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Merck

E1132

17β-Estradiol

ER agonist

Synonim(y):

1,3,5-Estratriene-3,17β-diol, 17β-Estradiol, 3,17β-Dihydroxy-1,3,5(10)-estratriene, Dihydrofolliculin

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1 VIAL

574,00 zł

5 VIALS

2170,00 zł

574,00 zł


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Informacje o tej pozycji

Wzór empiryczny (zapis Hilla):
C18H24O2
Numer CAS:
Masa cząsteczkowa:
272.38
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352104
EC Number:
200-023-8
MDL number:
Beilstein/REAXYS Number:
1914275
Quality level:

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Nazwa produktu

β-Estradiol, analytical standard

InChI key

VOXZDWNPVJITMN-ZBRFXRBCSA-N

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

SMILES string

O[C@H]1CC[C@@]2([H])[C@]3([H])CCC4=CC(O)=CC=C4[C@@]3([H])CC[C@@]21C

grade

analytical standard

packaging

vial of 250 mg

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

Quality Level

mp

176-180 °C (lit.)

application(s)

pharmaceutical

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Ta pozycja
E2257PHR1353E2758
Quality Level

200

Quality Level

200

Quality Level

300

Quality Level

200

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

cell culture | mammalian: suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

cell culture | mammalian: suitable, single cell analysis: suitable

grade

analytical standard

grade

-

grade

certified reference material, pharmaceutical secondary standard

grade

-

packaging

vial of 250 mg

packaging

-

packaging

-

packaging

-

mp

176-180 °C (lit.)

mp

176-180 °C (lit.)

mp

176-180 °C (lit.)

mp

176-180 °C (lit.)

application(s)

pharmaceutical

application(s)

-

application(s)

pharmaceutical (small molecule)

application(s)

-

Biochem/physiol Actions

The major estrogen secreted by the premenopausal ovary.
The major estrogen secreted by the premenopausal ovary. Estrogens direct the development of the female phenotype in embryogenesis and during puberty by regulating gene transcription and, thus, protein synthesis. It also induces the production of gonadotropins which, in turn, induce ovulation. Exposure to estradiol increases breast cancer incidence and proliferation.

Packaging

Supplied in amber screw-cap vials
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pictograms

Health hazardEnvironment

signalword

Danger

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Lact. - Repr. 1A

Klasa składowania

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


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Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

H R Andersen et al.
Environmental health perspectives, 107 Suppl 1, 89-108 (1999-05-07)
The aim of this study was to compare results obtained by eight different short-term assays of estrogenlike actions of chemicals conducted in 10 different laboratories in five countries. Twenty chemicals were selected to represent direct-acting estrogens, compounds with estrogenic metabolites
Yun Zhu et al.
PloS one, 12(2), e0171390-e0171390 (2017-02-06)
Mammalian lignans or enterolignans are metabolites of plant lignans, an important category of phytochemicals. Although they are known to be associated with estrogenic activity, cell signaling pathways leading to specific cell functions, and especially the differences among lignans, have not
Sarah B Putman et al.
PloS one, 10(10), e0140373-e0140373 (2015-10-16)
Because of poor reproduction after the lifting of an 8-year breeding moratorium, a biomedical survey of female lions in U.S. zoos was initiated in 2007. Fecal estrogen (FEM), progestagen (FPM) and glucocorticoid (FGM) metabolites were analyzed in samples collected 3-4
Nobutada Sakagami et al.
The Journal of veterinary medical science, 76(10), 1403-1405 (2014-07-01)
The influences of glucose supplementation on early development of bovine embryos in BSA-free synthetic oviduct fluid were examined. Among the groups supplemented with 1.5, 2.0, 4.0 or 5.6 mM glucose either at 0, 72 or 144 hr after fertilization, blastocysts
Hirotaka Ishii et al.
The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry, 13(4), 323-334 (2007-07-24)
It is believed that sex hormones are synthesized in the gonads and reach the brain via the blood circulation. In contrast with this view, the authors have demonstrated that sex hormones are also synthesized locally in the hippocampus and that

Questions

  1. Can I just confirm that this product is water soluble, please? Thank you.

    1 answer
    1. The solubility of this product in water has not been determined. However, various sources report a solubility rate of 3.6 - 3.9 mg/L in water. Please see the link below to review these sources from PubChem:
      https://pubchem.ncbi.nlm.nih.gov/compound/Estradiol#section=Solubility

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