- Estradiol
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- $10.00 / 1ASSAYS
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2026-05-11
- CAS:57-91-0
- Min. Order: 1ASSAYS
- Purity: 99%
- Supply Ability: 1 ton
- 17α-Estradiol
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- $0.00 / 1kg
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2026-05-11
- CAS:57-91-0
- Min. Order: 1kg
- Purity: 99%min
- Supply Ability: 50kg/month
- 17a-estradiol
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- $0.00 / 1kg
-
2026-05-10
- CAS:57-91-0
- Min. Order: 1kg
- Purity: 0.99
- Supply Ability: 1000kg
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| | Estradiol Basic information |
| Product Name: | Estradiol | | Synonyms: | 1,3,5-estratriene-3,17-alpha-diol;1,3,5-Estratriene-3,17alpha-diol;17alpha-Oestradiol;3,17alpha-Dihydroxyestra-1,3,5(10)-triene;3,17-alpha-dihydroxyoestra-1,3,5(10)-triene;3,17alpha-Dihydroxyoestra-1,3,5(10)-triene;5(10)-triene-3,17-diol,(17-alpha)-estra-3;epiestradial | | CAS: | 57-91-0 | | MF: | C18H24O2 | | MW: | 272.39 | | EINECS: | 200-354-8 | | Product Categories: | Steroids;Intermediates & Fine Chemicals;Pharmaceuticals;APIs;57-91-0 | | Mol File: | 57-91-0.mol |  |
| | Estradiol Chemical Properties |
| Melting point | 176-180 °C(lit.) | | Boiling point | 355.44°C (rough estimate) | | alpha | D20 +53 to +56° (c = 0.9 in dioxane) | | density | 1.0708 (rough estimate) | | refractive index | 1.4800 (estimate) | | storage temp. | Sealed in dry,Room Temperature | | solubility | ethanol: 50 mg/mL, clear, colorless | | form | powder | | pka | 10.27±0.60(Predicted) | | color | white with slight yellow | | biological source | synthetic (organic) | | Water Solubility | 3.9mg/L(25 ºC) | | Merck | 14,3704 | | InChI | 1S/C18H24O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-17,19-20H,2,4,6-9H2,1H3/t14-,15-,16+,17-,18+/m1/s1 | | InChIKey | VOXZDWNPVJITMN-SFFUCWETSA-N | | SMILES | [H][C@]12CC[C@]3(C)[C@H](O)CC[C@@]3([H])[C@]1([H])CCc4cc(O)ccc24 | | CAS DataBase Reference | 57-91-0(CAS DataBase Reference) | | NIST Chemistry Reference | Estra-1,3,5(10)-triene-3,17alpha-diol(57-91-0) | | EPA Substance Registry System | Estra-1,3,5(10)-triene-3,17-diol, (17.alpha.)- (57-91-0) |
| Hazard Codes | T,Xn | | Risk Statements | 45-48-40 | | Safety Statements | 53-45-24/25-22 | | RIDADR | UN 2811 6.1/PG 2 | | WGK Germany | 3 | | RTECS | KG3750000 | | F | 8-10 | | HS Code | 29372390 | | Storage Class | 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects | | Hazard Classifications | Aquatic Chronic 1
Carc. 2
Lact.
Muta. 2
Repr. 1A |
| | Estradiol Usage And Synthesis |
| Chemical Properties | White Solid | | Uses | Estradiol (known as α-Estradiol or 17 α-Estradiol) is a biologically active estrogen in human breast cancer cells in tissue culture. 17-Εstradiol and its selective receptor, ER-X, are not part of a classical hormone/receptor endocrine system but of a system with important autocrine/paracrine functions in the developing and adult brain. 17-Estradiol may have enormous implications for hormone replacement strategies at the menopause and in the treatment of such neurodegenerative disorders as Alzheimer’s disease and ischemic stroke. | | Definition | ChEBI: An estradiol that is estra-1,3,5(10)-triene substituted by hydroxy groups at positions 3 and 17 (the 17alpha stereoisomer). | | Biological Activity | Endogenous estrogen receptor ligand (K i values are 0.2 and 1.2 nM for ER α and ER β receptors respectively). | | Biochem/physiol Actions | Estradiol (known as alpha Estradiol or 17 alpha Estradiol) is a biologically active estrogen in human breast cancer cells in tissue culture.17-estradiol and its selective receptor, ER-X, are not part of a classical hormone/receptor endocrine system but of a system with important autocrine/paracrine functions in the developing and adult brain. 17-Estradiol may have enormous implications for hormone replacement strategies at the menopause and in the treatment of such neurodegenerative disorders as Alzheimer′s disease and ischemic stroke. | | target | Beta Amyloid | Bcl-2/Bax | Caspase | PARP | Estrogen receptor | GABA Receptor | Progestogen receptor | | storage | Room temperature | | Purification Methods | 17-Estradiol recrystallises from aqueous EtOH (80%) as the hemihydrate and differs from the -anomer (below) by not precipitating with digitonin in 80% aqueous EtOH. The diacetate [1474-52-8] crystallises from aqueous EtOH in needles with m 139-140o. The 3-benzoate crystallises in three forms m 158o, 153o and 63o. |
| | Estradiol Preparation Products And Raw materials |
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