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|CAS:||89778-27-8||Other Name:||FC 1157A; Fareston; NK 622; NSC 613680|
|Storage:||Shading, Confined Preservation||Standard:||Enterprise Standard|
|Usage:||Anti-Cancer||Drug Class:||Injectable Steroid, Bodybuilding Steroid, Bulking Steroids|
Estrogen Blocker Steroids,
Pharma Grade Steroids
Anti-Cancer White Toremifene Citrate Powder 89778-27-8 Fareston for Bodybuilding
(toremifene citrate), a.k.a. Fareston, is an oral SERM which helps oppose estrogen activity in your system. It is FDA-accepted for use in progressive breast cancer and is being assessed for prostate cancer prevention. It's a non-steroidal SERM that connects to different estrogen receptors to avoid estrogen hormones from escalating.
Product Name: Toremifene Citrate
Synonyms: FC 1157A; Fareston; NK 622; NSC 613680
Grade: Pharmaceutical Grade
Drug Class: Injectable steroid, bodybuilding steroid, bulking steroids
Storage: Shading, confined preservation
Place of Origin: China
Brand name: LSW
Certification: SGS, ISO9001, KOSHER
|Description||White Crystal Powder||Conforms|
|Solubility||Soluble in methanol,stightly soluble in water,And tn acetone||Conforms|
|Loss On Drying||Not more than 0.5%||0.23%|
|Residue on ignition||Not more than 0.2%||0.06%|
|Iron||Not more than 0.005%||0.0017%|
|Heavy metals||Not more than 0.001%||0.0006%|
|Related Substance||Total:Not more than 1.0% Individual:Not more than 0.5%||0.16%|
|E-isonet||Not more than 0.3%||0.25%|
|Acetone||Not more than 0.5%||0.128%(G/G)|
|Assay||Between 99.0% to 101.0%||99.73%|
Toremifene Citrate was originally patented as Fareston by the Orion Corporation of Finland, and approved for the treatment of breast cancer in Europe in 1996. In September of 1999, Roberts Pharmaceutical Corporation was granted the rights to market the drug in the United States of America.
Usage of Toremifene Citrate and Other SERMs:
Toremifene citrate (Fareston) is yet another SERM, which means Toremifene citrate (Fareston) will display both estrogen antagonist / agonist properties in the body. This puts Toremifene citrate (Fareston) in the same category as Nolvadex and Clomid, the two most popular drugs in Toremifene citrate (Fareston)s category.
At the hypothalamus and pituitary, estrogen acts in cooperation with the male body's negative feedback loop to send a signal to decrease the secretion of LH, and when LH secretion is lowered, so are natural testosterone levels. SERMs, like Fareston, possibly act as an estrogen antagonist in the hypothalamus and pituitary, in order to increase testosterone production. Thus, although it hasn't been studied to any great degree, it's highly likely that Fareston is capable of increasing testosterone in the same way that Nolvadex it, as it's androgenicity:estrogenicity ratio is 5x that of Nolvadex. It may also be better than Nolvadex for reasons that are of particular interest to steroid using athletes and bodybuilders.
Fareston differs from Nolvadex in several ways, however- even though it's very similar to it in others. Firstly, the risk of certain side effects (although relatively rare with Nolvadex) is actually quite a bit lower with Fareston. However unlikely these risks are in the first place, the risk of stroke, pulmonary embolism, and cataract is probably lower with Fareston than with Nolvadex. This is going to be of interest to people who have issues with "floaters" in their vision, which is sometimes caused by Nolvadex and Clomid, as this product may represent significantly less occular toxicity. It also differs slightly from Nolvadex in its potent with regards to improving lipid (cholesterol) profiles. In terms of improving bone mineral density, Fareston is roughly equal to Nolvadex.
Although anecdotal evidence on this compound is rare, bodybuilders who have already experimented with this stuff seem satisfied. In my estimation, it would seem to be a more potent and safer alternative to Nolvadex, for those who are worried about side effects. I'm also predicting that it may provide a greater increase in LH and therefore testosterone levels, in men when compared to Nolvadex (when an appropriate dose of each is utilized). This makes its use a strong possibility for PCT in the future, when studies on its ability to elevate testosterone is more fully studied and understood.
For bodybuilding purposes, a dose of 40-60mgs per day seems to be a good starting point. If the user is trying to fight existing gynecomastia (bitch tits), they may choose to double the dose and add an aromatase inhibitor like Aromasin with it. For PCT, some users will kick-start with 100-120mgs per day and then lower to 40-60mgs per day for 4-6 weeks.
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