Ethynyl estradiol structure
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Common Name | Ethynyl estradiol | ||
|---|---|---|---|---|
| CAS Number | 57-63-6 | Molecular Weight | 296.403 | |
| Density | 1.2±0.1 g/cm3 | Boiling Point | 457.2±45.0 °C at 760 mmHg | |
| Molecular Formula | C20H24O2 | Melting Point | 182-183 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 211.2±23.3 °C | |
| Symbol |
GHS07, GHS08 |
Signal Word | Danger | |
Use of Ethynyl estradiolEthynyl 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 this purpose. Transdermal ethinyl estradiol carries a greater risk of clot formation and venous thromboembolism than 17 beta estradiol, which some have theorized to be related to different amounts of hepatic metabolism after absorption. The same contraindications and precautions apply for EE as with other estrogen medications.Estinyl was a preparation of EE alone that was used for the management of menopausal symptoms and female hypogonadism. EE is released into the environment as a xenoestrogen from the urine and feces of people who take it as a medication. The major concern with unopposed estrogen is of endometrial cancer. As such, the medication is generally prescribed with progesterone in the setting of birth control. The first orally active semisynthetic steroidal estrogen, EE (17α-ethynylestradiol), the 17α-ethynyl analog of E2, was synthesized in 1938 by Hans Herloff Inhoffen and Walter Hohlweg at Schering AG in Berlin. |
This table lists Chinese names, IUPAC names and various aliases of this chemical substance.
| Name | 17α-ethynylestradiol |
|---|---|
| Synonym | More Synonyms |
This table contains bioactivity, target information and biological‑assay experimental data of this compound.
| 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 this purpose. Transdermal ethinyl estradiol carries a greater risk of clot formation and venous thromboembolism than 17 beta estradiol, which some have theorized to be related to different amounts of hepatic metabolism after absorption. The same contraindications and precautions apply for EE as with other estrogen medications.Estinyl was a preparation of EE alone that was used for the management of menopausal symptoms and female hypogonadism. EE is released into the environment as a xenoestrogen from the urine and feces of people who take it as a medication. The major concern with unopposed estrogen is of endometrial cancer. As such, the medication is generally prescribed with progesterone in the setting of birth control. The first orally active semisynthetic steroidal estrogen, EE (17α-ethynylestradiol), the 17α-ethynyl analog of E2, was synthesized in 1938 by Hans Herloff Inhoffen and Walter Hohlweg at Schering AG in Berlin. |
|---|---|
| Related Catalog | |
| Target |
Human Endogenous Metabolite |
| References |
[1]. Djerassi C. Chemical birth of the pill. 1992. Am J Obstet Gynecol. 2006 Jan;194(1):290-8. |
This table shows physicochemical parameters including melting point, boiling point, density, solubility and optical rotation. Missing data is marked as N/A.
| Density | 1.2±0.1 g/cm3 |
|---|---|
| Boiling Point | 457.2±45.0 °C at 760 mmHg |
| Melting Point | 182-183 °C(lit.) |
| Molecular Formula | C20H24O2 |
| Molecular Weight | 296.403 |
| Flash Point | 211.2±23.3 °C |
| Exact Mass | 296.177643 |
| PSA | 40.46000 |
| LogP | 4.52 |
| Vapour Pressure | 0.0±1.2 mmHg at 25°C |
| Index of Refraction | 1.624 |
| InChIKey | BFPYWIDHMRZLRN-SLHNCBLASA-N |
| SMILES | C#CC1(O)CCC2C3CCc4cc(O)ccc4C3CCC21C |
| Storage condition | -20°C Freezer |
| Water Solubility | ethanol: 50 mg/mL, clear, slightly yellow |
This table provides MSDS information including hazard classification, first‑aid, fire‑fighting, spill handling, operation and storage instructions.
This table summarizes toxicological test data, acute & chronic toxicity and ecological hazard parameters for this chemical.
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
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This table covers safety warnings, protective measures, incompatible substances and disposal guidelines for this compound.
| Symbol |
GHS07, GHS08 |
|---|---|
| Signal Word | Danger |
| Hazard Statements | H302-H350 |
| Precautionary Statements | P201-P308 + P313 |
| Personal Protective Equipment | Eyeshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges |
| Hazard Codes | T:Toxic |
| Risk Phrases | R45;R22 |
| Safety Phrases | S53-S36/37/39-S45 |
| RIDADR | 2811.0 |
| WGK Germany | 3 |
| RTECS | RC8925000 |
| HS Code | 2937290090 |
This table presents publicly reported synthetic routes, reaction conditions, reactants and product information of the compound.
