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4.customs synthesis
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cloprostenol sodium basic information
product name: | cloprostenol sodium |
synonyms: | 15-epi cloprostenol;15(s)-cloprostenol;16-(3-chlorophenoxy)-9,11,15r-trihydroxy-17,18,19,20-tetranorprosta-5z,13e-dien-1-oic acid sodium salt;(+)-16-m-chlorophenoxy tetranor prostaglandin f2alpha sodium salt;16-(m-chlorophenoxy)-tetranor-prostaglandin-f2alpha, sodium salt;(+/-)-9alpha,11alpha,15-trihydroxy-16-(3-chlorophenoxy)-17,18,19,20-tetranor-prosta-5z,13e-dien-1-oic acid, sodium salt;(+/-)-9alpha,11alpha,15s-trihydroxy-16-(3-chlorophenoxy)-17,18,19,20-tetranor-prosta-5z,13e-dien-1-oic acid;(+)-9alpha,11alpha,15r-trihydroxy-16-(3-chlorophenoxy)-17,18,19,20-tetranor-prosta-5z,13e-dien-1-oic acid, sodium salt |
cas: | 55028-72-3 |
mf: | c22h28clo6.na |
mw: | 446.9 |
einecs: | 259-439-3 |
product categories: | pharmaceutical raw materials;prostaglandins;chiral reagents;intermediates & fine chemicals;pharmaceuticals;other apis |
mol file: | 55028-72-3.mol |
cloprostenol sodium chemical properties |
mp | 68-70 °c |
storage temp. | −20°c |
solubility | h2o: >10 mg/ml |
form | solid |
color | light brown |
cas database reference | 55028-72-3(cas database reference) |
safety information |
hazard codes | t |
risk statements | 60-22-36/37/38 |
safety statements | 53-26-36/37/39-45 |
wgk germany | 3 |
usage | aryl-oxymethyl analog of prostaglandin f2a |
biological activity | water-soluble prostaglandin f 2 α (pgf 2 α ) analog; acts as a potent fp receptor agonist (ec 50 = 0.84 nm). potently inhibits differentiation of adipocyte precursor cells. luteolytic agent in vivo . |