An Analytical Reference Material
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  • This product is qualified as a Reference Material that has been manufactured and tested to meet ISO/IEC 17025 and ISO 17034 international standards
  • This product is intended to be used as an analytical reference standard
  • Bulk material is available for qualified institutions; please contact our sales department for pricing
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Despropionyl meta-Fluorofentanyl

Item No. 20125

Product Insert (PDF)GC-MS (PDF)Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • m-fluoro 4-ANPP
  • meta-fluoro 4-ANPP
  • Despropionyl m-FF
  • Despropionyl meta-FF
  • Despropionyl m-Fluorofentanyl
Technical Information
Formal Name
N-(3-fluorophenyl)-1-(2-phenylethyl)-4-piperidinamine
CAS Number
416881-38-4
Molecular Formula
C19H23FN2
Formula Weight
298.4
Purity
≥98%
Formulation
A neat solid
SMILES
FC1=CC=CC(NC2CCN(CCC3=CC=CC=C3)CC2)=C1
InChi Code
InChI=1S/C19H23FN2/c20-17-7-4-8-19(15-17)21-18-10-13-22(14-11-18)12-9-16-5-2-1-3-6-16/h1-8,15,18,21H,9-14H2
InChi Key
NDGQTNDWAZPEQV-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Despropionyl meta-fluorofentanyl (Item No. 20125) is an analytical reference material that is structurally similar to known opioids. Despropionyl meta-fluorofentanyl is a precursor to meta-fluorofentanyl and meta-fluorobutyryl fentanyl and a potential impurity in illicit preparations of this class of compounds. It is also a potential metabolite of meta-fluorofentanyl and meta-fluorobutyryl fentanyl based on the published metabolism of fentanyl.1,2,3,4,5 At the time despropionyl meta-fluorofentanyl (Item No. 20125) was made available for purchase, specific metabolism data had not been published. Contact us if updated information on this molecule is now available. 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. Pease, J.P., LePine, A.J., and Smith, C.M. Methods for preparing fentanyl and fentanyl intermediates. Patent Application Publication US2013/0281702A1, (2013).

    2. Watanabe, S., Vikingsson, S., Roman, M., et al. In vitro and in vivo metabolite identification studies for the new synthetic opioids acetylfentanyl, acrylfentanyl, furanylfentanyl, and 4-fluoro-isobutyrylfentanyl. AAPS J. 19(4), 1102-1122 (2017).

    3. Labroo, R.B., Paine, M.F., Thummel, K.E., et al. Fentanyl metabolism by human hepatic and intestinal cytochrome P450 3A4: Implications for interindividual variability in disposition, efficacy, and drug interactions. Drug Metab. Dispos. 25(9), 1072-1079 (1997).

    4. Melent'ev, A.B., Kataev, S.S., and Dvorskaya, O.N. Identification and analytical properties of acetyl fentanyl metabolites. J. Anal. Chem. 70(2), 216-224 (2015).

    5. Steuer, A.E., Williner, E., Staeheli, S.N., et al. Studies on the metabolism of the fentanyl-derived designer drug butyrfentanyl in human in vitro liver preparations and authentic human samples using liquid chromatography-high resolution mass spectrometry (LC-HRMS). Drug Test Anal. 9(7), 1085-1092 (2017).