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N4007

Sigma-Aldrich

N-Nitroso-N-methylbutylamine

Synonym(s):

Methylbutylnitrosamine

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500 MG
SEK 2,020.00
1 G
SEK 3,660.00
5 G
SEK 11,910.00

SEK 2,020.00

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500 MG
SEK 2,020.00
1 G
SEK 3,660.00
5 G
SEK 11,910.00

About This Item

Empirical Formula (Hill Notation):
C5H12N2O
CAS Number:
7068-83-9
Molecular Weight:
116.16
MDL number:
MFCD00056645
UNSPSC Code:
12352116
PubChem Substance ID:
24897361
NACRES:
NA.25

SEK 2,020.00

Please contact Customer Service for Availability
Request a Bulk Order

form

liquid

Quality Level

200

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

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1 of 4

This Item
C8822C6277C6767
New Coccine Dye content 75 %

199737

New Coccine

Crocein Scarlet 7B

C8822

Crocein Scarlet 7B

Congo Red certified by the Biological Stain Commission, BioXtra

C6277

Congo Red

Congo Red Dye content ≥35 %

C6767

Congo Red

form

powder

form

powder

form

powder

form

powder

solubility

water: 1 mg/mL, clear

solubility

H2O: 1 mg/mL

solubility

H2O: 10 mg/mL

solubility

H2O: 1 mg/mL

composition

Dye content, 75%

composition

Dye content, ~65-85%

composition

Dye content, ≥85%

composition

Dye content, ≥35%

storage temp.

room temp

storage temp.

room temp

storage temp.

room temp

storage temp.

room temp

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

Packaging

Bulk package

Pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

Signal Word

Danger

Hazard Statements

H301,H310 + H330,H350

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 2 Dermal - Acute Tox. 3 Oral - Carc. 1B

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves
  • Specification Sheet

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    Certificates of Analysis (COA)

    Lot/Batch Number
    084F0565
    107F0471

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    K E Appel et al.
    Carcinogenesis, 7(4), 659-663 (1986-04-01)
    To demonstrate whether there are any pathways of nitrite formation from N-nitrosamines other than reductive denitrosation by cytochrome P-450 we performed the following experiments. An esterified alpha-hydroxylated nitrosamine was incubated in a microsomal system to test if nitrite generation is
    J G Farrelly et al.
    Cancer research, 42(6), 2105-2109 (1982-06-01)
    With the use of rat liver preparations, the in vitro microsomal metabolism of methylethylnitrosamine, methyl-n-butylnitrosamine, and methyl(2-phenylethyl)nitrosamine labeled with deuterium in the methyl and alpha-methylene positions has been compared with that of the parent (unlabeled) compounds. All three forms of
    M Lee et al.
    Cancer research, 49(6), 1470-1474 (1989-03-15)
    Metabolic activation may be a key step in determining the tissue specificity of carcinogenic nitrosamines. In previous work, we characterized P450IIE1 (an acetone/ethanol-inducible form of cytochrome P-450) as the major enzyme for the metabolic activation of N-nitrosodimethylamine. In this work
    T Gichner et al.
    Mutagenesis, 1(2), 107-109 (1986-03-01)
    The organic solvents dimethylsulphoxide (DMSO), acetone, ethanol and dimethylformamide inhibited the mutagenic activity of the promutagens dimethylnitrosamine and methylbutylnitrosamine in a higher plant Arabidopsis thaliana. In contrast, the direct-acting mutagens N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) and N-methyl-N-nitrosourea (MNU) were not affected by the
    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
    View All Related Papers

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