Hydroxychloroquine
Also called oxychlorochine.
An antimalarial also used for lupus and rheumatoid arthritis. It became a focus of controversy during the COVID-19 pandemic.
Sources and notes
- The introductionfrom sourceMoleculeFinder curated
- Other namesfrom sourceWikidataIts English label and aliases on 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
Dispensed on prescription, not sold on a shelf. Hydroxychloroquine on the product labels we hold.
Medicines
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 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.
An O-H on a carbon that is not part of an aromatic ring, the group that makes a molecule an alcohol. It both gives and accepts hydrogen bonds, which helps the molecule mix with water.
From: standard chemistry.
Fluorine, chlorine, bromine or iodine bonded to carbon. Each pulls electrons toward itself, and each is larger than the hydrogen the carbon would otherwise carry.
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.
Properties and sources
Calculated by PubChem
- Molecular formula
- C18H26ClN3O
- Molecular weight
- 335.9 g/mol
- XLogP3octanol/water, log units
- 3.6
- Polar surface areatopological
- 48.4 Ų
- H-bond donors
- 2
- H-bond acceptors
- 4
- Rotatable bonds
- 9
- Complexity
- 331
Reported Hazard label (GHS), ECHA via PubChem
Warning Irritant pictogram (GHS07); hazard statements H302
Reported Licence
The US Food and Drug Administration licenses Hydroxychloroquine for human use (NDA 009768, authorized April 18, 1955), as Plaquenil. Drugs@FDA
Groups it belongs to
- Category
- Prescription medicine
- Family
- Antiparasitics
- Chemical groups
- Alcohols, Amines, Aromatics, Halogenated
- Hazard classes
- Irritant, GHS Warning
CCN(CCCC(C)NC1=C2C=CC(=CC2=NC=C1)Cl)CCOPubChem CID 3652 · Wikidata Q421094 · InChIKey XXSMGPRMXLTPCZ-UHFFFAOYSA-N · Data refreshed
Questions
- What is Hydroxychloroquine?
- An antimalarial also used for lupus and rheumatoid arthritis. It became a focus of controversy during the COVID-19 pandemic.
- How toxic is Hydroxychloroquine?
- Its GHS hazard label carries the signal word Warning and the hazard pictogram Irritant. from source
- What kind of molecule is Hydroxychloroquine?
- Hydroxychloroquine has the formula C18H26ClN3O and a molecular weight of 335.9 g/mol. MoleculeFinder files it under antiparasitics, in the prescription medicine group. from sourcefrom sourcefrom sourcefrom source
- What else is Hydroxychloroquine called?
- Hydroxychloroquine is also called oxychlorochine. from source
- Who licenses Hydroxychloroquine as a medicine?
- The US Food and Drug Administration licenses Hydroxychloroquine for human use (NDA 009768, authorized April 18, 1955), as Plaquenil. from source
Sources and notes
- Calculated valuescomputedPubChemComputed from the structure, so no laboratory conditions apply; complexity is PubChem's own structural score.
- 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