Chlordehydromethytestosterone – Turinabol
Turinabol is a powerful derivative of Dianabol, available in 10mg doses. This oral steroid combines the structural characteristics of methandrostenolone and clostebol (4-chlorotestosterone), sharing Dianabol’s base while featuring a unique 4-chloro modification. Compared to its renowned counterpart, chlorodehydromethyltestosterone exhibits reduced estrogenic and significantly lower androgenic activity, providing a balanced anabolic-to-androgenic ratio. As a result, users can expect muscle growth with fewer androgenic side effects.
Structural Characteristics
Chlorodehydromethyltestosterone is a modified testosterone variant distinguished by: 1) a methyl group at carbon 17-alpha, protecting the hormone for oral use, 2) a double bond between carbons 1 and 2 (1-ene), favoring anabolic effects, and 3) a chloro group at carbon 4 to inhibit aromatization, minimizing androgenicity.
Side Effects (Estrogenic)
Purchase chlorodehydromethyltestosterone with confidence, as it is not aromatized in the body and lacks measurable estrogenic effects. There’s no need for an anti-estrogen, greatly reducing concerns about gynecomastia—even for sensitive users. Water retention, typically associated with estrogen, is absent, leading to a leaner, more defined physique, making it ideal for cutting cycles.
Side Effects (Androgenic)
Despite being classified as an anabolic steroid, androgenic side effects like oily skin, acne, and increased body/facial hair growth may occur with elevated dosages. Additionally, anabolic steroids may worsen male pattern baldness and could lead to virilization in women, including voice deepening and menstrual irregularities. Chlorodehydromethyltestosterone’s metabolism is unaffected by 5-alpha reductase, retaining its androgenic profile.
Side Effects (Hepatotoxicity)
Procure chlorodehydromethyltestosterone, knowing it’s a c17-alpha alkylated compound, which prevents liver enzymatic breakdown, allowing higher blood concentration post-ingestion. However, such steroids may pose a risk of hepatotoxicity. Extended exposure might lead to liver damage, necessitating regular medical check-ups during usage. Dosage duration is typically limited to 6–8 weeks to mitigate liver strain.
Side Effects (Cardiovascular)
Anabolic and androgenic steroids can adversely impact cholesterol levels, reducing HDL (good cholesterol) and elevating LDL (bad cholesterol), potentially raising the risk for arteriosclerosis. The steroid’s impact on serum lipids depends on dosage, administration route, and type of steroid. Chlorodehydromethyltestosterone’s inherent resistance to hepatic breakdown and its non-aromatizable nature can significantly affect cholesterol management, raising cardiovascular concerns.
Side Effects (Testosterone Suppression)
Any sufficiently dosed anabolic steroid is likely to suppress endogenous testosterone levels. Generally, testosterone levels can normalize within 1–4 months post-cessation without intervention, though prolonged hypogonadotrophic hypogonadism may require medical assistance due to steroid misuse.
Administration (Men)
The typical clinical dosage of chlorodehydromethyltestosterone is estimated at 5mg daily; guidelines vary. Athletes commonly utilize 30-80mg daily in cycles of no longer than 6-8 weeks to limit hepatotoxic risks. This dosage effectively promotes muscle mass and strength increases, particularly for bodybuilding pre-contest or cutting due to its lack of estrogenicity, favoring speed-focused sports.
Administration (Women)
The standard clinical dosage for women is approximately 1-2.5mg daily; specific guidelines are sparse. Athletes typically take a single 5mg tablet daily in cycles of 4-6 weeks to minimize hepatotoxicity, with virilizing effects being unlikely at this level. Historically, excessive dosing in female athletes has led to significant virilization.
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