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TESTOSTERONE UNDECANOATE ANDRIOL TEST U RAW ROIDS

1, Testosterone Undecanoate/ Andriol Identification:
Appearance: White Crystalline Powder
Purity: 98.85% by HPLC
Melting point: 61-63ºC
Categories: Steroid and Hormone; API; testosterone steroids
Usage: It can be used as pharmaceutical material. Its main function is to promote metabolism. Anabolic effects include growth of muscle mass and strength, increased bone density and strength, and stimulation of linear growth and bone maturation.testosterone undecanoate powder

2, Applications of Testosterone Undecanoate/ Andriol:

Testosterone undecanoate (brand names Aveed, Andriol, Androxon, Cernos Depot, Nebido, Panteston, Restandol, Nebido-R, Reandron 1000, Undestor), or testosterone undecylate, is an androgen and anabolic steroid and a testosterone ester. It is used in androgen replacement therapy primarily for the treatment of male hypogonadism, and has also been investigated for use as a male contraceptive or as hormone replacement therapy in transgender men. Unlike other testosterone esters, testosterone undecanoate is available in both oral and intramuscular formulations.

Testosterone undecanoate (TU) has a decade-plus history of research and use in treating male hypogonadism (low testosterone). It is the preferred mode of hormone replacement for many men’s health specialists, due to its pharmacokinetic properties. TU is capable of maintaining a steady concentration of testosterone for 12 weeks in most users, up to 14 weeks in some.5-7 To reach a steady state, a 4 ml depot of TU in castor oil is injected, with a follow-up injection six weeks later; from then on, testosterone concentration is typically maintained with a 4 ml depot injected every 12 weeks.

Andriol is an oral steroid that produces mild gains and extremely mild unwanted side effects. Unfortunately, it is also an expensive steroid and to make it worthwhile for athletes and bodybuilders to see results from its use, a lot needs to be taken.
With Andriol, this was accomplished by making a form of testosterone that would be absorbed through the lymphatic system. This is due to its high fat solubility brought about by the ester, and its suspension in oil. Having the compound absorbed this way was thought to be very advantageous, as it allows the steroid to bypass the destructive first-pass through liver. This should permit the compound to enter the blood stream intact, without the need for a harsh chemical alteration. The ester breaks off once it is in circulation of course, yielding free active Pharmacokinetics of Oral Testosterone. In design this steroid appears to be undecanoate that of a completely liver safe and orally active form of testosterone.