Tbol dosage

Regardless of your Dbol dosage, four to six weeks of use is about all anyone will ever need; some may extend to eight weeks total, but this should be rare and is normally not recommended. The reason for such short-term use once again revolves around this steroid's strong hepatotoxic nature, and if you ignore the recommended time frames you will put your liver at risk. Of course, as seen from the Dbol only cycle link, your total cycle should extend past this point of use or you will risk losing all your gains. A solid plan is an injectable or two with your Dianabol for six weeks, and then continuing the two injectable steroids for another twelve weeks.

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presents you another cutting cycle for summer which will make you look hard and solid. As a base we will use testosterone enanthate however you may replace it with testosterone propionate as in some individuals enanthate will make visible water retention but I dont think this is a problem as you dont prepare for the contest, right? 🙂 On the other hand switching to propionate will bring you another headache as you will have to inject it EOD plus you will inject Primobolan ( Methenolone Enanthate) 2-3 times per week so having to inject primo and test propionate will keep you really busy and will not give your injection sites enough time to rest.

Hormones are esterified to slow their release into the bloodstream and prolong their duration of action by increasing their fat solubility. The esters used are just carbon chains of varying shapes and sizes, with a carboxyl group bound to and cleaved from the alcohol on the D ring of the parent steroid. Generally speaking: the larger the carbon chain, the more nonpolar/hydrophobic the compound meaning the depot will stick around longer and the ester will be cleaved at a slower rate by the body's esterase enzymes. So testosterone propionate, having a three carbon ester, will be released bound and metabolized more quickly than testosterone enanthate which has a seven carbon chain attached. In addition to altering the rate of release, the ester in use will alter the relative amount of hormone per weight of total compound. IIRC test prop is ~84% test by weight while test e is ~72% which I think is where you're getting your 15% number. But I'm not solid on those numbers. Anyway, so those are the two big ways that the ester used alters the curve and AUC of hormone release. That's good that you used the same dose location because injection site does play a role in the release as well, and I'm not trying to downplay your effort. but precise consistency between blood samples would take some serious doing. What I think you're overlooking though is that while each ester has an accepted window for when to get your blood drawn, these times aren't perfect and still won't always give equivalent values as far as where along the curve of hormone release your value lies. That was convoluted but I can't think of how to explain it any better.

Tbol dosage

tbol dosage

Hormones are esterified to slow their release into the bloodstream and prolong their duration of action by increasing their fat solubility. The esters used are just carbon chains of varying shapes and sizes, with a carboxyl group bound to and cleaved from the alcohol on the D ring of the parent steroid. Generally speaking: the larger the carbon chain, the more nonpolar/hydrophobic the compound meaning the depot will stick around longer and the ester will be cleaved at a slower rate by the body's esterase enzymes. So testosterone propionate, having a three carbon ester, will be released bound and metabolized more quickly than testosterone enanthate which has a seven carbon chain attached. In addition to altering the rate of release, the ester in use will alter the relative amount of hormone per weight of total compound. IIRC test prop is ~84% test by weight while test e is ~72% which I think is where you're getting your 15% number. But I'm not solid on those numbers. Anyway, so those are the two big ways that the ester used alters the curve and AUC of hormone release. That's good that you used the same dose location because injection site does play a role in the release as well, and I'm not trying to downplay your effort. but precise consistency between blood samples would take some serious doing. What I think you're overlooking though is that while each ester has an accepted window for when to get your blood drawn, these times aren't perfect and still won't always give equivalent values as far as where along the curve of hormone release your value lies. That was convoluted but I can't think of how to explain it any better.

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