resulting U-100 draw
- Concentration
- 5 mg/mL
- BAC added
- 1 mL
A short-acting GHRH analogue name that does not map to the long-acting DAC-linked CJC-1295 used in the best-known human trials.
Quantities below reproduce their stated source context—label, human study, laboratory work or educational guide. They do not assess suitability, product equivalence or individual risk.
Community-reported schedule
Community-reported · not a validated scheduleA single community-provenance subcutaneous line from forum reports - no-DAC CJC-1295 clustering near 100-200 mcg daily, paired with ipamorelin and cycled. Community reports only, not a validated or trial-verified schedule.
Vial-aware arithmetic
Choose the vial quantity and BAC water first. The diagram and results below update for the selected 200 mcg reported quantity. Higher-strength vials may naturally land outside the 20-30 unit band.

Basic example limit: 3 mL maximum. Check the actual vial and product-specific limits.
resulting U-100 draw
resulting U-100 draw
resulting U-100 draw
Shown in the diagram. Closest of these examples to 25 units.
Formula: draw units = selected mg × BAC mL ÷ vial mg × 100. The 20-30 unit band is a measurement reference, not a recommendation. Results are mathematical examples, not preparation instructions.
Each card states what the quantities are based on. A third-party or animal schedule is not a validated human dose.
100 mcg daily in weeks 1-2, 150 mcg in weeks 3-4, 200 mcg in weeks 5-6 and 250-300 mcg in weeks 7-12
No matched human no-DAC dose-finding trial validates this schedule. The published CJC-1295 study used the pharmacologically different long-acting DAC-linked molecule.
View sourceThe human study evaluated DAC-linked CJC-1295, not the no-DAC compound named on this page
This is an evidence-boundary card rather than a transferable dose. Its amounts and intervals must not be imported into no-DAC products.
View sourceReports cluster around 100 mcg no-DAC CJC-1295 plus 100-200 mcg ipamorelin once or twice daily, sometimes five days on and two days off
The archive admits the cycling rationale lacks evidence and records wider dosing. Its opening spotlight is explicitly described later as an erroneous AI placeholder; raw/peptide-education/pe-cjc-1295.md:8-26, 114-154 and 1133-1140.
View sourceSubcutaneous quantities cluster around 100-200 mcg of no-DAC CJC-1295, most often paired one-to-one with ipamorelin at 200/200 or 300/300 mcg, dosed before bed or fasted pre-workout and commonly cycled five days on and two off or in eight-to-twelve week blocks; some split 150/150 twice daily for the short half-life and titrate against IGF-1 testing
Forum provenance from an authenticated archive with usernames omitted. The archive keeps no-DAC CJC-1295 / Mod-GRF 1-29 separate from the long-acting DAC-linked molecule, notes the cycling rationale is convention rather than evidenced, and records conflicting quantities. These are community provenance, not controlled human dose finding.
View sourceA short-acting GHRH analogue name that does not map to the long-acting DAC-linked CJC-1295 used in the best-known human trials.
The protocol basis is a formulation mismatch. The human study proves that DAC-linked CJC-1295 affects GH and IGF-1, but it cannot validate a no-DAC schedule.
An authenticated research-forum archive records subcutaneous no-DAC CJC-1295 quantities clustering around 100-200 mcg, most often paired one-to-one with ipamorelin and dosed before bed or fasted before training, with five-days-on/two-off and multi-week block cycling both described. The archive treats no-DAC CJC-1295 / Mod-GRF 1-29 as separate from the long-acting DAC-linked molecule and admits the cycling rationale is convention rather than evidence. Reported quantities conflict, usernames are omitted, and figures are logged as community provenance without endorsement. The planner above reproduces the arithmetic of these reported quantities; it does not validate them.
The identity behind retail no-DAC naming, human pharmacokinetics, validated intervals and clinical outcomes remain uncertain.

Shared across protocols
Keep the universal checklist short. Product-specific labelling and source documentation always take priority over a general guide.
Select the labelled vial quantity used in the calculation.
View Peppys vialUse only a diluent appropriate to the research method and formulation.
View Peppys BAC waterUse a new sterile device for every entry. Source locally.
Source locallyPlan clean handling and immediate sharps disposal. Source locally.
Source locallyDo not apply a universal refrigerator rule. Follow the product, diluent and study documentation for temperature, light and expiry.
CDC injection-safety guidance calls for a new sterile needle and syringe for each injection and entry into a medication container.
Do not infer a post-mixing lifetime from BAC water alone. Discard material when identity, integrity or sterility is in doubt.