24-Crown 8-Ether TCI C1736

Chemical Identity

Other names: 1,4,7,10,13,16,19,22-Octaoxacyclotetracosane
CAS No.: 33089-37-1
PubChem: CID 10893545·SID 87566703
Formula: C16H32O8
Molecular weight: 352.42 g/mol
Purity: >95.0%(GC)
Storage: 0-10°C
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 1,4,7,10,13,16,19,22-octaoxacyclotetracosane
SMILES: C1COCCOCCOCCOCCOCCOCCOCCO1
InChIKey: BGYBONWLWSMGNV-UHFFFAOYSA-N
MDL: MDL00054528

Rp 11.686.500,00

~~Rp 8.187.900,00~~ Rp 11.686.500,00

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24-Crown 8-Ether is a synthetic reagent widely used in laboratory settings for its ability to form stable complexes with metal ions. This compound, with its unique molecular structure containing eight oxygen atoms, is highly effective in chelation reactions. Its stability and strong binding capacity make it a preferred choice in various chemical applications, including organic synthesis and metal ion analysis. In Indonesian laboratories, this reagent is essential for research and educational purposes, supporting both academic and industrial chemical studies. Its availability in standard packaging ensures ease of use and accessibility for researchers and students.

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Willey et al. (2000). Crown ether complexation of p-block metal halides: synthesis and structural characterisation of [InI2(dibenzo-24-crown-8)(H2O)][InI4], [(SnBr4)2(dibenzo-24-crown-8)]·MeCN, [(SbCl3)2(dibenzo-24-crown-8)]·MeCN, [(BiCl3)2(dibenzo-24-crown-8)]·MeCN and [(SbBr3)2(dibenzo-24-crown-8)]. Inorganica Chimica Acta doi:10.1016/s0020-1693(00)00029-3
Frańska et al. (2018). Gas-phase relative stabilities of Tl + -crown ether complexes and Rb + -crown ether complexes. European Journal of Mass Spectrometry doi:10.1177/1469066717752794
Tunca (1996). Synthesis of polymers containing crown ether and ferrocene units. Polymer doi:10.1016/0032-3861(96)00628-3

References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.