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2C-G (hydrochloride)

Item No. 14064

Restricted Product (Schedule I)
Product Insert (PDF)GC-MS (PDF)Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • 3,4-Dimethyl-2,5-dimethoxyphenethylamine
Technical Information
Formal Name
2,5-dimethoxy-3,4-dimethyl-benzeneethanamine, monohydrochloride
CAS Number
327175-14-4
Molecular Formula
C12H19NO2 • HCl
Formula Weight
245.7
Purity
≥95%
Formulation
A crystalline solid
Solubility(Learn about Variance in Solubility)
DMF: 20 mg/mlDMSO: 20 mg/mlEthanol: 30 mg/mlMethanol: 1 mg/mlPBS (pH 7.2): 5 mg/ml
SMILES
COC1=C(CCN)C=C(OC)C(C)=C1C.Cl
InChi Code
InChI=1S/C12H19NO2.ClH/c1-8-9(2)12(15-4)10(5-6-13)7-11(8)14-3;/h7H,5-6,13H2,1-4H3;1H
InChi Key
LSTJMRNIFGGQEH-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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    5 mg

    $62

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    50 mg

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    Product Description

    A series of 2,5-phenethylamines, collectively referred to as 2Cs, have psychoactive effects; many are scheduled as illegal substances. 2C-G is described formally as 3,4-dimethyl-2,5-dimethoxyphenethylamine. It is analogous to the psychoactive, monomethylated compound 2C-D, which is a Schedule I Controlled Substance in the United States.1,2 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. Moya, P.R., Berg, K.A., Gutiérrez-Hernandez, M.A., et al. Functional 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).

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