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Application Area
Environmental
Environmental

Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.

Clinical diagnostic
Clinical diagnostic

In addition to treating various diseases, isotopes are used for imaging, diagnosis, and newborn screening.

Organic Chemistry
Organic Chemistry

Small molecule compounds labeled with stable isotopes can be used as chemical reference for chemical identification, qualitative, quantitative, detection, etc. Various types of NMR solvents can be used to study the structure, reaction mechanism and reaction kinetics of compounds.

Metabolic Research
Metabolic Research

Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.

Estriol-[d]

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General Information
Catalog: BLP-010803
CAS: 55727-98-5
Molecular Formula: C18H23DO3
Molecular Weight: 289.39
Chemical Structure
Estriol-[d]
Description Estriol-[d] is the labelled analogue of Estriol, which is a metabolite of Estradiol.
Synonyms Estriol D1; (16α,17β)-Estra-1,3,5[10]-triene-3,16,17-triol-d1; Acifemine-d1; Colpogyn-d1; Destriol-d1; Ovesterin-d1; Ovestin-d1; Tridestrin-d1; Tricovex-d1
IUPAC Name (8R,9S,13S,14S,16R,17R)-17-deuterio-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthrene-3,16,17-triol
Related CAS 50-27-1 (unlabelled)
Canonical SMILES CC12CCC3C(C1CC(C2O)O)CCC4=C3C=CC(=C4)O
InChI InChI=1S/C18H24O3/c1-18-7-6-13-12-5-3-11(19)8-10(12)2-4-14(13)15(18)9-16(20)17(18)21/h3,5,8,13-17,19-21H,2,4,6-7,9H2,1H3/t13-,14-,15+,16-,17+,18+/m1/s1/i17D
InChI Key PROQIPRRNZUXQM-JATCHCLRSA-N
Melting Point >248°C (dec.)
Purity ≥98%; ≥99% atom D
Solubility Slightly soluble in DMSO (Sonicated), Ethanol (Heated, Sonicated), Methanol
Appearance White to Off-white Solid
Application An estrogenic metabolite considerably less potent than the hormone Estradiol.
Storage Store at -20°C
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