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    Fladrafinil (CRL-40,941) molecular structure

    Fladrafinil (CRL-40,941)

    NootropicsPreclinical

    Also known as: CRL-40,941, CRL 40941, Fluorafinil, Bisfluoroadrafinil, 2-[bis(4-fluorophenyl)methylsulfinyl]-N-hydroxyacetamide

    Fladrafinil, coded CRL-40,941, is the N-hydroxy analog of flmodafinil and the difluorinated counterpart of adrafinil. Flmodafinil was conceived at Laboratoire L.

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    $0.025/mg$74.99 for 3000mg

    at Disguised Alpha

    Half-life: Not established in humansRoute: OralMW: 325.3 g/molCAS: 90212-80-9
    Last reviewed:

    Overview

    At A Glance

    Mechanism

    Fladrafinil is the N-hydroxy analog of flmodafinil and behaves as a prodrug: after oral administration to humans it is converted to flmodafinil, which is then oxidized to the inactive derivatives flmodafinil acid and flmodafinil sulfone, mirroring the way adrafinil is converted t…

    Half-Life
    Not established in humans; after a single 20 mg oral dose in six volunteers, urinary fladrafinil peaked at 2 to 4 h and stayed detectable for up to 12 h, while the metabolite flmodafinil was detectable for about 8 days and the acid and sulfone metabolites for about two weeks (PMID: 42210629)
    Routes
    Oral
    Potential Benefits
    Longer wake duration in male C57BL/6J mice than modafinil, with no rebound hypersomnia, for lauflumide (NLS-4), which is flmodafinil, the active metabolite of fladrafinil (PMID: 30158846)Less non-REM sleep and less delta activity during recovery sleep in mice than after modafinil, suggesting a lower recovery need despite longer induced wakefulness (PMID: 30158846)Confirmed conversion to flmodafinil in six healthy human volunteers after a single 20 mg oral dose, establishing that the prodrug step works in people (PMID: 42210629)For the class parent modafinil, dopamine transporter occupancy and increased brain dopamine in 10 healthy men, the presumed basis of the class effect (PMID: 19293415)

    Overview

    Fladrafinil, coded CRL-40,941, is the N-hydroxy analog of flmodafinil and the difluorinated counterpart of adrafinil. Flmodafinil was conceived at Laboratoire L. Lafon, the French company behind adrafinil and modafinil, and was never developed as a medicine (PMID: 30158846); the CRL-40,941 code of fladrafinil places it in the same series. Fladrafinil is sold today only as a research chemical or as an ingredient in unapproved supplements marketed for wakefulness and focus, and interest in it grew alongside the off-label use of modafinil as a cognitive enhancer (PMID: 27928893). Its pharmacology is best understood as prodrug chemistry. In a human administration study published in 2026, six volunteers each took a single 20 mg dose and gave urine and dried blood spot samples; fladrafinil was converted to flmodafinil, which was then oxidized to flmodafinil acid and flmodafinil sulfone, the same pattern adrafinil follows toward modafinil (PMID: 42210629). The activity therefore belongs mostly to flmodafinil rather than to the parent compound. For flmodafinil there is one useful animal study, published under the compound names lauflumide and NLS-4. In male C57BL/6J mice with EEG and EMG recording, an intraperitoneal dose of 64 mg/kg produced longer wakefulness than modafinil at 150 mg/kg, without hyperlocomotion and without rebound hypersomnia, and recovery sleep afterwards involved less non-REM sleep and less delta activity than after modafinil (PMID: 30158846). No comparable study exists for fladrafinil itself. Nothing about efficacy in people has been tested. The single human study measured concentrations and detection windows, not attention, wakefulness or performance (PMID: 42210629). For the class parent, positron emission tomography in ten healthy men showed that modafinil occupied dopamine transporters in caudate, putamen and nucleus accumbens and raised extracellular dopamine, a finding the authors linked to abuse potential (PMID: 19293415). Whether the fluorinated analogs behave the same way at the same exposures has not been measured in humans. Two practical points come out of the doping-control work. Product labels are unreliable: one supplement bought for that study was labeled at 50 mg/mL of flmodafinil and assayed at 95.7 mg/mL, close to double the stated content (PMID: 42210629). And anyone tested in sport should know that fladrafinil and flmodafinil were added to the 2026 World Anti-Doping Agency Prohibited List under class S6 stimulants and are prohibited in competition, with detection windows of up to a week for the parent compounds and about two weeks for the metabolites (PMID: 42210629). A retrospective screen of about 2000 in-competition samples collected in 2023 and 2024 found none of these compounds, so current use among tested athletes appears low. There is no FDA or EMA authorization for fladrafinil, no published safety trial, and no pregnancy, cardiac or hepatic data. It is a research-use-only compound in the US market, and the gap between what is claimed for it online and what has actually been measured is wide.

