Chlordehydromethytestosterone – Turinabol
Is a powerful derivative of Dianabol. Purchase Turinabol 10mg, as this oral steroid is uniquely structured as a blend of methandrostenolone and clostebol (4-chlorotestosterone). Its base structure resembles Dianabol, enhanced with a 4-chloro modification from clostebol. This modification offers a milder alternative to Dianabol, resulting in minimal estrogenic and significantly reduced androgenic activities when compared to its more well-known counterpart. Although chlorodehydromethyltestosterone has slightly lower anabolic potency than Dianabol, it boasts a more favorable ratio of anabolic to androgenic effects. Thus, at any assigned dose for muscle growth, chlorodehydromethyltestosterone is less prone to inducing androgenic side effects.
Structural Characteristics
Chlorodehydromethyltestosterone is a modified variant of testosterone, characterized by: 1) a methyl group at carbon 17-alpha, preserving the hormone through oral administration, 2) a double bond between carbons 1 and 2 (1-ene), enhancing the anabolic-to-androgenic ratio, and 3) a chloro group at carbon 4, which curbs steroid aromatization and lowers relative androgenicity.
Side Effects (Estrogenic)
Obtain chlorodehydromethyltestosterone, which does not aromatize within the body, making it virtually estrogen-free. An anti-estrogen is unnecessary while using this steroid, as risks of gynecomastia are minimal, even for sensitive users. Since estrogen typically leads to water retention, this steroid encourages a lean, aesthetically pleasing physique without excess subcutaneous fluid retention. Consequently, it’s a favored choice during cutting cycles, where water and fat retention are critical concerns.
Side Effects (Androgenic)
While classified as an anabolic steroid, chlorodehydromethyltestosterone can still cause androgenic side effects, including oily skin, acne, and enhanced body/facial hair growth. Elevated doses increase the likelihood of such reactions. Additionally, anabolic/androgenic steroids may exacerbate male pattern hair loss. Women should be aware of potential virilization effects, including voice deepening, menstrual irregularities, alterations in skin texture, facial hair growth, and clitoral enlargement. Chlorodehydromethyltestosterone is minimally affected by the 5-alpha reductase enzyme, hence its androgenic nature remains relatively stable even with finasteride use.
Side Effects (Hepatotoxicity)
Purchase chlorodehydromethyltestosterone, a c17-alpha alkylated compound that safeguards the drug from liver deactivation, ensuring a high percentage reaches the bloodstream after oral intake. However, c17-alpha alkylated anabolic/androgenic steroids may pose risks of hepatotoxicity. Extended or high doses could lead to liver damage, and in rare cases, severe complications may arise. Regular medical check-ups are advisable during each cycle to monitor liver health. The intake of c17-alpha alkylated steroids is often limited to 6-8 weeks to help mitigate liver stress.
Side Effects (Cardiovascular)
Anabolic/androgenic steroids can adversely affect serum cholesterol levels. They may reduce HDL (good cholesterol) while elevating LDL (bad cholesterol), potentially altering the HDL to LDL ratio and increasing the risk of arteriosclerosis. The degree of impact on serum lipids varies based on dosage, administration route (oral vs. injectable), steroid type (aromatizable vs. non-aromatizable), and resistance to liver metabolism. Due to its structural resilience against liver breakdown, non-aromatizable nature, and oral route of administration, chlorodehydromethyltestosterone significantly influences cholesterol management. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, impair endothelial relaxation, and support left ventricular hypertrophy, collectively raising the risk of cardiovascular disease and myocardial infarction.
Side Effects (Testosterone Suppression)
All anabolic/androgenic steroids at doses promoting muscle gain are likely to suppress natural testosterone production. Testosterone levels typically normalize within 1-4 months post-drug cessation, barring interventions with testosterone-stimulating substances. Note the possibility of prolonged hypogonadotropic hypogonadism requiring medical attention due to steroid misuse.
Administration (Men)
A standard clinical dose of chlorodehydromethyltestosterone is about 5mg daily; formal prescribing standards are unavailable. Athletes often utilize a daily dosage between 30-80mg, cycling for no more than 6-8 weeks to limit hepatotoxicity. This dosage sufficiently promotes increases in lean muscle mass and strength and is primarily utilized as a pre-contest or cutting steroid in bodybuilding, lacking estrogenic properties. Athletes focused on speed also favor chlorodehydromethyltestosterone, gaining substantial anabolic advantages without unnecessary water or fat weight.
Administration (Women)
The typical clinical dose of chlorodehydromethyltestosterone is estimated to be 1-2.5mg daily; concrete prescribing guidelines are lacking. In sports, women generally take a single 5mg tablet daily, in cycling periods lasting no longer than 4-6 weeks to minimize hepatotoxicity risks. At this dosage, virilizing effects are unlikely. However, considerably higher dosages were utilized by female athletes in the past GDR doping programs, often leading to significant virilizing side effects.
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