An internal standard for the quantification of spiroxamine
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Unlabeled Version(s)
25823Spiroxamine
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Spiroxamine-d4

Item No. 39604

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
8-(1,1-dimethylethyl)-N-ethyl-N-propyl-1,4-dioxaspiro[4.5]decane-2-methanamine-6,6,10,10-d4
CAS Number
2469272-82-8
Molecular Formula
C18H31D4NO2
Formula Weight
301.5
Purity
≥99% deuterated forms (d1-d4)
Formulation
A neat oil
Solubility(Learn about Variance in Solubility)
Chloroform: slightly solubleMethanol: slightly soluble
SMILES
CCN(CC1COC2(C([2H])([2H])CC(C(C)(C)C)CC2([2H])[2H])O1)CCC
InChi Code
InChI=1S/C18H35NO2/c1-6-12-19(7-2)13-16-14-20-18(21-16)10-8-15(9-11-18)17(3,4)5/h15-16H,6-14H2,1-5H3/i10D2,11D2
InChi Key
PUYXTUJWRLOUCW-MKQHWYKPSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    1 mg

    $325

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    Product Description

    Spiroxamine-d4 is intended for use as an internal standard for the quantification of spiroxamine (Item No. 25823) by GC- or LC-MS. Spiroxamine is a tertiary amine fungicide.1 It inhibits the growth of N. parvum, B. dothidea, D. seriata, and L. theobromae isolates from grape vines (EC50s = 0.97-10.28 mg/L).2 Spiroxamine reduces mean firing and burst rates in rat cortical cultures (EC50s = 90 and 110 nM, respectively).3 It is also cytotoxic to MDA-kb2 breast cancer cells (EC20 = 9.29 μM).4

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Sui, G., Zhang, W., Zhou, K., et al. Trialkylamine derivatives containing a triazole moiety as promising ergosterol biosynthesis inhibitor: Design, synthesis, and antifungal activity. Chem. Pharm. Bull. (Tokyo) 65(1), 82-89 (2017).

    2. Amponsah, N.T., Jones, E., Ridgway, H.J., et al. Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines. Pest Manag. Sci. 68(5), 676-683 (2012).

    3. Frank, C.L., Brown, J.P., Wallace, K., et al. Developmental neurotoxicants disrupt activity in cortical networks on microelectrode arrays: Results of screening 86 compounds during neural network formation. Toxicol. Sci. 160(1), 121-135 (2017).

    4. Orton, F., Rosivatz, E., Scholze, M., et al. Widely used pesticides with previously unknown endocrine activity revealed as in vitro antiandrogens. Environ. Health Perspect. 119(6), 794-800 (2011).