    Potential Research Fields

    Wakefulness-promoting agentsAnti-doping analysisDrug metabolismCognitive enhancement

    Chemical Information

    IUPAC Name

    Not yet available

    CAS Number

    90212-80-9

    Molecular Formula

    C15H13F2NO3S

    Molecular Mass

    325.3 g/mol

    Dosing & Protocols

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    Research

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    Interactions

    Contraindications

    Mechanism-based: fladrafinil is converted to a compound of the modafinil class, and modafinil occupies dopamine transporters and raises brain dopamine in humans, an effect the investigators linked to abuse potential in vulnerable people (PMID: 19293415). Athletes subject to anti-doping testing should treat it as prohibited in competition (PMID: 42210629). No pregnancy, hepatic or cardiac safety data exist for fladrafinil in any species.

    Research Disclaimer

    This interaction data is compiled from published research and community reports. It may not be exhaustive. Always consult a healthcare professional before combining compounds.

    Best Price

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    Best $/mg

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    Vendors Selling Fladrafinil (CRL-40,941)

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    9-Me-BC (9-Methyl-β-carboline)

    NootropicsPreclinical

    9-Methyl--carboline (9-Me-BC) is a synthetic -carboline alkaloid that has drawn nootropic-community interest for a preclinical property that is genuinely unusual among -carbolines: in rodent and cell-culture studies it appears to stimulate the dopaminergic phenotype - raising tyrosine hydroxylase, the number of differentiated dopamine neurons and dopamine content - while also showing neuroprotective, neurorestorative and anti-inflammatory effects, plus in-vitro MAO-A/MAO-B inhibition [PMID:17913302, PMID:20374418, PMID:32285253].

    t½ Not characterized in humans (no pharmacokinetic data). Community/anecdotal only: ~5-25 mg per day, oral. No validated or approved human dose exists.
    6 PubMedView Profile

    Aniracetam

    NootropicsApproved (Italy)

    Aniracetam is a pyrrolidinone in the racetam family, developed by Hoffmann-La Roche under the code Ro 13-5057.

    t½ About half an hour for the parent drug in humans. Plasma elimination half-life was 0.47 to 0.49 hours after a single 400 mg oral dose in 20 healthy male volunteers (PMID: 19025058). Aniracetam is extensively metabolized to N-anisoyl-GABA and anisic acid; in six elderly hospitalized patients with cerebrovascular disease and reduced creatinine clearance, metabolite half-life was 4 to 7 times longer than in young volunteers (PMID: 9062694).
    PreclinicalView Profile

    Bemethyl (bemitil)

    NootropicsApproved (Russia)

    Bemethyl, known in the Russian literature as bemitil and sold in the region under names including Metaprot, Bemactor and Antihot, is 2-ethylthiobenzimidazole, normally handled as the hydrobromide salt.

    t½ Not established in humans; in healthy volunteers given a single 250 mg oral dose of the Metaprot capsule form, peak serum ethylthiobenzimidazole averaged 0.91 microg/mL at about 1.06 h, and no terminal half-life was reported (PMID: 21870773)
    PreclinicalView Profile

    Bromantane

    NootropicsRussia Approved

    Bromantane is an atypical psychostimulant and anxiolytic developed in the 1980s at the Zakusov Institute of Pharmacology of the Russian Academy of Medical Sciences, originally created as an adaptogen for Soviet military and elite athletic use and later approved in Russia for the treatment of neurasthenic and asthenic disorders under the trade name Ladasten.

