Chlordehydromethytestosterone – Turinabol
Is a powerful derivative of Dianabol. Purchase Turinabol 10mg; this oral steroid showcases a unique structure, merging methandrostenolone with clostebol (4-chlorotestosterone). With a base structure identical to Dianabol, the distinctive 4-chloro modification renders chlorodehydromethyltestosterone a milder relative, exhibiting negligible estrogenic effects and reduced androgenic activity compared to its more renowned predecessor. Although its anabolic activity is lower than that of Dianabol, it offers a more favorable anabolic-to-androgenic balance. This suggests that chlorodehydromethyltestosterone minimizes the risk of androgenic side effects while promoting muscle growth.
Structural Characteristics
Chlorodehydromethyltestosterone is a modified testosterone variant, featuring: 1) the addition of a methyl group at carbon 17-alpha, protecting the hormone during oral intake; 2) a double bond between carbons 1 and 2 (1-ene), enhancing the anabolic-to-androgenic ratio; and 3) a chloro group at carbon 4, which inhibits aromatization and reduces androgenicity.
Side Effects (Estrogenic)
Buy Chlorodehydromethyltestosterone, a non-aromatizing steroid with no significant estrogenic properties. Users need not worry about gynecomastia—even those sensitive to estrogen. As typical estrogen-related water retention is eliminated, this compound fosters a lean physique, making it ideal for cutting cycles, where excess water and fat retention is a concern.
Side Effects (Androgenic)
While classified as an anabolic steroid, chlorodehydromethyltestosterone may still induce androgenic side effects, such as oily skin, acne, and hair growth. Higher dosages are more likely to exacerbate these effects. Additionally, anabolic steroids can worsen male pattern baldness and pose virilizing risks for women, including voice deepening and menstrual irregularities. Chlorodehydromethyltestosterone’s metabolism is minimally influenced by the 5-alpha reductase enzyme, lessening its androgenic impact when combined with finasteride.
Side Effects (Hepatotoxicity)
Chlorodehydromethyltestosterone is a C17-alpha alkylated compound, preserving the drug’s efficacy during oral administration. However, C17-alpha alkylated steroids can present hepatotoxic risks; prolonged exposure may lead to liver damage or severe dysfunction. Regular physician check-ins during cycles are crucial for monitoring liver health, and usage is typically limited to 6-8 weeks to mitigate strain.
Side Effects (Cardiovascular)
Anabolic steroids can adversely affect serum cholesterol, potentially lowering HDL (good) cholesterol while raising LDL (bad) cholesterol, increasing the risk of arteriosclerosis. The extent of this impact is influenced by dose, administration route (oral vs. injectable), and steroid type. Chlorodehydromethyltestosterone significantly affects cholesterol management due to its resistant structure, increasing the likelihood of cardiovascular complications like hypertension or myocardial infarction.
Side Effects (Testosterone Suppression)
All anabolic steroids, when taken in sufficient doses, are expected to suppress natural testosterone production. Typically, testosterone levels normalize within 1-4 months post-use if no stimulating substances are introduced. Prolonged hypogonadism may arise from steroid misuse, necessitating medical attention.
Administration (Men)
The standard clinical dose of chlorodehydromethyltestosterone is approximately 5mg daily, although precise guidelines are lacking. In athletic usage, effective dosages range from 30-80mg daily, adhering to cycles limited to 6-8 weeks to minimize hepatotoxicity. This dosage promotes significant gains in lean muscle and strength, making it a preferred choice as a pre-contest or cutting agent—with little estrogenic activity making it unsuitable for bulking. Athletes seeking speed benefit from chlorodehydromethyltestosterone, gaining anabolic advantages without added water or fat.
Administration (Women)
The common clinical dosage for women is about 1-2.5mg daily; in practice, many women take one 5mg tablet daily, in cycles of 4-6 weeks to reduce hepatotoxicity. This dosing level minimizes virilizing effects. Higher doses, historically used in doping programs, often resulted in adverse virilizing outcomes.
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