Lol yeah guess soso microwaving gear is g2g
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Lol yeah guess soso microwaving gear is g2g
I would still stay away from it.so microwaving gear is g2g
I would still stay away from it.
Because I would. Feel free to put as much gear in the microwave as you want.Why?
Because I would. Feel free to put as much gear in the microwave as you want.
Then what were you asking me why about? My response was clearly towards putting gear in the microwave. I've heated crashed gear. I just don't microwave it.I wouldn't put it in the microwave at all but I sure would reheat it before pinning as many times as I had to before throwing it away.
Then what were you asking me why about? My response was clearly towards putting gear in the microwave. I've heated crashed gear. I just don't microwave it.
Dude. What are you even reading? I never once suggested he toss it. I simply said I wouldn't microwave my own gear.So he microwaved it a couple times, no big deal. If it was a 100ml vial and he microwaved it 50x for 2 minutes each then you have a point but to toss it over a couple instances is excessive.
Dude. What are you even reading? I never once suggested he toss it. I simply said I wouldn't microwave my own gear.
It's all good man.I misread your post #42 on this page then. When you said you'd stay away from it I thought you meant from the gear bc you'd toss it. I realize now you meant to stay away from the microwave. My apologies Whoremoans.
I am slightly worried that every time I do this (microwaving) I may be degrading the potency.
The short answer is IDK bc there are no studies on the subject, that I'm aware of (and I just scanned MedLine)
The long answer; MW is very unlikely to significantly alter the potency bc the chemical structure of oil soluble AAS are inherently VERY STABLE.
ALL AAS are relatively SMALL polycyclic compounds that are bound thru COVALENT or HYDROGEN bonds.
The relatively small size of AAS
limits their ability to twist or fold about an axis.
While the former covalent bonds are the strongest type of any involved in human physiologic processes, the latter hydrogen bond is relatively weak.
Fortunately for you microwavers, although it's quite likely some of the hydrogen bonds are lysed during the heating process the byproduct is even more unstable than its parent compound.
Moreover the fact parenteral AAS are well solubilized in OIL greatly limits the tendency of any dissociated Hydrogen to remain "free" in solution.
This solubility factor would facilitate the return of any "free" hydrogen to its original position within the AAS molecule
By contrast the INSTABILITY of POLY-PEPTIDE hormones such as GH and Slin, forbid all but passive heating measures.
The difference once again lies in the structural features of polypeptide hormones, as these compounds are amide based AND develop specific FUNCTIONAL folding patterns.
Really it's seems that portion of an AAS molecule which is most susceptible to heating is the ester group, which may be converted to its conjugate acid thru heating of any kind.
Oh another factor to bear in mind MW primarily heats the SOLVENT rather than the solute per say!
Jim
Fuck yeah, go test!The short answer is IDK bc there are no studies on the subject, that I'm aware of (and I just scanned MedLine)
The long answer; MW is very unlikely to significantly alter the potency bc the chemical structure of oil soluble AAS are inherently VERY STABLE.
ALL AAS are relatively SMALL polycyclic compounds that are bound thru COVALENT or HYDROGEN bonds.
The relatively small size of AAS
limits their ability to twist or fold about an axis.
While the former covalent bonds are the strongest type of any involved in human physiologic processes, the latter hydrogen bond is relatively weak.
Fortunately for you microwavers, although it's quite likely some of the hydrogen bonds are lysed during the heating process the byproduct is even more unstable than its parent compound.
Moreover the fact parenteral AAS are well solubilized in OIL greatly limits the tendency of any dissociated Hydrogen to remain "free" in solution.
This solubility factor would facilitate the return of any "free" hydrogen to its original position within the AAS molecule
By contrast the INSTABILITY of POLY-PEPTIDE hormones such as GH and Slin, forbid all but passive heating measures.
The difference once again lies in the structural features of polypeptide hormones, as these compounds are amide based AND develop specific FUNCTIONAL folding patterns.
Really it's seems that portion of an AAS molecule which is most susceptible to heating is the ester group, which may be converted to its conjugate acid thru heating of any kind.
Oh another factor to bear in mind MW primarily heats the SOLVENT rather than the solute per say!
Jim
NOOOO my 100ml jug!!Oh crap I forgot to mention one proviso, my comments exclude testosterone![]()
This settles it. Dr Jim has spokenThe short answer is IDK bc there are no studies on the subject, that I'm aware of (and I just scanned MedLine)
The long answer; MW is very unlikely to significantly alter the potency bc the chemical structure of oil soluble AAS are inherently VERY STABLE.
ALL AAS are relatively SMALL polycyclic compounds that are bound thru COVALENT or HYDROGEN bonds.
The relatively small size of AAS
limits their ability to twist or fold about an axis.
While the former covalent bonds are the strongest type of any involved in human physiologic processes, the latter hydrogen bond is relatively weak.
Fortunately for you microwavers, although it's quite likely some of the hydrogen bonds are lysed during the heating process the byproduct is even more unstable than its parent compound.
Moreover the fact parenteral AAS are well solubilized in OIL greatly limits the tendency of any dissociated Hydrogen to remain "free" in solution.
This solubility factor would facilitate the return of any "free" hydrogen to its original position within the AAS molecule
By contrast the INSTABILITY of POLY-PEPTIDE hormones such as GH and Slin, forbid all but passive heating measures.
The difference once again lies in the structural features of polypeptide hormones, as these compounds are amide based AND develop specific FUNCTIONAL folding patterns.
Really it's seems that portion of an AAS molecule which is most susceptible to heating is the ester group, which may be converted to its conjugate acid thru heating of any kind.
Oh another factor to bear in mind MW primarily heats the SOLVENT rather than the solute per say!
Jim
