Chlordehydromethyltestosterone – Turinabol
Discover Turinabol 10mg, a powerful derivative of Dianabol that merges the structures of methandrostenolone and clostebol (4-chlorotestosterone). This unique oral steroid offers a milder alternative to Dianabol, boasting minimized estrogenic and reduced androgenic effects. Although its anabolic activity is slightly lower than Dianabol, chlorodehydromethyltestosterone maintains a superior balance of anabolic to androgenic effects, reducing the likelihood of androgenic side effects while still promoting impressive muscle growth.
Structural Characteristics
Chlorodehydromethyltestosterone is a modified steroid that showcases distinct structural features: 1) a methyl group at carbon 17-alpha for oral administration protection, 2) a double bond between carbons 1 and 2 (1-ene) enhancing the anabolic ratio, and 3) a chloro group at carbon 4 that inhibits aromatization and effectively lowers androgenicity.
Side Effects (Estrogenic)
When you buy chlorodehydromethyltestosterone, rest assured it does not convert to estrogen within the body. Consequently, no need for anti-estrogens arises, and concerns over gynecomastia are minimized, even among sensitive users. Unlike other steroids that may induce water retention, this compound promotes a clean, lean physique, making it ideal for cutting cycles where minimizing water and fat retention is crucial.
Side Effects (Androgenic)
Though classified as an anabolic steroid, chlorodehydromethyltestosterone can still elicit androgenic side effects, such as oily skin, acne, and increased body or facial hair. Higher dosages heighten the risk of these effects. Additionally, male pattern baldness may be exacerbated. Female users should also be cautious of potential virilizing effects, including voice deepening and menstrual irregularities. Notably, chlorodehydromethyltestosterone’s androgenic activity remains relatively stable under finasteride treatment.
Side Effects (Hepatotoxicity)
As a c17-alpha alkylated compound, chlorodehydromethyltestosterone is shielded from liver deactivation, ensuring a significant portion enters the bloodstream upon oral intake. However, c17-alpha alkylated anabolic steroids can pose hepatotoxic risks, potentially leading to liver damage with prolonged or high use. Regular physician check-ups are advisable during cycles to monitor liver health, as such steroids are generally recommended for use within 6 to 8-week durations.
Side Effects (Cardiovascular)
Anabolic steroids can adversely affect cholesterol levels, lowering HDL and raising LDL, potentially increasing arteriosclerosis risk. The impact of chlorodehydromethyltestosterone on serum lipids depends on dosage, method of administration (oral vs. injectable), and its inherent resistance to liver metabolism. This steroid significantly influences cholesterol management and may also elevate blood pressure and triglycerides, compounding cardiovascular risks.
Side Effects (Testosterone Suppression)
All anabolic steroids, including chlorodehydromethyltestosterone, can suppress natural testosterone production when used in sufficient doses for muscle gain. Without testosterone-stimulating aids, normal testosterone levels should resume within 1 to 4 months following discontinuation. Prolonged use may lead to hypogonadotrophic hypogonadism, necessitating medical attention.
Administration (Men)
Typically, a dose of chlorodehydromethyltestosterone for clinical use is around 5mg daily; however, for athletic purposes, effective dosages range from 30 to 80mg daily over cycles of no longer than 6 to 8 weeks to mitigate hepatotoxic risk. This dosage is adequate for substantial gains in lean muscle mass and strength, often utilized in pre-contest or cutting phases due to its non-estrogenic nature. Athletes focusing on speed also favor this steroid for its anabolic benefits without additional water or fat weight.
Administration (Women)
Women typically see clinical dose estimates of 1 to 2.5mg daily; in practice, athletes commonly take one 5mg tablet daily for 4 to 6 weeks to avoid hepatotoxicity. At these dosages, virilizing effects are unlikely. Higher doses, historically utilized in the former GDR doping program, often resulted in undesirable virilization outcomes.
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