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Assay: 99% by HPLC
Standard: Enterprise standard.
Minimum order quantity(MOQ): 10g
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Halodrol (CDMA) is a derivative of the anabolic steroid testosterone. Halodrol bears a striking structural resemblance to another anabolic steroid known as Turinabol. Often referred to as Oral Turinabol, T-bol or OT, its an altered version of the legendary Dianabol. Both Halodrol and T-bol possess much lower androgenic activity levels than Dianabol, along with a better balanced ratio between anabolic and androgenic effects. Consequently, they both provide noticeable increases in quality lean muscle, as opposed to D-bols bloated muscle development.
|Appearance||: White Or Practically White Crystalline Powder||White Crystalline Powder|
|Melting range||: ≥145ºC||145-147ºC|
|Loss on drying||: 0.5%max||0.29%|
|Assay(by GLC)||: 98.00%min||99.00%|
|Conclusion||The specification conform with enterprize standard|
For bodybuilding or athletic purposes Halodrol increases testosterone levels which induce substantial increases in bodily shape and size, largely due to its ability to increase your number of muscle fibers. The most obvious physical effects will be greater muscle strength and size, improved vascularity, and aggressive muscular pumps.
These benefits alone make Halodrol a formidable androgen, but it also encompasses other traditional steroid properties like: increased red blood cell (RBC) production; improved endurance during exercise via better lactic acid clearing; enhanced oxygen and nutrient delivery to working muscles for greater endurance; better muscle glycogen restoration after exercise for faster recovery and; the inhibition of catabolism (muscle destruction).
Gains from Halodrol generally take a few weeks to notice, and its recommended dosage is 100-150 mg/day as a stand-alone compound, and 50-100 mg/day when stacked within a steroid cycle.
Halodrols average cycle length is 4-6 weeks, and because of its 17-alpha alkylated (a modification that permits the drug to pass through the liver and into the bloodstream without being deactivated, thereby making it effective for oral administration) property it possesses a high level of hepatotoxicity (liver toxicity), thus more than 8 weeks of continuous administration is not recommended.