| Weight | 137.118 g/mol |
|---|---|
| Formula | C6H5N2O2- |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
CUPFERRON (135-20-6)
Score:
#1139 in Biochemistry
,
#3624 in Chemistry
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- Selective determination of trace uranium by stripping voltammetry following adsorptive accumulation of the uraniumcupferron complex (Analytica Chimica Acta, 1992)
- Determination of trace aluminium by adsorptive stripping voltammetry on a preplated bismuth-film electrode in the presence of cupferron (Talanta, 2006)
- Measurement of ultratrace levels of chromium by adsorptivecatalytic stripping voltammetry in the presence of cupferron (Analyst, 1992)
- Adsorptive-catalytic stripping measurements of ultratrace vanadium in the presence of cupferron and bromate. (Talanta, 1992)
- Adsorptive Stripping Voltammetric Determination of Trace Uranium with a Bismuth-Film Electrode Based on the U(VI)U(V) Reduction Step of the Uranium-Cupferron Complex (Electroanalysis, 2006)
- Inhibitory effects of cupferron on the monophenolase and diphenolase activity of mushroom tyrosinase (The International Journal of Biochemistry & Cell Biology, 2003)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H350: May cause cancer
Danger Carcinogenicity - Category 1A, 1B -
SMILESC1=CC=C(C=C1)N(N=O)[O-]
-
InChIKeyDTPFDWCBDYPUHO-UHFFFAOYSA-N
- Pubchem - CUPFERRON
- Wikipedia - cupferron
Cupferron, the ammonium salt of N-nitroso-N-phenylhydroxylamine, is a common reagent for the complexation of metal ions. Its formula is NH4[C6H5N(O)NO]. The anion binds to metal cations through the two oxygen atoms, forming five-membered chelate rings.
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