Identification | Back Directory | [Name]
BETA-ESTRADIOL 17-ACETATE | [CAS]
1743-60-8 | [Synonyms]
Estradiol acetate oestradiol acetate B-ESTRADIOL 17-ACETATE β-Estradiol 17-Acetate Estradiol 17-Monoacetate BETA-ESTRADIOL 17-ACETATE (17β)-Estradiol 17-acetate 17-BETA-ESTRADIOL 17-ACETATE β-Estradiol 17-acetate crude 17β-Acetoxyestra-1,3,5(10)-trien-3-ol 17BETA-ESTRADIOL 17-ACETATE VETRANAL100 1,3,5(10)-estratriene-3,17β-diol 17-acetate 1,3,5(10)-Estratriene-3,17b-diol 17-acetate 1,3,5(10)-ESTRATRIEN-3,17BETA-DIOL 17-ACETATE 1,3,5[10]-ESTRATRIENE-3,17BETA-DIOL 17-ACETATE (17β)-Estra-1,3,5(10)-triene-3,17-diol 17-Acetate 3,17BETA-DIHYDROXY-1,3,5[10]-ESTRATRIENE 17-ACETATE Estra-1,3,5(10)-triene-3,17-diol (17β)-, 17-acetate Acetic acid 3-hydroxyestra-1(10),2,4-triene-17β-yl ester Acetic acid 3-hydroxyestra-1,3,5(10)-triene-17β-yl ester 1,3,5(10)-Estratriene-3,17β-diol 17-acetate, 3,17β-Dihydroxy-1,3,5(10)-estratriene 17-acetate β-Estradiol 17-acetate,1,3,5(10)-Estratriene-3,17β-diol 17-acetate, 3,17β-Dihydroxy-1,3,5(10)-estratriene 17-acetate (8R,9S,13S,14S,17S)-3-hydroxy-13-Methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthren-17-yl acetate | [EINECS(EC#)]
605-722-5 | [Molecular Formula]
C20H26O3 | [MDL Number]
MFCD00056537 | [MOL File]
1743-60-8.mol | [Molecular Weight]
314.42 |
Chemical Properties | Back Directory | [Melting point ]
210 °C | [Boiling point ]
450.5±45.0 °C(Predicted) | [density ]
1.18±0.1 g/cm3(Predicted) | [storage temp. ]
-20°C Freezer, Under inert atmosphere | [solubility ]
Chloroform (Sparingly), Ethyl Acetate (Slightly), Methanol (Slightly), DMSO (Slightly) | [form ]
neat | [pka]
10.26±0.60(Predicted) | [color ]
White to Off-White | [PH]
6.96 at 24.1℃ and 10g/L | [BRN ]
2625732 | [LogP]
4 at 25℃ and pH5 |
Hazard Information | Back Directory | [Chemical Properties]
White Solid | [Uses]
Protected Estradiol. | [Definition]
ChEBI: Beta-Estradiol 17-acetate is a steroid ester. | [Brand name]
Femring(Galen); Femtrace (Warner Chilcott). | [Biochem/physiol Actions]
β-Estradiol is a steroid hormone involved in a number of organ functions. It is significantly associated with brain functions including neuroprotection, neurogenesis and synaptic plasticity. β-Estradiol maintains bone homeostasis, and hence is preferred for osteoporosis therapy. 17-β-Estradiol is the most active estrogen generated in our body. During postmenopausal, 17-β-estradiol inhibits oxidative modification in low density lipoprotein. This indicates that estrogen replacement therapy might be useful in treating cardiovascular disease. |
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