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Finasteride 5 mg Accord

Accord

35,00

In Stock (100 available)

Finasteride 5 mg Accord (5 mg) — Finasteride — selective 5α-reductase type-II inhibitor. Scalp DHT protection for testosterone-based cycles; ineffective against DHT-derivative AAS like tren or masteron.

100 in stock

This product is for laboratory research use only. Not for human consumption.

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Description

Finasteride 5 mg Accord — finasteride from Accord at 5 mg. Type II 5-alpha-reductase inhibitor. Reduces scalp and prostate DHT (70%+ reduction). Ineffective against DHT-derivative AAS like masteron, winstrol, or anavar.

Key Benefits

  • 5α-reductase type-II inhibitor — suppresses scalp DHT
  • Clinical standard for male-pattern hair loss
  • On-cycle hair protection during testosterone-based protocols
  • Not effective against DHT-derived AAS (trenbolone, masteron, oxandrolone)
  • Sexual side-effects documented in a minority of users
  • Each unit dosed at 5 mg — see Recommended Dosage below for protocol-specific intake

Recommended Dosage

Research dosing: 1 mg/day for hair protection. Higher doses (5 mg) for BPH. Oral tablet, single daily dose.

How It Works

Selective 5α-reductase type-II inhibitor. Prevents conversion of testosterone to dihydrotestosterone (DHT) at scalp and prostate. Does not affect type-I isoform — whole-body DHT reduction around 70%.

Pharmacokinetics

Plasma half-life approximately 6 hours. Once-daily dosing. Scalp DHT reduction persists longer than plasma half-life suggests.

Potential Side Effects

Sexual side-effects (libido, ED) in a minority (2–8% in trials). Depression documented but rare. Does NOT protect against DHT-derivative AAS like tren, masteron, winstrol, anavar — those bypass 5α-reductase entirely.

Cycle & Stacking Guide

On-cycle daily with testosterone-based protocols if hair concerns exist. Pointless alongside DHT-derivative AAS. Consider dutasteride (type I + II inhibition) for more complete coverage if needed.

Manufacturer Notes

Accord is an independent producer in the research-compound market. Before first use, request the batch-specific Certificate of Analysis and confirm the vial’s tamper-evident seal is intact.

Storage & Handling

Store at recommended temperature (15–25°C; peptides and HGH at 2–8°C after reconstitution). Protect from light and moisture. Keep out of reach of children. For research and educational purposes only.

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Finasteride

Physical & Chemical Properties for Research Purposes
Chemical structure of Finasteride (C23H36N2O2) for laboratory analysis
2D structural representation · PubChem CID 57363 ↗
Chemical Identity
# CAS Registry Number 98319-26-7
Σ IUPAC Name N-tert-butyl-3-oxo-4-aza-5alpha-androst-1-ene-17beta-carboxamide
F Molecular Formula C23H36N2O2
M Molecular Weight 372.55 g/mol
SMILES CC(C)(C)NC(=O)[C@H]1CC[C@@H]2[C@@]1(C)CC[C@H]3[C@H]2CC[C@@H]4NC(=O)C=C[C@]34C
InChIKey DBEPLOCGEIEOCV-WSBQPABSSA-N
Melting Point 252-254 °C
Solubility Freely soluble in chloroform, ethanol; practically insoluble in water
Biological Half-life 5-6 hours (oral)
PubChem CID 57363 ↗
Pharmacological Profile
Aromatization None
Hepatotoxicity Low
Known trade names: Propecia, Proscar, Finasteride

Data sourced from published pharmacological literature and authoritative chemical databases (PubChem, DrugBank, ChEBI). Provided for identification and research reference only.