An internal standard for the quantification of climbazole
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Unlabeled Version(s)
27968(±)-Climbazole
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(±)-Climbazole-d4

Item No. 27616

Technical Information
Formal Name
1-(4-chlorophenoxy-2,3,5,6-d4)-1-(1H-imidazol-1-yl)-3,3-dimethylbutan-2-one
CAS Number
1185117-79-6
Molecular Formula
C15H13ClD4N2O2
Formula Weight
Purity
≥99% deuterated forms (d1-d4)
A solid
Chloroform: solubleMethanol: sparingly soluble
SMILES
CC(C)(C)C(C(OC1=C([2H])C([2H])=C(Cl)C([2H])=C1[2H])N2C=CN=C2)=O
InChi Code
InChI=1S/C15H17ClN2O2/c1-15(2,3)13(19)14(18-9-8-17-10-18)20-12-6-4-11(16)5-7-12/h4-10,14H,1-3H3/i4D,5D,6D,7D
InChi Key
OWEGWHBOCFMBLP-UGWFXTGHSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    (±)-Climbazole-d4 is intended for use as an internal standard for the quantification of climbazole by GC- or LC-MS. Climbazole is an imidazole antifungal.1 It inhibits the growth of C. albicans (MIC = 0.29 μg/ml) and various strains of M. pachydermatis (MICs = <0.06-1 μg/ml).2,3 (±)-Climbazole (80 mg/kg) increases the levels of cytochrome P450 in rat liver.4 Formulations containing climbazole have been used in the treatment of dandruff.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Paz-Alvarez, M., Pudney, P.D.A., Hadgraft, J., et alTopical delivery of climbazole to mammalian skin. Int. J. Pharm. 549(1-2), 317-324 (2018).

    2. Stylianou, M., Kulesskiy, E., Lopes, J.P., et alAntifungal application of nonantifungal drugs. Antimicrob. Agents Chemother. 58(2), 1055-1062 (2014).

    3. Schmidt, A. In vitro activity of climbazole, clotrimazole and silver-sulphadiazine against isolates of Malassezia pachydermatis. Zentralbl. Veterinarmed. B 44(4), 193-197 (1997).

    4. Kobayashi, Y., Suzuki, M., Ohshiro, N., et alClimbazole is a new potent inducer of rat hepatic cytochrome P450. J. Toxicol. Sci. 26(3), 141-150 (2001).