CAS 95-55-6
:2-Aminophenol
Description:
2-Aminophenol, with the CAS number 95-55-6, is an organic compound characterized by the presence of both an amino group (-NH2) and a hydroxyl group (-OH) attached to a benzene ring. It appears as a white to light brown crystalline solid and is soluble in water, alcohol, and ether, which enhances its utility in various applications. The compound exhibits a melting point that typically falls within a specific range, indicating its solid state under standard conditions. 2-Aminophenol is primarily used in the synthesis of dyes, pharmaceuticals, and as a developer in photographic processes. It also serves as an intermediate in the production of various chemical compounds. The presence of the amino and hydroxyl groups contributes to its reactivity, allowing it to participate in electrophilic substitution reactions. However, it is important to handle this compound with care, as it may pose health risks, including skin and respiratory irritation. Proper safety measures should be observed when working with 2-aminophenol in laboratory or industrial settings.
Formula:C6H7NO
InChI:InChI=1/C6H7NO/c7-5-3-1-2-4-6(5)8/h1-4,8H,7H2
InChI key:InChIKey=CDAWCLOXVUBKRW-UHFFFAOYSA-N
SMILES:NC1=C(O)C=CC=C1
Synonyms:- (2-Hydroxyphenyl)amine
- 1-Amino-2-hydroxybenzene
- 1-Hydroxy-2-aminobenzene
- 2-Amino Phenol
- 2-Amino-1-hydroxybenzene
- 2-Aminofenol
- 2-Aminophenyl alcohol
- 2-Hydroxyaniline
- 2-Hydroxybenzenamine
- BASF Ursol 3GA
- Benzofur GG
- Fouramine OP
- Nako Yellow 3GA
- Nsc 1534
- Nsc 226261
- O-Amino Phenol
- O-Aminophenol
- Ortho Amino Phenol
- Oxidation Base 17
- Paradone Olive Green B
- Pelagol 3GA
- Pelagol Grey GG
- Phenol, 2-amino-
- Phenol, o-amino-
- Rodol 2G
- Zoba 3GA
- o-Aminohydroxybenzene
- o-Hydroxyaniline
- o-Hydroxyphenylamine
- C.I. 76520
- C.I. Oxidation Base 17
- 2-Aminophenol
- LABOTEST-BB LTBB000484
- benzofurgg
- AKOS BBS-00004290
- OAP
- 2-Hydroxyaniline H
- 2-Hydroxyanaline
- Benzene, 1hydroxy-2-amine-
- 2-amino-pheno
- See more synonyms
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Found 12 products.
2-Aminophenol
CAS:Formula:C6H7NOPurity:>99.0%(GC)Color and Shape:White to Brown powder to crystalMolecular weight:109.132-Aminophenol, 99%
CAS:<p>2-Aminophenol is used to make dyes and pharmaceuticals. It is also used as a reagent for the synthesis of heterocyclic compounds. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy b</p>Formula:C6H7NOPurity:99%Color and Shape:Crystals or powder or crystalline powder, White to grey to brownMolecular weight:109.13MESALAZINE IMPURITY C CRS
CAS:<p>MESALAZINE IMPURITY C CRS</p>Formula:C6H7NOMolecular weight:109.12592-Aminophenol
CAS:Formula:C6H7NOPurity:≥ 98.0%Color and Shape:White to off-white, beige, grey or brown crystals or powderMolecular weight:109.13Mesalazine (Mesalamine) EP Impurity C
CAS:Formula:C6H7NOColor and Shape:Grey SolidMolecular weight:109.132-Aminophenol
CAS:<p>2-Aminophenol</p>Purity:99%Color and Shape:Brown PowderMolecular weight:109.13g/molMesalazine EP Impurity C
CAS:Controlled ProductFormula:C6H7NOColor and Shape:BeigeMolecular weight:109.132-Aminophenol
CAS:<p>Impurity Mesalazine EP Impurity C<br>Applications 2-Aminophenol is an isomer of 4-Aminophenol (A618920) and is used as a reagent for the synthesis of heterocyclic compounds and dyes.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Pan, E., et al.: Chem. Sci., 4, 482 (2013); Meek, A.R., et al.: Can. J. Chem., 90, 865 (2012); Kiorpelidous, E., et al.: Chem. Res. Toxicol., 25, 2054 (2012);<br></p>Formula:C6H7NOColor and Shape:BeigeMolecular weight:109.132-Aminophenol
CAS:<p>2-Aminophenol is a water soluble redox catalyst that is used in wastewater treatment. It has been shown to be a potent antimicrobial agent against bacteria, fungi, and viruses. 2-Aminophenol is active against the Gram-positive bacteria Staphylococcus aureus and Enterococcus faecalis. The mechanism of the reaction of 2-aminophenol with picolinic acid is believed to be due to intramolecular hydrogen bonding between nitrogen atoms (N) and amines (NH). The binding site for this reaction is not well understood, but it may involve an electrochemical mechanism such as constant pressure or electrochemical impedance spectroscopy. 2-Aminophenol also participates in electron transfer reactions involving NAD+/NADH or cytochrome c/cytochrome c oxidase.</p>Formula:C6H7NOPurity:Min. 98 Area-%Color and Shape:Brown White PowderMolecular weight:109.13 g/mol











