Bluedark

Tramadol
Tramadol
Salts
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Tramadol hydrobromide
Tramadol hydrobromide
Tramadol hydrochloride
Tramadol hydrochloride
Molecular structure via molpic
Molecular formulaC16H25NO2
Molecular mass263.37 g/mol
Predicted LogP2.6
Melting point178-181 °C
DecompositionWhen heated to decomposition it emits very toxic fumes of /nitrogen oxides/.
Solubility>39.5 [ug/mL] (The mean of the results at pH 7.4)
Chiralityracemic
Identifiers
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IUPAC name(1R,2R)-2-[(dimethylamino)methyl]-1-(3-methoxyphenyl)cyclohexan-1-ol
SMILESCN(C)C[C@H]1CCCC[C@@]1(C2=CC(=CC=C2)OC)O
InChIInChI=1S/C16H25NO2/c1-17(2)12-14-7-4-5-10-16(14,18)13-8-6-9-15(11-13)19-3/h6,8-9,11,14,18H,4-5,7,10,12H2,1-3H3/t14-,16+/m1/s1
InChIKeyTVYLLZQTGLZFBW-ZBFHGGJFSA-N
Dosing
Oral
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Threshold1 - 50 mg
Light50 mg
Common50 - 100 mg
Strong100 - 200 mg
Heavy200 - 250 mg
Statistically derived dosages by Sernyl

Tramadol

Tramadol (also known as (+)-Tramadol, 27203-92-5, Ralivia flashtab, Ralivia ER, Tramadon, Racemic tramadol, Tramadolum [INN-Latin], Biomadol, Contramid or Labesfal)

Chemistry

Tramadol is typically found in the form of its hydrobromide and hydrochloride salts.

Stereochemistry

Tramadol is a racemic mixture of the optical stereoisomers.

See also