A Certified Reference Material
Features
  • This product is intended for customers who require an alternate batch for (±)-cannabichromene (CRM) (Item No. ISO60163)
  • 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
Related Products
Alternative(s)
ISO60163(±)-Cannabichromene (CRM)
Analytical Standard(s)
26252(±)-Cannabichromene
Isomer(s)
9003416(+)-Cannabidiol 38947(+)-cis-Cannabidiol 35329(+)-Δ8-THC 33453(+)-Δ9-THC 34628(+)-Δ9-THC (exempt preparation) 9002438(±)-Cannabicyclol42627(±)-Cannabicyclol (Alt. Batch CRM) 22036(±)-Cannabicyclol (CRM) 9003741(±)-Cannabidiol 27074(±)-cis-Δ9-THC 42464(±)-cis-Δ9-THC (CRM) 9003740(±)-Δ9-THC 34629(±)-Δ9-THC (exempt preparation) 41814(6aR,9R)-Δ10-THC (Alt. Batch CRM) 33011(6aR,9R)-Δ10-THC (CRM) 42625(6aR,9S)-Δ10-THC (Alt. Batch CRM) 33012(6aR,9S)-Δ10-THC (CRM) 37046(9,10a)-anti-Δ6a,7-THC 41297(9,10a)-anti-Δ6a,7-THC (exempt preparation) 37047(9,10a)-syn-Δ6a,7-THC 41298(9,10a)-syn-Δ6a,7-THC (exempt preparation) 426299(R)-Δ6a,10a-THC (Alt. Batch CRM) 330139(R)-Δ6a,10a-THC (CRM) 340769(R)-Δ7-THC 391879(R)-Δ7-THC (CRM) 421419(S)-Δ6a,10a-THC (Alt. Batch CRM) 330149(S)-Δ6a,10a-THC (CRM) 340779(S)-Δ7-THC 393179(S)-Δ7-THC (CRM) 10004259Abnormal Cannabidiol 37475Cannabicitran 41377Cannabicitran (Alt. Batch CRM) 21295Cannabicitran (CRM) 90080Cannabidiol 41217Cannabidiol (Alt. Batch CRM) ISO60156Cannabidiol (CRM) 41216exo-THC (Alt. Batch CRM) 36898exo-THC (CRM) 33862Δ4-iso-THC 33863Δ4(8)-iso-THC 39955Δ4(8)-iso-THC (CRM) 43198Δ8-cis-iso-THC 33864Δ8-iso-THC 39000Δ8-iso-THC (CRM) 14042Δ8-THC 41193Δ8-THC (Alt. Batch CRM) ISO60158Δ8-THC (CRM) 12068Δ9-THC 42138Δ9-THC (Alt. Batch CRM) ISO60157Δ9-THC (CRM) 43003Δ9-THC (CRM) 45655Δ9-THC (CRM) 9003771Δ9-THC (solution)
Labeled Version(s)
21294(±)-Cannabichromene-d9 (CRM)
Metabolite(s)
40857(±)-6',7'-dihydroxy Cannabichromene 40854(±)-6',7'-epoxy Cannabichromene 40853(±)-8'-hydroxy Cannabichromene
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(±)-Cannabichromene (Alt. Batch CRM)

A 1 mg/ml solution in methanol

Item No. 41376

Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • CBC
  • NSC 291831
  • Pentylcannabichromene
Technical Information
Formal Name
2-methyl-2-(4-methyl-3-penten-1-yl)-7-pentyl-2H-1-benzopyran-5-ol
CAS Number
20675-51-8
Molecular Formula
C21H30O2
Formula Weight
Formulation
A 1 mg/ml solution in methanol
SMILES
CCCCCC1=CC2=C(C=CC(CC/C=C(C)/C)(C)O2)C(O)=C1
InChi Code
InChI=1S/C21H30O2/c1-5-6-7-10-17-14-19(22)18-11-13-21(4,23-20(18)15-17)12-8-9-16(2)3/h9,11,13-15,22H,5-8,10,12H2,1-4H3
InChi Key
UVOLYTDXHDXWJU-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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Certificates of Analysis & Batch Specific Data

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    Product Description

    This product is intended for customers who require an alternate batch for (±)-cannabichromene (CRM) (Item No. ISO60163). (±)-Cannabichromene (Alt. Batch CRM) (Item No. 41376) is a certified reference material categorized as a phytocannabinoid.1,2 (±)-Cannabichromene induces catalepsy, hypothermia, hypolocomotion, and antinociception in the mouse tetrad assay for cannabimimetic activity.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. DeLong, G.T., Wolf, C.E., Poklis, A., et alPharmacological evaluation of the natural constituent of Cannabis sativa, cannabichromene and its modulation by Δ9-tetrahydrocannabinol. Drug Alcohol Depend. 112(1-2), 126-133 (2010).

    2. Rosenthaler, S., Pöhn, B., Kolmanz, C., et alDifferences in receptor binding affinity of several phytocannabinoids do not explain their effects on neural cell cultures. Neurotoxicol. Teratol. 46, 49-56 (2014).