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Comparison

Bromantane vs Modafinil

Side-by-side of Bromantane and Modafinil. Every row below is pulled from the compound schema and will update as our data grows. For deeper reads, follow through to each compound page.

Effects at a glance

Bromantane

  • Russian RCT base (Voznesenskaya 2010, n=728) supports 50 mg daily for asthenia and fatigue over 4 weeks
  • Atypical actogenic mechanism: induces tyrosine hydroxylase rather than direct monoamine release
  • Subjective profile is anxiolytic plus mildly motivating, distinct from classical stimulants
  • Long half-life of around 11 hours supports once-daily morning dosing
  • WADA-banned since 1996; relevant for tested athletes
  • Western evidence base is thin; most published trials are Russian-language and not independently replicated

Modafinil

  • FDA approved in 1998 for narcolepsy, with later additions for shift-work sleep disorder and OSA residual sleepiness
  • Schedule IV controlled substance in the US; prescription-only in EU, UK, Australia
  • Increases wakefulness via weak dopamine reuptake inhibition plus histaminergic, noradrenergic, and orexinergic activation
  • Long half-life of 12 to 15 hours requires morning dosing to avoid sleep disruption
  • Modest cognitive enhancement signal in non-sleep-deprived adults at 100 to 200 mg (Battleday meta-review 2015)
  • Substantial CYP3A4 induction reduces hormonal contraceptive efficacy; barrier methods recommended

Side-by-side

Attribute Bromantane Modafinil
Category nootropic pharmaceutical
Also known as Ladasten, ADK-709, N-(4-bromophenyl)adamantan-2-amine Provigil, Modalert, Modvigil, diphenylmethylsulfinyl-acetamide
Half-life (hr) 11 13
Typical dose (mg) 75 200
Dosing frequency daily, morning daily, morning
Routes oral oral
Onset (hr) 3 1
Peak (hr) 168 3
Molecular weight 280.21 273.35
Molecular formula C16H20BrN C15H15NO2S
Mechanism Indirect dopaminergic and serotonergic actogenic activity via induction of tyrosine hydroxylase and selective increases in serotonin synthesis in hippocampus and hypothalamus. Weak dopamine reuptake inhibition plus downstream activation of histaminergic, noradrenergic, and orexinergic wake-promoting systems.
Legal status Approved in Russia (Ladasten); unscheduled and unapproved in US, EU, UK Schedule IV (US); prescription-only globally; not a supplement
WADA status banned banned
DEA / Rx Not scheduled in the US Schedule IV
Pregnancy Not recommended Not recommended
CAS 87913-26-6 68693-11-8
PubChem CID 9576456 4236
Wikidata Q4093816 Q422968

Safety profile

Bromantane

Common side effects

  • mild GI upset
  • headache
  • skin rash
  • occasional insomnia at higher doses

Contraindications

  • pregnancy
  • lactation
  • severe hepatic impairment
  • severe renal impairment
  • pediatric use

Interactions

  • MAOIs: theoretical additive dopaminergic and serotonergic activity(major)
  • levodopa and dopamine agonists: additive dopaminergic activity(moderate)
  • SSRIs and other serotonergic drugs: theoretical serotonergic additivity(moderate)
  • classical stimulants: theoretical additive activity, undocumented(moderate)

Modafinil

Common side effects

  • headache
  • nausea
  • anxiety
  • insomnia (with late-day dosing)
  • dry mouth
  • mild blood pressure elevation

Contraindications

  • recent myocardial infarction
  • unstable angina
  • left ventricular hypertrophy
  • significant arrhythmia
  • history of Stevens-Johnson syndrome
  • psychotic disorders
  • pregnancy
  • concurrent MAOI use

Interactions

  • hormonal contraceptives: CYP3A4 induction reduces contraceptive efficacy; use barrier method(major)
  • cyclosporine: reduced cyclosporine levels via CYP3A4 induction(major)
  • warfarin: CYP2C9 inhibition raises INR(moderate)
  • phenytoin: CYP2C19 inhibition raises phenytoin levels(moderate)
  • MAOIs: potential hypertensive reaction(major)
  • classical stimulants (amphetamine, methylphenidate): additive cardiovascular and sleep-disruption effects(moderate)

Which Should You Take?

Modafinil comes out ahead for most readers on the criteria we weight: 3 catalogued goals, controlled substance, oral dosing, with a Tier-A outcome catalogued. Bromantane is the right call when one of the conditionals below applies.

  • If your priority is stress and HPA-axis regulation, pick Bromantane.
  • If your priority is wakefulness, pick Modafinil.
  • If your priority is focus or working memory, pick Modafinil.

Default choice: Modafinil. Wider use case, a Tier-A evidence outcome catalogued, and broader goal coverage. Reach for Bromantane only if your priority sits squarely in the goals it owns above.

This verdict is generated from each compound's schema (goals, legal status, evidence outcomes, dosing route). It updates automatically as our compound data evolves; the deeper read sits on each individual compound page.

Common questions

What is the difference between Bromantane and Modafinil?

Bromantane and Modafinil differ in category (nootropic vs pharmaceutical), mechanism, and typical dosing. See the side-by-side table for full details.

Which has a longer half-life, Bromantane or Modafinil?

Bromantane half-life is 11 hours; Modafinil half-life is 13 hours.

Can you stack Bromantane with Modafinil?

Stack compatibility depends on mechanism overlap, legal status, and individual response. Check each compound page for specific interactions and contraindications before combining.

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