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Propionyl chloride (CAS 79-03-8)

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Alternate Names:
Propionic acid chloride
Application:
Propionyl chloride is an acid halide
CAS Number:
79-03-8
Purity:
≥97%
Molecular Weight:
92.52
Molecular Formula:
C3H5ClO
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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Propionyl chloride is an acid halide. It functions as an intermediate for dyes, textile auxiliaries, and peroxide compounds. Additionally, it serves as a crop protecting agent.


Propionyl chloride (CAS 79-03-8) References

  1. Sidewall functionalization of single-walled carbon nanotubes through electrophilic addition.  |  Tagmatarchis, N., et al. 2002. Chem Commun (Camb). 2010-1. PMID: 12357754
  2. Intramolecular chiral relay at stereogenic nitrogen. Synthesis and application of a new chiral auxiliary derived from (1R,2S)-norephedrine and acetone.  |  Hitchcock, SR., et al. 2004. J Org Chem. 69: 714-8. PMID: 14750795
  3. Catalytic, asymmetric synthesis and diastereoselective aldol reactions of dipropionate equivalents.  |  Calter, MA., et al. 2004. J Org Chem. 69: 1270-5. PMID: 14961680
  4. Insights into photodissociation dynamics of propionyl chloride from ab initio calculations and molecular dynamics simulations.  |  Chen, SL. and Fang, WH. 2006. J Phys Chem A. 110: 944-50. PMID: 16419994
  5. Products and mechanism of the reaction of Cl with butanone in N2/O2 diluent at 297-526 K.  |  Kaiser, EW., et al. 2009. J Phys Chem A. 113: 2424-37. PMID: 19228051
  6. Products and mechanism of the reaction of chlorine atoms with 3-pentanone in 700-950 torr of N(2)/O(2) diluent at 297-515 K.  |  Kaiser, EW., et al. 2010. J Phys Chem A. 114: 343-54. PMID: 19883042
  7. Some geometric and electronic structural effects of perfluorinating propionyl chloride.  |  Grubbs, GS., et al. 2010. J Phys Chem A. 114: 8009-15. PMID: 20666547
  8. Synthesis and pharmacological evaluation of carvacrol propionate.  |  de Santana, MT., et al. 2014. Inflammation. 37: 1575-87. PMID: 24710701
  9. Rapid esterification of wheat straw hemicelluloses induced by microwave irradiation.  |  Xu, F., et al. 2008. Carbohydr Polym. 73: 612-20. PMID: 26048228
  10. Syntheses and antibacterial activities of 4 linear nonphenolic diarylheptanoids.  |  Demİr, ŞB., et al. 2020. Turk J Chem. 44: 589-601. PMID: 33488179
  11. Design, synthesis, molecular docking, and some metabolic enzyme inhibition properties of novel quinazolinone derivatives.  |  Tokalı, FS., et al. 2021. Arch Pharm (Weinheim). 354: e2000455. PMID: 33537994
  12. Anticancer Evaluation of Novel Quinazolinone Acetamides: Synthesis and Characterization.  |  Hakim, F., et al. 2022. Anticancer Agents Med Chem. 22: 926-932. PMID: 34030622
  13. Automated chemoenzymatic synthesis of no-carrier-added [carbonyl-11C]propionyl L-carnitine for pharmacokinetic studies.  |  Davenport, RJ., et al. 1997. Appl Radiat Isot. 48: 917-24. PMID: 9376826
  14. Synthesis of 1-[11C]methylpiperidin-4-yl propionate ([11C]PMP) for in vivo measurements of acetylcholinesterase activity.  |  Snyder, SE., et al. 1998. Nucl Med Biol. 25: 751-4. PMID: 9863562

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Propionyl chloride, 25 g

sc-236483
25 g
$62.00

Propionyl chloride, 500 g

sc-236483A
500 g
$112.00