Metaradrine

Salts []
Metaraminol bitartrate

Molecular structure via molpic
Conformer structure via 3Dmol.js
Molecular formula	C9H13NO2
Molecular mass	167.20 g/mol
Predicted LogP	-0.4
Melting point	107.5 °C
Decomposition	When heated to decomposition it emits toxic fumes of nitroxides.
Solubility	SOLUBILITY IN ALCOHOL: 1 G/100 ML /BITARTRATE/
Chirality	absolute

Identifiers []
IUPAC name	3-[(1R,2S)-2-amino-1-hydroxypropyl]phenol
SMILES	C[C@@H]([C@@H](C1=CC(=CC=C1)O)O)N
InChI	InChI=1S/C9H13NO2/c1-6(10)9(12)7-3-2-4-8(11)5-7/h2-6,9,11-12H,10H2,1H3/t6-,9-/m0/s1
InChIKey	WXFIGDLSSYIKKV-RCOVLWMOSA-N

Dosing

Metaraminol

Metaraminol (also known as Hydroxynorephedrine, m-Hydroxypropadrine, Pressonex, m-Hydroxy norephedrine, 1-Metaraminol, (-)-Erythro-metaraminol, Pressorol, m-Hydroxyphenylpropanolamine, Icoral B or Metaraminolum) is a sympathomimetic substance of the phenylethanolamine class.

Chemistry

Metaraminol is typically found in the form of its bitartrate salt.

Stereochemistry

Legal status

• Australia: Metaraminol is a S4 substance.
• United Kingdom: Metaraminol is a prescription only substance.
• United States: Metaraminol is a prescription only substance.

See also

• Phenylethanolamine
• Substituted phenylethanolamines
• Bluedark

External links

• Metaraminol (Wikipedia)
• Metaraminol (Wikidata)
• Metaraminol (DrugBank)
• Metaraminol (PubChem)
• Metaraminol (ChEMBL)
• Metaraminol (ChEBI)
• Metaraminol (Common Chemistry)
• Metaraminol (HMDB)
• Metaraminol (KEGG)
• Metaraminol (UNII)
• Metaraminol (EPA DSSTox)