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Sigma-Aldrich

Europium(III) chloride hexahydrate

99.9% trace metals basis

Synonym(s):

Europium chloride hexahydrate, Europium trichloride hexahydrate, Europium(3+) chloride hexahydrate

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About This Item

Linear Formula:
EuCl3 · 6H2O
CAS Number:
13759-92-7
Molecular Weight:
366.41
EC Number:
233-040-4
MDL number:
MFCD00149701
UNSPSC Code:
12352302
PubChem Substance ID:
24852751
NACRES:
NA.23

Assay

99.9% trace metals basis

form

crystals and lumps

reaction suitability

reagent type: catalyst
core: europium

impurities

≤2000.0 ppm Trace Rare Earth Analysis

density

4.89 g/mL at 25 °C (lit.)

SMILES string

O.O.O.O.O.O.Cl[Eu](Cl)Cl

InChI

1S/3ClH.Eu.6H2O/h3*1H;;6*1H2/q;;;+3;;;;;;/p-3

InChI key

AWDWVTKHJOZOBQ-UHFFFAOYSA-K

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Application

Europium(III) chloride hexahydrate can be used as a precursor to synthesize novel luminescent europium(III) terpyridyl chelate.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Uri Hananel et al.
Proceedings of the National Academy of Sciences of the United States of America, 116(23), 11159-11164 (2019-05-18)
Symmetry plays a crucial part in our understanding of the natural world. Mirror symmetry breaking is of special interest as it is related to life as we know it. Studying systems which display chiral amplification, therefore, could further our understanding
Eitam Vinegrad et al.
ACS nano, 13(1), 601-608 (2018-12-07)
The occurrence of biological homochirality is attributed to symmetry-breaking mechanisms which are still debatable. Studies of symmetry breaking require tools for monitoring the population ratios of individual chiral nano-objects, such as molecules, polymers, or nanocrystals. Moreover, mapping their spatial distributions
Mona Sharar et al.
Analytical and bioanalytical chemistry, 409(8), 2015-2027 (2017-01-18)
Oxidative transformation of cysteine thiol groups into different functional groups is considered a significant posttranslational modification of great importance in pathological and physiological processes. A cysteine sulfenic acid (SA) residue is the transient state for thiol group oxidation and it
Marie Anne van de Haar et al.
The journal of physical chemistry letters, 11(3), 689-695 (2020-01-11)
Phosphors have been used successfully for both research and commercial applications for decades. Eu3+-doped materials are especially promising, because of their extremely stable, efficient, and narrow red emission lines. Although these emission properties are ideal for lighting applications, weak absorption
Hassan A Azab et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 148, 114-124 (2015-04-16)
This work describes the application of time resolved fluorescence in microtiter plates for investigating the interactions of europium-allyl-3-carboxycoumarin with pesticides chlorpyrifos, endosulfan and crotoxyphos. Stern-Volmer studies at different temperatures for chlorpyrifos and crotoxyphos shows dynamic and static quenching mechanisms respectively.
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