An Analytical Reference Standard
Related Products
Parent Compound(s)
154895-fluoro AMB16421MA-CHMINACA
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Methyl 2-(1H-indazole-3-carboxamido)-3-methylbutanoate

Item No. 25580

Product Insert (PDF)GC-MS (PDF)Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • Methyl (1H-indazole-3-carbonyl)-L-valinate
  • MMB-INACA
Technical Information
Formal Name
N-(2H-indazol-3-ylcarbonyl)-L-valine, methyl ester
CAS Number
1563540-10-2
Molecular Formula
C14H17N3O3
Formula Weight
275.3
Purity
≥98%
Formulation (Request formulation change)
A crystalline solid
Solubility(Learn about Variance in Solubility)
DMF: 30 mg/mlDMSO: 30 mg/mlEthanol: 30 mg/ml
SMILES
O=C(N[C@H](C(OC)=O)C(C)C)C1=NNC2=CC=CC=C21
InChi Code
InChI=1S/C14H17N3O3/c1-8(2)11(14(19)20-3)15-13(18)12-9-6-4-5-7-10(9)16-17-12/h4-8,11H,1-3H3,(H,15,18)(H,16,17)/t11-/m0/s1
InChi Key
MGMCMSGDELHUGP-NSHDSACASA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Certificates of Analysis & Batch Specific Data

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    Product Description

    Methyl 2-(1H-indazole-3-carboxamido)-3-methylbutanoate (Item No. 25580) is an analytical reference standard that is structurally similar to known synthetic cannabinoids. Methyl 2-(1H-indazole-3-carboxamido)-3-methylbutanoate is a precursor in the synthesis of synthetic cannabinoids, including AMB (Item No. 15488), 5-fluoro AMB (Item No. 15489), MMB-4en-PINACA (Item No. 29750), MMB-FUBINACA (Item No. 9001960), and MA-CHMINACA (Item No. 16421). It is also a metabolite of 5-fluoro AMB and MA-CHMINACA.1 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. Franz, F., Jechle, H., Wilde, M., et al. Structure-metabolism relationships of valine and tert-leucine-derived synthetic cannabinoid receptor agonists: A systematic comparison of the in vitro phase I metabolism using pooled human liver microsomes and high-resolution mass spectrometry. Forensic Toxicol. 37, 316-329 (2019).