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2,4-Diaminophenol

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Name

2,4-Diaminophenol

EINECS N/A
CAS No. 95-86-3 Density 1.343g/cm3
PSA 72.27000 LogP 1.71900
Solubility N/A Melting Point 79°C (rough estimate)
Formula C6H8 N2 O Boiling Point 347.4°Cat760mmHg
Molecular Weight 124.142 Flash Point 163.9°C
Transport Information N/A Appearance N/A
Safety Poison by intraperitoneal route. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx. See also AMINES and PHENOL. Risk Codes N/A
Molecular Structure Molecular Structure of 95-86-3 (2,4-diaminophenol) Hazard Symbols N/A
Synonyms

2,4-Diaminophenol;4-Hydroxy-1,3-benzenediamine

Article Data 80

2,4-Diaminophenol Synthetic route

51-28-5

2,4-Dinitrophenol

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%
99-65-0

meta-dinitrobenzene

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;
67329-17-3

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

A

95-86-3

2,4-diaminophenol

B

121-57-3

4-aminobenzene sulfonic acid

Conditions
ConditionsYield
bei der Reduktion;
bei der Reduktion;
99-09-2

3-nitro-aniline

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

95-86-3

2,4-diaminophenol

Conditions
ConditionsYield
With sodium sulfite
7664-93-9

sulfuric acid

99-09-2

3-nitro-aniline

aluminium

aluminium

95-86-3

2,4-diaminophenol

51-28-5

2,4-Dinitrophenol

7664-93-9

sulfuric acid

95-86-3

2,4-diaminophenol

Conditions
ConditionsYield
at 85 - 90℃; Electrolysis;
51-28-5

2,4-Dinitrophenol

iodophosphorus

iodophosphorus

95-86-3

2,4-diaminophenol

51-28-5

2,4-Dinitrophenol

hydrogen

hydrogen

nickel

nickel

95-86-3

2,4-diaminophenol

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

meta-dinitrobenzene

7664-93-9

sulfuric acid

platinum cathode

platinum cathode

95-86-3

2,4-diaminophenol

Conditions
ConditionsYield
durch elektrolytische Reduktion;
durch elektrolytische Reduktion;

2,4-Diaminophenol Chemical Properties

Empirical Formula: C6H8N2O
Molecular Weight: 124.1405 g/mol
EINECS: 202-459-4 
Index of Refraction: 1.722
Density: 1.343 g/cm3
Flash Point: 163.9 °C
Enthalpy of Vaporization: 61.51 kJ/mol
Boiling Point: 347.4 °C at 760 mmHg
Vapour Pressure: 2.68E-05 mmHg at 25 °C
Structure of 2,4-Diaminophenol (CAS NO.95-86-3):
               
IUPAC Name: 2,4-Diaminophenol

2,4-Diaminophenol Uses

Its dihydrogen chloride salt is used as a photographic developer. As amidol ages 2,4-Diaminophenol (CAS NO.95-86-3) changes color to a dark red-brown. Developing dishes and equipment used to prepare amidol solutions are also frequently stained brown, a stain that is very persistent.

2,4-Diaminophenol Toxicity Data With Reference

1.    

mma-sat 10 µg/plate

    BCPCA6    Biochemical Pharmacology. 26 (1977),729.
2.    

ipr-mus LDLo:50 mg/kg

    RBPMAZ    Revue Belge de Pathologie et de Medecine Experimentale. 22 (1952),1.

2,4-Diaminophenol Safety Profile

Poison by intraperitoneal route. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx. See also AMINES and PHENOL.

2,4-Diaminophenol Specification

 2,4-Diaminophenol ,its cas register number is 95-86-3. It also can be called Amidol ; and Phenol, 2,4-diamino- . 2,4-Diaminophenol (CAS NO.95-86-3) was introduced as a developing agent for photographic papers in 1892, and is unusual amongst developers as it works most effectively in slightly acid conditions rather than the strongly alkaline conditions required for most other developers.

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