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4-cyano MMB-BUTINACA N-butanoic acid 3-methylbutanoic acid metabolite

Item No. 33836

Synonyms
Synonyms
  • MMB-4CN-BUTINACA ester hydrolysis N-butanoic acid metabolite
Technical Information
Formal Name
(1-(3-carboxypropyl)-1H-indazole-3-carbonyl)-L-valine
Molecular Formula
C17H21N3O5
Formula Weight
Purity
≥98%
Formulation
A solution in acetonitrile
Acetonitrile: 50 mg/ml
SMILES
O=C(N[C@H](C(O)=O)C(C)C)C1=NN(CCCC(O)=O)C2=C1C=CC=C2
InChi Code
InChI=1S/C17H21N3O5/c1-10(2)14(17(24)25)18-16(23)15-11-6-3-4-7-12(11)20(19-15)9-5-8-13(21)22/h3-4,6-7,10,14H,5,8-9H2,1-2H3,(H,18,23)(H,21,22)(H,24,25)/t14-/m0/s1
InChi Key
MYJZLMBLSRIDMA-AWEZNQCLSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    4-cyano MMB-BUTINACA N-butanoic acid 3-methylbutanoic acid metabolite (Item No. 33836) is an analytical reference standard that is structurally similar to known synthetic cannabinoids. 4-cyano MMB-BUTINACA N-butanoic acid 3-methylbutanoic acid metabolite is a potential metabolite of 4-cyano MMB-BUTINACA N-butanoic acid metabolite (Item No. 33835) and 4-cyano MMB-BUTINACA (Item No. 33334) based on the published metabolism of 5-fluoro AMB (Item No. 15489) and 4-cyano CUMYL-BUTINACA (Item No. 20194).1,2 At the time 4-cyano MMB-BUTINACA N-butanoic acid 3-methylbutanoic acid metabolite (Item No. 33836) 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. Haschimi, B., Mogler, L., Halter, S., et alDetection of the recently emerged synthetic cannabinoid 4F-MDMB-BINACA in "legal high" products and human urine specimens. Drug Test Anal. 11(9), 1377-1386 (2019).

    2. Åstrand, A., Vikingsson, S., Lindstedt, D., et alMetabolism study for CUMYL-4CN-BINACA in human hepatocytes and authentic urine specimens: Free cyanide is formed during the main metabolic pathway. Drug Test. Anal. 10(8), 1270-1279 (2018).