AOD-9604
Price range: $59 through $69
2MG, 5MG
AOD-9604 is dosed at 300 mcg–500 mcg daily via subcutaneous injection in educational protocols. A 2 mg vial reconstituted with bacteriostatic water yields about 0.667 mg/mL. This information is for research and educational use only.
In stock | ≥99% catalog purity
Description
Product specification
Analytical Profile
Catalog data is presented for material identification and laboratory planning. Batch-specific documentation governs the supplied vial.
| RESEARCH NAME | AOD-9604 · Peptide Fragment 176–191 |
| FORMAT | Lyophilised powder |
| MOLECULAR FORMULA | C209H322N54O64 |
| MOLECULAR MASS | 1815.1 g/mol |
| CAS REGISTRY | 221231-10-3 |
| ANALYTICAL IDENTITY | HPLC 98.6% · LC–MS confirmed |
| CATALOG CONDITION | Lyophilised · −20°C |
PROTOCOL LITERACY
Reconstitution Sequence
01
Metabolic
Prepare 1.0 mL of bacteriostatic water with sterile equipment.
02
INTRODUCE SLOWLY
Direct the liquid toward the inside wall of the vial to limit foaming.
03
DISSOLVE GENTLY
Roll or swirl with care until the material is dissolved; do not shake.
04
LABEL AND PROTECT
Record the preparation date and keep the vial protected from light.
05
COLD STORAGE
Refrigerate at 2-8°C and use within the four-week reference window.
UNRECONSTITUTED MATERIAL
-20°C
After reconstitution
2-8°C
Handling principle
DO NOT FREEZE
Avoid repeated freeze–thaw cycles and maintain appropriate refrigerated storage after reconstitution.
PROTOCOL LITERACY
AOD-9604 DOSAGE CHART
VIAL CONTENT
5 MG
+
REFERENCE DILUENT
3.0 MG
=
STOCK CONCENTRATION
1.667 MG/ML
U-100 SCALE
1 UNIT = 0.01 ML = 16.67 MCG
01
GRADUAL 8MG MODEL
02
12 MG TRIAL CONTEXT
EDUCATIONAL REFERENCE
GRADUAL DAILY MODEL
| STUDY INTERVAL | STAGE | WEEKLY DOSE | U-100 REFERENCE | SOLUTION VOLUME |
|---|---|---|---|---|
|
01
WEEKS 1-4
|
INITIATION | 300 MG | 18 UNITS | 0.18 ML |
|
02
WEEKS 5-12
|
MAINTENANCE | 500 MCG | 30 UNITS | 0.30 ML |
01
REFERENCE ASSUMPTIONS
Every unit and volume value shown assumes a 10 mg vial prepared to a total reference volume of 1.0 mL.
02
MATERIAL BOUNDARY
This table does not provide preparation or administration instructions.
03
PROTOCOL CONTROL
Trial documentation and qualified clinical oversight—not this chart—must govern all dosing decisions.
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