Library

Flmodafinils

Flmodafinil (CRL-40,940; bisfluoromodafinil; lauflumide) is a bis(4-fluoro) derivative of modafinil with enhanced dopamine transporter affinity and improved lipophilicity. Unlike modafinil, it does not induce CYP3A4 or CYP3A5 enzymes, reducing drug-drug interactions. Animal studies demonstrate robust wake-promoting activity without classic amphetamine-like locomotor sensitisation. Human anecdotes report shorter subjective duration (6-8 hours) with crisper onset but potential late-phase anxiety spike 6-8 hours post-dose. Keeping daily use at or below 100 mg and finishing doses before 10 a.m.

Flmodafinils molecular structure
Flmodafinils molecular structure diagram from the DrugsPRO substance library.

Also known as: Nls-4, Lauflumide, Crl-40,940, Bisfluoromodafinil, Fluoromodafinil, Flodafinil

Classification

  • Psychoactive: Nootropic
  • Psychoactive: Stimulant
  • Tag: Diphenylmethylsulfinylacetamide
  • Tag: Eugeroic
  • Tag: Research-Chemical
  • Tag: Tentative

Effects

  • Increased Heart Rate
  • Vasoconstriction
  • Stimulation
  • Loss Of Appetite
  • Insomnia
  • Headache
  • Wakefulness Enhancement
  • Focus Enhancement
  • Motivation Enhancement
  • Anxiety
  • Analysis Enhancement
  • Cognitive Euphoria
  • Appetite Suppression
  • Dehydration
  • Light Sensitivity
  • Photophobia
  • Increased Music Appreciation
  • Increased Libido

Routes of Administration

Oral / Sublingual

Dosage

  • Threshold: 15-20 mg
  • Light: 20-50 mg
  • Common: 50-100 mg
  • Strong: 100-150 mg
  • Heavy: 150 mg

Duration

  • Onset: 0.33-0.67 h
  • Comeup: 0.5-1 h
  • Peak: 2-4 h
  • Offset: 2-4 h
  • After Effects: 6 h

Insufflated

Dosage

  • Threshold: 5–10 mg
  • Light: 10–20 mg
  • Common: 15-30 mg
  • Strong: 30-50 mg
  • Heavy: 50 mg+

Duration

  • Onset: 0.08-0.25 h
  • Comeup: 0.33-0.5 h
  • Peak: 1.5-3.5 h
  • Offset: 2-4 h
  • After Effects: 9-15 h
  • Total Duration: 6-9 h

Rectal (Solution)

Dosage

  • Threshold: 10 mg
  • Light: 10-25 mg
  • Common: 25-60 mg
  • Strong: 60-90 mg
  • Heavy: 90 mg

Duration

  • Onset: 0.25-0.5 h
  • Comeup: 0.5-1 h
  • Peak: 2-4 h
  • Offset: 2-4 h
  • After Effects: 6 h

Oral

Dosage

  • Common: 50–100 mg
  • Light: 20-40 mg
  • Strong: 100–150 mg
  • Heavy: 150 mg+
  • Threshold: 10–20 mg

Duration

  • Onset: 0.33-0.67 h
  • Peak: 2-4 h
  • Offset: 6-10 h
  • After Effects: 10-16 h
  • Total Duration: 6-10 h

Sublingual

Dosage

  • Heavy: 120 mg+
  • Light: 15–40 mg
  • Common: 40–80 mg
  • Strong: 80–120 mg
  • Threshold: 10–15 mg

Duration

No data available for this section yet.

Rectal

Dosage

  • Heavy: 90 mg+
  • Light: 15–30 mg
  • Common: 30–60 mg
  • Strong: 60–90 mg
  • Threshold: 10–15 mg

Duration

No data available for this section yet.

Harm Reduction

Check interactions before mixing substances, pay attention to dose spacing and hydration, and treat all dosage guidance as approximate rather than guaranteed safe.

Sources

Substance data is aggregated from the following public harm-reduction and reference sources.

Links

This static page is intended as a readable non-JS and prerender-friendly library export.

Get the full DrugsPRO experience

Open the interactive DrugsPRO app for search, saved items, interactions, and deeper harm reduction tools.

Get the PRO test kit. The simple, quick and reliable drug checking test kit. Visit https://protestkit.eu

Flmodafinil - DrugsPRO vielu ceļvedis

Flmodafinil: Flmodafinil (CRL-40,940; bisfluoromodafinil; lauflumide) is a bis(4-fluoro) derivative of modafinil with enhanced dopamine transporter affinity and improved lipophilicity. Unlike modafinil, it does not induce CYP3A4 or CYP3A5 enzymes, reducing drug-drug interactions. Animal studies demo

Related pages