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4-methoxy-α-Pyrrolidinopropiophenone (hydrochloride)

Item No. 10394

Product Insert (PDF)GC-MS (PDF)Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • 4-MeO-α-PPP
  • 4-MeOPPP
  • MOPPP
Technical Information
Formal Name
1-(4-methoxyphenyl)-2-(1-pyrrolidinyl)-1-propanone, monohydrochloride
CAS Number
1794760-01-2
Molecular Formula
C14H19NO2 • HCl
Formula Weight
269.8
Purity
≥98%
Formulation
A crystalline solid
Solubility(Learn about Variance in Solubility)
DMF: 3 mg/mlDMSO: 5 mg/mlEthanol: 3 mg/mlMethanol: 1 mg/mlPBS (pH 7.2): 10 mg/ml
λmax
224, 288 nm
SMILES
COC1=CC=C(C(C(N2CCCC2)C)=O)C=C1.Cl
InChi Code
InChI=1S/C14H19NO2.ClH/c1-11(15-9-3-4-10-15)14(16)12-5-7-13(17-2)8-6-12;/h5-8,11H,3-4,9-10H2,1-2H3;1H
InChi Key
FTNXEPKGUANWLT-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    4-methoxy-α-Pyrrolidinopropiophenone (hydrochloride) (Item No. 10394), also known as MOPPP, is an analytical reference standard that is structurally categorized as a cathinone. It is a designer drug that has appeared on the illicit drug market.1 Its metabolism in rats has been described.1,2 The physiological and toxicological properties of this compound are not known. This product is intended for research and forensic applications.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Springer, D., Fritschi, G., and Maurer, H.H. Metabolism and toxicological detection of the new designer drug 4'-methoxy-α-pyrrolidinopropiophenone studied in rat urine using gas chromatography-mass spectrometry. J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. 793(2), 331-342 (2003).

    2. Staack, R.F., and Maurer, H.H. Metabolism of designer drugs of abuse. Curr. Drug Metab. 6(3), 259-274 (2005).

    Product Citations

    Tremeau-Cayel, L., Carnes, S., Schandield, M.S., et al. A comparison of single quadrupole mass detection and diode array ultraviolet detection interfaced to ultra-high performance supercritical chromatography for the quantitative analysis of synthetic cathinones. J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 1091, 96-100 (2018).