Chlordehydromethytestosterone – Turinabol
As a powerful derivative of Dianabol, Turinabol 10mg offers a unique oral steroid experience. This anabolic compound is a structural hybrid of methandrostenolone and clostebol (4-chlorotestosterone), maintaining the core structure of Dianabol while incorporating a 4-chloro modification. This adjustment grants chlorodehydromethyltestosterone a milder profile, featuring minimal estrogenic and significantly reduced androgenic activities compared to its renowned predecessor. While its anabolic potency is slightly less than that of Dianabol, it presents a more favorable anabolic to androgenic effect ratio, greatly lowering the risk of androgenic side effects during muscle enhancement.
Structural Characteristics
Chlorodehydromethyltestosterone is a modified variant of testosterone characterized by: 1) a methyl group addition at carbon 17-alpha for oral protection, 2) a double bond between carbons 1 and 2 (1-ene) enhancing the anabolic ratio, and 3) a chloro group at carbon 4, which curbs aromatization and mitigates androgenic potency.
Side Effects (Estrogenic)
Choose Chlorodehydromethyltestosterone, a compound that remarkably avoids aromatization, resulting in negligible estrogenic effects. Users need not worry about gynecomastia, even those sensitive to estrogens. This steroid promotes a lean physique without excess subcutaneous fluid retention, making it an ideal candidate for cutting cycles where water and fat retention are primary concerns.
Side Effects (Androgenic)
While classified as an anabolic steroid, users should remain mindful of possible androgenic side effects from chlorodehydromethyltestosterone, such as oily skin, acne, and increased body/facial hair growth. Elevated doses heighten these risks, as does the potential for accelerated male pattern hair loss. Women should also exercise caution due to the risk of virilization manifested in voice deepening, menstrual irregularities, and skin changes. Notably, chlorodehydromethyltestosterone is minimally affected by the 5-alpha reductase enzyme, making concurrent finasteride use less impactful.
Side Effects (Hepatotoxicity)
Acquiring Chlorodehydromethyltestosterone means acknowledging its C17-alpha alkylated nature, which affords high bioavailability but raises hepatotoxicity risks. Extended or high-dose use may lead to liver damage, necessitating medical supervision during cycles. Usage duration should generally be limited to 6 to 8 weeks to mitigate liver strain.
Side Effects (Cardiovascular)
Anabolic/androgenic steroids can negatively influence cholesterol levels. Users may experience decreased HDL (good cholesterol) and increased LDL (bad cholesterol), potentially elevating arteriosclerosis risk. The effects vary based on dosage, administration method (oral vs. injectable), steroid type (aromatizable or not), and metabolic resistance. Due to its structure, chlorodehydromethyltestosterone significantly impacts hepatic cholesterol management, with implications for blood pressure and overall cardiovascular health.
Side Effects (Testosterone Suppression)
Like all anabolic/androgenic steroids, chlorodehydromethyltestosterone suppresses endogenous testosterone production at muscle-building doses. Typically, testosterone levels may normalize within 1 to 4 months post-use, but prolonged hypogonadotropic hypogonadism is a risk associated with misuse, requiring medical attention.
Administration (Men)
The recommended clinical dosage for chlorodehydromethyltestosterone is approximately 5mg daily. Athletes often utilize a dosage of 30 to 80mg per day in 6 to 8-week cycles to avoid hepatotoxic effects, achieving significant gains in strength and lean muscle. It is particularly favored in cutting phases due to its non-estrogenic nature, helping athletes maintain a lean physique without excess water retention.
Administration (Women)
For women, a common clinical dose of chlorodehydromethyltestosterone falls between 1 to 2.5mg daily. In athletic practice, a single 5mg tablet daily, extended over 4 to 6 weeks, minimizes hepatotoxicity with minimal risk of virilizing effects. While historical high doses seen in former GDR doping practices resulted in adverse virilization, moderate usage is typically safer and more effective.
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