Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

E9252

Sigma-Aldrich

β-Estradiol 17-hemisuccinate

Synonym(s):

1,3,5(10)-Estratriene-3,17β-diol 17-hemisuccinate, 3,17β-Hydroxy-1,3,5(10)-estratriene 17-hemisuccinate

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C22H28O5
CAS Number:
7698-93-3
Molecular Weight:
372.45
MDL number:
MFCD00056186
UNSPSC Code:
12352200
PubChem Substance ID:
24894692
form:
powder
Assay:
≥98.00% (TLC)

Assay

≥98.00% (TLC)

form

powder

solubility

methanol: 9.80-10.20 mg/mL, clear, colorless to faintly yellow

shipped in

ambient

storage temp.

room temp

SMILES string

[H][C@]12CC[C@]3(C)[C@H](CC[C@@]3([H])[C@]1([H])CCc4cc(O)ccc24)OC(=O)CCC(O)=O

InChI

1S/C22H28O5/c1-22-11-10-16-15-5-3-14(23)12-13(15)2-4-17(16)18(22)6-7-19(22)27-21(26)9-8-20(24)25/h3,5,12,16-19,23H,2,4,6-11H2,1H3,(H,24,25)/t16-,17-,18+,19+,22+/m1/s1

InChI key

YJPIDPAGJSWWBE-FNIAAEIWSA-N

Pictograms

Health hazardExclamation mark
GHS08,GHS07

Signal Word

Warning

Hazard Statements

H302 + H312 + H332,H351

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
061F4013V
061F4013

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

C Christiansen et al.
Calcified tissue international, 35(6), 720-722 (1983-09-01)
Bone loss in postmenopausal women can be treated by hormonal substitution therapy. We investigated whether rapid bone losers (as opposed to nonrapid losers) respond sufficiently to estrogen treatment. A sample of 88 early postmenopausal women was followed up for a
S S Smith et al.
Brain research, 422(1), 40-51 (1987-09-29)
The purpose of this study was to test whether 17 beta-estradiol (E2) could alter neuronal activity or responsiveness to iontophoretically applied amino acid neurotransmitters in an area not reported to contain classical E2 receptors. Such a region is the cerebellum
K W Kan et al.
Calcified tissue international, 35(6), 740-744 (1983-09-01)
Using the dextran charcoal method, a specific steroid receptor for dexamethasone, but not 17 beta-estradiol or 17 alpha-methyltrienolone, was demonstrated in cytosol prepared from mid-gestation fetal calf growth cartilage. Zonal analysis of cytoplasmic receptor levels showed that tissue sections from
Maia M Cherney et al.
Biochimica et biophysica acta, 1784(11), 1625-1632 (2008-07-01)
We have determined the X-ray crystal structure of the Mycobacterium tuberculosis (Mtb) gene product encoded by the open reading frame Rv0760c at 1.50 A resolution by single-wavelength anomalous dispersion (SAD) phasing of diffraction data from crystals of the selenomethionine-substituted protein.
J T Haskins et al.
Brain research bulletin, 7(5), 479-485 (1981-11-01)
This paper reports preliminary data obtained from the combination of extracellular single unit recording, microiontophoretic testing and intracellular staining of single neurons in the diencephalon of the anesthetized rat. Sixty neurons were recorded extracellularly and iontophoretically tested with glass multibarrelled
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service