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Synonyms
Synonyms
  • 2,5-Dimethoxy-4-nitrophenethylamine
Technical Information
Formal Name
2,5-dimethoxy-4-nitro-benzeneethanamine
CAS Number
261789-00-8
Molecular Formula
C10H14N2O4
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
DMF: 20 mg/mlDMF:PBS(pH 7.2)(1:1): 0.5 mg/mlDMSO: 3 mg/mlEthanol: 13 mg/ml
λmax
220, 275, 361 nm
SMILES
COC1=C(CCN)C=C(OC)C([N+]([O-])=O)=C1
InChi Code
InChI=1S/C10H14N2O4/c1-15-9-6-8(12(13)14)10(16-2)5-7(9)3-4-11/h5-6H,3-4,11H2,1-2H3
InChi Key
ZMUSDZGRRJGRAO-UHFFFAOYSA-N
Regulatory Information
DEA Schedule
I
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    A series of 2,5-phenethylamines, collectively referred to as 2Cs, have psychoactive effects.1,2 The most effective 2C compounds are 2,5-dimethoxy-4-substituted phenethylamines; many are regulated as illegal substances.3,4 2C-N is described formally as 2,5-dimethoxy-4-nitrophenethylamine and is structurally analogous to the psychedelic drug 2C-B. 2C-N potently stimulates arachidonic acid release through the serotonin receptors 5-HT2C (pEC50 = 5.91) and 5-HT2A (pEC50 = 4.78).2 This product is intended for forensic and research applications.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Bruno, R., Matthews, A.J., Dunn, M., et alEmerging psychoactive substance use among regular ecstasy users in Australia. Drug Alcohol Depend. 124(1-2), 19-25 (2012).

    2. Moya, P.R., Berg, K.A., Gutiérrez-Hernandez, M.A., et alFunctional selectivity of hallucinogenic phenethylamine and phenylisopropylamine derivatives at human 5-hydroxytryptamine (5-HT)2A and 5-HT2C receptors. J. Pharmacol. Exp. Ther. 321(3), 1054-1061 (2007).

    3. Meyer, M.R., and Maurer, H.H. Metabolism of designer drugs of abuse: An updated review. Curr. Drug Metab. 11(5), 468-482 (2010).

    4. Nagai, F., Nonaka, R., and Satoh Hisashi Kamimura, K. The effects of non-medically used psychoactive drugs on monoamine neurotransmission in rat brain. Eur. J. Pharmacol. 559(2-3), 132-137 (2007).