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855871

Sigma-Aldrich

Mestranol

99%

Synonym(s):

(17α)-3-Methoxy-19-norpregna-1,3,5(10)-trien-20-yn-17-ol, 17α-Ethynyl-1,3,5(10)-estratriene-3,17β-diol 3-methyl ether, 17α-Ethynylestradiol 3-methyl ether, 3-Methoxy-17α-ethynylestradiol, NSC 84032

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About This Item

Empirical Formula (Hill Notation):
C21H26O2
CAS Number:
72-33-3
Molecular Weight:
310.43
Beilstein:
2625905
EC Number:
200-777-8
MDL number:
MFCD00003689
UNSPSC Code:
12352112
PubChem Substance ID:
24888219
NACRES:
NA.22

Quality Level

100

Assay

99%

form

solid

optical activity

[α]15/D +3°, c = 2 in dioxane

mp

153-155 °C (lit.)

SMILES string

COc1ccc2C3CC[C@@]4(C)C(CC[C@@]4(O)C#C)C3CCc2c1

InChI

1S/C21H26O2/c1-4-21(22)12-10-19-18-7-5-14-13-15(23-3)6-8-16(14)17(18)9-11-20(19,21)2/h1,6,8,13,17-19,22H,5,7,9-12H2,2-3H3/t17-,18-,19+,20+,21+/m1/s1

InChI key

IMSSROKUHAOUJS-MJCUULBUSA-N

Gene Information

human ... ESR1(2099)

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Related Categories

Pictograms

Health hazardExclamation mark
GHS08,GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H351

Hazard Classifications

Carc. 2 - Eye Irrit. 2 - Skin Irrit. 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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Yuegang Zuo et al.
Chemosphere, 63(9), 1583-1590 (2005-11-26)
17alpha-Ethinylestradiol (EE2), a major constituent of common contraceptive pills, and three other estrogenic hormones, estrone (E1), 17beta-estradiol (E2) and mestranol (MeEE2) have been determined in Acushnet River Estuary seawater using a GC-MS technique. Among three estrogenic compounds detected, EE2 has
Dennis R Doose et al.
Epilepsia, 44(4), 540-549 (2003-04-12)
To study the pharmacokinetics of a combination oral contraceptive (OC) containing norethindrone and ethinyl estradiol during OC monotherapy, concomitant OC and topiramate (TPM) therapy, and concomitant OC and carbamazepine (CBZ) therapy in order to comparatively evaluate the pharmacokinetic interaction, which
Yuegang Zuo et al.
Journal of chromatography. A, 1148(2), 211-218 (2007-04-03)
A rapid microwave-accelerated derivatization process for the GC-MS analysis of steroid estrogens, estrone (E1), 17beta-estradiol (E2), estriol (E3), 17alpha-ethynylestradiol (EE2) and mestranol (MeEE2), was developed. Under microwave irradiation, the five estrogenic hormones studied were simultaneously derivatized with N,O-bis(trimethylsilyl)trifluoroacetamide (BSTFA)+trimethylchlorosilane (TMCS)
Dóra Kovács et al.
Steroids, 77(11), 1075-1085 (2012-05-23)
Regioselective 1,3-dipolar cycloadditions of different aryl nitrile oxides to mestranol were carried out to furnish novel steroidal 17α-isoxazoles in good to excellent yields. Copper(I) was found to be an efficient catalyst, accelerating the intermolecular ring-closures and leading exclusively to 3,5-disubstituted
A sesquineolignan with a spirodienone structure from Pinus sylvestris L.
Jari Sinkkonen et al.
Angewandte Chemie (International ed. in English), 46(22), 4148-4150 (2007-04-25)
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