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N7382

Sigma-Aldrich

Nitrosomorpholin

Synonym(e):

NMOR

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About This Item

Empirische Formel (Hill-System):
C4H8N2O2
CAS-Nummer:
59-89-2
Molekulargewicht:
116.12
MDL-Nummer:
MFCD00039710
UNSPSC-Code:
41116105
PubChem Substanz-ID:
24897824
NACRES:
NA.25

Form

solid

Qualitätsniveau

100

SMILES String

O=NN1CCOCC1

InChI

1S/C4H8N2O2/c7-5-6-1-3-8-4-2-6/h1-4H2

InChIKey

ZKXDGKXYMTYWTB-UHFFFAOYSA-N

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Biochem./physiol. Wirkung

Tumor initiator in rodent liver, trachea, nasal cavity, esophagus, kidney, lung, and thyroid.

Verpackung

Bulk package

Piktogramme

Skull and crossbonesHealth hazard
GHS06,GHS08

Signalwort

Danger

H-Sätze

H301,H351

Gefahreneinstufungen

Acute Tox. 3 Oral - Carc. 2

Lagerklassenschlüssel

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
MKCT1742
MKCR8362
MKCN2923
MKCN2922
MKCM6477

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Wenn Sie eine bestimmte Version benötigen, können Sie anhand der Lot- oder Chargennummer nach einem spezifischen Zertifikat suchen.

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40060

N-Nitrosodiphenylamin -Lösung

N-Nitrosodiethylamin ISOPAC®

Sigma-Aldrich

N0258

N-Nitrosodiethylamin

N-Nitrosodiethylamin ≥99.0% (GC)

Sigma-Aldrich

73861

N-Nitrosodiethylamin

N-Nitroso-N-methylbutylamine

Sigma-Aldrich

N4007

N-Nitroso-N-methylbutylamine

W Lijinsky et al.
In vivo (Athens, Greece), 5(2), 85-89 (1991-03-01)
A number of nitrosamines that have been studied by administration to rats as solutions in drinking water have been examined by gavage administration of similar doses, for assessment of the role of pharmacokinetics in organ-specific carcinogenesis. Methylnitrosoethylamine was more effective
W Lijinsky et al.
Carcinogenesis, 3(8), 911-915 (1982-01-01)
A comparison was made of the carcinogenic effectiveness of some cyclic nitrosamines containing oxygen in the ring. The compounds were administered to F344 rats at approximately equimolar concentrations in drinking water. Nitrosomorpholine, nitroso-1,3-oxazolidine and nitrosotetrahydro-1,3-oxazine were of similar potency and
Jutta Groos et al.
Mathematical biosciences, 202(2), 248-268 (2006-04-11)
Several hypotheses are established to describe the formation and progression of foci of altered hepatocytes (FAH). A common model of hepatocarcinogenesis is the mutation model (MM), which is based on the assumption that cells have to undergo multiple successive changes
Yong-Cang Wang et al.
Hepato-gastroenterology, 58(112), 2032-2035 (2012-01-12)
Concern that much controversy exists with respect to the role of estrogen in hepatocarcinogenesis prompted us to examine the effect of estrogen, at physiological concentrations, on our established HCC rat model induced by diethylnitrosamine and N-nitrosomorpholine. Female Sprague-Dawley rats were
Olga Teufelhofer et al.
Electrophoresis, 27(20), 4112-4120 (2006-10-21)
Comparative proteome data of normal and diseased tissue samples are difficult to interpret. Proteins detected in tissues are derived from different cell types and blood constituents. Pathologic or toxicant-induced aberrations may affect the proteome profile of tissues in several ways
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