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    Cyclazodone

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    Dihexa

    NootropicsPreclinical

    Dihexa is a synthetic peptide analogue of the angiotensin IV metabolite LVV-hemorphin-7, developed at Washington State University.

    t½ Not characterized in humans. Dihexa was engineered for metabolic stability (resistant to plasma and enzymatic degradation) and blood-brain-barrier penetration; in preclinical work its central procognitive effects appear to outlast its plasma presence. 5 to 40 mg oral per day (anecdotal range; no established human dose)
    1 PubMedView Profile

    View Full Dosage Guide →

    Protocols, calculator & safety for Fladrafinil (CRL-40,941)

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    1 vendor · 1 listing

    Research Score

    30

    0 PubMed results

    Quality Indicators

    Data Completeness

    63%
    Description
    Mechanism of Action
    Chemical Data
    Dosing Protocols
    Safety Profile
    PubMed Results
    Interactions
    Vendor Listings

    COA Verification

    0

    Verified COAs

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    Vendors w/ COA

    Latest test: 9/16/2026

    Quick Facts

    Half-Life

    Not established in humans; after a single 20 mg oral dose in six volunteers, urinary fladrafinil peaked at 2 to 4 h and stayed detectable for up to 12 h, while the metabolite flmodafinil was detectable for about 8 days and the acid and sulfone metabolites for about two weeks (PMID: 42210629)

    Molecular Weight

    325.3 g/mol

    Administration

    Oral

    CAS Number

    90212-80-9

    Trial Phase

    Preclinical

    Research Disclaimer

    This information is for educational and research purposes only. Not intended as medical advice. Consult a healthcare professional before use.

    Frequently Asked Questions

    What is Fladrafinil (CRL-40,941) used for in research?

    Fladrafinil, coded CRL-40,941, is the N-hydroxy analog of flmodafinil and the difluorinated counterpart of adrafinil. Flmodafinil was conceived at Laboratoire L. Lafon, the French company behind adrafinil and modafinil, and was never developed as a medicine (PMID: 30158846); the CRL-40,941 code of fladrafinil places it in the same series. Fladrafinil is sold today only as a research chemical or as an ingredient in unapproved supplements marketed for wakefulness and focus, and interest in it grew alongside the off-label use of modafinil as a cognitive enhancer (PMID: 27928893).

    Its pharmacology is best understood as prodrug chemistry. In a human administration study published in 2026, six volunteers each took a single 20 mg dose and gave urine and dried blood spot samples; fladrafinil was converted to flmodafinil, which was then oxidized to flmodafinil acid and flmodafinil sulfone, the same pattern adrafinil follows toward modafinil (PMID: 42210629). The activity therefore belongs mostly to flmodafinil rather than to the parent compound.

    For flmodafinil there is one useful animal study, published under the compound names lauflumide and NLS-4. In male C57BL/6J mice with EEG and EMG recording, an intraperitoneal dose of 64 mg/kg produced longer wakefulness than modafinil at 150 mg/kg, without hyperlocomotion and without rebound hypersomnia, and recovery sleep afterwards involved less non-REM sleep and less delta activity than after modafinil (PMID: 30158846). No comparable study exists for fladrafinil itself.

    Nothing about efficacy in people has been tested. The single human study measured concentrations and detection windows, not attention, wakefulness or performance (PMID: 42210629). For the class parent, positron emission tomography in ten healthy men showed that modafinil occupied dopamine transporters in caudate, putamen and nucleus accumbens and raised extracellular dopamine, a finding the authors linked to abuse potential (PMID: 19293415). Whether the fluorinated analogs behave the same way at the same exposures has not been measured in humans.

    Two practical points come out of the doping-control work. Product labels are unreliable: one supplement bought for that study was labeled at 50 mg/mL of flmodafinil and assayed at 95.7 mg/mL, close to double the stated content (PMID: 42210629). And anyone tested in sport should know that fladrafinil and flmodafinil were added to the 2026 World Anti-Doping Agency Prohibited List under class S6 stimulants and are prohibited in competition, with detection windows of up to a week for the parent compounds and about two weeks for the metabolites (PMID: 42210629). A retrospective screen of about 2000 in-competition samples collected in 2023 and 2024 found none of these compounds, so current use among tested athletes appears low.

    There is no FDA or EMA authorization for fladrafinil, no published safety trial, and no pregnancy, cardiac or hepatic data. It is a research-use-only compound in the US market, and the gap between what is claimed for it online and what has actually been measured is wide.

