COMPOUNDS / STIMULANT / MDPV
STIMULANT

MDPV

HIGH RISK
BEST FOR:Stimulation●○○○○○○○○○1/10
MDPV · 3,4-METHYLENEDIOXYPYROVALERONE · METHYLENEDIOXYPYROVALERONE · MDPK · MD-PV
StimulantSynthetic CathinoneDesigner DrugBath SaltsNPS

Synthetic cathinone and potent dopamine-norepinephrine reuptake inhibitor with high abuse liability and severe toxicity.

ROUTE / DOSAGE
LOW4-8mg
STANDARD8-14mg
HIGH14-25mg
Note: Onset 15-30 min; effects can last 3-6 hours
CYCLE
Avoid redosing high compulsive redosing and addiction risk
BIOAVAILABILITY
variable oral (~50-70%) high intranasal (~80%)
ACTIVE DURATION
3-6h (subjective)
STORAGE
Room temperature dry away from light keep sealed to prevent degradation
HALF-LIFE
3-4h (plasma)
DURATION BREAKDOWN
Total3-6h
Onset5-30min
Come up15-45min
Peak1-3h
Offset1-2h
After effects2-8h
Duration varies by route, dose, and individual. Source: community reports.
§ 01 — EFFECTS
8 documented
Intense stimulation and euphoria
Increased alertness and vigilance
Decreased appetite
Suppressed need for sleep
Elevated heart rate and blood pressure
Compulsive redosing urge
Anxiety and paranoia at higher doses
Severe crash and dysphoria during withdrawal
§ 02 — RISKS
Acute intoxication and fatalities documented in humans
Severe cardiovascular effects including tachycardia, hypertension, and cardiac arrhythmias
High addiction liability with compulsive use patterns
Severe withdrawal symptoms including anxiety, depression, hypersomnia, and panic attacks
Neuroimmune dysregulation and cytokine elevation during withdrawal
Psychiatric symptoms including paranoia, hallucinations, and perceptual disturbances
§ 03 — INTERACTIONS
No interaction with your stack
VIEW STACK
CAUTION
Alcohol
MXE
Dissociatives
AVOID · DANGEROUS
25x-NBOMe
25x-NBOH
Tramadol
MAOIs
DXM
MDMA
Stimulants
§ 04 — SCIENCE

MDPV is a synthetic cathinone (β-keto amphetamine analogue) that emerged as a component of so-called bath salts products and has caused serious medical consequences including acute intoxications and fatalities. Preclinical studies demonstrate that MDPV functions as a powerful reinforcer in self-administration paradigms, with potency exceeding that of cocaine. MDPV displays rapid pharmacokinetics with peak plasma concentrations achieved within 10-20 minutes after injection and quick decline thereafter. Metabolism involves CYP2C19, CYP1A2, and CYP2D6 isoenzymes, producing metabolites such as 3,4-catechol-PV and 4-OH-3-MeO-PV, though motor activation correlates with parent drug concentrations rather than metabolites. Withdrawal from MDPV produces anxiety-like effects and dysregulation of cytokine and glutamate systems in mesocorticolimbic regions. Evidence is largely preclinical; human pharmacological data remain limited and derive primarily from case reports of intoxication and fatality.

§ 06 — SOURCES
[1]
PubMed PMID 29030166 - MDPV and α-PVP use in humans: The twisted sisters
pubmed.ncbi.nlm.nih.gov ↗
[2]
PubMed PMID 27830575 - Neuropharmacology of MDPV, Its Metabolites, and Related Analogs
pubmed.ncbi.nlm.nih.gov ↗
[3]
PubMed PMID 35470552 - Interactions between impulsivity and MDPV self-administration in rats
pubmed.ncbi.nlm.nih.gov ↗
[4]
PubMed PMID 33236170 - MDPV self-administration in female rats
pubmed.ncbi.nlm.nih.gov ↗
[5]
PubMed PMID 22112374 - MDPV epidemic?
pubmed.ncbi.nlm.nih.gov ↗
[6]
PubMed PMID 36871847 - Cyanidin prevents MDPV withdrawal-induced anxiety-like effects
pubmed.ncbi.nlm.nih.gov ↗
[7]
PubMed PMID 27142261 - Neurobiology of MDPV and α-PVP
pubmed.ncbi.nlm.nih.gov ↗
[8]
PubMed PMID 33809599 - Acute MDPV Binge Paradigm on Mice Emotional Behavior
pubmed.ncbi.nlm.nih.gov ↗
[9]
PsychonautWiki - MDPV
psychonautwiki.org ↗
Disclaimer. Protokol.wiki is an informational reference. Nothing on this site is medical advice. Compounds listed may be unapproved, unregulated, or illegal in your jurisdiction. Consult a licensed physician before use. Data compiled from peer-reviewed literature.
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