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~78%
Ethynyl estradiol CAS#:57-63-6 |
| Literature: Rao, Pemmaraju N.; Cessac, James W.; Kim, Hyun K. Steroids, 1994 , vol. 59, # 11 p. 621 - 627 |
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Ethynyl estradiol CAS#:57-63-6 |
| Literature: US2265976 , ; DE681869 , ; DRP/DRBP Org.Chem. |
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Ethynyl estradiol CAS#:57-63-6 |
| Literature: Pharmazie, , vol. 39, # 1 p. 27 - 29 |
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Ethynyl estradiol CAS#:57-63-6 |
| Literature: FR809819 , ; |
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Ethynyl estradiol CAS#:57-63-6 |
| Literature: Chemische Berichte, , vol. 77/79, p. 121,125 |
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Ethynyl estradiol CAS#:57-63-6 |
| Literature: Chemische Berichte, , vol. 77/79, p. 121,125 |
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Ethynyl estradiol CAS#:57-63-6
Detail
Learn More
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| Literature: Steroids, , vol. 36, # 3 p. 255 - 282 |
This table lists upstream starting materials and downstream derivative products related to this chemical.
| Precursor 7 | |
|---|---|
| DownStream 10 | |
This table shows customs‑related data including HS‑code, tariff and regulatory conditions for import and export.
| HS Code | 2937290090 |
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This table lists relevant public references with title, journal and publication metadata for this compound.
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Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species.
Chem. Res. Toxicol. 23 , 171-83, (2010) Drug-induced liver injury is one of the main causes of drug attrition. The ability to predict the liver effects of drug candidates from their chemical structures is critical to help guide experimental... |
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Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
J. Sci. Ind. Res. 65(10) , 808, (2006) Drug-induced liver injury (DILI) is a significant concern in drug development due to the poor concordance between preclinical and clinical findings of liver toxicity. We hypothesized that the DILI typ... |
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The Japanese toxicogenomics project: application of toxicogenomics.
Mol. Nutr. Food. Res. 54 , 218-27, (2010) Biotechnology advances have provided novel methods for the risk assessment of chemicals. The application of microarray technologies to toxicology, known as toxicogenomics, is becoming an accepted appr... |
This table collects all English aliases, systematic names and CAS‑related synonyms of the compound.
| Estinyl |
| Prosexol |
| diprol |
| Gynolett |
| eed |
| LYNORAL |
| Estigyn |
| Dufaston |
| Kolpolyn |
| MFCD00003690 |
| Anovlar |
| Ertonyl |
| Ethynyl estradiol |
| Estoral |
| Esteed |
| Ethinyl estradiol |
| (17α)-19-Norpregna-1(10),2,4-trien-20-yne-3,17-diol |
| (8R,9S,13S,14S,17R)-17-Ethinyl-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthren-3,17-diol |
| 17α-ethynylestradiol |
| Progylut |
| Ethynylestradiol |
| Ethinyloestradiol |
| (8R,9S,13S,14S,17R)-17-éthynyl-13-méthyl-7,8,9,11,12,13,14,15,16,17-décahydro-6H-cyclopenta[a]phénanthrène-3,17-diol |
| (17α)-19-Norpregna-1,3,5(10)-trien-20-yne-3,17-diol |
| Etinilestradiol |
| 17alpha-ethynylestradiol |
| (17b)-17-ethynylestra-1(10),2,4-triene-3,17-diol |
| 17-Ethynyloestra-1,3,5(10)-triene-3,17β-diol |
| EINECS 200-342-2 |
| Ylestrol |
| Progynon M |
| Ethinyl estradiol (USP) |
| Etivex |
| 17a-Ethynyl-1,3,5(10)-estratriene-3,17b-diol |
| Ethinyl Estradial |
This section contains frequently‑asked‑questions about this compound, including basic parameters, properties, storage conditions and corresponding answers.
| Q: What is the CAS number of 17α-ethynylestradiol? |
| A: CAS number of 17α-ethynylestradiol is 57-63-6. |
| Q: What is the boiling point of 17α-ethynylestradiol? |
| A: Boiling point of 17α-ethynylestradiol is 457.2±45.0 °C at 760 mmHg. |
| Q: What is the molecular formula of 17α-ethynylestradiol? |
| A: Molecular formula of 17α-ethynylestradiol is C20H24O2. |
| Q: What are the upstream materials of 17α-ethynylestradiol? |
| A: Related upstream materials(CAS) of 17α-ethynylestradiol: 68-22-4;1111-63-3;28913-23-7;53-16-7;74-86-2;4301-14-8;72-33-3. |
| Q: What is the LogP of 17α-ethynylestradiol? |
| A: LogP of 17α-ethynylestradiol is 4.52. |
| Q: What is the polar surface area (PSA) of 17α-ethynylestradiol? |
| A: Polar surface area (PSA) of 17α-ethynylestradiol is 40.46000. |
| Q: How is the water solubility of 17α-ethynylestradiol? |
| A: Water solubility of 17α-ethynylestradiol: ethanol: 50 mg/mL, clear, slightly yellow. |
| Q: What is the SMILES notation of 17α-ethynylestradiol? |
| A: SMILES notation of 17α-ethynylestradiol is C#CC1(O)CCC2C3CCc4cc(O)ccc4C3CCC21C. |
| Q: What is the molecular weight of 17α-ethynylestradiol? |
| A: Molecular weight of 17α-ethynylestradiol is 296.403. |
| Q: What are the storage conditions for 17α-ethynylestradiol? |
| A: Storage conditions for 17α-ethynylestradiol: -20°C Freezer. |
This table lists manufacturers and suppliers of this compound, including vendor names and product supply reference information.
| Shanghai Nianxing Industrial Co., Ltd |
| Dayang Chem (Hangzhou) Co., Ltd. |
| Henan Tianfu Chemical Co., Ltd. |