Date published: 2026-4-30

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Dichloromethane-d2 (CAS 1665-00-5)

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Alternate Names:
Dideuteromethylenechloride; Methylene chloride-d2
Application:
Dichloromethane-d2 is labelled Methylene Chloride used in organic chemical reactions as a general solvent
CAS Number:
1665-00-5
Purity:
≥99%
Molecular Weight:
86.94
Molecular Formula:
CD2Cl2
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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Dichloromethane-d2, also known as deuterated dichloromethane, is a variant of dichloromethane. Deuterated solvents like dichloromethane-d2 are used in nuclear magnetic resonance (NMR) spectroscopy, a powerful analytical technique for determining the structure of organic compounds. The use of deuterated solvents is in NMR because they exhibit significantly lower NMR signal interference compared to their non-deuterated counterparts, thereby providing clearer, more interpretable NMR spectra of the solutes being studied. Similar to regular Dichloromethane, Dichloromethane-d2 has a relatively low boiling point, making it easy to remove from a sample after analysis or reaction by simple evaporation under reduced pressure. Dichloromethane-d2 is chemically stable under a wide range of conditions, making it suitable for use in various chemical reactions and analytical procedures without undergoing significant decomposition or reaction with solutes.


Dichloromethane-d2 (CAS 1665-00-5) References

  1. Hyperpolarisation of weakly binding N-heterocycles using signal amplification by reversible exchange.  |  Rayner, PJ., et al. 2021. Chem Sci. 12: 5910-5917. PMID: 34168816
  2. Heterobimetallic Coinage Metal-Ruthenium Complexes Supported by Anionic N-Heterocyclic Carbenes.  |  Planer, S., et al. 2021. Chemistry. 27: 15217-15225. PMID: 34342923
  3. Selective Oxidation of Clopidogrel by Peroxymonosulfate (PMS) and Sodium Halide (NaX) System: An NMR Study.  |  Krake, EF. and Baumann, W. 2021. Molecules. 26: PMID: 34641465
  4. Azolium Control of the Osmium-Promoted Aromatic C-H Bond Activation in 1,3-Disubstituted Substrates.  |  Cancela, L., et al. 2021. Organometallics. 40: 3979-3991. PMID: 34924674
  5. Diverse synthesis of C2-linked functionalized molecules via molecular glue strategy with acetylene.  |  Yang, B., et al. 2022. Nat Commun. 13: 1858. PMID: 35388000
  6. Novel [FeFe]-Hydrogenase Mimics: Unexpected Course of the Reaction of Ferrocenyl α-Thienyl Thioketone with Fe3(CO)12.  |  Daraosheh, AQ., et al. 2022. Materials (Basel). 15: PMID: 35454560
  7. Real-Time High-Sensitivity Reaction Monitoring of Important Nitrogen-Cycle Synthons by 15N Hyperpolarized Nuclear Magnetic Resonance.  |  Rayner, PJ., et al. 2022. J Am Chem Soc. 144: 8756-8769. PMID: 35508182
  8. Repercussion of a 1,3-Hydrogen Shift in a Hydride-Osmium-Allenylidene Complex.  |  Esteruelas, MA., et al. 2021. Organometallics. 40: 1523-1537. PMID: 35693112
  9. Asymmetric Phenyl Substitution: An Effective Strategy to Enhance the Photosensitizing Potential of Curcuminoids.  |  Vesco, G., et al. 2022. Pharmaceuticals (Basel). 15: PMID: 35890142
  10. Calix[4]pyrrolato gallate: square planar-coordinated gallium(iii) and its metal-ligand cooperative reactivity with CO2 and alcohols.  |  Sigmund, LM., et al. 2022. Chem Sci. 13: 11215-11220. PMID: 36320463
  11. Acetylides for the Preparation of Phosphorescent Iridium(III) Complexes: Iridaoxazoles and Their Transformation into Hydroxycarbenes and N,C(sp3),C(sp2),O-Tetradentate Ligands.  |  Benítez, M., et al. 2022. Inorg Chem. 61: 19597-19611. PMID: 36416194
  12. An Organic Molecular Nanobarrel that Hosts and Solubilizes C60.  |  Bera, S., et al. 2023. Angew Chem Int Ed Engl. 62: e202216540. PMID: 36469042
  13. Multicolor emission based on a N, N'-Disubstituted dihydrodibenzo [a, c] phenazine crown ether macrocycle.  |  Ma, CS., et al. 2022. Front Chem. 10: 1087610. PMID: 36545215
  14. Sensitizer-controlled photochemical reactivity via upconversion of red light.  |  Glaser, F. and Wenger, OS. 2022. Chem Sci. 14: 149-161. PMID: 36605743
  15. A molecular descriptor of intramolecular noncovalent interaction for regulating optoelectronic properties of organic semiconductors.  |  Liu, M., et al. 2023. Nat Commun. 14: 2500. PMID: 37127693

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Dichloromethane-d2, 5 g

sc-257331
5 g
$122.00

Dichloromethane-d2, 10 g

sc-257331A
10 g
$224.00