04 / RECONSTITUTION
Preparation Protocol
// 10MG VIAL — STANDARD RECONSTITUTION
10,000 mcg ÷ 300 units BAC water = 33.3 mcg per unit
Add 3.0 mL (300 units) bacteriostatic water to 10mg lyophilized vial.
| TARGET DOSE |
UNITS TO DRAW |
VOLUME |
NOTE |
| LOW200 mcg |
6 units |
0.06 mL |
Sensitive users; intro dose |
| STANDARD500 mcg |
15 units |
0.15 mL |
Daily cognitive enhancement |
| HIGH1,000 mcg |
30 units |
0.30 mL |
Intensive cognitive work; clinical range |
Intranasal Preferred: Reconstituted Semax can be administered intranasally (using a nasal spray bottle). 200–600mcg per nostril (divide total dose across both nostrils). Faster onset (5–15 min) via olfactory/BBB penetration. Many users find IN route more convenient and effective than SC. Use appropriate sterile nasal spray pump bottles.
Storage: Lyophilized — refrigerate (2–8°C). Reconstituted: refrigerate, use within 30 days. If using intranasal spray: refrigerate the spray bottle between uses. Semax is moderately stable once reconstituted.
08 / CYCLE PROTOCOL
Recommended Cycle
5 on/2 off
WEEKLY SCHEDULE
Standard Cycle: 300–500mcg SC or intranasal, AM fasted, Monday–Friday. Run 4–6 weeks, then 1–2 weeks off. Within 3–7 days of starting, most users notice significantly improved focus and cognitive clarity. By week 2–3, BDNF-driven neuroplasticity benefits accumulate (better learning retention, mood improvement).
Intensive Protocol (Learning/High-Demand Period): 1000mcg SC/IN AM during 4–6 week intensive study/work period. Higher dose amplifies BDNF response and cognitive enhancement. Take 1–2 weeks off after intensive cycle to allow neurotrophin levels to normalize.
Complete Russian Nootropic Stack:
AM: Semax 300mcg (IN or SC) — activating, focusing, dopaminergic
PM: Selank 500mcg (IN or SC) — calming, anxiolytic, serotonergic
Both: BDNF upregulation from complementary mechanisms
Result: clear-headed focus during the day, calm and restorative evenings, progressive neuroplasticity building over weeks.
Research Compound Notice: Semax is an approved prescription drug in Russia with 30+ years of clinical use and extensive safety data from Russian clinical trials. It has not been approved by the FDA. The compound has an excellent safety profile — no serious adverse effects documented across decades of Russian clinical practice. No reported dependence, withdrawal, or cognitive impairment. Mild temporary headache and nasal irritation (intranasal) are the most commonly reported side effects. Avoid evening dosing to prevent sleep disruption. Consult a healthcare provider.