δ-Cadinol
Based on 1 Customer Validation
δ-Cadinol ((-)-Torreyol) is a sesquiterpenoid compound and fungicide produced by the basidiomycete Boreostereum vibrans. δ-Cadinol is used for the research of fungal infections.
For research use only. We do not sell to patients.
- Purity: 98.0%
- CAS No.: 19435-97-3
- Formula: C15H26O
- Molecular Weight:222.37
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Storage:
-20°C, sealed storage, away from moisture and light
* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
Biological Activity
δ-Cadinol (compound 26) is a juniperane-type sesquiterpene with bactericidal activity, and its 9-thio analog thio-δ-cadinol can be obtained via terpene synthase-mediated biotransformation[1].
δ-Cadinol (compound 6) serves as the major product of the reaction between purified recombinant δ-cadinene synthase and farnesyl diphosphate[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 19435-97-3
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Appearance Solid
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Molecular Weight 222.37
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Formula C15H26O
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Color White to off-white
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SMILES
CC([C@H]1[C@@]2([H])[C@@](CCC(C)=C2)([H])[C@](O)(CC1)C)C
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Synonyms
(-)-Torreyol
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Structure Classification
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Initial Source
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
-20°C, sealed storage, away from moisture and light
* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
Purity & Documentation
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Data Sheet (271 KB)
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SDS (252 KB)
- English - EN (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Portuguese - PT (252 KB)
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Handling Instructions (2659 KB)
References
[1]. Jäger B, et al. Chemoenzymatic Generation of Thio-analogues of δ-Cadinene, δ-Cadinol, and a Thio-diquinane Using 8-Thio-farnesylpyrophosphate. J Nat Prod. 2025;88(7):1653-1662. [Content Brief]
[2]. Zhou H, et al. Identification and Characterization of a δ-Cadinol Synthase Potentially Involved in the Formation of Boreovibrins in Boreostereum vibrans of Basidiomycota. Nat Prod Bioprospect. 2016;6(3):167-171. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)