Ethinylestradiol Dimer

SZ CAT No:	SZ-E007015
CAS No	NA
Mol.F.	C40H46O4
Mol.Wt.	590.8
Inv. Status	In Stock

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Chemical Name: (13S,17R)-17-Ethynyl-2-(((13S,17R)-17-ethynyl-17-hydroxy-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthren-3-yl)oxy)-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthrene-3,17-diol compound with (13S,17R)-17-ethynyl-4-(((13S,17R)-17-ethynyl-17-hydroxy-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthren-3-yl)oxy)-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthrene-3,17-diol (1:1)

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Smiles: OC1=CC=C2C(CCC3C2CC[C@@]4(C)C3CC[C@]4(C#C)O)=C1OC5=CC(CCC6C7CC[C@@]8(C)C6CC[C@@]8(O)C#C)=C7C=C5.C#C[C@]9(O)CCC%10C(C%11CC[C@@]%109C)CCC%12=C%11C=CC(OC%13=C(O)C=C(CCC%14C%15CC[C@@]%16(C)C%14CC[C@]%16(C#C)O)C%15=C%13)=C%12

Reversed-phase high-performance liquid chromatographic determination of Norethindrone acetate and ethinyl estradiol in pharmaceutical formulation
By Koneru, Ajitha; Kimbahune, Ritu; Mubeen, G.; Lalitha, N.; Chakraborty, Krishnasis
From Indo American Journal of Pharmaceutical Research (2015), 5(6), 2442-2449

Analytical method development and validation for simultaneous determination and quantification of Ethinyl Estradiol and Gestodene in combined tablet dosage form by RP-HPLC
By Nautiyal, Kanchan; Ramakrishna, K.
From Journal of Chemical and Pharmaceutical Research (2014), 6(10), 74-80

Simultaneous determination of ethinyl estradiol and drospirenone in oral contraceptive by high performance liquid chromatography
By Silva, Viviane Benevenuti; Galdos, Angel Arturo Gaona; Mothe, Cintia Maria Alves; Pallastrelli, Michele Bacchi; Prado, Maria Segunda Aurora; Singh, Anil Kumar; Kedor-Hackmann, Erika Rosa Maria; Santoro, Maria Ines Rocha Miritello
From Brazilian Journal of Pharmaceutical Sciences (2013), 49(3), 521-528

New oxidative decomposition mechanism of estradiol through the structural characterization of a minute impurity and its degradants
By Beni, Zoltan; Hada, Viktor; Varga, Emese; Maho, Sandor; Aranyi, Antal; Szantay, Csaba, Jr.
From Journal of Pharmaceutical and Biomedical Analysis (2013), 78-79, 183-189

Ethinylestradiol Dimer is chemically (13S,17R)-17-Ethynyl-2-(((13S,17R)-17-ethynyl-17-hydroxy-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthren-3-yl)oxy)-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthrene-3,17-diol compound with (13S,17R)-17-ethynyl-4-(((13S,17R)-17-ethynyl-17-hydroxy-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthren-3-yl)oxy)-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthrene-3,17-diol (1:1). Ethinylestradiol Dimer is supplied with detailed characterization data compliant with regulatory guideline. Ethinylestradiol Dimer can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Ethinyl Estradiol .

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.

Ethinylestradiol Dimer

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