Colterol

Salts []
Colterol mesylate

Esters []
Colterol acetate

Molecular structure via molpic
Conformer structure via 3Dmol.js
Molecular formula	C12H19NO3[1]
Molecular mass	225.28 g/mol[1]
Predicted LogP	-0.4[1]
Chirality	racemic[2]

Identifiers []
IUPAC name	4-[2-(tert-butylamino)-1-hydroxyethyl]benzene-1,2-diol[1]
SMILES	CC(C)(C)NCC(C1=CC(=C(C=C1)O)O)O[1]
InChI	InChI=1S/C12H19NO3/c1-12(2,3)13-7-11(16)8-4-5-9(14)10(15)6-8/h4-6,11,13-16H,7H2,1-3H3[1]
InChIKey	PHSMOUBHYUFTDM-UHFFFAOYSA-N[1]

Dosing

Colterol

Colterol (also known as Colterolum, (+-)-N-tert-Butylarterenol, (+-)-N-t-Butylnoradrenaline, dl-N-tert-Butylnorepinephrine, (+-)-tert-Butyl noradrenaline, KWD 2026, WIN-5563, S 1541, S-1541 or dl-1-(3,4-Dihydroxyphenyl)-2-tert-butylaminoethanol) is a sympathomimetic substance of the phenylethanolamine class.

Chemistry

Colterol is typically found in the form of its mesylate salt or its acetate ester.

Stereochemistry

(RS)-Colterol is a racemic mixture of the optical stereoisomers:

Stereoisomers []
(+)-Colterol (-)-Colterol

See also

• Phenylethanolamine
• Substituted phenylethanolamines
• Substituted catecholamines
• Anodyne

External links

• Colterol (Wikipedia)
• Colterol / (+)-Colterol / (-)-Colterol (Wikidata)
• Colterol / (+)-Colterol / (-)-Colterol (PubChem)
• Colterol / (-)-Colterol (ChEMBL)
• Colterol (ChEBI)
• Colterol / (+)-Colterol / (-)-Colterol (Common Chemistry)
• Colterol / (+)-Colterol / (-)-Colterol (UNII)
• Colterol (EPA DSSTox)