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TA-1 Cloudy

Scheduled Pinned Locked Moved Peptide Discussion
researchingthymosin-alpha-1
7 Posts 5 Posters 492 Views 2 Watching
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  • D Offline
    D Offline
    diegoc
    wrote on last edited by
    #1

    I think I lost y first peptide ever...lol

    I had always reconstruted my TA-1 with Bac water NEVER had a problem.

    I was readig online that TA-1 should be reconstituted with Acetic Acid, well that didnt work out.

    @randy NEED Randys help on this one.

    Scratch the BRO science and use the METHOD

    If it aint broke dont fix it?

    WisGal64W 1 Reply Last reply
    0
    • RandyR Online
      RandyR Online
      Randy
      wrote on last edited by
      #2

      if you ask chat gpt the same thing enough times it will give you the answer you want. Thats whats happening with the peptide influencers.

      Ive never had ta-1 go cloudy but ive only played with a kit over the course of my research. Ive never heard the "use acetic acid" line on that one before.

      Did you use acedic acid or bac to make it turn?

      "If it doesnt come in a needle. It doesn't work"

      1 Reply Last reply
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      • D Offline
        D Offline
        diegoc
        wrote on last edited by
        #3

        I have always used Bac, never had a problem, ever.

        Usually TA-1 comes in 10mg vials and typical protocol in the winter months is 1.5mg 3x a week.

        Im done with a bottle in less than a month.

        Ppl saying its jelliing up and saying it had to be Acetic Acid like in AOD.

        Im so freaking stupid i ordered Acetic Shit Acid and added 1ml and the shit went cloudy.

        So my bad for not asking Randy if this was a myth or buster.

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        0
        • D diegoc

          I think I lost y first peptide ever...lol

          I had always reconstruted my TA-1 with Bac water NEVER had a problem.

          I was readig online that TA-1 should be reconstituted with Acetic Acid, well that didnt work out.

          @randy NEED Randys help on this one.

          Scratch the BRO science and use the METHOD

          If it aint broke dont fix it?

          WisGal64W Online
          WisGal64W Online
          WisGal64
          wrote on last edited by
          #4

          @diegoc I just recently had a vial go bad on me halfway through, and another previous one gel up on towards the end. I used Hospira, which I'm starting to think has too high of a PH for TA based on reading various articles. This article in particular says:

          "Thymosin Alpha 1 exhibits its highest stability in a pH range of 5 to 6.[5] Acetate buffer is a suitable buffer system to maintain this pH range."

          [https://pdf.benchchem.com/15623/Thymosin_Alpha_1_Stability_and_Degradation_A_Technical_Support_Center.pdf](link url)

          I think Hospira is between 4 and 7? Someone on another forum suggested to try to try adding about .2 - .3% after dissolving it in Bac water. But I haven't tried it yet.

          “Currently in a committed relationship with my plateau. Waiting for my receptor reset to file for divorce”

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          • S Offline
            S Offline
            SEOCoder
            wrote on last edited by
            #5

            Use 0.6% acetic acid solution made for reconstitution from reputable source. No BAC at all. Keeps it at the right pH. Trying to mix them together is the problem. Use either all BAC and hope it doesn’t gel. Or all AA solution.

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            • P PeptideCritic moved this topic from Immune & Bioregulators on
            • vpeptidesV Online
              vpeptidesV Online
              vpeptides
              wrote last edited by vpeptides
              #6

              So, I reconstituted TA-1 today and it went cloudy. I used Hospira BW, but the vial was recently taken from the freezer, maybe that was the issue.
              Anyway, I filtered it after that, and it became clear. I want to confirm my TA-1 is useless now, or maybe it has something in it still?

              Anyone? @randy ?

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              • vpeptidesV Online
                vpeptidesV Online
                vpeptides
                wrote last edited by
                #7

                Ok, I asked the Omniscience AI and it stated the obvious:

                Cloudiness indicates that the TA-1 molecules clumped together instead of dissolving. When you reconstituted the freezing cold powder, a significant portion of the Thymosin Alpha-1 molecules collapsed and clumped together (precipitated) because cold temperatures decrease peptide solubility. Because these clumps were large enough to scatter light, the 0.22-micron filter likely trapped and removed those un-dissolved clumps.

                Because an unpredictable amount of the peptide clumps was filtered out, your final solution is likely under-dosed. You cannot accurately know how many milligrams of TA-1 are left per milliliter.

                Because the solution was originally cloudy from being mixed while cold, the exact composition of your clear 5 mg/mL solution (10 mg in 2 mL BAC water) remains highly unpredictable.

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