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Estriol

ID:521918 View:1127 Collection
Date Listed: 2017-09-28 11:27:12 Country: China»Guangdong»Guangzhou
Poster: Laura Company: Kafen Biotech Co.,Ltd
Location: No.128,Hanxing East Rd,Zhongcun,Panyu District,Guangzhou,Guangdong,China Website: Kafen Biotech Co.,Ltd
Email: laura@rawroid.com Mobile: +8613332873040
Fax: +8613332873040 MSN:

99% High Purity Prohormones Steroids Raw Powder Estriol CAS 50-27-1 Basic Info. Estriol Synonyms: 50-27-1, steroid powder, Estriol CAS No.: 50-27-1 Formula: C18H24O3 Molecular Weight: 288.39 EINECS: 200-022-2 Density: 1.255 g/cm3 Melting Point: 280-282 ° C(lit. ) Boiling Point: 469 ° C at 760 mmHg Flash Point: 220.8 ° C Purity: 99% Appearance: White crystalline powder Description: Estradiol, or more precisely, 17β-estradiol, is a human sex hormone and steroid, and the primary female sex hormone. It is named for and is important in the regulation of the estrous and menstrual female reproductive cycles. Estradiol is essential for the development and maintenance of female reproductive tissues but it also has important effects in many other tissues including bone. While estrogen levels in men are lower compared to women, estrogens have essential functions in men as well. Estradiol is found in most vertebrates as well as many crustaceans, insects, fish, and other animal species. Estradiol or oestradiol (American or British English usages), derives from estra-, Gk. οστρο? (oistros, literally meaning "verve or inspiration") and -diol, a chemical name and suffix indicating that this form of steroid and sex hormone is a type of alcohol bearing two hydroxyl groups. Estradiol is produced especially within the follicles of female ovaries, but also in other endocrine (i.e., hormone-producing) and non-endocrine tissues (e.g., including fat, liver, adrenal, breast, and neural tissues). Estradiol is biosynthesized from progesterone (arrived at in two steps from cholesterol, via intermediate pregnenolone). One principle pathway then converts progesterone to its 17-hydroxy-derivative, and then to androstenedione via sequential cytochrome P450-catalyzed oxidations.Action of aromatase on this dione generates estrone, and action of a dehydrogenase on this gives the title compound, 17β-estradiol. Application: Hormonal contraception: A chemi

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