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E6375

Sigma-Aldrich

Estriol-3-Sulfat Natriumsalz

≥98% (TLC)

Synonym(e):

1,3,5(10)-Oestratrien-3,16α,17β-triol-3-sulfat, 3,16α,17β-Trihydroxy-1,3,5(10)-oestratrien-3-sulfat

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About This Item

Lineare Formel:
C18H23O6SNa
CAS-Nummer:
5150-64-1
Molekulargewicht:
390.43
MDL-Nummer:
MFCD00056547
UNSPSC-Code:
12171500
PubChem Substanz-ID:
24894625
NACRES:
NA.47

Qualitätsniveau

200

Assay

≥98% (TLC)

Form

powder

Enthält

~30% methylglucamine as stabilizer

Löslichkeit

methanol: 19.60-20.40 mg/mL, clear, colorless to faintly yellow

Anwendung(en)

diagnostic assay manufacturing
hematology
histology

Versandbedingung

ambient

Lagertemp.

room temp

SMILES String

[Na].[H][C@]12CC[C@]3(C)[C@@H](O)[C@H](O)C[C@@]3([H])[C@]1([H])CCc4cc(OS(O)(=O)=O)ccc24

InChI

1S/C18H24O6S.Na.H/c1-18-7-6-13-12-5-3-11(24-25(21,22)23)8-10(12)2-4-14(13)15(18)9-16(19)17(18)20;;/h3,5,8,13-17,19-20H,2,4,6-7,9H2,1H3,(H,21,22,23);;/t13-,14-,15+,16-,17+,18+;;/m1../s1

InChIKey

NGMCHEUPKPRHNC-XZEIGEQDSA-N

Verwandte Kategorien

Verpackung

Packungsgrösse basiert auf dem Steroidgehalt

Piktogramme

Health hazard
GHS08

Signalwort

Warning

H-Sätze

H351

P-Sätze

P281

Gefahreneinstufungen

Carc. 2

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

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

Analysenzertifikate (COA)

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T Tanaka et al.
Steroids, 46(1), 649-657 (1985-07-01)
A highly specific anti-estriol 3-sulfate antiserum was treated with 50% ammonium sulfate, and the crude globulin fraction was coupled to CNBr-activated Sepharose-4B. Addition of 0.1M Tris-HC1 buffer (pH 8.3) containing 0.1M glutamine to the solution of antigen-antibody enabled assaying without
J R Pasqualini et al.
Annals of the New York Academy of Sciences, 595, 106-116 (1990-01-01)
Different estrogen-3-sulfates (estrone-3-sulfate, estradiol-3-sulfate, and estriol-3-sulfate) can provoke important biologic responses in different mammary cancer cell lines; there is a significant increase in progesterone receptor. However, no significant effect was observed with estrogen-17-sulfates. The reason for the biologic response of
M Levitz et al.
Journal of steroid biochemistry, 20(4B), 971-974 (1984-04-01)
Estriol (E3), the most abundant estrogen in pregnancy is produced predominantly in the placenta from androgen precursors of fetal origin. The estriol so formed is secreted efficiently into the maternal circulation where it is converted to 4 conjugates--estriol-3-sulfate (E3-3S), estriol-16-glucosiduronate
T Tanaka et al.
Steroids, 43(3), 235-242 (1984-03-01)
Antisera were raised in male guinea pigs against 6-oxoestriol 3-sulfate O-carboxymethyloxime-bovine serum albumin (BSA) conjugate. The antisera to this antigen exhibited high affinity (Ka=4.7 X 10(9)M-1) and excellent specificity for estriol 3-sulfate, showing slight cross-reactions (less than 0.43%) with other
Estriol-3-sulfate in human breast cyst fluid. Concentrations, possible origin, and physiologic implications.
U Raju et al.
Annals of the New York Academy of Sciences, 586, 83-87 (1990-01-01)
Alle zugehörigen Dokumente anzeigen

Artikel

UHPLC Analysis of Conjugated Estrogens on Ascentis ® Express C18

Separation of Estriol 3-(β-D-glucuronide) sodium salt; β-Estradiol 3-(β-D-glucuronide) 17-sulfate dipotassium salt; Estriol 3-sulfate sodium salt; β-Estradiol 3,17-disulfate dipotassium salt, ≥95%; β-Estradiol 17-(β-D-glucuronide) sodium salt; β-Estradiol 3-(β-D-glucuronide) sodium salt; Estrone 3-(β-D-glucuronide) sodium salt; β-Estradiol 3-sulfate sodium salt, ≥93%; Estriol, ≥97%; Estrone 3-sulfate sodium salt, contains ~35% Tris as stabilizer; β-Estradiol, ≥98%; α-Estradiol, powder, ≥98% (TLC); Estrone, ≥99%

Verwandter Inhalt

UHPLC Analysis of Conjugated Estrogens on Titan™ C18

The Titan C18 column provided efficient and rapid resolution of thirteen related estrogenic compounds. Ultra Ultra high purity solvents provided robust operation.

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