One Pharma: Bulk Cyp

Here is what is going to happen:

I believe the results were correct when they stated this is indeed Test Cyp. Hard to argue with that as that is the one actual thing that was tested. However, I do not believe purity could be calculated with what was performed and I do not believe the purity. This batch will be sold same as last based on a 180mg/mL purity. I am hoping to see some bloods to clear a lot of this up.
Thanks to all for their input, especially the WKM like Dr Jim and flenser. members like these keep facts straight.
 
ANYONE who tells you they have raws that exceed 95% purity is FOS. Now guys that means don't even consider buying raws from companies that make such outlandish claims bc they are KNOWINGLY lying to your face.

(Please don't give me this BS but, but, but, Jim maybe they didn't know, then WHY IN THE F are they making such an absurd claim. In legal circles it's referred to as KNOWN OR SHOULD HAVE KNOWN, thus they have a responsibility TO KNOW!)

Why? Bc the extraction process can be VERY costly.

That's bc to achieve such high purity levels, AT LEAST 5 extractions are required and the closer one gets to 100% purity the greater the amount that remains, and is lost, in the supernatant above the desired precipitate.

As many know I just purchased roughly 15 RESEARCH grade AAS standards and the purity ranges between 95-98% !

Understand these standards came from a DEA certified lab that manufactures ANY AAS a researcher could want and that includes DESIGNER AAS!


Producing standards with a cholesterol skeleton for research centers is ALL this company does!

With respect to the question of size and the reliability of AAS blood levels, the total blood volume has VERY little to do with the level obtained.

Why?
Bc the PRIMARY factor which determines the level achieved is what is referred to as the VOLUME OF DISTRIBUTION.

Ok so there are TWO forms of AAS, those that are fat soluble (injectables) and those that are not

The more fat soluble an AAS is the longer it will take to achieve Steady State levels.

So Orals that are not very fat soluble have a much shorter half life and reliable levels would be available after roughly 5-7 DAYS, or 5-7 half lives.

While essentially all injectables being less soluble in blood (which is mostly water) require a considerably longer interval.

Thus unless we are talking about the difference in those with SIX liters of blood vs those with THREE, absolute blood volume has only a minor influence on the absolute level obtained.

Regs
Jim

A rhetorical question, what happens to the overwhelming majority of most drugs including AAS once they enter the blood stream, I mean where is most medication "stored" sort of speak.

It's one reason for MANY drugs total blood volume does not impact serum levels significantly ESPECIALLY once steady state levels are achieved.

As an incentive, whomever posts the correct answer will receive $250 bucks worth of FREE testing! Oh crap I'm already doing that :)

Hint: it is a MAJOR contributor to the volume of distribution I mentioned earlier.

Jim
 
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A rhetorical question, what happens to the overwhelming majority of most drugs including AAS once they enter the blood stream, I mean where is most medication "stored" sort of speak.

It's one reason for MANY drugs total blood volume does not impact serum levels significantly ESPECIALLY once steady state levels are achieved.

As an incentive, whomever posts the correct answer will receive $250 bucks worth of FREE testing! Oh crap I'm already doing that :)

Jim

Fat Cells.
 
Fat Cells.

Now that's an excellent choice BUT for something to be stored in fat cells it has to be what we call "lipo-phillic" or "hydro-phobic". And that is why this particular X is so important bc it can "store" either lipophillic or hydrophillic drugs!

Here is another HINT: The absolute amount people have is proportionally their blood volume!
 
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Now that's an excellent choice BUT for something to be stored in fat cells it has to be what we call "lipo-phillic" or "hydro-phobic". And that is why this particular X is so important bc it can "store" either lipophillic or hydrophillic drugs!

Here is another HINT: The absolute amount people have is proportionally their blood volume!
Red blood cells?
 


CORRECT almost all drugs are bound to albumin, some more than others, but is THE PRIMARY extracellular "storage compartment" for AAS is indeed albumin.

Fact is a bound vs non-bound equilibrium MUST be reached between albumin and the extravascular sapce before SS levels are ever achieved.

Obviously then ALBUMIN is a huge contributor to what is referred to as the volume of distribution!!

PM me Harry and I'll ensure any 2 samples of your choosing are tested by HPLC!

 
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