Boldenone Undecylenate – injectable steroid that demonstrates strong anabolic and moderate androgenic properties. Undecylenate ester extends the work of the drug so that injections can be performed every 3-4 weeks. Well-balanced anabolic and androgenic properties of this drug are greatly appreciated by athletes who believe that it is a little more alternative androgen nandrolone decanoate. Generally it is cheaper and might replace nandrolone decanoate in most courses. Boldenone Undecylenate also known as the drug that increases the production of red blood cells, although all AAS have this feature.
History:
The company has patented Ciba boldenone as a synthetic anabolic steroid in 1949. During the 1950s and 1960s, the company produced several experimental preparation of esters and finally released a long-acting form – Boldenone Undecylenate. It is sold under the name parenabol that apparently celebrated its route of administration. Parenabol had some clinical use in the 1960s and 1970s, mainly for the treatment of dystrophies and increase bone mass in osteoporosis. Boldenone Undecylenate was briefly on the official market, and its production was discontinued in the late 1970s. In the veterinary market, the drug was introduced under the name Equipoise and produced by Squibb. In veterinary medicine it is used primarily in horses, but it was used in other animals. There was a clear effect in the form of increase in dry weight, improve appetite and general condition of the animal. Equipoise by Squibb sold to 1985 while Squibb was acquired by Solvay, which in turn was later acquired by Wyeth in 1995. Veterinary division moved to Fort Dodge, and continues to produce and sell Equipoise in the U.S. and other markets. Many other companies produce boldenone Undecylenate, because the timing of patents have long expired.
Structural features:
Boldenone is a modified form of testosterone. It is characterized by the addition of a double bond between carbons 1 and 2, which reduces the relative estrogen and androgen. Equipoise has boldenone associated with the carboxylic acid ester in 17-beta hydroxyl group. Etherized steroids are less polar than the free steroids, and absorbed more slowly from the injection site. Once in the bloodstream, the ether is cleaved in the blood and travels free boldenone. Etherized steroids have been developed to prolong the therapeutic effect after injection, to inject at least compared with injections of free steroids. Boldenone Undecylenate was developed to provide a peak separation of boldenone in a few days, and prolonged secretion of the hormone for 21-28 days. It is interesting to note that boldenone and methandrostenolone is structurally almost identical. In the case of boldenone, Undecylenate ether used in position 17 beta, while in the methandrostenolone the same effect is achieved by adding a methyl group at position 17 alpha. In general, the molecules are identical. Of course, they work slightly differently in the body, given that the 17-alpha methylation, the drug can be absorbed when taken orally.
Boldenone aromatizes in the human body to estradiol. Increased estrogen levels can cause side effects such as increased water retention, increase body fat and gynecomastia. Boldenone is regarded as mildly estrogenic steroid. Studies aromatization suggest that the level of conversion to estradiol – about half of the aromatization of testosterone. The development of significant estrogenic side effects with boldenone is slightly higher than with nandrolone, but significantly lower than with testosterone. Estrogenic side effects usually do not show if the drug is taken in doses of no more than 200-400mg per week. Anti-estrogens such as clomiphene citrate or tamoxifen citrate can be used to mitigate these adverse effects, if they occur. You can alternately use an aromatase inhibitor such as Arimidex, but it’s more expensive option, and this may adversely affect the level of lipids in the blood.
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