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CAS 89778 27 8 Toremifene Citrate Powder For Antiestrogen
Place of Origin | China |
---|---|
Brand Name | MALL |
Certification | TESTING |
Model Number | 89778 27 8 |
Minimum Order Quantity | 10g |
Price | negotiable |
Packaging Details | 10g,50g,1kg bag |
Delivery Time | 1-3 working days to ship, then about 5-12 working days for delivery |
Payment Terms | , , T/T, Bank transfer and BTC or Another Payment Method |
Supply Ability | 1000 kg per month |
Purity | 99% Min | Grade Standard | Medical Grade |
---|---|---|---|
MW | 598.08 | Other Names | Fareston |
Cas No. | 89778 27 8 | Shelf Life | 2 Years |
MF | C32H36ClNO8 | Assay | HPLC 99% |
Color | White Powder | Type | Auxiliaries And Other Medicinal Chemicals |
High Light | Antiestrogen Toremifene Citrate Powder,Antiestrogen 89778 27 8,Toremifene Citrate Powder |
CAS 89778 27 8 Toremifene Citrate raw Steroid Powder Fareston powder
Toremifene Citrate CAS 89778-27-8
Toremifene Citrate Synonyms: FC 1157a; Fareston; NK 622; NSC 613680
Toremifene Citrate Molecular Formula: C26H28ClNO·C6H8O7
Toremifene Citrate Molecular Weight: 598.09
Toremifene Citrate Melting Point: 158-164 ºC
Toremifene Citrate Boiling Point: 535.1 ºC at 760 mmHg
Toremifene Citrate Density: 1.045g/cm3
Toremifene Citrate Refractive index: 1,416-1,418
Toremifene Citrate Appearance: White or almost white powder
Toremifene Citrate Drug Class: Selective Estrogen Receptor Modulator
Toremifene Citrate Active Life: 5-7 days
Toremifene Citrate Use: An antiestrogen and antineoplastic. Nonsteroidal antiestrogen structurally similar to Tamoxifen.
Toremifene Citrate Descriptions:
Fareston will display both estrogen antagonist / agonist properties in the body. This puts Fareston in the same category as Nolvadex and Clomid, the two most popular drugs in Farestons category. FARESTON is an estrogen agonist/antagonist indicated for the treatment of metastatic breast cancer in postmenopausal women with estrogen-receptor positive or unknown tumors.
Toremifene administration for a period of 3 months in men with idiopathic oligozoospermia is associated with significant improvements of sperm count, motility, and morphology, mediated by increased gonadotropin secretion and possibly a direct beneficial effect of toremifene on the testes. The above findings are also indicative of a better testicular exocrine (improved sperm parameters) response to treatment in men whose partners achieved pregnancy compared with those who did not. Further randomized, placebo-controlled trials should be conducted to determine whether this particular selective estrogen receptor modulator can be useful as an initial approach in men with oligozoospermia.
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