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About This Item
Empirical Formula (Hill Notation):
C16H25NO6
CAS Number:
Molecular Weight:
327.37
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5296463
grade
technical
Quality Level
assay
99.9%
form
powder
reaction suitability
core: crown ether
impurities
≤10% water
functional group
ether
storage temp.
2-8°C
SMILES string
Nc1ccc2OCCOCCOCCOCCOCCOc2c1
InChI
1S/C16H25NO6/c17-14-1-2-15-16(13-14)23-12-10-21-8-6-19-4-3-18-5-7-20-9-11-22-15/h1-2,13H,3-12,17H2
InChI key
PZXYILUXRGTFGD-UHFFFAOYSA-N
General description
4′-Aminobenzo-18-crown-6 is a cyclic compound. It is widely used as an ionophore. It coordinates with metal ions more readily than other ligands because of its planar oxygen atoms which provide a strong negative potential barrier.
Application
4′-Aminobenzo-18-crown-6 can be easily functionalized with magnetic nanoparticles and used as a solid-phase extraction adsorbent for the determination of Pb2+. It can also be used as a metal complexing agent to prepare a variety of molecular complexes.
Other Notes
Derivative of 18-crown-6 which can be derivatized by alkylation or acylation
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Articles
Crown ethers and cryptands, complexing agents able to selectively bind metal cations, are vital for diverse synthesis and analytical applications.
S. Shinkai et al.
Journal of the American Chemical Society, 109, 4458-4458 (1987)
Bulletin of the Chemical Society of Japan, 61, 4385-4385 (1988)
E. Ozeki et al.
Journal of the Chemical Society. Chemical Communications, 1353-1353 (1988)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| I15807-25G | 04061833847855 |
| 06913-500MG | 04061833278642 |
| 06913-100MG | 04061833278635 |
