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Dextromethorphan Hydrobromide (CAS 125-69-9)

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Alternate Names:
(9S,13S,14S)-3-Methoxy-17-methylmorphinan hydrobromide
Application:
Dextromethorphan Hydrobromide is a potentially useful NMDA receptor agonist
CAS Number:
125-69-9
Purity:
≥98%
Molecular Weight:
352.31
Molecular Formula:
C18H25NO•HBr
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Dextromethorphan hydrobromide, a synthetic derivative of morphine, is extensively utilized in research laboratories, primarily for its neuropharmacological properties. In the realm of neuroscientific research, it serves as useful for studying NMDA (N-methyl-D-aspartate) receptors, a class of receptors that play a role in synaptic plasticity, memory function, and neurodevelopment. By acting as an antagonist at these receptors, dextromethorphan hydrobromide helps researchers understand the mechanisms of diseases like Alzheimer′s and Parkinson′s, where NMDA receptor dysfunction is implicated. Additionally, its sigma-1 receptor agonist activity makes it useful in investigating the role of these receptors in neuroprotection, neuroplasticity, and mood regulation. This chemical is also employed in studies exploring cough reflex pathways, aiding in the understanding of the central processing of cough reflexes. Moreover, its application extends to research in drug abuse and addiction, offering insights into the neurochemical pathways involved in substance dependency. In psychopharmacological studies, dextromethorphan hydrobromide is used to simulate certain aspects of psychosis, thereby enabling the exploration of potential antipsychotic treatments. Furthermore, its impact on glutamate neurotransmission is a subject of investigation in studies related to excitotoxicity and neurodegenerative disorders. Overall, dextromethorphan hydrobromide′s multifaceted pharmacological profile renders it a versatile agent in neuroscience and pharmacology research, providing a deeper understanding of various neurobiological processes and pathologies.


Dextromethorphan Hydrobromide (CAS 125-69-9) References

  1. Modulation of nicotine self-administration in rats by combination therapy with agents blocking alpha 3 beta 4 nicotinic receptors.  |  Glick, SD., et al. 2002. Eur J Pharmacol. 448: 185-91. PMID: 12144940
  2. Plasma profile and pharmacokinetics of dextromethorphan after intravenous and oral administration in healthy dogs.  |  Kukanich, B. and Papich, MG. 2004. J Vet Pharmacol Ther. 27: 337-41. PMID: 15500572
  3. LC-MS/MS analysis of dextromethorphan metabolism in human saliva and urine to determine CYP2D6 phenotype and individual variability in N-demethylation and glucuronidation.  |  Lutz, U., et al. 2004. J Chromatogr B Analyt Technol Biomed Life Sci. 813: 217-25. PMID: 15556536
  4. Enhancing the uptake of dextromethorphan in the CNS of rats by concomitant administration of the P-gp inhibitor verapamil.  |  Marier, JF., et al. 2005. Life Sci. 77: 2911-26. PMID: 15964599
  5. The simultaneous assay of triprolidine, pseudoephedrine and dextromethorphan in combined preparations by derivative-difference spectrophotometry.  |  Davidson, AG. and Mkoji, LM. 1988. J Pharm Biomed Anal. 6: 449-60. PMID: 16867391
  6. Sigma ligands, but not N-methyl-D-aspartate antagonists, reduce levodopa-induced dyskinesias.  |  Paquette, MA., et al. 2008. Neuroreport. 19: 111-5. PMID: 18281903
  7. Involvement of sigma-1 receptors in the antidepressant-like effects of dextromethorphan.  |  Nguyen, L., et al. 2014. PLoS One. 9: e89985. PMID: 24587167
  8. Characterization of pulmonary sigma receptors by radioligand binding.  |  Lever, JR., et al. 2015. Eur J Pharmacol. 762: 118-26. PMID: 26004528
  9. Dextromethorphan and neuromodulation: old drug coughs up new activities.  |  Tortella, FC., et al. 1989. Trends Pharmacol Sci. 10: 501-7. PMID: 2694543
  10. Illicit and Counterfeit Drug Analysis by Morphologically Directed Raman Spectroscopy.  |  Koutrakos, AC., et al. 2018. Methods Mol Biol. 1810: 13-27. PMID: 29974414
  11. Dextrorphan and levorphanol selectively block N-methyl-D-aspartate receptor-mediated neurotoxicity on cortical neurons.  |  Choi, DW., et al. 1987. J Pharmacol Exp Ther. 242: 713-20. PMID: 3039122
  12. Role of calcium in sigma-mediated neuroprotection in rat primary cortical neurons.  |  Klette, KL., et al. 1995. Brain Res. 704: 31-41. PMID: 8750959
  13. Thin layer chromatographic analysis of some common over the counter (OTC) cough–cold preparations  |  MK Chahal, PK Yadav, GS Bumbrah. 2016. Egyptian Journal of Forensic Sciences. 6(4): 351-360.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Dextromethorphan Hydrobromide, 5 g

sc-204716
5 g
$75.00

Dextromethorphan Hydrobromide, 10 g

sc-204716A
10 g
$135.00

Dextromethorphan Hydrobromide, 50 g

sc-204716B
50 g
$496.00

What is the boiling point of this compound

Asked by: suhail
Thank you for your question. This product, sc-204716 (Dextromethorphan Hydrobromide) is a solid. Here is a link to the CoA for our latest lot: http://datasheets.scbt.com/coa/coa.php?sc=sc-204716&lot=L1416 If you have any further questions, please contact our Asia Technical Service team. You can reach them by phone at (86 21) 6093-6350, by email at: asia@scbio.cn or by live chat directly on our website, www.scbt.com
Answered by: Tech Service
Date published: 2017-09-25
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Rated 5 out of 5 by from WuWu, K. et al. (PubMed 23400250) reported that the NMDA receptor agonist Dextromethorphan inhibits osteoclast differentiation by suppressing RANKL-induced NF- B activation. -SCBT Publication Review
Date published: 2015-02-14
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Dextromethorphan Hydrobromide is rated 5.0 out of 5 by 1.
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