Date published: 2026-5-3

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Methan(ol-d) (CAS 1455-13-6)

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Alternate Names:
Deuteromethanol
CAS Number:
1455-13-6
Molecular Weight:
33.05
Molecular Formula:
CH3OD
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Methanol-d is a stable isotope of methanol, used as a solvent and reagent in various chemical reactions and processes. Its primary function is to serve as a deuterated substitute for regular methanol. Methanol-d′s mechanism of action involves replacing the hydrogen atoms in methanol with deuterium, which alters the spectroscopic properties of the molecule. This modification enables the ability to study the behavior and interactions of methanol in biological, chemical, and environmental systems with enhanced precision and accuracy. By incorporating methanol-d into their experiments, the ability to monitor the mechanisms and pathways involving methanol, contributing to a deeper understanding of various processes and phenomena at the molecular level.


Methan(ol-d) (CAS 1455-13-6) References

  1. Pd-catalyzed copolymerization of methyl acrylate with carbon monoxide: structures, properties and mechanistic aspects toward ligand design.  |  Nakamura, A., et al. 2011. J Am Chem Soc. 133: 6761-79. PMID: 21480592
  2. Addition of reagents to the sheath liquid: a novel concept in capillary electrophoresis-mass spectrometry.  |  Causon, TJ., et al. 2014. J Chromatogr A. 1343: 182-7. PMID: 24751556
  3. Using sheath-liquid reagents for capillary electrophoresis-mass spectrometry: application to the analysis of phenolic plant extracts.  |  Maringer, L., et al. 2015. Electrophoresis. 36: 348-54. PMID: 25308871
  4. Influence of sulfur for oxygen substitution in the solvolytic reactions of chloroformate esters and related compounds.  |  D'Souza, MJ. and Kevill, DN. 2014. Int J Mol Sci. 15: 18310-32. PMID: 25310653
  5. Mechanistic Studies of the Solvolyses of Carbamoyl Chlorides and Related Reactions.  |  D'Souza, MJ. and Kevill, DN. 2016. Int J Mol Sci. 17: PMID: 26784185
  6. Phytotoxic Potential of Secondary Metabolites and Semisynthetic Compounds from Endophytic Fungus Xylaria feejeensis Strain SM3e-1b Isolated from Sapium macrocarpum.  |  García-Méndez, MC., et al. 2016. J Agric Food Chem. 64: 4255-63. PMID: 27159617
  7. Hydrogen bond competition in the ethanol-methanol dimer.  |  Finneran, IA., et al. 2016. Phys Chem Chem Phys. 18: 22565-72. PMID: 27472828
  8. Concurrent Cationic Vinyl-Addition and Coordination Ring-Opening Copolymerization via Orthogonal Propagation and Transient Merging at the Propagating Chain End.  |  Higuchi, M., et al. 2017. ACS Macro Lett. 6: 365-369. PMID: 35610844
  9. Reaction mechanism studies involving the correlation of the rates of solvolysis of benzoyl and p-nitrobenzoyl p-toluenesulfonates  |  Kevill, D. N., & Ryu, Z. H. 2014. Journal of Chemical Research. 38(7): 387-395.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Methan(ol-d), 25 g

sc-250314
25 g
$71.00