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Cupferron

Name: Cupferron
Brand: ALDRICH

97%, reagent grade

Synonym(s):

N-Nitroso-N-phenylhydroxylamine ammonium salt

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About This Item

Linear Formula:

C₆H₅N(NO)ONH₄

CAS Number:

135-20-6

Molecular Weight:

155.15

UNSPSC Code:

12352100

NACRES:

NA.21

PubChem Substance ID:

24885293

EC Number:

205-183-2

Beilstein/REAXYS Number:

3919107

MDL number:

MFCD00078422

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Properties

grade

reagent grade

Quality Level

200

assay

97%

form

solid

technique(s)

titration: suitable

mp

150-155 °C (dec.) (lit.)

shipped in

wet ice

storage temp.

2-8°C

SMILES string

[H][N+]([H])([H])[H].[O-]N(N=O)c1ccccc1

InChI

1S/C6H5N2O2.H3N/c9-7-8(10)6-4-2-1-3-5-6;/h1-5H;1H3/q-1;/p+1

InChI key

GDEBSAWXIHEMNF-UHFFFAOYSA-O

Description

General description

Cupferron (Cup) is an ammonium salt of N-nitroso-N-phenylhydroxylamine. It acts as an organic chelation reagent by co-ordinating through the oxygen atoms. Its radiomimetic effect is reported to be affected by the pH and temperature of the treatment solution.

Application

A solvothermal route to ZnO and Mn-doped ZnO nanoparticles using the cupferron complex as the precursor.: This research presents a novel method to produce zinc oxide and manganese-doped zinc oxide nanoparticles using cupferron as a precursor, showcasing its application in material synthesis in analytical chemistry (Ghosh et al., 2004).

Determination of tellurium in geochemical materials by flameless atomic-absorption spectroscopy.: Demonstrates the role of cupferron in enhancing the analytical methodologies for tellurium determination, underpinning its significance in geochemical studies (Sighinolfi et al., 1979).

Extraction of vanadium into isobutyl methyl ketone.: Outlines a method for extracting vanadium using cupferron, which plays a crucial role in the development of methods for the quantitative analysis of vanadium in various samples (Crump-Wiesner and Purdy, 1969).

Substituted hydroxylamines as analytical reagents.: Discusses the application of substituted hydroxylamines, including cupferron, as reagents in chemical analysis, illustrating the compound′s adaptability and utility in analytical chemistry (Shendrikar, 1969).