3a,5a-Tetrahydronorethisterone D5

Product Name 3a,5a-Tetrahydronorethisterone D5
Alternate Names Norethisterone Stable Isotopes, Stable Isotopes of Norethisterone
CAT No. CS-T-87315
CAS No. 122605-87-2
Category Stable Isotopes
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Norethisterone
Smileys C#C[C@]1(O)CC[C@@]2([H])[C@]3([H])CC[C@@]4([H])C([2H])([2H])[C@@](O)([2H])C([2H])([2H])C[C@]4([H])[C@@]3([H])CC[C@]12C
Controlled No
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3a,5a-Tetrahydronorethisterone D5 is a synthetic steroid hormone that belongs to the class of progestins. It is a deuterated analogue of norethindrone, which is commonly used as a hormonal contraceptive. This compound is used in various scientific researches as a stable isotope-labeled internal standard for the quantification of norethisterone in biological matrices. It is also used as a reference standard for the identification and quantification of norethisterone in pharmaceutical formulations. The chemical formula of 3a,5a-Tetrahydronorethisterone D5 is C20H25D5O2, and its molecular weight is 311.50 g/mol. It is a white to off-white powder that is soluble in organic solvents such as ethanol, methanol, and chloroform. This compound has a melting point of 210-215°C and a boiling point of 495.3°C at 760 mmHg. 3a,5a-Tetrahydronorethisterone D5 is a potent progestin that binds to the progesterone receptor and exhibits progestational activity. It is also known to have antiandrogenic and antigonadotropic effects. This compound is metabolized in the liver and excreted in the urine and feces. It has a half-life of approximately 8-12 hours in the body. In conclusion, 3a,5a-Tetrahydronorethisterone D5 is a useful compound for scientific research that involves the quantification and identification of norethisterone in biological matrices and pharmaceutical formulations. Its stable isotope-labeled nature makes it an ideal internal standard for accurate and precise measurements.

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