Dimethyl Sulfoxide-d₆ (DMSO-d₆): The Heavyweight Solvent for Challenging NMR Samples
When it comes to NMR spectroscopy, solvent choice is critical—not just for solubility, but for spectrum clarity and accuracy. Among deuterated solvents, DMSO-d₆ (Dimethyl sulfoxide-d₆) stands out for its unique solubility range, thermal stability, and ability to handle polar and high-melting compounds.
In this post, we’ll explore what DMSO-d₆ is, how it’s used in spectroscopy and research, and what precautions are necessary when working with it.
What Is DMSO-d₆?
DMSO-d₆ is the deuterated form of dimethyl sulfoxide (DMSO), where all six hydrogen atoms in the methyl groups are replaced with deuterium (²H or D). This significantly reduces its signal in proton NMR, making it ideal for analyzing organic compounds without solvent interference.
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Chemical Formula: (CD₃)₂SO
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Molecular Weight: 84.17 g/mol
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Appearance: Colorless, hygroscopic liquid
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Boiling Point: ~189°C
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Melting Point: ~18.5°C
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Density: ~1.19 g/cm³ at 20°C
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Deuterium Content: ≥ 99.9% D (typical for spectroscopy-grade DMSO-d₆)
Why Use DMSO-d₆ in NMR Spectroscopy?
DMSO-d₆ is especially useful in NMR when dealing with compounds that:
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Have low solubility in less polar solvents like CDCl₃
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Are highly polar, ionic, or hydrogen-bonded
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Need to be analyzed at elevated temperatures
Benefits in NMR:
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Minimal interference in proton spectra due to deuteration
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Excellent solvent for polar and ionic compounds (e.g., salts, peptides, sugars)
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Stable under a wide range of temperatures
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Often used in ¹H, ¹³C, and multinuclear NMR (e.g., ¹⁹F, ³¹P)
Residual Peaks in NMR
Even deuterated solvents contain trace amounts of non-deuterated material. For DMSO-d₆:
Spectrum Type | Residual Peak Position |
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¹H NMR | ~2.50 ppm (singlet) |
¹³C NMR | ~39.5 ppm (septet due to ¹³C–²H coupling) |
These peaks serve as convenient internal standards for chemical shift referencing.
Solubility and Compatibility
DMSO-d₆ is miscible with water, alcohols, acetonitrile, and many organic and inorganic salts. It's an ideal choice for:
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Biomolecules (e.g., peptides, nucleotides)
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Ionic compounds
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Hydrogen bonding studies
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Hydrolytically sensitive compounds, if moisture is carefully excluded
How Is DMSO-d₆ Made?
DMSO-d₆ is typically synthesized via:
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Exchange of methyl protons with deuterium using D₂O in the presence of a base or catalyst.
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Subsequent distillation and purification to reach the required deuterium enrichment for NMR use.
The high cost reflects this energy-intensive and careful preparation.
Handling and Storage
Though generally safe and non-volatile, DMSO-d₆ requires some precautions:
Storage Tips
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Store in airtight, amber bottles
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DMSO-d₆ is hygroscopic—it absorbs water from air, which can degrade NMR performance
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Desiccators or dry boxes are recommended for long-term storage
Handling Tips
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Always use dry pipettes or syringes to prevent contamination
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Avoid skin contact—DMSO can carry small molecules through the skin, including toxins or drugs
Safety Notes
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Low toxicity but unusual transdermal properties
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May cause skin irritation or interact with other substances if absorbed
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Use gloves and lab coat, especially if working with bioactive or hazardous samples
DMSO-d₆ vs. Other Deuterated Solvents
Property | DMSO-d₆ | CDCl₃ | Acetone-d₆ | D₂O |
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Polarity | High | Low | Moderate | Very high |
Boiling Point | 189°C | 61°C | 56°C | 100°C |
Hydrogen Bonding | Excellent | Poor | Moderate | Excellent |
Water Solubility | Miscible | Slight | Miscible | N/A (it's water) |
Best for | Polar compounds | Non-polar organics | Keto compounds | Ionic/aqueous |
Applications Beyond NMR
While DMSO-d₆ is mainly used for spectroscopy, its non-deuterated version (DMSO) is used in:
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Cryopreservation
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Drug delivery systems
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Polymer science
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Electrochemistry and battery research
Conclusion
DMSO-d₆ is the go-to deuterated solvent when standard NMR solvents like CDCl₃ or acetone-d₆ fall short—especially for polar, high-melting, or ionic compounds. Its high boiling point, broad solubility, and clean spectral properties make it a must-have for complex NMR work.
Just be mindful of its hygroscopic nature and transdermal effects, and it will serve as a reliable ally in both academic and industrial research.
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