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N-Nitrosomorpholine

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N-nitrosomorpholine
Names
Other names 4-nitrosomorpholine, alpha-acetoxy-N-nitrosomorpholine, nitrosomorpholine, NMOR, 4-nitroso-morpholine, NNM
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.155.913 Edit this at Wikidata
EC Number
  • 627-564-6
KEGG
PubChem CID
UNII
UN number 2810 3077
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C4H8N2O2/c7-5-6-1-3-8-4-2-6/h1-4H2Key: ZKXDGKXYMTYWTB-UHFFFAOYSA-N
SMILES
  • C1COCCN1N=O
Properties
Chemical formula C4H8N2O2
Molar mass 116.120 g·mol
Appearance Pale yellow powder
Melting point 29 °C (84 °F; 302 K)
Boiling point 435 to 436 °F at 747 mmHg
Solubility in water greater than or equal to 100 mg/mL in water at 66 °F
Hazards
Occupational safety and health (OHS/OSH):
Main hazards hepatocarcinogen
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

N-Nitrosomorpholine (NNM, NMOR) is an organic compound which is known to be a carcinogen and mutagen.

Chemistry

NMOR is a pale yellow sand-like powder below 84°F. NMOR is most commonly produced from morpholine, but can also be made by the reaction of dimorpholinomethane in fuming nitric acid. Few reactions using NMOR as a starting material are reported in the organic synthesis literature, but it can be used as a precursor to a nitrogen-centered radical.

Occurrence

NMOR is generally not used intentionally, but is instead created by the nitrosation of morpholine or morpholine derivatives which are used for several industrial purposes.

Rubber

2-(Morpholinothio)benzothiazole is used as an accelerator/stabilizer for vulcanization, or the manufacture of rubber products. It is the precursor to NMOR in the vulcanization process, as it is nitrosated by ambient sources of the nitro group present in the manufacturing process. As such, workers and others exposed to the rubber industry or its byproducts are exposed to higher levels of NMOR than the general population, raising their risk of cancer.

Tobacco products

NMOR is a component of tobacco products. As of 2014, detectable levels of NMOR are present in tobacco products in the United States and China. The presence of NMOR and other n-nitrosoamines is not limited to cigarettes, but is found in smokeless tobacco products (snuff tobacco, Snus, etc.) as well. Volatile nitrosamines, including NMOR, are detectable in the urine of tobacco smokers.

Food

Morpholine oleate is used in glazing wax which covers fruit. NMOR can be generated by the nitration of morpholine, causing its presence in waxed fruits.Health Canada, the Canadian governmental department of public health, has stated in 2002 that this does not pose a risk to human health.

Consumption of nitrate-rich diets is correlated with levels of salivary and urinary NMOR. The presence of NMOR can also be observed in gastric juices.

Other

NMOR has been found in several cosmetic products.

Health hazards

The mechanisms of carcinogenesis are not completely clear in humans. NMOR and its metabolites may induce DNA damage by directly forming reactive oxygen species or compounds which crosslink DNA. In a rat model in 2013, it was observed that NMOR is hydroxylated, probably by a P450 enzyme, alpha to the N-nitroso moiety. This then decomposes into a diazonium-containing aldehyde which is capable of crosslinking DNA.

Endogenous synthesis from morpholine in the digestive system is observed. NMOR can be generated from N-nitrosating species formed by salivary nitrite and stomach acid, potentially leading to more damage in individuals with acid reflux. H. pylori does not induce NMOR formation in vitro, though this has yet to be confirmed in vivo.

NMOR is in fact used to generate liver cancer models in rats. Along with N-diethylnitrosamine, it is the gold standard for producing hepatocarcinoma with 100% lung metastasis.

See also

References

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