Epithalon

Epithalon

$59

10MG

Epitalon is dosed at 5 mg daily via subcutaneous injection in educational protocols. A Epithalon reconstituted with bacteriostatic water yields about 5 mg/mL. This information is for research and educational use only.

In stock   |   ≥99% catalog purity

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Description

Product specification

Analytical Profile

Catalog data is presented for material identification and laboratory planning. Batch-specific documentation governs the supplied vial.

RESEARCH NAME Epithalon · LY3437943
FORMAT Lyophilised powder · 10 mg vial
MOLECULAR FORMULA C209H322N54O64
MOLECULAR MASS 390.35 g/mol
CAS REGISTRY 307297-39-8
ANALYTICAL IDENTITY HPLC + LC–MS
CATALOG CONDITION Sealed · light-protected · 2–8°C

PROTOCOL LITERACY

Reconstitution Sequence

This source-derived sequence assumes a 10 mg vial and a final reference volume of 1.0 mL. The supplied product documentation remains the controlling instruction.

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

Keep frozen, dry, sealed, and protected from direct light for long-term storage.

After reconstitution

2-8°C

Keep refrigerated and light-protected. Use within 2–4 weeks and avoid temperature fluctuations.

Handling principle

ONE THAW

If frozen aliquots are required by an approved research protocol, avoid repeated freeze–thaw cycles.

PROTOCOL LITERACY

Epithalon DOSAGE CHART

A designed reference covering concentration, weekly schedule models, reconstitution, supply planning, storage, mechanism, study observations, and administration context. It is educational material—not an individualized regimen.

VIAL CONTENT

1.0 MG

+

REFERENCE DILUENT

1.0 MG

=

STOCK CONCENTRATION

1.0 MG/ML

U-100 SCALE

1 Unit = 0.01 ml 100 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 Days 1–20
(Cycle On)
INITIATION 5 mg 100 UNITS 1.00 ML
02 Weeks 4–26
(Cycle Off)
ESCALATION 01 0 mcg - 0.40 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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