83-4

2-(2,4-dichlorophenyl)benzo[d]oxazol-5-amine

Conditions
ConditionsYield
With polyphosphoric acid at 110 - 120℃; for 16h;95%
2,4-diaminophenol
95-86-3

2,4-diaminophenol

para-chlorobenzoic acid
74-11-3

para-chlorobenzoic acid

2-(4-chlorophenyl)benzo[d]oxazol-5-amine
54995-51-6

2-(4-chlorophenyl)benzo[d]oxazol-5-amine

Conditions
ConditionsYield
With polyphosphoric acid Heating;95%
With polyphosphoric acid at 170℃;
With polyphosphoric acid at 170℃; for 12h;
2,4-diaminophenol
95-86-3

2,4-diaminophenol

methyl iodide
74-88-4

methyl iodide

2,4-Diaminoanisole
615-05-4

2,4-Diaminoanisole

Conditions
ConditionsYield
With methyl tributylmethylammonium carbonate; sodium hydroxide at 35 - 55℃; for 7h; Temperature; Inert atmosphere;88.8%
2,3-Dichloro-1,4-naphthoquinone
117-80-6

2,3-Dichloro-1,4-naphthoquinone

2,4-diaminophenol
95-86-3

2,4-diaminophenol

10-amino-6-chlorobenzo[a]phenoxazin-5-one

10-amino-6-chlorobenzo[a]phenoxazin-5-one

Conditions
ConditionsYield
Stage #1: 2,4-diaminophenol With sodium carbonate In N,N-dimethyl-formamide; benzene for 0.5h; Reflux;
Stage #2: 2,3-Dichloro-1,4-naphthoquinone In N,N-dimethyl-formamide; benzene for 5h; Reflux;
85%
Stage #1: 2,4-diaminophenol With potassium hydroxide In methanol at 20℃; for 0.5h;
Stage #2: 2,3-Dichloro-1,4-naphthoquinone In methanol at 20℃; for 6h;
41%
2,3-dichlorbenzoic acid
50-45-3

2,3-dichlorbenzoic acid

2,4-diaminophenol
95-86-3

2,4-diaminophenol

2-(2,3-dichlorophenyl)benzo[d]oxazol-5-amine
339197-79-4

2-(2,3-dichlorophenyl)benzo[d]oxazol-5-amine

Conditions
ConditionsYield
With polyphosphoric acid at 110 - 120℃; for 16h;83%
1,4-cyclohexanedione-2,5-di-carboxylic acid methyl ester
27712-87-4

1,4-cyclohexanedione-2,5-di-carboxylic acid methyl ester

2,4-diaminophenol
95-86-3

2,4-diaminophenol

dimethyl 2,5-bis-(3-amino-4-hydroxylanilino)-1,4-cyclohexadiene-1,4-dicarboxylate

dimethyl 2,5-bis-(3-amino-4-hydroxylanilino)-1,4-cyclohexadiene-1,4-dicarboxylate

Conditions
ConditionsYield
With 1-ethyl-piperidine In various solvent(s) at 105℃; for 7h;80%
1H-indene-1,3(2H)-dione
606-23-5

1H-indene-1,3(2H)-dione

2,4-diaminophenol
95-86-3

2,4-diaminophenol

C24H16N2O3
1352954-41-6

C24H16N2O3

Conditions
ConditionsYield
In ethanol for 8h; Reflux;77%
2,4-diaminophenol
95-86-3

2,4-diaminophenol

diphenyl acetylene
501-65-5

diphenyl acetylene

2,3-diphenyl-4H-benzo[b][1,4]oxazin-6-amine

2,3-diphenyl-4H-benzo[b][1,4]oxazin-6-amine

Conditions
ConditionsYield
With [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; copper diacetate In N,N-dimethyl-formamide at 100℃; for 4h;77%
phenylacetic acid
103-82-2

phenylacetic acid

2,4-diaminophenol
95-86-3

2,4-diaminophenol

2-benzyl-5-aminobenzoxazole
313527-44-5

2-benzyl-5-aminobenzoxazole

Conditions
ConditionsYield
With PPA at 150 - 160℃; for 2.5h;66%
2,4-diaminophenol
95-86-3

2,4-diaminophenol

2,5-dichlorobenzoic acid
50-79-3

2,5-dichlorobenzoic acid

2-(2,5-dichlorophenyl)benzo[d]oxazol-5-amine
293737-84-5

2-(2,5-dichlorophenyl)benzo[d]oxazol-5-amine

Conditions
ConditionsYield
With polyphosphoric acid at 110 - 120℃; for 16h;66%
2,4-diaminophenol
95-86-3

