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4-Nitrosomorpholine

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Identification
Molecular formula
C4H8N2O2
CAS number
598-93-6
IUPAC name
4-nitrosomorpholine
State
State

4-Nitrosomorpholine exists as a solid at room temperature. It is often available in the form of a crystalline powder.

Melting point (Celsius)
32.00
Melting point (Kelvin)
305.15
Boiling point (Celsius)
267.00
Boiling point (Kelvin)
540.15
General information
Molecular weight
116.12g/mol
Molar mass
130.1310g/mol
Density
1.2800g/cm3
Appearence

4-Nitrosomorpholine is typically a pale yellow to a yellow-orange compound. It is generally available in solid form, often presented in crystalline or powder form. The color may vary slightly depending on the level of purity and specific synthesis method used.

Comment on solubility

Solubility of 4-nitrosomorpholine

4-nitrosomorpholine, with the chemical formula C4H8N2O2, is an intriguing compound when it comes to solubility. Here are some key points regarding its solubility characteristics:

  • Polar Nature: The presence of the nitroso group and hydroxyl functionality within its structure contributes to the compound's polar nature.
  • Solvent Compatibility: This polarity suggests that 4-nitrosomorpholine is likely to be soluble in polar solvents such as water and alcohols.
  • Limited Solubility: However, it's important to note that the actual solubility may vary, and experimental data is essential for an accurate assessment.

In summary, while 4-nitrosomorpholine exhibits properties that suggest it should be soluble in polar solvents, its true solubility may depend on factors such as temperature and concentration. Understanding its solubility is crucial for its applications in various chemical processes.

Interesting facts

Interesting Facts About 4-Nitrosomorpholine

4-Nitrosomorpholine is a fascinating compound that has garnered attention in various scientific fields due to its unique properties and implications. Below are some notable points about this compound:

  • Chemical Significance: 4-Nitrosomorpholine is a nitrosamine, a class of compounds widely studied for their potential carcinogenic effects. Understanding how these compounds behave can provide insights into their effects on human health.
  • Formation: This compound is often formed through the reaction of morpholine (a cyclic amine) with nitrous acid. Its synthesis in the laboratory raises questions regarding the conditions that favor nitrosamine formation.
  • Toxicology: Research has indicated that 4-nitrosomorpholine can induce tumors in laboratory animals, making it a subject of regulatory scrutiny. The implications of its toxicity necessitate careful handling and study in various applications.
  • Detection: Analytical techniques such as gas chromatography/mass spectrometry (GC/MS) are commonly employed to identify and quantify 4-nitrosomorpholine in various samples, including environmental and biological specimens.
  • Regulatory Considerations: Due to its potential health risks, 4-nitrosomorpholine is subject to stringent regulations, particularly in industries where nitrosamines might form as by-products.

In the words of scientists studying this compound, "In our quest for knowledge, we must tread carefully with compounds that hold both promise and peril." This balance between utility and safety is an essential consideration in the ongoing dialogues surrounding 4-nitrosomorpholine.

4-Nitrosomorpholine serves as a reminder of the complexity within organic chemistry and underscores the importance of ongoing research into chemical safety and health impacts.

Synonyms
N-NITROSOMORPHOLINE
59-89-2
4-Nitrosomorpholine
Nitrosomorpholine
Morpholine, 4-nitroso-
NMOR
N-Nitrosomorpholin
Morpholine, N-nitroso-
N-Nitrosomorfolin
N-Nitrosomorfolin [Czech]
NSC 139
NCI-C02164
4-Nitroso-morpholine
N-Nitrosomorpholin [German]
CCRIS 473
HSDB 4308
UNII-3L25FO7FN7
BRN 0112139
3L25FO7FN7
DTXSID4021056
CHEBI:76326
NSC-139
DTXCID001056
NSC139
N-NITROSOMORPHOLINE [MI]
N-NITROSOMORPHOLINE [HSDB]
N-NITROSOMORPHOLINE [IARC]
67587-56-8
N-NITROSOMORPHOLINE (IARC)
N-NITROSOMORPHOLIN (GERMAN)
CAS-59-89-2
Molsidomine impurity B
NNitrosomorfolin
NNitrosomorpholin
alpha-acetoxy-N-nitrosomorpholine
4Nitrosomorpholine
N-nitroso morpholine
Morpholine, Nnitroso
Morpholine, 4nitroso
4-NITOSOMORPHOLINE
N-Nitrosomorpholine solution
WLN: T6N DOTJ ANO
N-Nitrosomorpholine (NMOR)
N-Nitrosomorpholine (Standard)
CHEMBL165908
SCHEMBL1578515
Tox21_202132
Tox21_302867
MFCD00039710
MSK4918-100M
STL301087
AKOS015903272
MSK4918-1000M
HY-131123R
NCGC00249174-01
NCGC00256343-01
NCGC00259681-01
BS-17191
FN182145
SY052130
4-Nitrosomorpholine 0.1 mg/ml in Methanol
4-Nitrosomorpholine 1.0 mg/ml in Methanol
DB-053489
HY-131123
CS-0128913
N0466
NS00010254
C19283
N-Nitrosomorpholine 100 microg/mL in Methanol
T72681
EN300-7323775
N-Nitrosomorpholine Solution in Methanol, 100_g/mL
N-Nitrosomorpholine Solution in Methanol, 1000_g/mL
Q22138414
Z1255360497
Molsidomine impurity B, European Pharmacopoeia (EP) Reference Standard
627-564-6