Post your Analyzer test results!

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The test list is....
-Test suspension 100mg/ml water based, pharmacom
-test p 100mg/ml. Eurochemlabs
-test e 250mg/ml. Eurochemlabs
-nand deca 250mg/ml. Eurochemlabs
-The next one is a blend, test e200mg, test c100mg, bold(eq)300mg/ml total 600mg/ml. Eurochemlabs
-Then I had a cheap 1$/iu gh source tested. Godtropin. I have a IGF1 test already that was 480. If it passes this test I will really believe in it.
 
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Sample number one was pharmacom test suspension 100mg/ml, and was 102mg/ml. The sample also contained benzyl alcohol and benzyl benzoate. I will have that report tomorrow.

The tests are on the following products.
#2 eurochemlabs propioject 100mg/ml
#3 Eurochemlabs Enanject 250mg/ml
#4 Eurochemlabs Decaject 250mg/ml
#5 Eurochemlabs megastack 600mg/ml
The GH was godtropin and is labeled as 24iu.
The results on the test p, test e and deca were great.
The test on the megastack was pretty low at 516 total which is no where near the 600 listed. Also the test decanate is not listed as an ingredient. When I contacted EC about this they said. It was a temporary attempt to help with pip complaints. They will make label changes once they decide to make this blend the permanent mix. It’s still pretty concentrated but knowing it’s almost 100mg/ml low allows me to dose it properly.

To be honest I only understand the conversion from mg to iu for gh so there was 19iu with a percent purity. I am unsure how to read this. It’s purity is either high or low at 5.6% heavy proteins. Not sure how to read the purity.
 

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With the gh test. If I have it right there is actually 18.4iu after subtracting the 5.6 % from 19.4iu total. Is that how to calculate total content? That would calculate to $1.33/iu and that really cheap.
 
As the title says. If you had Analyzer test a product please post the results. Include everything, not just the analysis page.

Product type and manufacturer will be important as well as source if the rules will allow it. Also the date purchased and batch number.

Please include all the information on the product you have as far as the rules will allow.

Please keep the chatter in this thread to a minimum to keep it clean.

And go!
I have no results but I like the idea of a thread full of test results
 
Sample number one was pharmacom test suspension 100mg/ml, and was 102mg/ml. The sample also contained benzyl alcohol and benzyl benzoate. I will have that report tomorrow.

The tests are on the following products.
#2 eurochemlabs propioject 100mg/ml
#3 Eurochemlabs Enanject 250mg/ml
#4 Eurochemlabs Decaject 250mg/ml
#5 Eurochemlabs megastack 600mg/ml
The GH was godtropin and is labeled as 24iu.
The results on the test p, test e and deca were great.
The test on the megastack was pretty low at 516 total which is no where near the 600 listed. Also the test decanate is not listed as an ingredient. When I contacted EC about this they said. It was a temporary attempt to help with pip complaints. They will make label changes once they decide to make this blend the permanent mix. It’s still pretty concentrated but knowing it’s almost 100mg/ml low allows me to dose it properly.

To be honest I only understand the conversion from mg to iu for gh so there was 19iu with a percent purity. I am unsure how to read this. It’s purity is either high or low at 5.6% heavy proteins. Not sure how to read the purity.
Nice! Thank you for your contribution and I am more the happy you proved me wrong.
 
With the gh test. If I have it right there is actually 18.4iu after subtracting the 5.6 % from 19.4iu total. Is that how to calculate total content? That would calculate to $1.33/iu and that really cheap.


No,

It is approx 20iUs (19.4) per vial

According to EUR:

The European Pharmacopoeia (Pharmacopoeia Europaea, Ph. Eur.) is a pharmacopoeia that aims to provide common quality standards throughout Europe to control the quality of medicines and the substances used to manufacture them. It is a published collection of monographs that describe both the individual and general quality standards for ingredients, dosage forms and methods of analysis for medicines. These standards apply to medicines for both human and veterinary use.

RELATED PROTEINS
All of the non-hGH proteins coexist with the main ingredient (rhGH). Impurities influence the rhGH activity and cause side effects. The fewer impurities one product have, the better quality it has .
Testing method: HPLC (To assay the percentage of rhGH and the impure proteins in the product)
Standard: According to European Pharmacopoeia 5.0 (Page2463-2464), the content of related protein of somatropin should be no more than 6.0 %
Result:

DIMMER AND RELATED SUBSTANCES OF HIGHER MOLECULAR MASS TEST
Dimmer and related substances of higher molecular mass: rhGh aggregates that coexist with normal rhGh. They don't have biological activity and cause antibody of rhGH. The antibody combines to rhGH molecule. The antibody prevents the rhGH from combining to its receptor to stimulate growth, cause the biological activity of rhGH to decrease.
Testing method: HPLC (To assay the percentage of active protein and the impure proteins in the product) Standard: According to European Pharmacopoeia 5.0 (Page 2464), the content of dimer and related substances of higher molecular mass of somatropin should be no more than 4.0%


This is version 5.0

I believe there is a newer version with updated info (%)...but this helps to understand the results

@Analyzer could elaborate more

Very good testing !

Thanks
 
No,

It is approx 20iUs (19.4) per vial

According to EUR:

The European Pharmacopoeia (Pharmacopoeia Europaea, Ph. Eur.) is a pharmacopoeia that aims to provide common quality standards throughout Europe to control the quality of medicines and the substances used to manufacture them. It is a published collection of monographs that describe both the individual and general quality standards for ingredients, dosage forms and methods of analysis for medicines. These standards apply to medicines for both human and veterinary use.

RELATED PROTEINS
All of the non-hGH proteins coexist with the main ingredient (rhGH). Impurities influence the rhGH activity and cause side effects. The fewer impurities one product have, the better quality it has .
Testing method: HPLC (To assay the percentage of rhGH and the impure proteins in the product)
Standard: According to European Pharmacopoeia 5.0 (Page2463-2464), the content of related protein of somatropin should be no more than 6.0 %
Result:

DIMMER AND RELATED SUBSTANCES OF HIGHER MOLECULAR MASS TEST
Dimmer and related substances of higher molecular mass: rhGh aggregates that coexist with normal rhGh. They don't have biological activity and cause antibody of rhGH. The antibody combines to rhGH molecule. The antibody prevents the rhGH from combining to its receptor to stimulate growth, cause the biological activity of rhGH to decrease.
Testing method: HPLC (To assay the percentage of active protein and the impure proteins in the product) Standard: According to European Pharmacopoeia 5.0 (Page 2464), the content of dimer and related substances of higher molecular mass of somatropin should be no more than 4.0%


This is version 5.0

I believe there is a newer version with updated info (%)...but this helps to understand the results

@Analyzer could elaborate more

Very good testing !

Thanks
Thanks you for that. It is very informative. So this means all my gh test parameters are within industry standards.
 
Yes same email different handle. Thconcentrates is my other handle. But that’s an old one I don’t use any loner.
 
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