| Minoxidil | |
|---|---|
| Salts [] | |
|---|---|
| Minoxidil tartrate | |
| Molecular structure via molpic based on CDK |
| Physical properties [] | |
|---|---|
| Molecular mass | 209.25 g/mol [1] |
| Solubility | >31.4 [ug/mL] (The mean of the results at pH 7.4) [1] |
| Predicted LogP | 1.2 [1] |
| Structural Identifiers [] | |
|---|---|
| Molecular formula | C9H15N5O [1] |
| IUPAC name | 3-hydroxy-2-imino-6-piperidin-1-ylpyrimidin-4-amine [1] |
| SMILES | C1CCN(CC1)C2=NC(=N)N(C(=C2)N)O [1] |
| InChI | InChI=1S/C9H15N5O/c10-7-6-8(12-9(11)14(7)15)13-4-2-1-3-5-13/h6,11,15H,1-5,10H2 [1] |
| InChIKey | ZIMGGGWCDYVHOY-UHFFFAOYSA-N [1] |
| Pharmacokinetics[] | |
|---|---|
| Elimination half-life | 4.2 h |
Minoxidil
Minoxidil (also known as Rogaine, Loniten, Minoximen, Theroxidil, Alopexil, Alostil, Regaine, Tricoxidil, Lonolox or Normoxidil) is a
Chemistry
Salts []
Minoxidil is typically found in the form of its tartrate salt.
Stereochemistry []
Minoxidil is a achiral mixture
| Anodyne Usernotes [] | |
|---|---|
| 0xea / Minoxidil via Transdermal and Oral at 10-15mg oral |
|
Legal status
See also []
External links []
References []
National Center for Biotechnology Information. PubChem Compound Summary for CID 4201, Minoxidil. Accessed October 2, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/4201
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Minoxidil. UNII: 5965120SH1. Global Substance Registration System. Accessed October 2, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/5965120SH1
59445 WOMEN'S REGAINE EXTRA STRENGTH Minoxidil 5% application bottle. Accessed October 2, 2025. https://www.ebs.tga.gov.au/servlet/xmlmillr6?dbid=ebs/PublicHTML/pdfStore.nsf&docid=59445&agid=%28PrintDetailsPublic%29&actionid=1
Search the TGA website. Accessed October 2, 2025. https://tga-search.clients.funnelback.com/s/search.html?collection=tga-artg&profile=record&meta_i=79914
Anodyne