A Certified Reference Material
Features
  • This product is intended for customers who require an alternate batch for Cannabidoiolic Acid (CRM) (Item No. 18090)
  • This product is qualified as a Certified Reference Material (CRM) that has been manufactured and tested to meet ISO/IEC 17025 and ISO 17034 international standards
  • This CRM has been characterized by metrologically valid procedures and may be used as a quantitative analytical reference standard
  • Certificate of analysis provides the certified property values and the associated uncertainties, including a statement of metrological traceability for the certified values
  • Bulk material is available for qualified institutions; please contact our sales department for pricing
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Cannabidiolic Acid (Alt. Batch CRM)

A 1 mg/ml solution in acetonitrile

Item No. 41378

Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • CBDA
Technical Information
Formal Name
2,4-dihydroxy-3-[(1R,6R)-3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-6-pentyl-benzoic acid
CAS Number
1244-58-2
Molecular Formula
C22H30O4
Formula Weight
358.5
Formulation
A 1 mg/ml solution in acetonitrile
SMILES
OC1=C(C(O)=O)C(CCCCC)=CC(O)=C1[C@@H]2C=C(C)CC[C@H]2C(C)=C
InChi Code
InChI=1S/C22H30O4/c1-5-6-7-8-15-12-18(23)20(21(24)19(15)22(25)26)17-11-14(4)9-10-16(17)13(2)3/h11-12,16-17,23-24H,2,5-10H2,1,3-4H3,(H,25,26)/t16-,17+/m0/s1
InChi Key
WVOLTBSCXRRQFR-DLBZAZTESA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Dry ice in continental US; may vary elsewhere
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Certificates of Analysis & Batch Specific Data

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    1 mg

    $168

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    Product Description

    This product is intended for customers who require an alternate batch for cannabidoiolic acid (CRM) (Item No. 18090). Cannabidoiolic acid (Alt. Batch CRM) (Item No. 41378) is a certified reference material categorized as a phytocannabinoid.1,2 Cannabidiolic acid has anxiolytic-like and antinociceptive activities in mice.2,3 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. Taura, F., Morimoto, S., and Shoyama, Y. Purification and characterization of cannabidiolic-acid synthase from Cannabis sativa L.. Biochemical analysis of a novel enzyme that catalyzes the oxidocyclization of cannabigerolic acid to cannabidiolic acid. The Journal of Biological Chemisty 271(29), 17411-17416 (1996).

    2. ZagZoog, A., Mohamed, K.A., Kim, H.J.J., et al. In vitro and in vivo pharmacological activity of minor cannabinoids isolated from Cannabis sativa. Sci. Rep. 10(1), 20405 (2020).

    3. Vigli, D., Cosentino, L., Pellas, M., et al. Chronic treatment with cannabidiolic scid (CBDA) reduces thermal pain sensitivity in male mice and rescues the hyperalgesia in a mouse model of Rett syndrome. Neuroscience 453, 113-123 (2021).