Naloxone
Also called N-Allyl-noroxymorphone and n-Allylnoroxymorphone.
The opioid antagonist sold as Narcan, which reverses an opioid overdose in minutes and is now sold over the counter in the United States.
Sources and notes
- The introductionfrom sourceMoleculeFinder curated
- Other namesfrom sourcePubChem / Wikidata
- Formula and weightcomputedPubChem
- 2D drawingcomputedPubChem structure, drawn by RDKit
- 3D modelfrom sourcePubChem 3D conformerLoaded after the page has painted, and on a phone only when you ask for it; the 2D drawing shows until it arrives.
Where you encounter it
Sold over the counter, without a prescription. Naloxone on the product labels we hold.
Every product and list we hold
Sources and notes
- The product labels and their strengthsfrom sourceDailyMed (FDA label)Each label lists the molecule as an ingredient, and an active ingredient at the strength shown.
- How it gets therefrom sourceMoleculeFinder curatedEach mark is set by hand on our lists, never inferred; a label's ingredient is added by the maker. A row with no mark data says Not marked.
- The line abovefrom sourceMoleculeFinder curatedFrom the group the molecule belongs to.
Explore its structure
Choose a part to light it up.
A C=O with a carbon on each side. Its oxygen accepts hydrogen bonds but has no hydrogen to give, and it resists oxidation better than an aldehyde.
From: standard chemistry.
An O-H fixed directly to a benzene ring. The ring makes that hydrogen easier to give up than an ordinary alcohol's, which is why many phenols act as antioxidants.
From: standard chemistry.
A nitrogen bonded to three carbons, with no hydrogen of its own. Its spare pair of electrons can still pick up a hydrogen ion, so a tertiary amine is a base.
From: standard chemistry.
Sources and notes
- The drawingcomputedPubChem structure, drawn by RDKitThe page's one shipped drawing, with the chosen part lit in amber under it.
- The partscomputedFound by ruleEach part is found by a chemical pattern, never picked by hand atom by atom; its words say where they come from.
Compare a related molecule
Naloxone
Naltrexone
Naloxone reverses an opioid overdose within minutes, while naltrexone survives the gut and lasts many hours; both block the same opioid receptor.
Naloxone vs Naltrexone, side by sideSources and notes
- The sentencefrom sourceMoleculeFinder comparison notesThe pair's answer line.
- The two drawingscomputedPubChem structures, drawn by RDKitThe two drawings side by side.
Properties and sources
Calculated by PubChem
- Molecular formula
- C19H21NO4
- Molecular weight
- 327.4 g/mol
- XLogP3octanol/water, log units
- 2.1
- Polar surface areatopological
- 70 Ų
- H-bond donors
- 2
- H-bond acceptors
- 5
- Rotatable bonds
- 2
- Complexity
- 594
Measured LD50, HSDB via PubChem
90 mg/kg pure naloxone, mouse, intravenous
An LD50 is an animal study measurement, not a dose for a person.
Reported Hazard label (GHS), ECHA via PubChem
Danger Corrosive pictogram (GHS05) and Irritant pictogram (GHS07); hazard statements H302, H315, H318, H319, H335
Reported Licence
The US Food and Drug Administration licenses Naloxone for human use (NDA 208411, authorized November 18, 2015). Drugs@FDA
Groups it belongs to
- Category
- OTC medicine
- Elements
- Nitrogen
- Hazard classes
- Corrosive, Irritant, GHS Danger
C=CCN1CC[C@]23[C@@H]4C(=O)CC[C@]2([C@H]1CC5=C3C(=C(C=C5)O)O4)OPubChem CID 5284596 · Wikidata Q282902 · InChIKey UZHSEJADLWPNLE-GRGSLBFTSA-N · Data refreshed
Questions
- What is Naloxone?
- The opioid antagonist sold as Narcan, which reverses an opioid overdose in minutes and is now sold over the counter in the United States.
- How toxic is Naloxone?
- The reported LD50 of Naloxone is 90 mg/kg (mouse, iv). An LD50 is an animal study measurement, not a dose for a person. Its GHS hazard label carries the signal word Danger and the hazard pictograms Corrosive and Irritant. from sourcefrom source
- What kind of molecule is Naloxone?
- Naloxone has the formula C19H21NO4 and a molecular weight of 327.4 g/mol. MoleculeFinder files it under opioid antagonist, in the OTC medicine group. from sourcefrom sourcefrom sourcefrom source
- Who licenses Naloxone as a medicine?
- The US Food and Drug Administration licenses Naloxone for human use (NDA 208411, authorized November 18, 2015). from source
Sources and notes
- Calculated valuescomputedPubChemComputed from the structure, so no laboratory conditions apply; complexity is PubChem's own structural score.
- LD50from sourceHSDB via PubChemOther values the sources report: rat, intravenous, 107 mg/kg; rat, another route, 239 mg/kg; mouse, another route, 286 mg/kg; rat, another route, 500 mg/kg. The page shows the one LD50 the site uses everywhere.
- Hazard labelfrom sourceECHA via PubChemThe label combines these classifications.
- ECHAfrom sourceAttributionSource: European Chemicals Agency, echa.europa.eu.
- Licencefrom sourceDrugs@FDARead 2026-10-21.
- Data refreshedfrom sourceMoleculeFinder2026-11-09
Keep exploring
Sources and notes
- Compared side by sidefrom sourceMoleculeFinder comparison notesA molecule we compare it with on its own page.
- Similar in shapecomputedRDKit Morgan/TanimotoNeighbours by structural fingerprint; the sentence names the chemical groups the two share.
- The drawingscomputedPubChem structures, drawn by RDKit