Chlordehydromethytestosterone – Turinabol
Turinabol, a powerful derivative of Dianabol, is available as a convenient 10mg oral steroid. Structurally, it combines the elements of methandrostenolone and clostebol (4-chlorotestosterone), featuring the same foundational structure as Dianabol, enhanced by a 4-chloro modification. This unique alteration grants chlorodehydromethyltestosterone a milder profile compared to Dianabol, exhibiting no estrogenic properties and significantly reduced androgenic effects. Although its anabolic potency is lower than Dianabol’s, it maintains a preferable anabolic to androgenic balance, decreasing the likelihood of unwanted androgenic side effects during muscle-building activities.
Structural Characteristics
The chlorodehydromethyltestosterone compound is a specialized variation of testosterone characterized by several key modifications: 1) a methyl group at the 17-alpha position protects the hormone during oral use, 2) a double bond between the first and second carbons (1-ene) enhances the anabolic-to-androgenic ratio, and 3) the presence of a chloro group at carbon 4 inhibits steroid aromatization, minimizing relative androgenicity.
Side Effects (Estrogenic)
Purchasing Chlorodehydromethyltestosterone is advisable as it does not undergo aromatization, making estrogenic complications nonexistent. Users need not worry about gynecomastia, even those with heightened sensitivity. Unlike many steroids that typically cause water retention, this compound promotes a lean, aesthetic physique without unwanted subcutaneous fluid build-up, making it an optimal choice for cutting cycles where fat and water retention are critical concerns.
Side Effects (Androgenic)
Despite being classified as an anabolic steroid, potential androgenic side effects from chlorodehydromethyltestosterone may include oily skin, acne, and increased body/facial hair growth. Higher-than-recommended doses are associated with a higher risk of these side effects. Additionally, male pattern baldness may be worsened by anabolic/androgenic steroids. Women should also be cautious of possible virilizing effects such as voice deepening, irregular menstruation, changes in skin texture, facial hair growth, and clitoral enlargement. It is noteworthy that chlorodehydromethyltestosterone is not significantly metabolized by the 5-alpha reductase enzyme, thus not notably influenced by finasteride use.
Side Effects (Hepatotoxicity)
Consider purchasing Chlorodehydromethyltestosterone, a c17-alpha alkylated compound which protects the drug from liver breakdown, allowing substantial bloodstream entry post-oral administration. C17-alpha alkylated anabolic/androgenic steroids can lead to hepatotoxicity; prolonged use may result in liver damage, and severe cases can cause life-threatening dysfunction. Regular liver function check-ups with a physician are recommended during cycles. Use is typically limited to 6 to 8 weeks to minimize liver strain.
Side Effects (Cardiovascular)
Anabolic/androgenic steroids can adversely affect serum cholesterol levels, often reducing HDL (good cholesterol) and raising LDL (bad cholesterol), increasing arteriosclerosis risk. The effect of chlorodehydromethyltestosterone on serum lipids is contingent upon dosage, administration route (oral or injectable), type of steroid (aromatizable or non-aromatizable), and resistance to hepatic metabolism. Its significant impact on cholesterol due to structural resistance and oral administration heightens cardiovascular risks, including blood pressure elevation and left ventricular hypertrophy, potentially leading to heart disease and myocardial infarction.
Side Effects (Testosterone Suppression)
All anabolic/androgenic steroids can suppress natural testosterone production when used in muscle-building doses. Normal testosterone levels typically return within 1 to 4 months post-cessation, though prolonged hypogonadotrophic hypogonadism may necessitate medical intervention.
Administration (Men)
The usual clinical dose of chlorodehydromethyltestosterone is about 5mg per day; specific prescribing guidelines may be lacking. In athletic settings, effective dosages range from 30 to 80mg daily, taken in cycles lasting no longer than 6 to 8 weeks to limit hepatotoxicity. This dosage is effective for increasing lean muscle mass and strength, making it a preferred choice for cutting in bodybuilding competitions, rather than for bulking, due to its lack of estrogenic properties. Athletes in speed-focused sports often favor chlorodehydromethyltestosterone for its anabolic benefits without added weight from water or fat.
Administration (Women)
The estimated clinical dose of chlorodehydromethyltestosterone for women is approximately 1 to 2.5mg per day, though specific guidelines are not always clear. Female athletes typically use a single 5mg tablet daily, with cycles lasting no more than 4 to 6 weeks to mitigate hepatotoxicity. At this dosage, virilizing effects are rare, while significantly higher doses used historically in performance enhancement programs have led to notable virilizing side effects.
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