Euro-Pharmacies Turanabol 50 tabs (10 mg/tab)

Chlordehydromethytestosterone – Turinabol

Discover Turinabol, a powerful derivative of Dianabol. This oral steroid, available as a 10mg option, is structurally a unique blend of methandrostenolone and clostebol (4-chlorotestosterone), sharing Dianabol’s base formula with the crucial 4-chloro modification. This tweak renders chlorodehydromethyltestosterone a gentler version of Dianabol, characterized by negligible estrogenic and significantly lower androgenic activity, promoting a favorable anabolic-to-androgenic effect ratio. Consequently, users can enjoy muscle-building advantages with reduced risk of androgenic side effects.

Structural Characteristics

Chlorodehydromethyltestosterone is an enhanced form of testosterone, modified through three key alterations: 1) a methyl group attached at carbon 17-alpha safeguards the hormone for oral use, 2) a double bond is added between carbons 1 and 2 (1-ene), enabling a favorable anabolic dominance, and 3) a chloro group at carbon 4 prevents aromatization, thus minimizing androgenic properties.

Side Effects (Estrogenic)

Choose Chlorodehydromethyltestosterone, which avoids body aromatization and is largely devoid of estrogenic effects. This means no need for anti-estrogens, eliminating concerns such as gynecomastia, even for those who are typically sensitive. Instead, users experience a defined, lean physique with minimal risk of unwanted water retention, making it ideal for cutting cycles when fat and water retention are prioritized concerns.

Side Effects (Androgenic)

While Chlorodehydromethyltestosterone is primarily anabolic, potential androgenic side effects may still arise. These include oily skin, acne, and increased body or facial hair growth, especially at elevated doses. Additionally, male pattern hair loss can be exacerbated. Women should be cautious of virilizing effects, which could manifest as voice deepening, menstrual issues, skin texture changes, and facial hair growth. Despite its relative stability, concurrent use of finasteride does not significantly reduce androgenicity.

Side Effects (Hepatotoxicity)

When you buy chlorodehydromethyltestosterone, note that it is a c17-alpha alkylated compound that enhances bioavailability through oral administration. However, such steroids carry hepatotoxic risks, necessitating careful monitoring during prolonged use. Medical supervision is recommended to assess liver functioning, particularly during cycles lasting 6 to 8 weeks, to mitigate liver strain.

Side Effects (Cardiovascular)

Anabolic/androgenic steroids, including Chlorodehydromethyltestosterone, may adversely affect serum cholesterol, diminishing HDL (good) and elevating LDL (bad) cholesterol levels, increasing arteriosclerosis risk. The specific impact depends on dosage, administration route, and the steroid’s inherent metabolism resistance. This compound significantly influences cholesterol management, emphasizing the importance of cautious dosing and administration methods.

Side Effects (Testosterone Suppression)

All anabolic/androgenic steroids can suppress internal testosterone production when dosages promote muscle growth. With appropriate post-cycle intervention, testosterone levels typically normalize within 1 to 4 months. However, there is a risk of prolonged hypogonadotrophic hypogonadism from steroid abuse, necessitating medical attention.

Administration (Men)

The typical clinical dosage of chlorodehydromethyltestosterone is around 5mg daily; however, athletes may increase this to 30-80mg over 6-8 week cycles to enhance lean muscle mass and strength, effectively utilized during bodybuilding’s pre-contest phases. Its non-estrogenic nature renders it less suitable for bulking and is favored by athletes prioritizing speed, given the steroid’s advantage of minimal water retention.

Administration (Women)

For women, the common clinical dose of chlorodehydromethyltestosterone lies between 1-2.5mg daily, with sports enthusiasts typically consuming a single 5mg tablet for no more than 4-6 weeks. At this level, virilizing effects are unlikely, though notably higher doses employed by female athletes in previous doping regimes carried strong virilizing risks.