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Testosterone Undecanoate

ID:496480 View:183 Collection
Date Listed: 2017-01-17 11:40:08 Country: China»Hubei»WUHAN
Poster: Cherry Wang Company: Wuhan YC Medicine Co.ltd
Location: No.496,Zhongshan Road, Wuhan, Hubei, China Website: Wuhan YC Medicine Co.ltd
Email: wx@yccreate.com Mobile: 18149707080
Fax: 862788048077 MSN:

Prescription Raw Testosterone Undecanoate Powder , Andriol Steroids To Get Ripped 1. Quick Detail Product name Testosterone Undecanoate Other name Andriol CAS register number 5949-44-0 EINECS 227-712-6 Molecular formula C30H48O3 Molecular weight 456.70 Molecular structure Assay 97.0%~103.0% Appearance White crystalline powder Package 1kg/aluminium foil bag or as required Usage can be used as pharmaceutical material 2. Product description Andriol first became available in the early 1980′s. This compound contains 40 mg of testosterone undecanoate, based in oil (oleic acid) and sealed inside a capsule. Subtracting the ester weight, this equates to a dosage of approximately 25mg of raw testosterone per cap. The design of this steroid is quite different from that of most oral steroids. Drugs administered orally generally enter the blood stream through the liver. When a steroid compound is given this way without some form of structural protection, it will be quickly broken down during the "first pass". This process leaves very little steroid intact, basically deactivating the drug. Adding a methyl group (c-17 AA) to the structure is one way to protect it from this process, however stress is also placed on the liver as a result. In some instances this stress can lead to actual damage to liver tissues, so the designers of this steroid sought another way to protect the testosterone molecule. 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 o

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