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O-(2,4-dinitrophenyl)hydroxylamine

O-(2,4-dinitrophenyl)hydroxylamine Structure
CAS No.
17508-17-7
Chemical Name:
O-(2,4-dinitrophenyl)hydroxylamine
Synonyms
2,4-Dinitrophenylhydroxylamine;NSC 148499;2,4-NitrophenoxyaMine;2,4-DinitrophenoxyaMine;4-dinitrophenyl)hydroxylamine;1-aMinooxy-2,4-dinitro-benzene;O-(2,4-dinitrophenyl)hydroxylamine;HydroxylaMine,O-(2,4-dinitrophenyl)-;O-(2,4-Dinitrophenyl)hydroxylamine,98%;TIANFUCHEM--17508-17-7---O-(2,4-dinitrophenyl)hydroxylamine
CBNumber:
CB3922714
Molecular Formula:
C6H5N3O5
Molecular Weight:
199.12
MOL File:
17508-17-7.mol
MSDS File:
SDS
Modify Date:
2023/6/8 17:06:37

O-(2,4-dinitrophenyl)hydroxylamine Properties

Melting point 112.5°C
Boiling point 336.62°C (rough estimate)
Density 1.6937 (rough estimate)
refractive index 1.6910 (estimate)
storage temp. 2-8°C(protect from light)
solubility DMSO (Sparingly), Methanol (Slightly)
form solid
pka -1.07±0.70(Predicted)
color yellow

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
Risk Statements  22-36/37/38
Safety Statements  26
TSCA  No
HS Code  29221990
NFPA 704
0
2 2

O-(2,4-dinitrophenyl)hydroxylamine price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemicals (India) D5103 O-(2,4-Dinitrophenyl)hydroxylamine min. 97.0 % 17508-17-7 1G ₹2600 2022-05-26 Buy
TCI Chemicals (India) D5103 O-(2,4-Dinitrophenyl)hydroxylamine min. 97.0 % 17508-17-7 5G ₹7900 2022-05-26 Buy
Product number Packaging Price Buy
D5103 1G ₹2600 Buy
D5103 5G ₹7900 Buy

O-(2,4-dinitrophenyl)hydroxylamine Chemical Properties,Uses,Production

Chemical Properties

Light yellow solid

Uses

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 r esidue with concomitant release of 2,4-dinitrophenol.

Preparation

To a stirred solution of 13.3 gm (0.1 mole) of t-butyl JV-hydroxycar-bamate and 5.6 gm (0.1 mole) of potassium hydroxide in 200 ml of absolute ethanol is added 20.2 gm (0.1 mole) of 2,4-dinitrochlorobenzene. The resultant deep red solution is stirred at room temperature for 1 hr; then enough glacial acetic acid is added dropwise to produce a light yellow solution. The solution is poured into 1.5 liters of cold water. The yellow oil which separates is gradually converted to crystals. The solid ?-butyl JV-(2,4-dinitrophenoxy)carbamate is separated, dried, and recrystallized from an ethyl acetate-hexane mixture to afford 16.4 gm (53%), m.p. 74-75°C. To 15 ml of trifluoroacetic acid is added 4 gm (0.0133 mole) of the i-butyl J/V-(2,4-dinitrophenoxy)carbamate. After the evolution of carbon dioxide has subsided, the solution is poured into 100 ml of ice water. The resultant oily layer crystallizes on standing to afford 2.5 gm (95%), m.p. 112°C (from ethanol).
Preparation of O-(2,4-Dinitrophenyl)hydroxylamine-1
Recently it was discovered that the alkylation of ethyl JV-hydroxy-carbamate under alkaline conditions, particularly in a DMF medium at 60°C in the presence of sodium bicarbonate, leads to the ultimate formation of O-alkylated hydroxylamines. On the other hand, at 80-85°C, the direct alkylation without the presence of a base ultimately leads to N-alkylhydrox-ylamines (see Table I) [59]. The reaction of ethylazidoformate with an alcohol, while perhaps haz­ardous, may have some merit (Eqs. 31-33). The overall yield, based on ethyl chloroformate, is said to be on the order of 60%.
Preparation of O-(2,4-Dinitrophenyl)hydroxylamine-2

O-(2,4-dinitrophenyl)hydroxylamine Preparation Products And Raw materials

Raw materials

Preparation Products

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O-(2,4-dinitrophenyl)hydroxylamine Spectrum

HydroxylaMine,O-(2,4-dinitrophenyl)- 1-aMinooxy-2,4-dinitro-benzene 2,4-DinitrophenoxyaMine 2,4-NitrophenoxyaMine NSC 148499 O-(2,4-dinitrophenyl)hydroxylamine 4-dinitrophenyl)hydroxylamine TIANFUCHEM--17508-17-7---O-(2,4-dinitrophenyl)hydroxylamine 2,4-Dinitrophenylhydroxylamine O-(2,4-Dinitrophenyl)hydroxylamine,98% 17508-17-7 nitro-compound Amines Aromatics Inhibitors