CAS 100-65-2
:Benzenamine, N-hydroxy-
Description:
Benzenamine, N-hydroxy-, also known as N-hydroxyaniline, is an organic compound characterized by the presence of both an amino group (-NH2) and a hydroxyl group (-OH) attached to a benzene ring. This compound typically appears as a solid or liquid, depending on its purity and specific conditions. It is known for its role as an intermediate in the synthesis of various dyes, pharmaceuticals, and agrochemicals. The presence of the hydroxyl group enhances its reactivity, allowing it to participate in various chemical reactions, such as nitration and acylation. Benzenamine, N-hydroxy- is also recognized for its potential use in the production of antioxidants and stabilizers in polymer chemistry. 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 this substance in laboratory or industrial settings.
Formula:C6H7NO
InChI:InChI=1S/C6H7NO/c8-7-6-4-2-1-3-5-6/h1-5,7-8H
InChI key:InChIKey=CKRZKMFTZCFYGB-UHFFFAOYSA-N
SMILES:N(O)C1=CC=CC=C1
Synonyms:- Fenilhidroxilamina
- Hydroxyaminobenzene
- Hydroxylamine, N-phenyl-
- Hydroxylamine, β-phenyl-
- N-Hydroxyaniline
- N-Hydroxybenzenamine
- N-Phenylhydroxylamin
- N-Phenylhydroxylamine
- Nsc 223099
- Phenylhydroxyamine
- Phenylhydroxylamin
- Phenylhydroxylamine
- β-Phenylhydroxylamine
- CCRIS 5062
- Benzenamine, N-hydroxy-
- Benzenamine, N-hydroxy-
- NCI-C60093
- Benzene, hydroxylamino-
- Aniline, N-hydroxy-
- 4-15-00-00004 (Beilstein Handbook Reference)
- HSDB 2884
- See more synonyms
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Found 5 products.
Ref: IN-DA000071
1g41.00€5g110.00€10g171.00€25g302.00€250gTo inquire500gTo inquire100mg24.00€250mg25.00€N-Phenylhydroxylamine
CAS:<p>N-Phenylhydroxylamine</p>Formula:C6H7NOPurity:95%Color and Shape: light brown solidMolecular weight:109.13g/molN-Phenylhydroxylamine
CAS:<p>N-Phenylhydroxylamine is a chemical compound that is used in wastewater treatment. It is a hydrophobic compound that has been shown to irreversibly inhibit the nitrite reductase enzyme, which is responsible for converting nitrite ions into nitrate ions. This reaction mechanism was studied using in vitro assays with picolinic acid and nitrobenzene. N-Phenylhydroxylamine binds to the active site of the enzyme and blocks access by the substrate, preventing it from being converted into its product. The reaction can be reversed by adding hydrogen fluoride, which displaces the N-phenylhydroxylamine molecule from its binding site. N-Phenylhydroxylamine also binds to nitrogen atoms and participates in transfer reactions with other molecules, making it reactive and capable of reacting with other compounds. The sample preparation process should include separating N-phenylhydroxylamine from water samples after extraction because it will react with</p>Formula:C6H7NOPurity:Min. 95%Color and Shape:PowderMolecular weight:109.13 g/mol




