CAS No.
[155206-00-1 (Unlabeled)]
Therapeutic Uses
Prostaglandins
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
(Z)-7-((1R,2R,3R,5S)-3,5-dihydroxy-2-((S,E)-3-hydroxy-5-phenylpent-1-en-1-yl)cyclopentyl)-N-(ethyl-d5)hept-5-enamide
Application Notes
Useful research chemical for a range of applications
Purity by HPLC
Not less than 95 %
Hazard Compound
No -Refer MSDS for accurate information
Bimatoprost-d5 is a drug product that is used as an analytical standard for HPLC, as well as in research and development of drugs.
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Bimatoprost-d5 usage and description
Bimatoprost D5 is a synthetic prostamide that belongs to the category of prostaglandin analogues. It is a modified version of Bimatoprost, which is a medication used to treat glaucoma and hypotrichosis (insufficient eyelashes). Bimatoprost D5 is a deuterated form of Bimatoprost, meaning that five hydrogen atoms in the molecular structure have been replaced with deuterium atoms, making it a stable isotopologue.
Bimatoprost D5 is primarily used as a research tool to study the pharmacokinetics and metabolism of Bimatoprost in vivo and in vitro. It is also used as a reference standard in analytical chemistry to develop and validate analytical methods for the quantification of Bimatoprost.
The chemical formula of Bimatoprost D5 is C25H34D5NO4, and its molecular weight is 430.64 g/mol. It has a melting point between 62°C to 64°C and is soluble in organic solvents such as ethanol, methanol, and dimethyl sulfoxide.
Bimatoprost D5 works by activating the prostaglandin receptors in the eye, which reduces intraocular pressure by increasing the outflow of aqueous humor. It also stimulates the growth of eyelashes by prolonging the anagen (growth) phase of the hair follicles.
In conclusion, Bimatoprost D5 is a valuable tool for researchers and analytical chemists to study the pharmacokinetics and metabolism of Bimatoprost. Its stable isotopologue nature makes it an ideal reference standard in the development of analytical methods for the quantification of Bimatoprost.
