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
  • Bulk material is available for qualified institutions; please contact our sales department for pricing
Related Products
Certified Reference Material(s)
18930Mitragynine-d3 (CRM)
Unlabeled Version(s)
11151Mitragynine 18567Mitragynine (CRM)
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Mitragynine-d3

Item No. 18929

Product Insert (PDF)GC-MS (PDF)Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • 9-methoxy Corynantheidine-d3
Technical Information
Formal Name
(αE,2S,3S,12bS)-3-ethyl-1,2,3,4,6,7,12,12b-octahydro-8-methoxy-d3-α-(methoxymethylene)-indolo[2,3-a]quinolizine-2-acetic acid, methyl ester
CAS Number
2135473-75-3
Molecular Formula
C23H27D3N2O4
Formula Weight
401.5
Purity
≥97%
Formulation (Request formulation change)
A neat solid
SMILES
O=C(OC)/C([C@@H]1[C@H](CC)CN2CCC3=C(NC4=C3C(OC([2H])([2H])[2H])=CC=C4)[C@]2([H])C1)=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+/m1/s1/i3D3
InChi Key
LELBFTMXCIIKKX-MEQAAMGQSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    500 µg

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    Product Description

    Mitragynine-d3 (Item No. 18929) is an analytical reference material intended for use as an internal standard for the quantification of mitragynine (Item Nos. 11151 | 18567) by GC- or LC-MS. Mitragynine is 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

    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).