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Acetyl chloride-d3 (CAS 19259-90-6)

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CAS Number:
19259-90-6
Molecular Weight:
81.52
Molecular Formula:
CD3COCl
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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Acetyl chloride-d3 is a compound used as a reactant in the synthesis of various organic compounds. It functions as an acetylating agent, transferring the acetyl group to other molecules, thereby facilitating the formation of new chemical bonds. The deuterium-labeled form of acetyl chloride, it is particularly useful in tracing the movement and transformation of acetyl groups within complex organic systems. Its mechanism of action involves the substitution of the hydrogen atoms in the acetyl group with deuterium atoms, allowing for the tracking of acetyl group transfer and metabolic pathways in biological and chemical systems. It is useful in studies aimed at understanding the behavior and reactivity of acetyl groups in different chemical and biological processes, providing insights into the mechanisms underlying these reactions at a molecular level.


Acetyl chloride-d3 (CAS 19259-90-6) References

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  4. The Decomposition of Gaseous Chloroformates. II. Substitution and Elimination Stereochemistry1  |  Edward S. Lewis, William C. Herndon, and Donald C. Duffey. 1961,. J. Am. Chem. Soc. 83, 8,: 1959–1961.
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  7. Regioselective deuteriation kinetics of 2-, 4-, and 6-methyl groups in D2O solutions of pyrylium and N-methylpyridinium perchlorates possessing also 3-methyl or 3-phenyl groups  |   and Alexandru T. Balaban, Cornelia Uncuta, Filip Chiraleu. June 1982. Journal of Labelled Compounds and Radiopharmaceuticals. Volume19, Issue6: Pages 783-794.
  8. Alkylation of allylic derivatives. 10. Relative rates of reactions of allylic carboxylates with lithium dimethylcuprate  |  Harlan L. Goering, Steven S. Kantner, and Earl P. Seitz Jr. 1985. J. Org. Chem., 50, 26,: 5495–5499.
  9. A new method for generating trichlorotitanium(IV) ester homoenolates. Direct tin-titanium exchange  |  Ramanuj Goswami. 1985. J. Org. Chem., 50, 26,: 5907–5909.
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  11. Mechanism of ester formation in the photosensitized oxidation of diazomethanes. Carbonyl oxides do not isomerize to dioxiranes in solution  |  Katsuya Ishiguro, Yukimichi Hirano, and Yasuhiko Sawaki. 1988,. J. Org. Chem. 53, 23,: 5397–5405.
  12. Photolysis of matrix-isolated acetyl chloride and infrared spectrum of the 1:1 molecular complex of hydrogen chloride with ketene in solid argon  |  N Kogure, T Ono, E Suzuki, F Watari - Journal of molecular structure, 1993 - Elsevier. 1 July 1993,. Journal of Molecular Structure. Volume 296, Issues 1–2,: Pages 1-4.
  13. Photolysis of matrix-isolated acetyl bromide and the infrared spectrum of the 1:1 molecular complex of hydrogen bromide with ketene in solid argon  |  N Kogure, R Hatakeyama, E Suzuki, F Watari - Journal of molecular …, 1993 - Elsevier. 20 October 1993,. Journal of Molecular Structure. Volume 299,: Pages 105-109.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Acetyl chloride-d3, 10 g

sc-257062
10 g
$244.00