An Analytical Reference Standard
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Certified Reference Material(s)
38208Salvinorin A (CRM)
Labeled Version(s)
36410Salvinorin A-d3
Reference Material(s)
11487Salvinorin A
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Salvinorin A

Item No. 34779

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • Divinorin A
  • Sal A
Technical Information
Formal Name
(2S,4aR,6aR,7R,9S,10aS,10bR)-9-(acetyloxy)-2-(3-furanyl)dodecahydro-6a,10b-dimethyl-4,10-dioxo-2H-naphtho[2,1-c]pyran-7-carboxylic acid, methyl ester
CAS Number
83729-01-5
Molecular Formula
C23H28O8
Formula Weight
432.5
Purity
≥98%
Formulation
A crystalline solid
Solubility(Learn about Variance in Solubility)
DMF: 20 mg/mlDMSO: 20 mg/ml
SMILES
[H][C@@]12CC[C@@](C3[C@@]1(C)C[C@@H](C4=COC=C4)OC2=O)(C)[C@H](C(OC)=O)C[C@H](OC(C)=O)C3=O
InChi Code
InChI=1S/C23H28O8/c1-12(24)30-16-9-15(20(26)28-4)22(2)7-5-14-21(27)31-17(13-6-8-29-11-13)10-23(14,3)19(22)18(16)25/h6,8,11,14-17,19H,5,7,9-10H2,1-4H3/t14-,15-,16-,17-,19?,22-,23-/m0/s1
InChi Key
OBSYBRPAKCASQB-LKTZHPIXSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Salvinorin A (Item No. 34779) is an analytical reference standard categorized as an opioid and a diterpene.1 Salvinorin A has been found in S. divinorum, a plant with hallucinogenic properties.1,2,3,4 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. Roth, B.L., Baner, K., Westkaemper, R., et al. Salvinorin A: A potent naturally occurring nonnitrogenous κ opioid selective agonist. Proc. Natl. Acad. Sci. USA 99(18), 11934-11939 (2002).

    2. Harding, W.W., Tidgewell, K., Schmidt, M., et al. Salvinicins A and B, new neoclerodane diterpenes from Salvia divinorum. Org. Lett. 7(14), 3017-3020 (2005).

    3. Tsujikawa, K., Kuwayama, K., Miyaguchi, H., et al. Determination of salvinorin A and salvinorin B in Salvia divinorum-related products circulated in Japan. Forensic Sci. Int. 180(2-3), 105-109 (2008).

    4. Munro, T.A., Duncan, K.K., Xu, W., et al. Standard protecting groups create potent and selective κ opioids: Salvinorin B alkoxymethyl ethers. Bioorg. Med. Chem. 16(3), 1279-1286 (2008).