Trenbolone Hexahydrobenzylcarbonate 100 mg Cygnus
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Packaging video review Trenbolone Hexahydrobenzylcarbonate 100 mg Cygnus
Trenbolone hexahydrobenzylcarbonate is an anabolic steroid, it is dissolved in oil with hexahydrobenzylcarbonate ether attached through the 17-beta hydroxyl group, and this slows down the release of trenbolone from the injection area more strongly if compared with the acetate form of this steroid (17b-hydroxyestra-4,9,11-triene-3-one). Its half-life ranges from five to six days. Trenbolone is an altered form of nandrolone. It has a difference-the introduction of a double bond between carbons 9 and 11, this removes aromatization, nandrolone, for example, very slowly undergoes aromatization, despite the fact that it releases a certain amount of estrogen, this is not typical for trenbolone at all. The 11-12 bond slightly increases the binding to androgen receptors. Trenbolone is non-estrogenic, while it is more anabolic and androgenically active, compared to nandrolone. It is more like drostanolone than nandrolone. The drug is three times more androgen than testosterone, and it is one of the most powerful steroids that are produced.
In 1967, a large number of different forms of trenbolone were produced. The production of trenbolone hexahydrobenzylcarbonate was started by the French company Negma under the name parabolan. Trenbolone hexahydrobenzylcarbonate was the only trenbolone drug that was officially marketed for the treatment of people suffering from dystrophy and osteoporosis. Parabolan was found on the French market for a long time, almost until 1997. From that moment on, there was not a single trenbolone drug that was officially released.
Trenbolone hexahydrobenzylcarbonate has an anabolic and androgenic effect. For medical purposes, it was used to treat people suffering from osteoporosis and dystrophy. The drug has weakly expressed activity in the prostate, skin of the body and head of a person. Such side effects as acne, baldness, severe facial and body hair do not appear if the drug is used in the recommended doses, but if you use doses that exceed the optimal ones, such effects tend to manifest themselves. In addition, trenbolone has progestogenic activity, although not pronounced. Due to this fact, the drug can somewhat affect the weakening of libido, but in practice this was almost not found, on the contrary, the sexual desire of the athlete increased significantly, as well as physical strength (with the appropriate class of athlete). Trenbolone is 5 times stronger (when compared with testosterone) to stabilize the androgen receptor. This property indicates that the drug is an excellent anabolic. Just like testosterone, it has an anabolic effect, which is expressed in stimulating protein synthesis, reducing fat deposition, delaying the body’s potassium, phosphorus, and sulfur necessary for protein synthesis, increasing the fixation of calcium in the bones, and increasing muscle mass. In addition, it significantly increases the synthesis of IGF in the liver.
Steroid profile of Trenbolone hexahydrobenzylcarbonate
Activity of the substance: 10 days
Classification: Steroid of Anabolic / Androgenic origin
Method of use: by injection
Dosages: Men 100-300 mg per week. / Women do not advise
Acne: Yes Water
High blood pressure: Yes
Progestogenic activity: Present
DHT (Dehydrotestosterone) Conversion: None
Reduced HPTA function (production of own testosterone): Yes
Anabolic activity (400%)\ Androgen activity (200%)
The detection time is 6-7 weeks (approximately, due to the fact that the DC is making progress in finding methods for detecting prohibited substances, in addition, it depends on the athlete himself, whether he takes phenobarbital and furosemide in order to accelerate the withdrawal of the drug)
Effects of Trenbolone hexahydrobenzylcarbonate
Increases muscle mass (up to 10 kg for an 8-week course of trenbolone)
Increases strength indicators
It affects the increase in the level of insulin-like growth factor (aka somatomedin) by 200%
Promotes fat burning both independently and by stimulating the secretion of IGF
It affects an increase in libido during the course, a noticeable decrease after the course (if gonadotropin and nolvadex are not used, PCT (post-course therapy with tamoxifen (or its analogues, for example, toremifene or clomiphene citrate) and gonadotropin after a course of trenbolone is mandatory)
Affects a decrease in cortisol levels
Application of Trenbolone Hexahydrobenzylcarbonate
Reception (for men)
If you are working on the physique, the recommended dosage is 150-300mg per week (divided into several doses throughout the week), 6-8 weeks in a row. This dose is enough to significantly increase the strength and dry mass, while the risk of side effects is very low. The fact that the drug has no estrogenic component makes it one of the most important for performing athletes. It has an androgenic component that eliminates fat, in addition, trenbolone is a strong anabolic that is superior to testosterone and methandrostenolone. It is often found that trenbolone is recommended to be included in the mass-gathering course. It is likely that trenbolone is the most anabolic of all non-estrogenic commercial steroids. In addition, trenbolone is a universal drug. On drying, it is combined with stanozolol or primobolan, this removes excess water and gives hardness. Nandrolone or boldenone is used if a dry mass is needed. If simple weight gain is needed, trenbolone is combined with testosterone, oxymetalon, or methandrostenolone.
