Chlordehydromethytestosterone – Turinabol
Unlock the potential of Turinabol, a powerful derivative of Dianabol, available in 10mg tablets. This oral steroid uniquely combines the structures of methandrostenolone and clostebol, featuring a base structure akin to Dianabol with a distinctive 4-chloro modification. This modification equips chlorodehydromethyltestosterone with a milder profile, exhibiting no estrogenic and significantly lower androgenic activity compared to its well-known counterpart. While its anabolic effects may be slightly less potent, Turinabol offers a more favorable ratio of anabolic to androgenic effects, minimizing the likelihood of androgenic side effects during muscle-building activities.
Structural Characteristics
Chlorodehydromethyltestosterone is a refined version of testosterone, characterized by: 1) the addition of a methyl group at carbon 17-alpha, enhancing oral efficacy, 2) a double bond between carbons 1 and 2, favoring anabolic over androgenic action, and 3) a chloro group at carbon 4, which curbs aromatization and reduces androgenicity.
Side Effects (Estrogenic)
Purchase Chlorodehydromethyltestosterone confidently, knowing it is non-aromatizable with no significant estrogenic effects. This means users need not worry about gynecomastia, even those prone to sensitivity. As this steroid reduces water retention, it promotes a lean, defined physique, making it ideal for cutting cycles where excess fluid retention is a concern.
Side Effects (Androgenic)
Despite being classified as anabolic, chlorodehydromethyltestosterone can still trigger androgenic side effects including oily skin, acne, and hair growth. Higher dosages increase the risk of these effects. Men may also experience acceleration of male pattern baldness, while women should be cautious of potential virilization, which can include voice deepening and changes in skin texture. Notably, this steroid doesn’t significantly alter its androgenicity through 5-alpha reductase metabolism.
Side Effects (Hepatotoxicity)
Order Chlorodehydromethyltestosterone, a c17-alpha alkylated compound, which protects the steroid from liver degradation, ensuring high bioavailability post-oral administration. However, prolonged use or high doses may pose hepatotoxic risks; monitoring liver function during cycles is recommended. It’s often advised to limit usage to 6-8 weeks to mitigate potential liver strain.
Side Effects (Cardiovascular)
Be aware that anabolic/androgenic steroids can adversely affect cholesterol profiles, lowering HDL and raising LDL levels, increasing the risk of arteriosclerosis. The impact of chlorodehydromethyltestosterone on serum lipids is contingent upon dosage, administration route, and its inherent resistance to hepatic metabolism. Additionally, it can influence blood pressure and triglycerides, contributing to cardiovascular disease risk.
Side Effects (Testosterone Suppression)
All anabolic/androgenic steroids can inhibit natural testosterone production at sufficient dosages to foster muscle growth. Following discontinuation, testosterone levels typically return to normal within 1-4 months, although prolonged hypogonadism may necessitate medical intervention.
Administration (Men)
The standard clinical dose for chlorodehydromethyltestosterone is around 5mg daily, with athletic dosages ranging from 30-80mg per day, preferably in cycles of no more than 6-8 weeks to reduce hepatotoxicity risks. This enables significant muscle mass and strength gains. Athletes favor it for pre-contest or cutting phases, as it promotes an anabolic edge without excess water or fat accumulation.
Administration (Women)
For women, the typical clinical dosage of chlorodehydromethyltestosterone is approximately 1-2.5mg daily, with most female athletes opting for a single 5mg tablet over 4-6 week cycles to minimize liver toxicity. At this dosage, virilization risks are minimal, though higher doses experienced in former doping programs can lead to significant side effects.
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