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MIXING IPAMORELIN INTO A TESAMORELIN VIAL FOR AN EASIER DOSE WITH FEWER PINS.
HOW TO LAND 1MG TESA + 200mcg IPA EVERY DOSE
1. Neither peptide settles out — this is a real solution, not a suspension
3. Nothing exists that would let the peptides separate again
4. Which means every accurately measured volume holds the exact proportion
The Math, Step by Step
1. Reconstituting the Tesamorelin
10 mg of Tesamorelin + 1.6 ml of bac water
→ So the concentration = 10 mg ÷ 1.6 ml, which gives 6.25 mg/ml
2. Reconstituting the Ipamorelin
10 mg of Ipamorelin + 2 ml of bac water
→ Which gives a concentration of 5 mg/ml
3. Transferring it
Into the Tesamorelin vial, add 0.4 ml of the Ipamorelin solution.
Ipamorelin added = 0.4 ml × 5 mg/ml, which is 2 mg
4. The finished mixed vial
o Tesamorelin total = 10 mg
o Ipamorelin total = 2 mg
o Overall volume = 1.6 ml + 0.4 ml = 2.0 ml
What that leaves you with:
o Tesamorelin comes to 10 mg ÷ 2.0 ml = 5 mg/ml
o Ipamorelin comes to 2 mg ÷ 2.0 ml = 1 mg/ml
5. Drawing a shot
Pull 0.2 ml (20 units on a U-100 insulin syringe) out of the mixed vial.
What lands in the syringe:
o From Tesamorelin: 0.2 ml × 5 mg/ml = 1 mg
o From Ipamorelin: 0.2 ml × 1 mg/ml = 0.2 mg = 200 mcg
A perfect 1:1 ratio, every single time.
HOW TO LAND 1MG TESA + 200mcg IPA EVERY DOSE
1. Neither peptide settles out — this is a real solution, not a suspension
- Tesamorelin and Ipamorelin both come as acetate salts of peptides. In bacteriostatic water they are highly water-soluble.
- Once dissolved, the peptide molecules sit as individual molecules (or tiny solvated clusters) spread through the water.
- That makes it a true molecular solution, not a suspension of particles that could settle or clump.
- In any liquid at room temperature, molecules are constantly in random motion from thermal energy (this is called Brownian motion).
- That random movement spreads molecules out of high-concentration areas and into low-concentration ones until everything matches across the vial.
- The process follows Fick’s laws of diffusion. For peptides of this size in water, the diffusion coefficient is large enough that complete uniformity arrives within seconds to a few minutes of gentle swirling in a small 2–4 ml vial.
- Swirling also sets up convection currents, which speed the process up even more.
3. Nothing exists that would let the peptides separate again
- Both peptides are hydrophilic (water-loving) and behave similarly in bac water.
- No chemical reaction, precipitation, crystallization, or hydrophobic effect would push one peptide to clump or split away from the other.
- At this scale gravity does nothing meaningful to dissolved molecules (they do not “settle” like sand in water).
- Entropy (the natural drift toward disorder) in fact favors the mixed state.
4. Which means every accurately measured volume holds the exact proportion
- Concentration = peptide mass ÷ solution volume.
- Since the solution is homogeneous, any subsample (e.g. 0.2 ml) carries the exact same concentration as the whole vial.
- That is how pharmacies build compounded multi-peptide vials that deliver consistent doses from the first draw to the last.
The Math, Step by Step
1. Reconstituting the Tesamorelin
10 mg of Tesamorelin + 1.6 ml of bac water
→ So the concentration = 10 mg ÷ 1.6 ml, which gives 6.25 mg/ml
2. Reconstituting the Ipamorelin
10 mg of Ipamorelin + 2 ml of bac water
→ Which gives a concentration of 5 mg/ml
3. Transferring it
Into the Tesamorelin vial, add 0.4 ml of the Ipamorelin solution.
Ipamorelin added = 0.4 ml × 5 mg/ml, which is 2 mg
4. The finished mixed vial
o Tesamorelin total = 10 mg
o Ipamorelin total = 2 mg
o Overall volume = 1.6 ml + 0.4 ml = 2.0 ml
What that leaves you with:
o Tesamorelin comes to 10 mg ÷ 2.0 ml = 5 mg/ml
o Ipamorelin comes to 2 mg ÷ 2.0 ml = 1 mg/ml
5. Drawing a shot
Pull 0.2 ml (20 units on a U-100 insulin syringe) out of the mixed vial.
What lands in the syringe:
o From Tesamorelin: 0.2 ml × 5 mg/ml = 1 mg
o From Ipamorelin: 0.2 ml × 1 mg/ml = 0.2 mg = 200 mcg
A perfect 1:1 ratio, every single time.