Magnus Pharmaceuticals Turinabol 100 tabs (10 mg/tab)

Klordehüdrometütestosteroon - Turinabol

Discover Chlordehydromethytestosterone, a powerful derivative of Dianabol. Purchase Turinabol 10mg; this oral steroid is a structural fusion of methandrostenolone and clostebol (4-chlorotestosterone), with an identical base structure to Dianabol, augmented by a 4-chloro modification from clostebol. This modification presents chlorodehydromethyltestosterone as a gentler counterpart to Dianabol, exhibiting minimal estrogenic effects and significantly reduced androgenic activity compared to its renowned relative. While its anabolic potency is slightly less than that of Dianabol, it offers an enhanced anabolic-to-androgenic effect balance. This characteristic indicates that chlorodehydromethyltestosterone is less prone to induce androgenic side effects at equivalent muscle-building dosages.

Struktuurilised omadused

Chlorodehydromethyltestosterone is structurally altered testosterone, featuring: 1) the addition of a methyl group at the 17-alpha position for oral protection, 2) a double bond between carbons 1 and 2 (1-ene) to favor anabolic outcomes over androgenic, and 3) a chloro group at carbon 4 that mitigates steroid aromatization and lessens androgenicity.

Kõrvaltoimed (östrogeensed)

Purchase Chlorodehydromethyltestosterone, which is inherently non-aromatizable, boasting negligible estrogenic properties. Anti-estrogen supplements are unnecessary with this steroid—a significant benefit for those at risk of gynecomastia, even amongst sensitive individuals. Instead of causing water retention, this steroid fosters a streamlined physique, making it an optimal choice during cutting cycles where water and fat gain are major concerns.

Kõrvaltoimed (androgeensed)

Though mainly anabolic, chlorodehydromethyltestosterone could elicit androgenic side effects, such as oily skin, acne, and increased body or facial hair. Higher doses may intensify these reactions. Like other anabolic/androgenic steroids, it could potentially worsen male pattern baldness. Women should be aware of risks for virilizing symptoms, including voice deepening and irregular menstruation. Remarkably, chlorodehydromethyltestosterone exhibits minimal metabolism by the 5-alpha reductase enzyme, preserving its lower androgenic potential, even with finasteride use.

Kõrvaltoimed (hepatotoksilisus)

Acquire Chlorodehydromethyltestosterone, a c17-alpha alkylated compound shielding itself from hepatic degradation, facilitating significant absorption post-oral administration. However, c17-alpha alkylated steroids pose hepatotoxic risks; prolonged use or high doses may lead to liver damage, with severe cases potentially becoming life-threatening. Regular check-ups with a physician during cycles are recommended to monitor liver health, as intake is typically limited to 6-8 weeks to reduce liver strain.

Kõrvaltoimed (kardiovaskulaarsed)

Like many anabolic/androgenic steroids, chlorodehydromethyltestosterone can negatively affect cholesterol levels, typically lowering HDL (good) and raising LDL (bad) cholesterol, potentially increasing atherosclerosis risk. The impact on lipid profiles varies with dosage, administration method (oral vs. injectable), steroid type, and hepatic metabolism resistance. Chlorodehydromethyltestosterone possesses strong resistance to liver breakdown, significantly influencing cholesterol management. Additionally, it may adversely impact blood pressure and triglycerides, increase left ventricular hypertrophy, and consequently elevate cardiovascular disease and myocardial infarction risks.

Kõrvaltoimed (testosterooni supressioon)

All anabolic/androgenic steroids applied in muscle-building doses will suppress natural testosterone production. Absent testosterone-boosting measures, testosterone levels typically normalize within 1-4 months post-cycle. Be cautious of the potential for prolonged hypogonadotropic hypogonadism due to steroid misuse, which may require medical treatment.

Administratsioon (mehed)

The typical clinical dosage for chlorodehydromethyltestosterone is around 5mg daily; specific prescribing protocols are scarce. Athletes often take 30-80mg daily in cycles of no more than 6-8 weeks to minimize hepatotoxicity, which effectively enhances lean muscle mass and strength. This compound is primarily used as a pre-contest or cutting steroid in kulturismi due to its low estrogenic properties, making it less suitable for bulk gains. It’s especially favored among athletes focused on speed, offering robust anabolic advantages without excess fat or water weight.

Administration (Women)

The common clinical dosage for females taking chlorodehydromethyltestosterone is approximately 1-2.5mg daily; actual guidelines remain unavailable. Women typically utilize a single 5mg tablet daily in cycles lasting 4-6 weeks, mitigating hepatotoxicity risks. At these levels, virilizing effects are unlikely, although higher dosages used in past GDR doping programs often led to severe virilization.