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β-Estradiol, cell culture reagent

β-Estradiol, cell culture reagent

$32.85
β-Estradiol

SKU: 02194565-CF

Synonyms
1,3,5(10)-Estratriene-3,17β-diol; (17β)-Estra-1,3,5(10)-triene-3,17-diol; cis-estradiol; 3,17-epidihydroxyestratriene; dihydrofollicular hormone; dihydrofolliculin; dihydroxyestrin; dihydrotheelin; Dimenformon; Diogyn; Estrace; Estraderm; Estroclim; Evorel; Gynoestryl; Macrodiol; Menorest; Oestrogel; Ovocyclin; Ovocylin; Profoliol B; Progynon; Systen; Vagifem; Zumenon; 3,17β-Dihydroxy-1,3,5(10)-estratriene
CAS Number:
50-28-2
Molecular Formula:
C18H24O2
Molecular Weight:
272.388 g/mol
Beilstein Registry Number:
1914275
EC Number:
200-023-8
MDL Number:
MFCD00003693
Product Description

β-Estradiol

Application Notes

β-Estradiol is used to study cell differentiation and transformations (tumorigenicity).

Usage Statement

Research Use Only (RUO). Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

Key Applications

Tumorigenicity Studies

Specifications
SKU 02194565-CF
Alternate Names 1,3,5(10)-Estratriene-3,17β-diol; (17β)-Estra-1,3,5(10)-triene-3,17-diol; cis-estradiol; 3,17-epidihydroxyestratriene; dihydrofollicular hormone; dihydrofolliculin; dihydroxyestrin; dihydrotheelin; Dimenformon; Diogyn; Estrace; Estraderm; Estroclim; Evorel; Gynoestryl; Macrodiol; Menorest; Oestrogel; Ovocyclin; Ovocylin; Profoliol B; Progynon; Systen; Vagifem; Zumenon; 3,17β-Dihydroxy-1,3,5(10)-estratriene
Application Notes β-Estradiol is used to study cell differentiation and transformations (tumorigenicity).
Base Catalog Number 194565
Beilstein Registry Number 1914275
Biochemical Physiological Actions 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.
CAS # 50-28-2
EC Number 200-023-8
Extinction Coefficient EM(280 nm) = 1950 (lit.)
Format Powder
Grade Cell Culture Grade
Hazard Statements H351-H360Fd-H362
Melting Point 151-152
Molecular Formula C18H24O2
Molecular Weight 272.388 g/mol
Optical Rotation +76.8 (Concentration = 1, Solvent = Dioxane) (Lit.)
Personal Protective Equipment Eyeshields, Full-face particle respirator, Gloves, Respirator cartridge, Respirator filter
RTECS Number KG2975000
Safety Symbol GHS08
Solubility Water Solubility3.6 mg/L (at 27 °C)
Usage Statement Research Use Only (RUO). Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
Vapor Pressure 6.38X10-9 mm Hg at 25 deg C (est)
Documents

Certificates of Analysis

Certificates of Analysis
English (United States)
Certificates of Analysis
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Certificates of Analysis
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Certificates of Analysis
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Certificates of Analysis
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Certificates of Analysis
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Certificates of Analysis
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Certificates of Analysis
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Datasheets

Datasheets
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Material Safety Data Sheet

Material Safety Data Sheet
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Material Safety Data Sheet
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Material Safety Data Sheet
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Material Safety Data Sheet
English (United States)