Reception (for women)
Trenbolone is not recommended for women for sports purposes, as it has pronounced androgenic side effects.
Side effects of trenbolone hexahydrobenzylcarbonate
Trenbolone does not aromatize in the human body, nor does it have estrogenic activity. Trenbolone is similar to progesterone receptors. This can lead to the development of progesterone side effects, for example, to stop the production of testosterone and increase body fat. Progestins affect the increase in the stimulating effect of estrogen in the growth of breast tissue (in this regard, you should take antiprogestins-cabergoline). There is a very strong interaction here, gynecomastia can be triggered by progestins alone, without increasing the level of estrogen. The use of anti-estrogens can mitigate gynecomastia, which will cause progestogenic AAS. Progestin side effects may increase if you take flavoring drugs in parallel.
Trenbolone is referred to as anabolics, despite this, the probability of androgenic side effects is present. This can be increased fat content of the skin, acne, hair growth on the body and face, they can be caused by taking high doses. Anabolic steroids can lead to worse male-type hair loss. Women should be reminded of the likely virilizing effects of AAS (coarsening of the voice, irregular periods, changes in skin structure, facial hair growth, and clitoral enlargement). Trenbolone does not react with 5a-reductase, its androgenicity does not change in the case of combined administration of finasteride or dutasteride.
AAS can adversely affect blood cholesterol (for example, a decrease in the level of “good” HDL, a shift in the balance towards the risk of atherosclerosis). The relative effect of AAS on lipids depends on the dose, the route of administration, the type of steroid, and the level of resistance to hepatic metabolism. Trenbolone has a strong negative effect on hepatic cholesterol management, this is due to its non-aromatizing structure and resistance to metabolism. AAS can negatively affect blood pressure and triglycerides, reduce vascular endothelial relaxation, lead to ventricular hypertrophy, and this can potentially lead to an increased risk of cardiovascular disease and heart attack. To reduce the load on the cardiovascular system, it is recommended to minimize the intake of saturated fat, cholesterol and simple carbohydrates during the course of AAS. It is recommended to take supplements such as fish oil, lipid stable and similar products.
It inhibits the endogenous production of testosterone. If you do not take substances that stimulate the production of testosterone, it will come to its usual indicators in 1-4 months after the course. It should be noted that in a long period of hypogonadotropic hypogonadism can develop into a secondary one, and this may lead to the need for medical intervention. In experimental conditions, it was proved that trenbolone is three times more strongly inhibits gonadotropins, in comparison with testosterone. Decreased libido and a sluggish erection are very rare on the course itself (this is due to the pronounced androgenic effect of trenbolone), and testicular atrophy associated with inhibition of testosterone production is a very common side effect. For prevention, take gonadotropin (from the beginning of 2 weeks of the course and until the end of the reception) and on PCT with toremifene (3 weeks, 60 mg per day divided into morning and evening) or clomifene citrate (3 weeks, 150 mg per day (divided into morning and evening) or tamoxifen (3 weeks of taking 40 mg per day (20 mg in the morning and 20 mg in the evening) also 3000-5000 units of gonadotropin every 3rd day 5-7 days after the last injection of trenbolone). In addition, taking trenbolone, you should be prepared for insomnia and for the “trenov cough”.
There is no toxic effect on the kidneys. This effect is invented, it is associated with the fact that during the course of the metabolites are excreted and the urine turns red. Some athletes take this fact as a sign of kidney damage.