2,4-diaminophenol

methyl chloroformate
79-22-1

methyl chloroformate

4-hydroxy-1,3-bis(methoxycarbonylamino)benzene

4-hydroxy-1,3-bis(methoxycarbonylamino)benzene

Conditions
ConditionsYield
With pyridine at 20℃;61%
cyclohexanepropionic acid
701-97-3

cyclohexanepropionic acid

2,4-diaminophenol
95-86-3

2,4-diaminophenol

2-(2-Cyclohexyl-ethyl)-benzooxazol-5-ylamine
144037-45-6

2-(2-Cyclohexyl-ethyl)-benzooxazol-5-ylamine

Conditions
ConditionsYield
With PPA; Polyphosphoric acid (PPA) at 180℃; for 3h;59%
3-methoxy-2-hydroxybenzaldehyde
148-53-8

3-methoxy-2-hydroxybenzaldehyde

2,4-diaminophenol
95-86-3

2,4-diaminophenol

6,6'-((4-hydroxy-1,3-phenylene)bis(azanylylidene))bis(methanylylidene)bis(2-methoxyphenol)

6,6'-((4-hydroxy-1,3-phenylene)bis(azanylylidene))bis(methanylylidene)bis(2-methoxyphenol)

Conditions
ConditionsYield
In ethanol for 5h; Reflux;58%
4-(diethylamino)benzoic acid
5429-28-7

4-(diethylamino)benzoic acid

2,4-diaminophenol
95-86-3

2,4-diaminophenol

2-(4-(diethylamino)phenyl)benzo[d]oxazol-5-amine

2-(4-(diethylamino)phenyl)benzo[d]oxazol-5-amine

Conditions
ConditionsYield
With polyphosphoric acid Heating;57%
2,4-diaminophenol
95-86-3

2,4-diaminophenol

4-trifluoromethoxybenzoic acid
330-12-1

4-trifluoromethoxybenzoic acid

2-(4-(trifluoromethoxy)phenyl)benzo[d]oxazol-5-amine

2-(4-(trifluoromethoxy)phenyl)benzo[d]oxazol-5-amine

Conditions
ConditionsYield
With polyphosphoric acid Heating;53%
4-Fluorobenzoic acid
456-22-4

4-Fluorobenzoic acid

2,4-diaminophenol
95-86-3

2,4-diaminophenol

2-(4-fluorophenyl)benzo[d]oxazol-5-amine
116248-10-3

2-(4-fluorophenyl)benzo[d]oxazol-5-amine

Conditions
ConditionsYield
With polyphosphoric acid at 190℃; for 16h;52%
2,4-diaminophenol
95-86-3

2,4-diaminophenol

p-Fluorophenylacetic acid
405-50-5

p-Fluorophenylacetic acid

2-(4-fluorobenzyl)-5-aminobenzoxazole
959958-63-5

2-(4-fluorobenzyl)-5-aminobenzoxazole

Conditions
ConditionsYield
With PPA at 100℃; for 2.5h;45%
4-tolylacetic acid
622-47-9

4-tolylacetic acid

2,4-diaminophenol
95-86-3

2,4-diaminophenol

2-(4-methylbenzyl)-5-aminobenzoxazole
959958-62-4

2-(4-methylbenzyl)-5-aminobenzoxazole

Conditions
ConditionsYield
With PPA at 100℃; for 2.5h;41%
4-Aminosalicylic acid
65-49-6

4-Aminosalicylic acid

2,4-diaminophenol
95-86-3

2,4-diaminophenol

5-amino-2-(2'-hydroxy-4'-aminophenyl)benzoxazole

5-amino-2-(2'-hydroxy-4'-aminophenyl)benzoxazole

Conditions
ConditionsYield
With polyphosphoric acid Heating;37%
2,4-diaminophenol
95-86-3

2,4-diaminophenol

ortho-chlorobenzoic acid
118-91-2

ortho-chlorobenzoic acid

2-(2-chlorophenyl)benzo[d]oxazol-5-amine

2-(2-chlorophenyl)benzo[d]oxazol-5-amine

Conditions
ConditionsYield
With polyphosphoric acid Heating;8%
With polyphosphoric acid at 170℃;
With polyphosphoric acid at 170℃; for 12h;
acetic anhydride
108-24-7

acetic anhydride

2,4-diaminophenol
95-86-3

2,4-diaminophenol

N-(5-acetylamino-2-hydroxyphenyl)-acetamide
38847-62-0

N-(5-acetylamino-2-hydroxyphenyl)-acetamide

Conditions
ConditionsYield
With water
salicylaldehyde
90-02-8

salicylaldehyde

2,4-diaminophenol
95-86-3

2,4-diaminophenol

2,4-bis-salicylidenamino-phenol
4588-99-2

2,4-bis-salicylidenamino-phenol

Conditions
ConditionsYield
With ethanol
benzoyl chloride
98-88-4

benzoyl chloride

2,4-diaminophenol
95-86-3

2,4-diaminophenol

2,4-bis-benzoylamino-1-benzoyloxy-benzene
30716-60-0

2,4-bis-benzoylamino-1-benzoyloxy-benzene

Conditions
ConditionsYield
With alkali
benzoyl chloride
98-88-4

benzoyl chloride

2,4-diaminophenol
95-86-3

2,4-diaminophenol

N,N'-(4-hydroxy-m-phenylene)-bis-benzamide
174187-15-6

N,N'-(4-hydroxy-m-phenylene)-bis-benzamide

Conditions
ConditionsYield
With sodium sulfite; magnesium carbonate
CYANAMID
420-04-2

