An N-nitrosamine
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Product Type

Biochemicals
Synthetic Intermediates & Building Blocks

Research Area

N-Nitroso-N-ethylaniline

Item No. 21063

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
N-ethyl-N-nitroso-benzenamine
CAS Number
612-64-6
Synonyms
  • N-Ethyl-N-nitrosoaniline
  • NSC 405070
Molecular Formula
C8H10N2O
Formula Weight
150.2
Purity
≥98%
Formulation (Request formulation change)
A 10 mg/ml solution in ethanol
Solubility(Learn about Variance in Solubility)
DMSO: 5 mg/ml
λmax
217, 273 nm
SMILES
CCN(N=O)C1=CC=CC=C1
InChi Code
InChI=1S/C8H10N2O/c1-2-10(9-11)8-6-4-3-5-7-8/h3-7H,2H2,1H3
InChi Key
WXRXVZXYLBWKRG-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    1 mg

    $36

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    5 mg

    $128

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    10 mg

    $186

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    25 mg

    $294

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    Product Description

    N-Nitroso-N-ethylaniline is a member of the N-nitrosamine class of compounds, which are classified as carcinogens by the Environmental Protection Agency.1 However, N-nitroso-N-ethylaniline is non-carcinogenic in a survival assay using 2FR450 Rauscher leukemia virus-infected rat embryo cultures.2 It is a synthetic intermediate in the synthesis of 3-amino-4-hydrazine-cyclobut-3-ene-1,2-diones as antagonists of chemokine (C-X-C motif) receptor 2 (CXCR2).3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Park, J.-E., Seo, J.-E., Lee, J.-Y., et al. Distribution of seven N-nitrosamines in food. Toxicol. Res. 31(3), 279-288 (2015).

    2. Traul, K., Takayama, F., Kachevsky, V., et al. A rapid in vitro assay for carcinogenicity of chemical substances in mammalian cells utilizing an attachment-independence endpoint. 2 - Assay validation. J. Appl. Toxicol. 1(3), 190-195 (1981).

    3. Liu, S., Liu, Y., Wang, H., et al. Design, synthesis, and evaluation of novel 3-amino-4-hydrazine-cyclobut-3-ene-1,2-diones as potent and selective CXCR2 chemokine receptor antagonists. Bioorg. Med. Chem. Lett. 19(19), 5741-5745 (2009).