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CAS No.: | 40665-92-7 |
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Name: | CLOPROSTENOL |
Article Data: | 6 |
Molecular Structure: | |
Formula: | C22H29ClO6 |
Molecular Weight: | 424.922 |
Synonyms: | 5-Heptenoicacid, 7-[(1R,2R,3R,5S)-2-[(1E,3R)-4-(3-chlorophenoxy)-3-hydroxy-1-butenyl]-3,5-dihydroxycyclopentyl]-,(5Z)-rel- (9CI);5-Heptenoic acid,7-[2-[4-(3-chlorophenoxy)-3-hydroxy-1-butenyl]-3,5-dihydroxycyclopentyl]-, [1a(Z),2b(1E,3R*),3a,5a]-;Estrofan;Estrophan;Estrophane;Oestrophan;Oestrophane;Racemic cloprostenol;Cloprostenol; |
EINECS: | 255-028-8 |
Density: | 1.321 g/cm3 |
Boiling Point: | 628 °C at 760 mmHg |
Flash Point: | 333.6 °C |
Solubility: | Chloroform, DMSO, Methanol |
Appearance: | Yellow Oil |
PSA: | 107.22000 |
LogP: | 3.19500 |
Cloprostenol(40665-92-7), a synthetic prostaglandin analogue of F2α, exists as white amporphous powder. The sodium salt of cloprostenol(40665-92-7) is soluble in water, ethanol and methanol, insoluble in acetone.
Molecular Structure:
Molecular Formula: C22H29ClO6.
Molecular Weight: 424.96.
Density: 1.321 g/cm3.
Boiling Point: 628 ℃ at 760 mmHg.
Flash Point: 333.6 ℃.
Solubility: very slightly soluble in water.
Appearance: clear colorless to light yellowish liquid.
Cloprostenol(40665-92-7) is mainly used for functional and morphological regression of the corpus luteum (luteolysis) in cattles and horses followed by return to oestrus and normal ovulation.
Stimulates smooth muscle contractions. irritating to the mucous membranes and upper respiratory tract. May be harmful by inhalation, ingestion, or skin absorption. Cloprostenol(40665-92-7) has the potential to induce premature labor or abortion. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of Cl−.
Aryl-oxymethyl analog of prostaglandin F2α.