Magnus Pharmaceuticals Turinabol 100 tabs (10 mg/tab) EXPIRATION

Chlordehydromethytestosterone – Turinabol

Is a powerful derivative of Dianabol. Purchase Turinabol 10mg, an oral steroid featuring a structure that combines elements of methandrostenolone and clostebol (4-chlorotestosterone). This modification results in a milder steroid compared to Dianabol, exhibiting no estrogenic properties and significantly reduced androgenic activity. While the anabolic action of chlorodehydromethyltestosterone is less potent than Dianabol, it offers a more favorable anabolic-to-androgenic ratio, meaning lower risk of androgenic side effects during muscle enhancement.

Structural Characteristics

Chlorodehydromethyltestosterone is a modified testosterone derivative characterized by: 1) the addition of a methyl group at carbon 17-alpha for oral bioavailability, 2) a double bond between carbons 1 and 2 (1-ene), which improves the anabolic effect, and 3) a chloro group at carbon 4 that reduces aromatization and lowers androgenicity.

Side Effects (Estrogenic)

Buy Chlorodehydromethyltestosterone, which does not aromatize, rendering it non-estrogenic. No anti-estrogen is required during use, minimizing gynecomastia risks, even for sensitive users. Unlike steroids that cause water retention, this compound promotes a lean physique, making it an excellent choice for cutting phases where maintaining a dry appearance is crucial.

Side Effects (Androgenic)

Despite its anabolic classification, users may experience androgenic effects such as oily skin, acne, and increased body or facial hair. Higher dosages elevate these risks. Additionally, men may face exacerbated male pattern baldness, while women should be cautious of virilization symptoms, including voice deepening and menstrual irregularities. Chlorodehydromethyltestosterone’s metabolism by the 5-alpha reductase enzyme is minimal, maintaining its lower androgenic profile even with finasteride use.

Side Effects (Hepatotoxicity)

Invest in Chlorodehydromethyltestosterone, a c17-alpha alkylated compound that bypasses hepatic degradation, allowing it to enter circulation effectively. However, such steroids can be hepatotoxic; hence, prolonged or high doses may harm liver function. Routine medical evaluations during cycles are advisable, and duration is typically capped at 6–8 weeks to mitigate liver strain.

Side Effects (Cardiovascular)

Anabolic and androgenic steroids adversely affect serum cholesterol, often lowering HDL (good) cholesterol and raising LDL (bad) cholesterol, increasing arteriosclerosis risk. The impact varies based on dosage, administration route, and steroid type. Chlorodehydromethyltestosterone notably alters cholesterol management due to its resistance to liver breakdown while increasing cardiovascular risks through potential negative effects on blood pressure and triglycerides.

Side Effects (Testosterone Suppression)

Utilization of anabolic steroids typically suppresses natural testosterone production. Recovery to baseline levels generally occurs within 1–4 months post-cycle, but persistent hypogonadism due to abuse may require medical intervention.

Administration (Men)

For men, a common clinical dose of chlorodehydromethyltestosterone is around 5mg per day; however, athletic dosages range from 30–80mg daily, taken over 6–8 week cycles to limit hepatotoxicity. This regimen is effective for significant gains in lean muscle and strength, preferred for competitive bodybuilding and sports focused on speed, offering benefits without excess weight.

Administration (Women)

For women, the average clinical dose is 1–2.5mg daily, with athletes typically using a single 5mg tablet per day for 4–6 weeks to reduce hepatotoxic risk. At these levels, chances of virilization are minimal, although historical misuse in past doping programs often led to severe side effects in female athletes.