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73532

Supelco

2-Methoxyestrone

analytical standard

Synonym(s):

2-MeO-E1, 3-Hydroxy-2-methoxyestra-1,3,5(10)-trien-17-one

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About This Item

Empirical Formula (Hill Notation):
C19H24O3
CAS Number:
362-08-3
Molecular Weight:
300.39
EC Number:
206-645-6
MDL number:
MFCD00056413
UNSPSC Code:
41116107
PubChem Substance ID:
329764929

grade

analytical standard

Quality Level

100

Assay

≥97.0% (HPLC)

optical activity

[α]/D +182.5±7.5°, c = 0.5 in methanol

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

pharmaceutical

format

neat

storage temp.

2-8°C

SMILES string

C[C@@]12[C@](CCC2=O)([H])[C@]3([H])CCC4=CC(O)=C(OC)C=C4[C@@]3([H])CC1

InChI

1S/C19H24O3/c1-19-8-7-12-13(15(19)5-6-18(19)21)4-3-11-9-16(20)17(22-2)10-14(11)12/h9-10,12-13,15,20H,3-8H2,1-2H3/t12-,13+,15-,19-/m0/s1

InChI key

WHEUWNKSCXYKBU-QPWUGHHJSA-N

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictograms

Health hazardEnvironment
GHS08,GHS09

Signal Word

Warning

Hazard Statements

H351,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF0118
BCBX4110
BCBS2816V
BCBL8654V
BCBL8654

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Hannah Oh et al.
British journal of cancer, 117(7), 1070-1078 (2017-08-18)
Prolonged sitting and lower levels of physical activity have been associated with increased levels of parent oestrogens (oestrone and oestradiol), the key hormones in female cancers, in postmenopausal women. However, it is unknown whether sitting and physical activity are associated
Shiying Xu et al.
Ecotoxicology and environmental safety, 209, 111754-111754 (2020-12-16)
There are many kinds of estrogens, and endogenous estrogens produce a variety of estrogen metabolites with similar structure but with different physiological effects after metabolism in vivo. Studies have shown that estrone (E1) widely occurs in the environment and animal-derived
Daniela Pemp et al.
Archives of toxicology, 93(7), 1979-1992 (2019-05-24)
Despite being widely used to investigate 17β-estradiol (E2)-induced mammary gland (MG) carcinogenesis and prevention thereof, estrogen homeostasis and its significance in the female August Copenhagen Irish (ACI) rat model is unknown. Thus, levels of 12 estrogens including metabolites and conjugates
Frank Z Stanczyk et al.
Clinica chimica acta; international journal of clinical chemistry, 484, 223-225 (2018-06-01)
Higher circulating estradiol levels are generally obtained using conventional radioimmunoassays (RIA) compared to liquid chromatography/tandem mass spectrometry (LC-MS/MS) assays, and this has been attributed to the presence of estradiol metabolites that cross-react with the antibody used in the RIA. This
Rebecca Troisi et al.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 27(10), 1208-1213 (2018-07-28)
Background: Prenatal diethylstilbestrol (DES) exposure is associated with adverse reproductive outcomes and cancer of the breast and vagina/cervix in adult women. DES effects on estrogen metabolism have been hypothesized, but reproductive hormone concentrations and metabolic pathways have not been comprehensively
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