Testosterone Undecanoate
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Molecular Structure
Detailed Description
Its compound contains 40 mg of testosterone undecanoate based on oil and is sealed in capsules. Minus the ester weight, which is equivalent to about 25 mg of the testosterone dose per hat. This steroid is designed to be very different from most oral steroids. Oral administration of drugs usually flows through the liver into the bloodstream. When a steroid compound is administered in this manner without any form of structural protection .
This process leaves a very small steroid intact, essentially inactivating the drug. The addition of methyl (c-17AA) to the structure is a way to protect it from the process, but the results also apply pressure to the liver. In some cases, the stress can lead to actual damage to the liver tissue, so the designer of the steroid seeks another way to protect the testosterone molecule. With Andriol, which is produced by making a form of testosterone that will be absorbed through the lymphatic system. This is due to its high fat solubility caused by the ester and its suspension in the oil. It is believed that the absorption of the compound in this way is very advantageous because it allows the steroid to bypass the destructive first pass through the liver. This should allow the compound to enter the bloodstream completely without the need for harsh chemical changes. Once the ester breaks in the circulation, it produces the pharmacokinetics of free-acting oral testosterone. In the design, this steroid appears to be undecanoic, complete liver safe and oral active form of testosterone
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