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English Synonyms: | Anadrol , Oxymetholone | CAS NO.: | 434-07-1 |
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Purity: | 99.31% By HPLC | Melting Point: | 172.0~176.0°C |
Standard: | USP30 | Air & Water Reactions: | Insoluble In Water |
Appearance: | White Crystalline Powder | Minimum Order Quantity: | 10 Grams |
Email: | Lina_doublewin@foxmail.com | ||
High Light: | anabolic dianabol steroid,common anabolic steroids |
Legit Stable Quality Oral Anabolic Steroids Anadrol Raw Powder For Cutting
Oxymetholone, commonly known as Anadrol, stacking with other anabolic steroids gives dramatic improvements.
Anadrol can promote protein synthesis and inhibiting protein dysplasia, and oxymetholone can lower blood cholesterol, reduce calcium phosphorus excretion and reduce bone marrow suppression, promoting development, promote tissue freshmen and granulation.
Data of Oxymetholone Powder:
Alias: | Anadrol |
CAS ID: | 434-07-1 |
Melting point: | 172.0~176.0°C |
Purity: | 99.31% by HPLC |
Appearance: | Off-White to Pale Yellow Solid. |
More favorable offers will be according to your exact orders.
General Information of Oxymetholone Powder:
Oxymetholone, commonly known as Anadrol due to the first manufactured name of the steroid is derived from Dihydrotestosterone (DHT) and is a 17-Alpha-Alkylated steroid (17-aa.) The 17-aa alteration simply means the steroid has been chemically altered at the 17th carbon position to allow it to survive ingestion by surviving the first pass through the liver; without the 17-aa alteration the steroid would be destroyed before it ever entered the blood stream. The good news is by this alteration we are able to absorb a usable and powerful anabolic steroid; the bad news is this is toxic to the liver. As most oral steroids are 17-aa the toxic effect can be quite high but as it pertains to Anadrol this effect is more pronounced making it one of the most liver toxic steroids on the market.
How it works?
Once oxymetholone enters the body, which is allowed by its 17-aa form it will become active very quickly and the effects will be dramatically fast. As we understand anabolic androgenic steroids the half-life associated with them largely affects the initial potency; Oxymetholone has a very short half-life of approximately 8.5 hours making the steroids activity almost instant but with a very short active duration. For this reason many athletes will split their Oxymetholone dose into two doses per day in order to keep a peak amount of the steroid active in their system around the clock during periods of use. However, one dose per day will be enough to keep an active amount of the steroid functioning in the body, although not at peak levels.
Oxymetholone for Cutting:
It's easy to see why Oxymetholone is perfect for bulking as its attributes lend to this end and because of these very attributes very few individuals will use Anadrol during a cutting cycle. However, there is an exception and quite a large one in competitive bodybuilding. Many competitive bodybuilders will supplement with Anadrol the last few weeks before a show; by building up a large amount of the steroid in their body over a period of weeks they are able to make greater use of their carb up at the end. Through this process the competitor will possess a much fuller look but again, caution must be applied. An individual who is very sensitive to water retention from this steroid will need to stay away from this process but if ones diet is on point and such sensitivity is not a problem, coupled with a good AI and solid contest cycle a nice full effect can be gained.
Oxymetholone Anadrol stacking:
Anadrol stacking with other anabolic steroids gives dramatic improvements. For exmaple, adding Anadrol to 50 mg/day of Dianabol gives little added benefit to a steroid cycle;
in contrast, adding Anadrol to 50-100 mg/day trenbolone acetate or 60-80 mg/day Anavar (oxandrolone) gives dramatic improvement. In this its stacking behavior is similar to that of Dianabol, but not to that of trenbolone.
Likely this is because unlike trenbolone, oxymetholone does not bind strongly to the androgen receptor, and most of its anabolic effect is likely not genomically mediated via the AR.
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