A synthetic estrogen
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Estradiol Undecylate

Item No. 9004927

Product Insert (PDF)
Technical Information
Formal Name
estra-1,3,5(10)-triene-3,17-diol, 17β-undecanoate
CAS Number
3571-53-7
Synonyms
  • β-Estradiol Undecylate
  • 17β-Estradiol Undecylate
  • 17β-Oestradiol Undecylate
  • E2 Undecylate
Molecular Formula
C29H44O3
Formula Weight
Purity
≥95%
A solid
DMSO: Sparingly soluble: 1-10 mg/ml
SMILES
C[C@@]12[C@](CC[C@@H]2OC(CCCCCCCCCC)=O)([H])[C@@]3([H])[C@@](CC1)([H])C4=CC=C(O)C=C4CC3
InChi Code
InChI=1S/C29H44O3/c1-3-4-5-6-7-8-9-10-11-28(31)32-27-17-16-26-25-14-12-21-20-22(30)13-15-23(21)24(25)18-19-29(26,27)2/h13,15,20,24-27,30H,3-12,14,16-19H2,1-2H3/t24-,25-,26+,27+,29+/m1/s1
InChi Key
TXHUMRBWIWWBGW-GVGNIZHQSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Estradiol undecylate is a synthetic estrogen.1,2 It induces vaginal keratinization in ovariectomized rats when administered subcutaneously at a dose of 100 µg/animal.1 Estradiol undecylate (40 µg/animal) induces vaginal estrus for 80 days in ovariectomized rats.2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Van Wauwe, J., Van Nyen, G., Coene, M.C., et alLiarozole, an inhibitor of retinoic acid metabolism, exerts retinoid-mimetic effects in vivo. J. Pharmacol. Exp. Ther. 261(2), 773-779 (1992).

    2. Kuhl, H., and Taubert, H.D. A new class of long-acting hormonal steroid preparation: Synthesis of oligomeric estradiol derivatives. Steroids 22(1), 73-87 (1973).