DNP
Form | Oral Tablet |
Unit | 50 capsules |
Strength/mL | 200mg |
Substance | 2,4 - Dinitrophenol (DNP) |
Description:
DNP belongs to a small class of compounds that in many ways, while not 100% accurate can be labeled as manufactured toxins.It's mode of action, while strong is relatively simple by which the substance uncouples oxidative phosphorylation thereby increasing both body temperature and overall metabolic rate.So how does this work exactly?By its very nature DNP readily and rapidly destroys ATP, in-fact it thrives and fuels off of it and literally drains your muscle stores of all ATP.By this action the mitochondria are necessarily required to create more ATP to meet desired function or perhaps in most simplistic terms convert food into ATP.
To understand the benefits of DNP we really only need to say two words, "Fat Loss" beyond that there is no other benefit to this synthetic chemical.When you examine many of the other profiles here you'll find that most all anabolic steroids have a multitude of purposes as well as several of the non-steroidal compounds such as SERM's, AI's and Peptides, as well as many secondary functions;That simply isn't the case with DNP.When it comes to DNP we are not talking about an anabolic steroid, it is often talked about in conjunction, as both are generally and necessarily used at the same time but a steroid it is not.When we talk about DNP the truth is very simple, we're talking about fat loss plain and simple but when steroids are added we are assuredly talking about pure fat loss and not simple body weight loss.
Applications:
2,4-Dinitrophenol (2,4-DNP, or simply DNP) is an organic compound with the formula HOC6H3(NO2)2. It is a yellow, crystalline solid that has a sweet, musty odor. It sublimes, is volatile with steam, and is soluble in most organic solvents as well as aqueous alkaline solutions.It is a precursor to other chemicals and is biochemically active, inhibiting energy (ATP) production in cells with mitochondria and was once used as a diet aid.
2,4-Dinitrophenol is produced by hydrolysis of 2,4-dinitrochlorobenzene.
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