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25E-NBOMe (hydrochloride)

Item No. 14727

Product Insert (PDF)GC-MS (PDF)Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • 2C-E-NBOMe
Technical Information
Formal Name
4-ethyl-2,5-dimethoxy-N-[(2-methoxyphenyl)methyl]-benzeneethanamine, monohydrochloride
CAS Number
1539266-39-1
Molecular Formula
C20H27NO3 • HCl
Formula Weight
365.9
Purity
≥98%
Formulation
A crystalline solid
Solubility(Learn about Variance in Solubility)
DMF: 3 mg/mlDMSO: 5 mg/mlEthanol: 13 mg/mlPBS (pH 7.2): 10 mg/ml
λmax
220, 282 nm
SMILES
COC1=C(CCNCC2=C(OC)C=CC=C2)C=C(OC)C(CC)=C1.Cl
InChi Code
InChI=1S/C20H27NO3.ClH/c1-5-15-12-20(24-4)16(13-19(15)23-3)10-11-21-14-17-8-6-7-9-18(17)22-2;/h6-9,12-13,21H,5,10-11,14H2,1-4H3;1H
InChi Key
SSCHHVMAKLDXFM-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    2C-E, known formally as 2,5-dimethoxy-4-ethyl phenethylamine, is a psychoactive compound that is regulated as Schedule I in the United States.1,2 25E-NBOMe is a derivative of 2C-E having an N-(2-methoxybenzyl) addition at the amine. This addition on related phenethylamines increases the affinity and selectivity for the 5-HT2A receptor over other serotonin receptors.3 This product is intended for forensic and research purposes.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Blaazer, A.R., Smid, P., and Kruse, C.G. Structure-activity relationships of phenylalkylamines as agonist ligands for 5-HT2A receptors. ChemMedChem 3(9), 1299-1309 (2008).

    2. Maurer, H.H. Chemistry, pharmacology, and metabolism of emerging drugs of abuse. Ther. Drug Monit. 32(5), 544-549 (2010).

    3. Braden, M.R., Parrish, J.C., Naylor, J.C., et al. Molecular interaction of serotonin 5-HT2A receptor residues Phe3396.51 and Phe3406.52 with superpotent N-benzyl phenethylamine agonists. Mol. Pharm. 70(6), 1956-1965 (2006).