Oral Anti Estrogen Tamoxifen Citrate / Nolvadex For Breast Cancer Treatment CAS

New Effective Anti-estrogen Tamoxifen Citrate for Male/Female Health

Tamoxifen Citrate Chemical Name: (Z)-2-[4-(1,2-Diphenyl-1-butenyl)phenoxyl]-N,N-dimethyl-ethanamine-citrate;
1-p-beta-Dimethylaminoethoxyphenyl-trans-1,2-diphenylbut-1-ene citrate
Tamoxifen Citrate Molecular Formula: C26H29NO.C6H8O7
Tamoxifen Citrate Molecular weight: 563.64
Tamoxifen Citrate Molecular Structure:
Tamoxifen Citrate CAS NO.: 54965-24-1
Tamoxifen Citrate Appearance: white crystalline powder
Tamoxifen Citrate MP: 140-144 ºC

Nolvadex is the trade name for the drug tamoxifen citrate, it is a non-steroidal agent that demonstrates potent anti-estrogenic properties. The drug is technically an estrogen agonist/antagonist, which competitively binds to estrogen receptors in various target tissues. Since many forms of breast cancer are responsive to estrogen, the ability of tamoxifen citrate to block its action in such cells has proven to be a very effective treatment. It is also utilized successfully as a preventative measure, taken by people with an extremely high familial tendency for breast cancer.

Nolvadex is an estrogen agonist in the liver, capable of activating the estrogen receptor and mimicking the actions of this sex hormone in this region of the body. As such it can have a markedly positive impact on HDL (good) cholesterol values, as does estrogen.

In terms of dosing for combating gynecomastia that has begun to form, there is very little research. The limited research that does exist does point to the fact that doses of 20-40mgs per day are effective in treating the existing condition.
For use during post-cycle therapy users have anecdotally indicated that doses ranging between 20 and 40mgs per day are average. These doses have been shown to significantly raise levels of testosterone, luteinizing hormone and follicle stimulating hormone. Most users have reported when using tamoxifen citrate for their post-cycle therapy they will administer the drug for a minimum of three weeks. A maximum length has not necessarily been established due to the few side effects associated with the compound.

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