Date published: 2026-4-28

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1-Iodopropane (CAS 107-08-4)

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Alternate Names:
Propyl iodide
CAS Number:
107-08-4
Molecular Weight:
169.99
Molecular Formula:
CH3CH2CH2I
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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1-Iodopropane is a chemical compound that functions as an alkylating agent in development applications. Its mechanism of action involves the substitution of the iodine atom for a hydrogen atom in organic molecules, leading to the formation of new carbon-carbon bonds. This process is particularly useful in the synthesis of complex organic compounds, as it allows for the introduction of alkyl groups into specific positions within a molecule. 1-Iodopropane′s ability to undergo nucleophilic substitution reactions may be useful for the modification of organic molecules in experimental applications. Its mechanism of action at the molecular level involves the interaction of the iodine atom with electron-rich centers in organic substrates, leading to the formation of covalent bonds. 1-Iodopropane′s function as an alkylating agent enables the manipulation of molecular structures.


1-Iodopropane (CAS 107-08-4) References

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  2. Analysis of alkyl organoiodide mixtures by high-performance liquid chromatography using electrochemical detection with a post-column photochemical reactor.  |  Wu, CH., et al. 2002. J Chromatogr A. 976: 423-30. PMID: 12462636
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  6. The surface chemistry of propylene, 1-iodopropane, and 1,3-diiodopropane on MoAl alloy thin films formed on dehydroxylated alumina.  |  Gao, F., et al. 2006. J Phys Chem B. 110: 12555-71. PMID: 16800585
  7. Quantitative structure-activity relationships for toxicity and genotoxicity of halogenated aliphatic compounds: wing spot test of Drosophila melanogaster.  |  Chroust, K., et al. 2007. Chemosphere. 67: 152-9. PMID: 17113125
  8. Substrate specificity of haloalkane dehalogenases.  |  Koudelakova, T., et al. 2011. Biochem J. 435: 345-54. PMID: 21294712
  9. Metabolic studies with phenobarbitone, primidone and their N-alkyl derivatives: quantification of substrates and metabolites using chemical ionization gas chromatography-mass spectrometry.  |  Treston, AM. and Hooper, WD. 1990. J Chromatogr. 526: 59-68. PMID: 2341546
  10. Biochemical and biophysical characterisation of haloalkane dehalogenases DmrA and DmrB in Mycobacterium strain JS60 and their role in growth on haloalkanes.  |  Fung, HK., et al. 2015. Mol Microbiol. 97: 439-53. PMID: 25899475
  11. Evidence for Electron Transfer in the Reactions of Hydrated Monovalent First-Row Transition-Metal Ions M(H2O)n+, M = V, Cr, Mn, Fe, Co, Ni, Cu, and Zn, n < 40, toward 1-Iodopropane.  |  Gernert, I. and Beyer, MK. 2017. J Phys Chem A. 121: 9557-9566. PMID: 29179537
  12. Subpicosecond HI elimination in the 266 nm photodissociation of branched iodoalkanes.  |  Todt, MA., et al. 2020. Phys Chem Chem Phys. 22: 27338-27347. PMID: 33231219
  13. Disentangling sequential and concerted fragmentations of molecular polycations with covariant native frame analysis.  |  McManus, JW., et al. 2022. Phys Chem Chem Phys. 24: 22699-22709. PMID: 36106844

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1-Iodopropane, 5 g

sc-237575
5 g
$28.00

1-Iodopropane, 100 g

sc-237575A
100 g
$37.00