Ethinyl Estradiol
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Ethinyl Estradiol
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CAS No:
57-63-6
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Formula:
C20H24O2
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Chemical Name:
Ethinyl Estradiol
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Synonyms:
ETHINYL ESTRADIOL;LYNORAL;19-NORPREGNA-1,3,5(10)-TRIEN-20-YNE-3,17ALPHA-DIOL;19-NOR-1,3,5[10],17ALPHA-PREGNATRIEN-20-YNE-3,17-DIOL;1,3,5(10)-ESTRATRIEN-17-ALPHA-ETHYNYL-3,17-BETA-DIOL;ACETENYL ESTRADIOL;17ALPHA-ETHYNYL-DELTA1,3,5(10)-ESTRA-TRIENE-3,17BETA-DIOL;17ALPHA-ETHYNYLESTRADIOL
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CAS No:
Description
Ethynyl estradiol is an orally bio-active estrogen used in almost all modern formulations of combined oral contraceptive pills.Target: Estrogen ReceptorEthinyl estradiol (EE), also sometimes written as ethinylestradiol, ethynyl estradiol, or ethinyl estradiol, is a derivative of 17β-estradiol (E2), the major endogenous estrogen in humans. EE is an orally bioactive estrogen used in many formulations of combined oral contraceptive pills. It is one of the most commonly used medications for
Ethynyl estradiol (EE) is a synthetic form of estrogen that is majorly employed in numerous hormonal contraceptives in combination with progestins. Occasionally, it is also used as a constituent of menopausal hormone therapy with combination with progestins for treating menopausal symptoms. Previously, the drug was used solely for numerous indications such as treatment of prostate cancer and gynecological disorders.Ethynyl estradiol is a semisynthetic alkylated estradiol with a 17-alpha-ethinyl substitution. It is normally administred orally and is marketed mostly as a combination oral contraceptive under various brand names such as Alesse, Tri-cyclen, Yasmin, and Triphasil. A black box warning is normally labelled on the packaging that states that the drug should not be used in smoking women who are over 35 years old as it can lead to increased risk of serious cardiovascular side effects.
Off-White to Light-Yellow Crystalline Powder
Ethinylestradiol is a white to creamy-white powder. Odorless.
ChEBI: A 3-hydroxy steroid that is estradiol substituted by a ethynyl group at position 17. It is a xenoestrogen synthesized from estradiol and has been shown to exhibit high estrogenic potency on oral administration.
Ethinyl Estradiol Basic Attributes
296.41
296.40
2419975
200-342-2
TSCA listed
White to Light yellow to Light orange
29372390
Characteristics
40.46000
3.7
Ethinylestradiol is a fine white to creamy white powder. A synthetic steroid. Used in combination with progestogen as an oral contraceptive.
1.0944 (rough estimate)
182-183 °C(lit.)
378°C (rough estimate)
211.2ºC
-30 ° (C=0.4, Pyridine)
0.0113 mg/mL at 27 °C
Keep in a cool, dry, dark location in a tightly sealed container or cylinder. Keep away from incompatible materials, ignition so
1.95X10-9 mm Hg at 25 deg C (est)
LD50 oral in rat: 960mg/kg
Specific optical rotation: 3.5 deg at 24 °C/D (c = 2 in dioxane); -29.5 deg at 24 °C/D (c = 2 in pyridine)
Odorless
pKa 10.32 (Uncertain)
1.2×106mol/(m3Pa) at 25℃, HSDB (2015)
Air and light sensitive . Insoluble in water.
Ethynyl estradiol may react vigorously with strong oxidizing agents. May react exothermically with reducing agents to generate gaseous hydrogen.
room temp
Safety Information
Ⅲ
9
3077
3
T,F
53-36/37/39-45-36/37-16
RC8925000
T
Color Code—Blue: Health Hazard/Poison: Storein a secure poison location. Prior to working with thischemical you should be trained on its proper handling andstorage. Store in a refrigerator under an inert atmosphereand protect from exposure to light.
P201-P308 + P313
45-22-39/23/24/25-23/24/25-11
May react exothermically with reducing agents to generate flammable gaseous hydrogen. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, and epoxides.
UN1230 - class 3 - PG 2 - Methanol, solution
The flash point data for Ethynyl estradiol are not available. Ethynyl estradiol is probably combustible.
Drug Information
ACUTE/CHRONIC HAZARDS: When heated to decomposition Ethynyl estradiol emits acrid smoke and fumes.
Ethinyl Estradiol Use and Manufacturing
1. A metabolite of 17a-Ethynylestradiol
2. A synthetic steroid with high oral estrogenic potency
3. Estrogen, plus progestogen as oral contraceptive
4. A synthetic estradiol analog.
A synthetic estradiol analog.
A metabolite of 17a-Ethynylestradiol
A synthetic steroid with high oral estrogenic potency
estrogen, plus progestogen as oral contraceptive
Computed Properties
Molecular Weight:296.4
XLogP3:3.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:296.177630004
Monoisotopic Mass:296.177630004
Topological Polar Surface Area:40.5
Heavy Atom Count:22
Complexity:505
Defined Atom Stereocenter Count:5
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Drug Function and Efficacy
It inhibits ovulation, changes cervical secretions, makes the menstrual cycle more regular, relieves dysmenorrhea, reduces bleeding, and reduces the occurrence of iron deficiency. When combined with drospirenone, it helps to increase the level of sex hormone binding globulin (SHBG), which is beneficial for binding with endogenous androgens and inactivating them. It may reduce the incidence of ovarian cysts, pelvic inflammatory disease, benign breast disease and ectopic pregnancy (further confirmation is needed).
Registered Holders
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VALARY LAB PRIVATE LIMITED
Active
India
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ZHEJIANG XIANJU JUNYE PHARMACEUTICAL CO., LIMITED
Active
Hongkong, China
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Bayer Ag
Active
Finland
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