    What forms does Fladrafinil (CRL-40,941) come in?

    Fladrafinil (CRL-40,941) is available in liquid form.

    How do I compare Fladrafinil (CRL-40,941) vendors?

    Compare prices, payment methods, shipping, and COA scores across 1 vendor.

    How many vendors sell Fladrafinil (CRL-40,941), and what does it cost per mg?

    1 of the vendors BodyHackGuide tracks list Fladrafinil (CRL-40,941) (1 listing). Among BodyHackGuide's Fladrafinil (CRL-40,941) listings recorded as in stock with a milligram count, the lowest price per milligram is $0.025/mg at Disguised Alpha and the median is $0.025/mg. The Fladrafinil (CRL-40,941) prices on BodyHackGuide are vendors' listed prices as BodyHackGuide last recorded them, not transactions; the most recent recorded change to a Fladrafinil (CRL-40,941) listing is dated 7 September 2026.

    Which vendors have third-party COAs for Fladrafinil (CRL-40,941) on file at BodyHackGuide?

    BodyHackGuide holds 1 third-party certificate record for Fladrafinil (CRL-40,941), from Disguised Alpha. No editor has read any of BodyHackGuide's 1 certificate record for Fladrafinil (CRL-40,941). The laboratory named on BodyHackGuide's Fladrafinil (CRL-40,941) certificate record is Freedom Diagnostics Testing, and the test date on it is 16 September 2026. Each vendor page on BodyHackGuide shows how many certificate records BodyHackGuide holds for that vendor and links to each record that has its own page.

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    9-Me-BC (9-Methyl-β-carboline)

    NootropicsPreclinical

    9-Methyl--carboline (9-Me-BC) is a synthetic -carboline alkaloid that has drawn nootropic-community interest for a preclinical property that is genuinely unusual among -carbolines: in rodent and cell-culture studies it appears to stimulate the dopaminergic phenotype - raising tyrosine hydroxylase, the number of differentiated dopamine neurons and dopamine content - while also showing neuroprotective, neurorestorative and anti-inflammatory effects, plus in-vitro MAO-A/MAO-B inhibition [PMID:17913302, PMID:20374418, PMID:32285253].

    t½ Not characterized in humans (no pharmacokinetic data). Community/anecdotal only: ~5-25 mg per day, oral. No validated or approved human dose exists.
    6 PubMedView Profile

    Aniracetam

    NootropicsApproved (Italy)

    Aniracetam is a pyrrolidinone in the racetam family, developed by Hoffmann-La Roche under the code Ro 13-5057.

    t½ About half an hour for the parent drug in humans. Plasma elimination half-life was 0.47 to 0.49 hours after a single 400 mg oral dose in 20 healthy male volunteers (PMID: 19025058). Aniracetam is extensively metabolized to N-anisoyl-GABA and anisic acid; in six elderly hospitalized patients with cerebrovascular disease and reduced creatinine clearance, metabolite half-life was 4 to 7 times longer than in young volunteers (PMID: 9062694).
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    Bemethyl (bemitil)

    NootropicsApproved (Russia)

    Bemethyl, known in the Russian literature as bemitil and sold in the region under names including Metaprot, Bemactor and Antihot, is 2-ethylthiobenzimidazole, normally handled as the hydrobromide salt.

    t½ Not established in humans; in healthy volunteers given a single 250 mg oral dose of the Metaprot capsule form, peak serum ethylthiobenzimidazole averaged 0.91 microg/mL at about 1.06 h, and no terminal half-life was reported (PMID: 21870773)
    PreclinicalView Profile

    Bromantane

    NootropicsRussia Approved

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    34 PubMedView Profile

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    NootropicsPreclinical

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    PreclinicalView Profile

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    NootropicsPreclinical

    Dihexa is a synthetic peptide analogue of the angiotensin IV metabolite LVV-hemorphin-7, developed at Washington State University.

    t½ Not characterized in humans. Dihexa was engineered for metabolic stability (resistant to plasma and enzymatic degradation) and blood-brain-barrier penetration; in preclinical work its central procognitive effects appear to outlast its plasma presence. 5 to 40 mg oral per day (anecdotal range; no established human dose)
    1 PubMedView Profile

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