CAS 17508-17-7

O-(2,4-Dinitrophenyl)hydroxylamine

Description:

O-(2,4-Dinitrophenyl)hydroxylamine is an organic compound characterized by its dinitrophenyl group attached to a hydroxylamine functional group. It typically appears as a yellow to orange crystalline solid, reflecting the presence of the dinitrophenyl moiety, which is known for its strong electron-withdrawing properties. This compound is often used in organic synthesis and analytical chemistry, particularly in the identification and quantification of carbonyl compounds through the formation of stable derivatives. It is soluble in polar organic solvents, and its reactivity is influenced by the electron-withdrawing nature of the dinitrophenyl group, which enhances its nucleophilicity. Safety considerations are important when handling this compound, as it may pose health risks, including potential toxicity and environmental hazards. Proper laboratory practices, including the use of personal protective equipment and appropriate waste disposal methods, are essential when working with O-(2,4-Dinitrophenyl)hydroxylamine.

Formula: C₆H₅N₃O₅

InChI: InChI=1S/C6H5N3O5/c7-14-6-2-1-4(8(10)11)3-5(6)9(12)13/h1-3H,7H2

InChI key: InChIKey=YLACRFYIUQZNIV-UHFFFAOYSA-N

SMILES: N(=O)(=O)C1=C(ON)C=CC(N(=O)=O)=C1

Synonyms:

• 1-Aminooxy-2,4-dinitrobenzene
• 2,4-Dinitrophenoxyamine
• 2,4-Nitrophenoxyamine
• Dnpa
• Hydroxylamine, O-(2,4-dinitrophenyl)-；
• Nsc 148499
• O-(2,4-Dinitrophenyl)hydroxylamine

O-(2,4-Dinitrophenyl)hydroxylamine

CAS: 17508-17-7

Formula: C₆H₅N₃O₅

Purity: >97.0%(GC)

Color and Shape: Light yellow to Yellow to Orange powder to crystal

Molecular weight: 199.12

Ref: 3B-D5103

Hydroxylamine, O-(2,4-dinitrophenyl)-

CAS: 17508-17-7

Formula: C₆H₅N₃O₅

Purity: 97%

Color and Shape: Solid

Molecular weight: 199.1210

Ref: IN-DA00204Y

O-(2,4-Dinitrophenyl)hydroxylamine

CAS: 17508-17-7

O-(2,4-dinitrophenyl)hydroxylamine is a synthetic compound that binds to the enzyme bound site of the cap-dependent endonuclease. It is an inhibitor of influenza virus replication in vitro and has shown inhibitory activity against murine leukemia virus. O-(2,4-dinitrophenyl)hydroxylamine is also a model for the study of aminoglycoside antibiotics. The compound inhibits aminoglycoside-induced protein synthesis in eukaryotic cells and may be useful in understanding the mechanism of action and resistance to these antibiotics.

Formula: C₆H₅N₃O₅

Purity: Min. 98 Area-%

Color and Shape: Yellow Powder

Molecular weight: 199.12 g/mol

Ref: 3D-FD22435

O-(2,4-Dinitrophenyl)hydroxylamine

CAS: 17508-17-7

Applications O-(2,4-Dinitrophenyl)hydroxylamine is a rapid active-site-directed inhibitor of D-amino acid oxidase; modification results in specific incorporation of an amine group into an accessible nucleophilic residue with concomitant release of 2,4-dinitrophenol.
References D'Silva, C., et al.: Biochemi., 25, 5602 (1986),

Formula: C₆H₅N₃O₅

Color and Shape: Brown Solid

Molecular weight: 199.12

Ref: TR-D479985