Nitromethaqualone is a central nervous system (CNS) depressant of the quinazolinone class that acts as a sedative and hypnotic. Nitromethaqualone is a derivative of methaqualone, distinguished by the presence of a nitro group, which affects its pharmacological profile. While methaqualone gained popularity in the 1960s and 70s, nitromethaqualone has been studied less extensively but exhibits similar depressant effects.
Nitrometakwalon molecular structure diagram from the DrugsPRO substance library.
Classification
Chemical: Quinazolinone
Psychoactive: Depressant
Effects
Sedation
Motor Impairment
Anxiolytic
Sedative
Muscle Relaxation
Dystaxia
Reduced Anxiety
Amnesia
Euphoria
Language Impairment
Memory Impairment
Anxiety Suppression
Dulled Perception
Disinhibition
Blurred Vision
Increased Libido
Increased Music Appreciation
Changes In Felt Gravity
Routes of Administration
Oral
Dosage
Threshold: 10 mg
Light: 10 - 25 mg
Common: 25 - 50 mg
Strong: 50 - 60 mg
Heavy: 60 mg
Duration
No data available for this section yet.
Insufflated
Dosage
Threshold: 5 mg
Light: 5 - 10 mg
Common: 10 - 30 mg
Strong: 30 - 60 mg
Heavy: 60 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.
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
Nitromethaqualone - przewodnik po substancji DrugsPRO
Nitromethaqualone: Nitromethaqualone is a central nervous system (CNS) depressant of the quinazolinone class that acts as a sedative and hypnotic. Nitromethaqualone is a derivative of methaqualone, distinguished by the presence of a nitro group, which affects its pharmacological profile. While metha