Methadone | |
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Molecular structure via molpic based on CDK |
Conformer [] | |
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Conformer structure via JSmol |
Physical properties [] | |
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Molecular mass | 309.4 g/mol [1] |
Melting point | 99.5 °C [1] |
Decomposition | When heated to decomposition it emits toxic fumes of /nitrogen oxides/. [1] |
Solubility | Platelets from alcohol + ether; mp, 235 °C; bitter taste; UV maximum, 292 nm; solubility (g/100 mL) water, 12; alcohol, 8; isopropanol, 2.4; Practically insoluble in ether, glycerol; pH of a 1% aqueous solution is 4.5-5.6 /Methadone hydrochloride/ [1] |
Predicted LogP | 3.9 [1] |
Structural Identifiers [] | |
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Molecular formula | C21H27NO [1] |
IUPAC name | 6-(dimethylamino)-4,4-diphenylheptan-3-one [1] |
SMILES | CCC(=O)C(CC(C)N(C)C)(C1=CC=CC=C1)C2=CC=CC=C2 [1] |
InChI | InChI=1S/C21H27NO/c1-5-20(23)21(16-17(2)22(3)4,18-12-8-6-9-13-18)19-14-10-7-11-15-19/h6-15,17H,5,16H2,1-4H3 [1] |
InChIKey | USSIQXCVUWKGNF-UHFFFAOYSA-N [1] |
Oral [] | |
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Threshold | 0.5 - 1 mg |
Light | 1 - 5 mg |
Common | 5 - 10 mg |
Strong | 10 - 20 mg |
Heavy | 20 - 29.10000000000001 mg |
Statistically derived dosages by Sernyl |
Methadone
Methadone (also known as Diaminon, Dolophin, Phenadone, Heptadone, Amidone, Ketalgin, Methadon, Adanon, Physeptone or Algovetin)
Chemistry
Salts []
Stereochemistry []
Methadone is a racemic mixture of the optical stereoisomers