Date published: 2025-12-19

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1-Chloropentane (CAS 543-59-9)

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Alternate Names:
Amyl chloride
CAS Number:
543-59-9
Molecular Weight:
106.59
Molecular Formula:
C5H11Cl
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-Chloropentane is a chemical compound that functions as an alkylating agent in development applications. It acts by replacing a hydrogen atom in a molecule with an alkyl group, leading to the formation of new carbon-carbon bonds. This process can be utilized to modify the structure of organic compounds, allowing for the synthesis of various derivatives for experimental purposes. 1-Chloropentane′s mechanism of action involves its ability to undergo nucleophilic substitution reactions with nucleophiles such as amines, alcohols, and thiols. 1-Chloropentane′s role in experimental applications involves its use as a building block in organic synthesis, enabling the creation of diverse molecular structures. Its mechanism of action at the molecular level involves the substitution of the chlorine atom with other functional groups, leading to the generation of novel compounds for scientific investigation.


1-Chloropentane (CAS 543-59-9) References

  1. Imprinting self-assembled patterns of lines at a semiconductor surface, using heat, light, or electrons.  |  Harikumar, KR., et al. 2011. Proc Natl Acad Sci U S A. 108: 950-5. PMID: 20798058
  2. Stereo-isomerism controls surface reactivity: 1-chloropentane-pairs on Si(100)-2×1.  |  Harikumar, KR., et al. 2011. Chem Commun (Camb). 47: 12101-3. PMID: 22005512
  3. Selector screening for enantioseparation of DL-α-methyl phenylglycine amide by liquid-liquid extraction.  |  Schuur, B., et al. 2015. Chirality. 27: 123-30. PMID: 25319069
  4. Negative-mode ion mobility spectrometry-comparison of ion-molecule reactions and electron capture processes.  |  Budzyńska, E., et al. 2022. Anal Bioanal Chem. 414: 3719-3728. PMID: 35305117
  5. Degradation of n-haloalkanes and alpha, omega-dihaloalkanes by wild-type and mutants of Acinetobacter sp. strain GJ70.  |  Janssen, DB., et al. 1987. Appl Environ Microbiol. 53: 561-6. PMID: 3579270

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1-Chloropentane, 100 ml

sc-237530
100 ml
$48.00