N4007
N-Nitroso-N-methylbutylamine
Synonym(s):
Methylbutylnitrosamine
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About This Item
Empirical Formula (Hill Notation):
C5H12N2O
CAS Number:
Molecular Weight:
116.16
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352116
MDL number:
form
liquid
Quality Level
density
0.93 g/mL (lit.)
storage temp.
2-8°C
SMILES string
CCCCN(C)N=O
InChI
1S/C5H12N2O/c1-3-4-5-7(2)6-8/h3-5H2,1-2H3
InChI key
PKTSCJXWLVREKX-UHFFFAOYSA-N
Packaging
Bulk package
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 1 Inhalation - Acute Tox. 2 Dermal - Acute Tox. 3 Oral - Carc. 1B
Storage Class
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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E Suzuki et al.
Japanese journal of cancer research : Gann, 76(3), 184-191 (1985-03-01)
In order to compare the extents of metabolic alpha-hydroxylation of the two alkyl groups in unsymmetrical N-nitrosodialkylamines, N-nitroso-N-alkylbutylamines (alkyl = methyl, ethyl, propyl, butyl, and amyl) were incubated with liver microsomes prepared from phenobarbital- or polychlorinated biphenyl (PCB)-treated and untreated
B Ludeke et al.
IARC scientific publications, (105)(105), 286-293 (1991-01-01)
Aliphatic methylalkylnitrosamines with a chain length of three to six carbon atoms are powerful oesophageal carcinogens in rats and have been shown to methylate target organ DNA preferentially. This class of carcinogens is efficiently metabolized not only in the oesophageal
W Lijinsky et al.
Carcinogenesis, 1(2), 157-160 (1980-02-01)
Nitrosomethyl-n-butylamine and its derivatives, labeled with deuterium in the methyl group or at the alpha position of the butyl group, were given to rats in drinking water at equimolar doses for approximately 20 weeks. Two concentrations were used, 16 mg/l
T Kawanishi et al.
Cancer letters, 20(2), 157-164 (1983-09-01)
The effect of phenobarbital (PB) and 3-methylcholanthrene (MC) pretreatment on dealkylations of N-nitrosodimethylamine (NDMA), N-nitrosomethylbutylamine (NMBuA) and N-nitrosomethylbenzylamine (NMBeA) was investigated in rat hepatic microsomes. PB increased the demethylation and the debutylation of NMBuA and the debenzylation of NMBeA. MC
Q Huang et al.
Cancer letters, 69(2), 107-116 (1993-04-30)
We studied the metabolism of methyl-n-butyl-nitrosamine (MBN), a carcinogen for the rat esophagus and liver. The 2-, 3- and 4-hydroxy derivatives were identified as new metabolites of MBN. In studies on tissue slices freshly removed from MRC-Wistar rats, MBN metabolism
Global Trade Item Number
| SKU | GTIN |
|---|---|
| N4007-1ML | 04061834116417 |
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