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Cupferron

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Identification
Molecular formula
C6H6N2O2
CAS number
135-20-6
IUPAC name
N-(4-nitrosophenyl)hydroxylamine
State
State

At room temperature, Cupferron is typically a solid. It is stable under normal conditions but should be stored in a cool, dry place to maintain its stability. Exposure to air and moisture should be minimized to prevent decomposition.

Melting point (Celsius)
85.00
Melting point (Kelvin)
358.00
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.00
General information
Molecular weight
154.12g/mol
Molar mass
154.1410g/mol
Density
1.3025g/cm3
Appearence

Cupferron is a light pink crystalline solid. It is usually found as a powder and has a characteristic odor. Due to its nitroso group, it can also appear in varying shades of pink under certain light conditions, dependent on its concentration and physical form.

Comment on solubility

Solubility of N-(4-nitrosophenyl)hydroxylamine

N-(4-nitrosophenyl)hydroxylamine, with the chemical formula C6H7N3O, exhibits notable solubility characteristics that are essential for its applications in chemical reactions. The compound exhibits the following solubility behavior:

  • Solvent Compatibility: N-(4-nitrosophenyl)hydroxylamine is reported to be soluble in polar solvents, particularly water and ethanol. This property enhances its utility in various chemical processes where polar environments are favored.
  • Temperature Dependence: The solubility of this compound tends to increase with temperature. Thus, heating the solvent can promote higher dissolution rates.
  • pH Influence: The solubility can also be affected by the pH of the solution. In more acidic or basic conditions, the behavior of the compound may change, impacting its overall solubility.

In summary, N-(4-nitrosophenyl)hydroxylamine's solubility is influenced by a combination of solvent nature, temperature, and solution pH. Understanding these factors is critical for effectively utilizing this compound in various scientific applications.

Interesting facts

Interesting Facts about N-(4-nitrosophenyl)hydroxylamine

N-(4-nitrosophenyl)hydroxylamine is a fascinating compound that presents a variety of intriguing properties and applications. This compound, known for its unique structure, belongs to a class of chemicals called hydroxylamines, which includes a wide range of important derivatives.

Applications

Here are some notable applications of N-(4-nitrosophenyl)hydroxylamine:

  • Analytical Chemistry: It is often used in the detection and quantification of certain metal ions in various samples.
  • Pharmaceuticals: Compounds similar to N-(4-nitrosophenyl)hydroxylamine are studied for their potential therapeutic effects, including antibiotic properties.
  • Industrial Processes: This compound may serve as a reagent in organic synthesis, contributing to the creation of more complex molecules.

Toxicological Considerations

Despite its uses, the compound also raises important safety concerns. Understanding its toxicological profile is crucial:

  • Potential Mutagenicity: N-(4-nitrosophenyl)hydroxylamine has been studied for its potential mutagenic effects, demonstrating the need for careful handling.
  • Environmental Impact: As with many nitrogen-containing compounds, it can have implications for environmental health, particularly in relation to water quality.

Chemical Structure

With a nitroso group attached to an aromatic amine, the structure of N-(4-nitrosophenyl)hydroxylamine is both simple and complex. Its ability to donate electrons due to the nitrogen atom's electron-donating properties makes it a key player in various chemical reactions. As one scientist put it: "The balance of stability and reactivity in nitrogen compounds like this one is a perpetual source of intrigue."

In conclusion, N-(4-nitrosophenyl)hydroxylamine exemplifies the dual nature of many chemical compounds—offering both opportunities for innovation and challenges for safety. As research continues, this compound may unlock new realms in chemistry and medicine.

Synonyms
1,4-Benzoquinone dioxime
105-11-3
p-Benzoquinonedioxime
p-Quinone dioxime
P-BENZOQUINONE DIOXIME
Quinone dioxime
Benzoquinone dioxime
Actor Q
p-Quinone oxime
Dibenzo PQD
para-Benzoquinone dioxime
Paraquinondioxime
Dioxime p-benzoquinone
para-Quinone oxime
2,5-Cyclohexadiene-1,4-dione, dioxime
N-(4-nitrosophenyl)hydroxylamine
G-M-F
p-Benzoquinone, dioxime
NCI-C03850
Dioxime 1,4-cyclohexadienedione
1,4-Benzochinondioxim
NSC 4774
CCRIS 549
NSC 14433
1,4-Benzochinondioxim [Czech]
Dioxime 2,5-cyclohexadiene-1,4-dione
HSDB 2866
Vulnoc GM
EINECS 203-271-5
MGE6YH92Q2
BRN 2043234
C6H6N2O2
DTXSID8021222
AI3-52518
2,5-Cyclohexadiene-1,4-dione, 1,4-dioxime
NSC-4774
MFCD00063636
NSC-14433
PQD
DTXCID901222
QDO
BENZOQUINONE DIOXIME, P-
4-07-00-02074 (Beilstein Handbook Reference)
P-BENZOQUINONE DIOXIME [HSDB]
Dioxime 2,4-dione
2,4-dione, dioxime
WLN: L6Y DYJ AUNQ DUNQ
1,4-cyclohexadienedione dioxime
1,4-benzoquinonedioxime
UNII-MGE6YH92Q2
pQuinone oxime
pQuinone dioxime
paraQuinone oxime
para-quinone dioxime
Dioxime pbenzoquinone
PBQD
1,4Benzochinondioxim
1,4-quinone dioxime
p-quinone dioxime powder
1,4Benzoquinone dioxime
p-Nitrosophenylhydroxylamin
SCHEMBL93568
Dioxime 1,4cyclohexadienedione
Benzo-1,4-quinone dioxime #
SCHEMBL8005268
CHEMBL1585396
CHEBI:82404
NSC4774
DZCCLNYLUGNUKQ-UHFFFAOYSA-N
LNHURPJLTHSVMU-CGXWXWIYSA-N
LNHURPJLTHSVMU-SFECMWDFSA-N
LNHURPJLTHSVMU-UHFFFAOYSA-N
Dioxime 2,5cyclohexadiene1,4dione
NSC14433
2,5Cyclohexadiene1,4dione, dioxime
Tox21_200273
AKOS015901106
AKOS015920447
NCGC00091127-01
NCGC00091127-02
NCGC00248444-01
NCGC00248585-01
NCGC00257827-01
AS-19482
CAS-105-11-3
SY048766
B0090
NS00020047
C19345
p-Benzoquinone dioxime, technical, >=90% (TLC)
Q27155923
N-[(1E,4E)-4-(HYDROXYIMINO)CYCLOHEXA-2,5-DIEN-1-YLIDENE]HYDROXYLAMINE
203-271-5