Detail of > 125-69-9
- CAS Number:
- 125-69-9
- Name:
Morphinan,3-methoxy-17-methyl-, hydrobromide (1:1), (9a,13a,14a)-
- Superlist Name:
- Dextromethorphan hydrobromide
- Formula:
- C18H26BrNO
- Molecular Structure:

- Synonyms:
- Dextromethorphan Hydrobromide;Dextromethorphan HBr;(1S,9S,10S)-4-méthoxy-17-méthyl-17-azatétracyclo[7.5.3.01,10.02,7]heptadéca-2,4,6-triène bromhydrate;(1S,9S,10S)-4-methoxy-17-methyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2,4,6-triene hydrobromide;(1S,9S,10S)-4-Methoxy-17-methyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2,4,6-trienhydrobromid;(9a,13a,14a)-3-methoxy-17-methylmorphinan hydrobromide (1:1);(9α,13α,14α)-3-Methoxy-17-methylmorphinan hydrobromide (1:1);morphinan, 3-methoxy-17-methyl-, (9a,13a,14a)-, hydrobromide (1:1);morphinan, 3-methoxy-17-methyl-, (9α,13α,14α)-, hydrobromide;
- Molecular Weight:
- 352.3091
- EINECS:
- 204-750-1
- Boiling Point:
- 427.5 °C at 760 mmHg
- Flash Point:
- 212.3 °C
- Deleted CAS:
- 18651-95-1
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Reference
- Determination of dextrorphan in plasma and evaluation of bioavailability of dextromethorphan hydrobromide in humans
- Determination of dextrorphan in plasma and evaluation of bioavailability of dextromethorphan hydrobromide in humans. Ramachander, Gollamudi; Williams, Florence D.; Emele, Jane Frances (Warner-Lambert Res. Inst., Morris Plains, N. J., USA). J. Pharm. Sci., 66(7), 1047-8 (English) 1977. CODEN: JPMSAE. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacodynamics) A fluorescence method is described for the estn. of dextrorphan (I) [125-73-5], a metabolite of dextromethorphan, in plasma. The bioavailability of dextromethorphan-HBr [125-69-9] after 30 mg orally, as measured by the concn. of total (free and conjugated) I in the plasma, was detd. in 6 human volunteers with this procedure.
- Liquid chromatographic analysis of pharmaceutical syrups using pre-columns and salt-adsorption on Amberlite XAD-2
- Liquid chromatographic analysis of pharmaceutical syrups using pre-columns and salt-adsorption on Amberlite XAD-2. Mohammed, Hussain Y.; Cantwell, Frederick F. (Dep. Chem., Univ. Alberta, Edmonton, Alberta, Can.). Anal. Chem., 50(3), 491-6 (English) 1978. CODEN: ANCHAM. DOCUMENT TYPE: Journal CA Section: 64 (Pharmaceutical Analysis) Twenty-nine drug compds. are chromatographed in acidic, neutral, and alk. solns. contg. varying amts. of water and methanol on a column of Amberlite XAD-2 nonionic resin. Cationic conjugate acids of amine drugs are adsorbed via "salt-adsorption". Their retention vols. depend on concn. and type of anion (e.g. Cl-, ClO4-) added to the mobile phase as well as on its pH and solvent compn. Pharmaceutical sirups can be analyzed without prior treatment when short pre-columns contg. anion-exchange resin and XAD-2 are added. As examples, synthetic and com. sirups are analyzed for phenylephrine-HCl [61-76-7], acetaminophen [103-90-2], glyceryl guaiacolate [93-14-1], and dextromethorphan-HBr [125-69-9].
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