Sterling Knight Turinabol 100 tabs (10 mg/tab)

Chlordehydromethytestosterone – Turinabol

Discover the power of Turinabol, a potent derivative of Dianabol. This oral steroid, available in 10mg doses, combines the structural advantages of methandrostenolone and clostebol (4-chlorotestosterone), sharing the same base structure as Dianabol, enhanced by a unique 4-chloro modification. This tweaking results in a milder alternative to Dianabol, exhibiting none of the estrogenic effects and significantly lower androgenic activity. While chlorodehydromethyltestosterone maintains a slightly lower anabolic effect, it offers a favorable anabolic-to-androgenic balance, reducing the likelihood of androgenic side effects during muscle-building.

Structural Characteristics

Chlorodehydromethyltestosterone is a modified testosterone form characterized by: 1) a methyl group at carbon 17-alpha for enhanced oral administration, 2) a double bond between carbons 1 and 2 (1-ene) to favor an anabolic effect, and 3) a chloro group at carbon 4 to suppress steroid aromatization and decrease androgenicity.

Side Effects (Estrogenic)

Purchase Chlorodehydromethyltestosterone with confidence, as it is non-aromatizing and exhibits no measurable estrogenic properties. Users need not worry about gynecomastia, even those with sensitivities. This compound promotes a lean and fit physique, ensuring no excess water retention, making it an excellent choice for cutting cycles where fat and water retention are concerns.

Side Effects (Androgenic)

As a powerful anabolic steroid, chlorodehydromethyltestosterone may still lead to androgenic side effects, including oily skin, acne, and body or facial hair growth, especially at higher doses. Male pattern hair loss may worsen, and women should be aware of possible virilizing effects such as voice deepening or menstrual irregularities. Its metabolism is minimally influenced by the 5-alpha reductase enzyme, leaving androgenicity relatively unchanged when taken with finasteride.

Side Effects (Hepatotoxicity)

Buying Chlorodehydromethyltestosterone means understanding its C17-alpha alkylated nature, which preserves the drug in the bloodstream post-oral administration. However, use of C17-alpha alkylated steroids can lead to hepatotoxicity. Long-term use poses risks of liver damage, necessitating regular physician check-ups to monitor liver health. Cycling duration is typically limited to 6 to 8 weeks to alleviate liver strain.

Side Effects (Cardiovascular)

Anabolic/androgenic steroids like chlorodehydromethyltestosterone can adversely influence cholesterol levels, often reducing HDL (good) and increasing LDL (bad) cholesterol, heightening arteriosclerosis risk. Factors including dose and administration route impact lipid profiles. This steroid’s resistance to liver breakdown exacerbates its cholesterol management challenges and may further elevate cardiovascular disease risks.

Side Effects (Testosterone Suppression)

All anabolic/androgenic steroids, including Chlorodehydromethyltestosterone, may inhibit natural testosterone production when used in sufficient doses for muscle enhancement. Typically, testosterone levels normalize within 1 to 4 months post-cessation; however, prolonged use can lead to hypogonadotropic hypogonadism requiring medical treatment.

Administration (Men)

The recommended clinical dose for chlorodehydromethyltestosterone is approximately 5mg daily. In athletic circles, effective dosages range from 30 to 80mg daily over cycles no longer than 6 to 8 weeks to mitigate hepatotoxicity. This regimen effectively enhances lean muscle gains and strength, particularly beneficial for bodybuilders during pre-contest phases or in speed-focused sports inquiries where excess weight is undesirable.

Administration (Women)

For women, the standard clinical dose of chlorodehydromethyltestosterone is about 1 to 2.5mg daily, with common practice suggesting a single 5mg tablet monthly in cycles lasting no more than 4 to 6 weeks to reduce hepatotoxicity concerns. At this dosage, virilization risks are generally minimal, unlike higher doses previously used in the GDR doping program, which proved detrimental due to pronounced virilizing side effects.