Skip to Content
Merck
CN

Key Documents

View All Documentation

E5255

Estriol 16α-(β-D-glucuronide) sodium salt

≥95% (HPLC)

Synonym(s):

1,3,5(10)-Estratriene-3,16α,17β-triol 16-glucuronide, 3,16α,17β-Trihydroxy-1,3,5(10)-estratriene 16-glucuronide

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
C24H31O9Na
CAS Number:
1852-44-4
Molecular Weight:
486.49
NACRES:
NA.77
PubChem Substance ID:
24894610
UNSPSC Code:
12352200
MDL number:
MFCD00070061
Biological source:
synthetic (organic)
Form:
powder
Assay:
≥95% (HPLC)
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

biological source

synthetic (organic)

Quality Level

200

assay

≥95% (HPLC)

form

powder

technique(s)

radioimmunoassay: suitable

solubility

ethanol: water (1:1): 10 mg/mL, clear, colorless

shipped in

ambient

storage temp.

−20°C

SMILES string

[Na].CC12CCC3C(CCc4cc(O)ccc34)C1CC(OC5OC(C(O)C(O)C5O)C(O)=O)C2O

InChI

1S/C24H32O9.Na.H/c1-24-7-6-13-12-5-3-11(25)8-10(12)2-4-14(13)15(24)9-16(21(24)29)32-23-19(28)17(26)18(27)20(33-23)22(30)31;;/h3,5,8,13-21,23,25-29H,2,4,6-7,9H2,1H3,(H,30,31);;

InChI key

BEUFZMWTRVPJQV-UHFFFAOYSA-N

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Warning

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

Regulatory Information

新产品

This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
055K37761
055K3776
068H3790
025F3869
059H3856

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

M Höller et al.
Acta endocrinologica, 100(1), 57-62 (1982-05-01)
Equimolar concentrations of [4-14C]oestriol and [6,9-3H]oestriol 16 alpha-monoglucuronide were simultaneously perfused through isolated rat livers. Oestriol was hydroxylated to 2-hydroxyoestriol and 6 xi-hydroxyoestriol; 2-hydroxyoestriol was further methylated to 2-methoxyoestriol. Oxidoreduction of oestriol led to the formation of 16 alpha-hydroxyoestrone, 16-0xooestradio-17
K Musch et al.
Zeitschrift fur Geburtshilfe und Perinatologie, 185(5), 284-287 (1981-10-01)
A method based on the inhibition of hemagglutination for the determination of estriol-16-alpha-glucuronide is compared to the method of Kober and Ittrich. A sufficient degree of correlation (p less than 0.001) is found, when the daily estrogen production (Kober-Ittrich) in
W J Brock et al.
The Journal of pharmacology and experimental therapeutics, 229(1), 175-181 (1984-04-01)
The uptake of estradiol-17 beta(beta-D-glucuronide) (E(2)17G), estriol-16 alpha(beta-D-glucuronide (E(3)16G), estradiol-17 beta-3-(beta-D-glucuronide) (E(2)3G) and taurocholate (TC) into hepatocytes isolated from male and female rats was examined and found to be linear for at least 75 sec and to exhibit Michaelis-Menten kinetics.
H Okada et al.
Biological research in pregnancy and perinatology, 5(2), 68-73 (1984-01-01)
The maternal peripheral serum level of estradiol-17 beta (E2), which reaches a peak a few weeks before delivery, may play a role in initiating delivery. In this study, the steroidal activity regulated by both the production and conjugation was estimated
Use of [125I]-iodohistamine-labelled steroid derivatives as radioligands for radioimmunoassay of natural and synthetic steroids.
F Z Stanczyk et al.
Journal of steroid biochemistry, 14(1), 53-62 (1981-01-01)
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