CYANAMID

2,4-diaminophenol
95-86-3

2,4-diaminophenol

N,N'''-(4-hydroxy-m-phenylene)-di-guanidine
4405-09-8

N,N'''-(4-hydroxy-m-phenylene)-di-guanidine

4-Sulfamoyl-benzenediazonium
14289-29-3

4-Sulfamoyl-benzenediazonium

2,4-diaminophenol
95-86-3

2,4-diaminophenol

4-(2,4-diamino-5-hydroxy-phenylazo)-benzenesulfonic acid amide

4-(2,4-diamino-5-hydroxy-phenylazo)-benzenesulfonic acid amide

95-86-3Relevant articles and documents

Synthesis of magnetic silver cyclodextrin nanocomposite as catalyst for reduction of nitro aromatics and organic dyes

Nariya, Pratik,Das, Manita,Shukla, Falguni,Thakore, Sonal

, (2020)

Nanocomposites decorated with metallic nanoparticles in their matrix are important class of heterogeneous catalyst with high catalytic activity. Functionalized polymers are low cost materials which offer excellent supports for catalysts to render stability to metallic nanoparticles. Herein we report synthesis of Silver nanocomposite using β-cyclodextrin (b-CD) maleic anhydride crosslinked polymer anchored on the surface of magnetic nanoparticles. The nanocomposite was characterized using sophisticated analytical techniques and its role as a catalyst for reduction of nitroaromatics and organic dyes was investigated. This catalytic system exhibited comparatively lower Ea value of 18 kJ mol?1 and followed pseudo first order kinetics. Simultaneous reduction of 4-Nitrophenol and Methylene Blue could be achieved in a time interval of 7 minutes. Being magnetically separable, the catalyst exhibited high recycling efficiency (up to 5 cycles) and ease of operation under mild conditions.

Synthesis of graphene quantum dots stabilized bimetallic AgRh nanoparticles and their applications

Li, Ning,Chen, Weifeng,Shen,Chen, Shaona,Liu

, (2019)

The design and synthesis of highly efficient and ultrafine bimetallic nanoparticles catalysts is challenging. Here we report the synthesis of AgRh bimetallic nanoparticles (AgRh BNPs) stabilized by graphene quantum dots (GQDs) and their exceptional catalytic activities in the reduction of 4-nitrophenol, 2,4-dinitrophenol and 4-nitrobenzene diazonium tetrafluoroborate and generation of hydroxyl radicals. Construction of AgRh BNPs nanocomposites is accomplished by mixing of GQDs and sodium borohydride, followed by the addition of simple commercial Ag and Rh salt at 0 °C in water. Among them, AgRh BNPs 4 exhibits excellent catalytic performance owing to a positive synergistic effects between the Ag and Rh atoms on GQDs, and its catalytic activity is better than those of both monometallic counterparts.

-

Bradt

, p. 2711,2713 (1930)

-

Chemoselective reduction of nitro and nitrile compounds using an Fe3O4-MWCNTs?PEI-Ag nanocomposite as a reusable catalyst

Ansari, Sara,Khorshidi, Alireza,Shariati, Shahab

, p. 3554 - 3565 (2020/02/04)

Multi-walled carbon nanotubes (MWNTs) were modified with carboxylic acid functional groups (MWCNTs-(COOH)n) prior to decoration with Fe3O4 nanoparticles. A further modification step by polyethyleneimine (PEI) resulted in Fe3O4-MWCNTs?PEI which provided a suitable platform for coordination and in situ reduction of silver ions to obtain an Fe3O4-MWCNTs?PEI-Ag nanocomposite with highly dispersed Ag nanoparticles. The Fe3O4-MWCNTs?PEI-Ag hybrid material was characterized by various techniques such as Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), transmission electron microscopy (TEM), vibrating sample magnetometry (VSM), X-ray photoelectron spectroscopy (XPS) and thermogravimetric analysis (TGA), and was used as an efficient catalyst for chemoselective reduction of nitroaromatic and nitrile compounds to their corresponding amines in aqueous solution at ambient temperature. Nitrofurazone, a cytotoxic antibiotic, as a non-aromatic example was also reduced selectively at the nitro group without reduction of the other functionalities in the presence of Fe3O4-MWCNTs?PEI-Ag. The catalyst was magnetically recoverable and maintained its activity for at least six cycles without considerable loss of efficiency.

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