|Product Name||Estradiol Valerate EP Impurity A|
|Synonyms||Estradiol; Estra-1,3,5(10)-triene-3,17β-diol; Dihydrofolliculin; (17β)-Estra-1,3,5(10)-triene-3,17-diol; 3,17-Epidihydroxyestratriene; Ethinyl Estradiol Impurity D (EP); Estrofem; Estrogel|
|Related API||Estradiol Valerate|
Estradiol Valerate EP Impurity A product with CAS number 50-28-2 and catalog number SA14001 is related to Estradiol Valerate. This product is used for Abbreviated New Drug Application (ANDA) filing to FDA as well as for Quality Control (QC), toxicity studies and other analytical studies during commercial production of Estradiol Valerate.
Estradiol valerate is a medication which is a female hormone (estrogen). It is used by women to help reduce symptoms of menopause (such as hot flashes, vaginal dryness). These symptoms are caused by the body making less estrogen. If you are using this medication to treat symptoms only in and around the vagina, products applied directly inside the vaginashould be considered before medications that are taken by mouth, absorbed through the skin, or injected. This medication may also be used by women who are not able to produce enough estrogen (for example, due to hypogonadism, primary ovarian failure) and by men to treat prostate cancer.
All products / Impurities / standards are provided with certificate of analysis (CoA) along with the characterization data like 1H-NMR, MASS, HPLC Purity etc. (whatever relevant and possible). Moreover, additional data like 13C-NMR, 13C-DEPT NMR, GC, GC-MS, IC, Potency, TGA, etc. will be provided on request (extra charges may apply).
This product is for research and development (R&D) use only.
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