An Analytical Reference Material
Features
  • 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
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Mitragynine

Item No. 11151

Product Insert (PDF)GC-MS (PDF)Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • 9-methoxy Corynantheidine
Technical Information
Formal Name
(αE,2S,3S,12bS)-3-ethyl-1,2,3,4,6,7,12,12b-octahydro-8-methoxy-α-(methoxymethylene)-indolo[2,3-a]quinolizine-2-acetic acid, methyl ester
CAS Number
4098-40-2
Molecular Formula
C23H30N2O4
Formula Weight
398.5
Purity
≥98%
Formulation (Request formulation change)
A neat solid
SMILES
O=C(OC)/C([C@H]([C@H](CC)C1)CC(N1CC2)C3=C2C4=C(OC)C=CC=C4N3)=C/OC
InChi Code
InChI=1S/C23H30N2O4/c1-5-14-12-25-10-9-15-21-18(7-6-8-20(21)28-3)24-22(15)19(25)11-16(14)17(13-27-2)23(26)29-4/h6-8,13-14,16,19,24H,5,9-12H2,1-4H3/b17-13+/t14?,16-,19?/m0/s1
InChi Key
LELBFTMXCIIKKX-DVKZKMAMSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    Product Description

    Mitragynine (Item No. 11151) is an analytical reference material categorized as an opioid.1,2 Mitragynine and its derivatives have been identified in products sold as incense.3 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. Matsumoto, K., Mizowaki, M., Suchitra, T., et al. Central antinociceptive effects of mitragynine in mice: Contribution of descending noradrenergic and serotonergic systems. Eur. J. Pharmacol. 317(1), 75-81 (1996).

    2. Takayama, H., Ishikawa, H., Kurihara, M., et al. Studies on the synthesis and opioid agonistic activities of mitragynine-related indole alkaloids: Discovery of opioid agonists structurally different from other opioid ligands. J. Med. Chem. 45(9), 1949-1956 (2002).

    3. Kikura-Hanajiri, R., Uchiyama, N., and Goda, Y. Survey of current trends in the abuse of psychotropic substances and plants in Japan. Leg. Med. (Tokyo) 13(3), 109-115 (2011).

    Product Citations

    Kim, K., Shahsavarani, M., Garza-García., J.J.O., et al. Biosynthesis of kratom opioids. New Phytol. (2023).

    Basiliere, S., and Kerrigan, S. Identification of metabolites and potential biomarkers of kratom in urine. J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. 1140, 121971 (2020).