Injectable Steroids

Tren Mix 200 mg Vedi Pharma

Vedi Pharma

65,00

In Stock (100 available)

Tren Mix 200 mg Vedi Pharma (200 mg) — Vedi Pharma presents this pharmaceutical-grade compound — this Trenbolone blend combines multiple esters (typically Acetate, Ena…

100 in stock

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

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Description

This Vedi Pharma trenbolone acetate at 200 mg delivers the fastest trenbolone ester available. Effects noticeable within 48 hours; clearance quick if side-effects (trensomnia, night sweats) require withdrawal. Not a beginner compound — testosterone base required.

Key Benefits

  • Multi-ester 19-nor trenbolone — acute kick + sustained coverage
  • Typical mix: acetate + enanthate + hexahydrobenzylcarbonate
  • Injection frequency every 3–4 days sufficient
  • Active molecule identical to single-ester tren at AR level
  • Same side-effect burden as standalone tren — blend isn’t softer
  • Each unit dosed at 200 mg — see Recommended Dosage below for protocol-specific intake

Recommended Dosage

Research dosing: 150–300 mg/week split across 2–3 injections. The acetate fraction peaks within a day while longer esters build steady-state over 3–4 weeks. Cycles 10–12 weeks.

How It Works

Blend of trenbolone acetate, enanthate, and hexahydrobenzylcarbonate (parabolan) — all three are 19-nor derivatives with the same extreme AR affinity as single-ester trenbolone. Progestagenic. The blend provides staggered release: acetate in ~24 h, enanthate ~7 days, hexa ~10 days. At the receptor level the active molecule is identical across esters.

Pharmacokinetics

Composite release profile. Faster kick-in than pure enanthate, flatter serum than pure acetate. Injection frequency every 3–4 days adequate. Steady-state in 3–4 weeks.

Potential Side Effects

Identical to single-ester tren: prolactin rise, night sweats, insomnia, CV stress, aggression. Caber 0.25 mg 2×/week mandatory. Bloodwork including prolactin at week 6.

Cycle & Stacking Guide

Cutting and recomp cycles 10–12 weeks. Test E 300–500 mg/week + tren blend 200–300 mg/week. Attention to sleep, resting HR, and lipids throughout. Not for first or second cycles.

Manufacturer Notes

Vedi Pharma ships injectables in tamper-evident 10 ml vials with GMP-compliant batch numbering.

Storage & Handling

Store upright at 15–25 °C in the original box, protected from light and moisture. Oil-based injectables are shelf-stable for the duration printed on the vial when kept at controlled room temperature. Do not refrigerate — cold thickens the carrier oil and makes drawing/injecting harder. Keep out of reach of children. For research and educational purposes only.

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Trenbolone Acetate

Physical & Chemical Properties for Research Purposes
Chemical structure of Trenbolone Acetate (C20H24O3) for laboratory analysis
2D structural representation · PubChem CID 24822 ↗
Chemical Identity
# CAS Registry Number 10161-34-9
Σ IUPAC Name [(8S,13S,14S,17S)-13-methyl-3-oxo-2,3,6,7,8,14-hexahydro-1H-cyclopenta[a]phenanthrene-17-yl] acetate
F Molecular Formula C20H24O3
M Molecular Weight 312.41 g/mol
SMILES CC(=O)O[C@@H]1CC[C@@H]2C3=CC=C4CC(=O)CC[C@]4(C)[C@@H]3CC[C@]12C
InChIKey FNYKCQMZFXUVMA-LKBHZCJUSA-N
Melting Point 96-97 °C
Solubility Practically insoluble in water; soluble in oils and organic solvents
Biological Half-life 1 day (IM)
PubChem CID 24822 ↗
Pharmacological Profile
Anabolic Rating 500
Androgenic Rating 500
Aromatization None
Hepatotoxicity Low
Detection Time 5 months

Clinical Notes

19-nor 5alpha-reduced analogue of nandrolone. Non-aromatizable — AR-binding affinity roughly 5x testosterone, with measurable agonist activity at the progesterone receptor. The acetate ester generates fast serum peaks and drops; EOD administration is the floor for stable concentrations. Clinical picture: rapid lean-tissue accretion independent of caloric surplus, reduced adipose mass via direct AR signalling in adipocytes, pronounced lipid shift (HDL suppression 40–60%). Prolactin elevation occurs in a subset — cabergoline 0.25 mg twice weekly is the standard response. Renal biomarkers (creatinine, cystatin C) commonly shift upward; this reflects haem metabolite excretion in urine (brick-red pigment) rather than confirmed nephrotoxicity, but CKD-EPI readings should be interpreted with the confounding documented. Nocturnal sympathetic tone (insomnia, diaphoresis) is dose-dependent and resolves on cessation.

Known trade names: Finajet, Finaplix, Trenbol

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