| Weight | 124.143 g/mol |
|---|---|
| Formula | C6H8N2O |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2,4-DIAMINOPHENOL (95-86-3)
amidol · 2,4-diaminophenol hydrochloride · 2,4-diaminophenol dihydrochloride
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- The electrochemical copolymerization of aniline with 2,4-diaminophenol and the electric properties of the resulting copolymer (Electrochimica Acta, 2009)
- Method of producing 7-(substituted)-9-[(substituted glycyl)-amidol]-6-demethyl-6-deoxytetra-cyclines (1992)
- Synthesis and properties of aromatic polyamidebenzoxazoles from trimethylsilylsubstituted 2,4diaminophenol and aromatic dicarboxylic acid chlorides (Journal of Polymer Science Part A, 1991)
- Reagent-injection spectrophotometric determination of citric acid in beverages and pharmaceutical formulations based on its inhibitory effect on the iron(III) catalytic oxidation of 2,4-diaminophenol by hydrogen peroxide (Analytica Chimica Acta, 2001)
- Nanostructured poly(aniline-co-2,4-diaminophenol) synthesized via chemical copolymerization and the properties of the resulting copolymer (Synthetic Metals, 2009)
- Synthesis and properties of hydroxyl-containing aromatic polyimides from trimethylsilylated 2,4-diaminophenol and aromatic tetracarboxylic dianhydrides (Journal of Polymer Science Part A, 1993)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - amidol
- 2,4-diaminophenol hydrochloride
- 2,4-diaminophenol dihydrochloride
-
SMILESC1=CC(=C(C=C1N)N)O
-
InChIKeyXIWMTQIUUWJNRP-UHFFFAOYSA-N
- Pubchem - 2,4-DIAMINOPHENOL
- Wikipedia - 2,4-diaminophenol
Amidol is a colorless crystalline compound with the molecular structure C6H3(NH2)2OH. It is a dihydrogen chloride salt and is used as a photographic developer. It was introduced as a developing agent for photographic papers in 1892.
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2,4-DIAMINOPHENOL
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