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V900647

Sigma-Aldrich

15-Crown-5

Vetec, reagent grade, 98%

Synonym(s):

1,4,7,10,13-Pentaoxacyclopentadecane

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About This Item

Empirical Formula (Hill Notation):
C10H20O5
CAS Number:
Molecular Weight:
220.26
Beilstein/REAXYS Number:
1618144
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
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grade

reagent grade

product line

Vetec

assay

98%

refractive index

n20/D 1.465 (lit.)

bp

93-96 °C/0.05 mmHg (lit.)

density

1.113 g/mL at 20 °C (lit.)

SMILES string

O1CCOCCOCCOCCOCC1

InChI

1S/C10H20O5/c1-2-12-5-6-14-9-10-15-8-7-13-4-3-11-1/h1-10H2

InChI key

VFTFKUDGYRBSAL-UHFFFAOYSA-N

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Legal Information

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup


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Yong Xiang Wu et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 82(1), 340-344 (2011-08-16)
A novel fluoroionophore 1 based on 3,4-dimethylthieno[2,3-b]thiophene bearing two monoaza-15-crown-5 ethers at 3- and 4-positions was prepared. UV-vis and fluorescence responses of compound 1 upon the addition of alkali and alkaline earth metal cations were evaluated in acetonitrile solution. Receptor
Maxime A Siegler et al.
Acta crystallographica. Section B, Structural science, 64(Pt 6), 725-737 (2008-11-26)
Initial attempts to make [Ni(H2O)2(15-crown-5)](NO3)2, i.e. to insert the Ni2+ ion into the 15-crown-5 macrocycle, gave the mono- (two polymorphs) and dihydrate of a co-crystal of[Ni(H2O)6](NO3)2 and 15-crown-5 (1,4,7,10,13-pentaoxacyclopentadecane=15C5). Synthetic routes designed to restrict the water available to the Ni2+
Tao Liu et al.
Bioorganic & medicinal chemistry letters, 20(16), 4845-4849 (2010-07-14)
The electron transfer properties of supramolecular complexes of 15-crown-5 (15C5) with protonated adrenaline (PAd(+)) at different electrodes using cyclic voltammetry (CV) have been investigated in the article. The experimental results show that 15C5 will affect the electron transfer properties of
Naoshi Yamamoto et al.
The Journal of organic chemistry, 76(7), 2257-2260 (2011-03-09)
Acetylcholinesterase inhibitor (-)-homogalanthamine 3 was synthesized from μ opioid antagonist naltrexone (2) in 16% total yield. The synthesis features Grob fragmentation as a key reaction, which was especially accelerated in the presence of 15-crown-5.
Toshiaki Hattori et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 26(10), 1039-1045 (2010-10-19)
Two-dimensional real-time observation of potassium ion distributions was achieved using an ion imaging device based on charge-coupled device (CCD) and metal-oxide semiconductor technologies, and an ion selective membrane. The CCD potassium ion image sensor was equipped with an array of

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