A commonly confused with Dianabol, but effect-side effect technically more popular oral anabolic steroid is Oral Turinabol. Popular for decades with its users, it provides the user with an extremely potent effect, with reduced side effects compared to many other oral anabolic steroids. Everything you should know about this topic you can find here:
Oral Turinabol is the former official brand name for the active substance chlordehydromethyltestosterone. Oral Turinabol was used in the GDR in the 1960s to support doping programs of various Eastern block athletes until the 1970s and 1980s as anabolic steroid for muscle building. Within the framework of the state doping of the GDR, Oral Turinabol was partially administered to up to 10,000 athletes from all disciplines without their knowledge. This range of application and the fact that Oral Turinabol was no longer available since the discontinuation of Jenapharm production in the 1990s led to a cult around this steroid, which ultimately resulted in some underground laboratories introducing Oral Turinabol into their program. Since there is no officially approved drug on the market containing the anabolic androgenic steroid chlordehydromethyltestosterone, the potential user is dependent on products from underground laboratories.
The anabolic androgenic steroid chlordehydromethyltestosterone is structurally a steroid, which in its structure is a cross between the steroids Dianabol, i.e. Methandienon and Clostebol, 4-Chlorotestosteron. Oral Turinabol possesses the same basic structure as Dianabol, which was extended by the 4-chloro group of Clostebol. For this reason, Oral Turinabol is also often compared with Dianabol, but there are also significant differences in the effects and side effects of these two anabolic androgenic steroids, in addition to the similarities between Oral Turinabol and Dianabol.
Because of the absence of conversion into estrogen in Oral Turinabol and the lower androgenic effect of Oral Turinabol compared to Dianabol, it does not produce as dramatic increases in strength and mass as Dianabol. Its muscle-building effect is described by users as being somewhere between the corresponding effects of oxandrolone and Dianabol. However, the growth achieved by Oral Turinabol is of a much higher quality than muscle mass achieved with the aid of Dianabol. Due to the absence of estrogen-induced water retention, the muscle mass built up with the aid of Oral Turinabol is significantly harder and more definite than is the case after a build-up phase with Dianabol. Due to these characteristics, Oral Turinabol is used during the build-up phase as well as during the diet phase and competition preparation.
Apart from bodybuilders, Oral Turinabol is also very popular with other sportsmen, since chlordehydromethyltestosterone significantly increases strength and performance, without an excessive water-induced increase in weight.
The dosages observed in practice in bodybuilders are in the range of 20 to 40 mg per day. Even female bodybuilders use Oral Turinabol occasionally. Here, the dosages begin in practice at 5 mg per day, doses above 10 mg can lead to significant androgen-induced masculinities. Since the effect of Oral Turinabol with 16 hours is longer than that of Dianabol, most users take Oral Turinabol twice a day.
Oral Turinabol is often also considered a milder and more tolerable form of Dianabol, since it has fewer side effects than Dianabol. This is due, among other things, to the fact that Oral Turinabol is less strongly androgenic than Dianabol, which leads to less androgen-induced side effects such as greasy skin, acne, aggression and promotion of an existing hereditary hair loss. Furthermore, Oral Turinabol cannot be converted into estrogen by the attached 4-chloro group in the body like Dianabol by aromatase enzyme. Thus, when using Oral Turinabol, the estrogen-induced side effects such as increased water retention, hypertension and gynecomastia, which are often associated with the intake of Dianabol, are eliminated. Since Oral Turinabol as well as Dianabol is 17-alpha-alkylated, both substances have approximately the same potential for liver-damaging effects.