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.
Нитрометаквалон molecular structure diagram from the DrugsPRO substance library.
Classification
Chemical: Quinazolinone
Psychoactive: Depressant
Effects
Sedation
Motor Impairment
Muscle Relaxation
Physical Euphoria
Incoordination
Anxiolytic
Reduced Anxiety
Anxiety Suppression
Motor Control Loss
Amnesia
Thought Deceleration
Euphoria
Dulled Perception
Disinhibition
Blurred Vision
Tactile Enhancement
Open Eye Visuals
Increased Libido
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 - DrugsPRO vodič o supstancama
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