An internal standard for the quantification of corticosterone
Related Products
Unlabeled Version(s)
16063Corticosterone
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Corticosterone-d8

Item No. 28524

Technical Information
Formal Name
(11β)-11,21-dihydroxy-pregn-4-ene-3,20-dione-2,2,4,6,6,17,21,21-d8
CAS Number
1271728-07-4
Synonyms
  • 17-deoxy Cortisol-d8
  • 11β,21-DHP-d8
  • 11β,21-dihydroxy Progesterone-d8
Molecular Formula
C21H22D8O4
Formula Weight
Purity
≥99% deuterated forms (d1-d8)
Formulation
A solid
Ethanol: slightly solubleMethanol: slightly soluble
SMILES
O=C1C([2H])([2H])C[C@@]2(C)C(C([2H])([2H])C[C@]3([H])[C@]2([H])[C@@H](O)C[C@@]4(C)[C@@]3([H])CC[C@]4([2H])C(C([2H])([2H])O)=O)=C1[2H]
InChi Code
InChI=1S/C21H30O4/c1-20-8-7-13(23)9-12(20)3-4-14-15-5-6-16(18(25)11-22)21(15,2)10-17(24)19(14)20/h9,14-17,19,22,24H,3-8,10-11H2,1-2H3/t14-,15-,16+,17-,19+,20-,21-/m0/s1/i3D2,7D2,9D,11D2,16D
InChi Key
OMFXVFTZEKFJBZ-VWODBOJYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Certificates of Analysis & Batch Specific Data

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    Product Description

    Corticosterone-d8 is intended for use as an internal standard for the quantification of corticosterone (Item No. 16063) by GC- or LC-MS. Corticosterone is a steroid hormone produced in the cortex of the adrenal glands that binds to both glucocorticoid and mineralocorticoid receptors.1 It is produced in response to adrenocorticotropic hormone (ACTH) and is the precursor to aldosterone synthesis.2 Since the production of glucocorticoids is increased by stress, it is often used as a biomarker of stress.3 Plasma corticosterone levels have a circadian variation and corticosterone may be important in the regulation of the sleep-wake cycle.4,5

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Lu, N.Z., Wardell, S.E., Burnstein, K.L., et alInternational Union of Pharmacology. LXV. The pharmacology and classification of the nuclear receptor superfamily: Glucocorticoid, mineralocorticoid, progesterone, and androgen receptors. Pharmacol. Rev. 58(4), 782-797 (2006).

    2. Palme, R., Rettenbacher, C., Touma, C., et alStress hormones in mammals and birds: Comparative aspects regarding metabolism, excretion, and noninvasive measurement in fecal samples. Ann. N. Y. Acad. Sci. 1040(21), 162-171 (2005).

    3. Goymann, W., Möstl, E., and Gwinner, E. Corticosterone metabolites can be measured noninvasively in excreta of European stonechats (Saxicola torquata rubicola). Auk 119(4), 1167-1173 (2002).

    4. Vázquez-Palacios, G., Retana-Márquez, S., Bonilla-Jaime, H., et alFurther definition of the effect of corticosterone on the sleep-wake pattern in the male rat. Pharmacol. Biochem. Behav. 70(2-3), 305-310 (2001).

    5. Millspaugh, J.J., Washburn, B.E., Milanick, M.A., et alEffects of heat and chemical treatments on fecal glucocorticoid measurements: Implications for sample transport. Wildl. Soc. Bull. 31(2), 399-406 (2003).