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13759-89-2

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13759-89-2 Usage

Description

Yttrium(III) bromide hydrate is a compound that incorporates the rare earth element yttrium in its +3 oxidation state, linked with bromine ions in a hydrated state. Characterized by its white to pale yellow color and solubility in water, it is represented by the chemical formula YBr3·xH2O, where x denotes the variable number of water molecules associated with the yttrium bromide complex. YTTRIUM(III) BROMIDE HYDRATE serves as a versatile precursor for the creation of a variety of yttrium-based compounds and materials, as well as a catalyst in organic synthesis processes.

Uses

Used in Synthesis of Yttrium Compounds:
Yttrium(III) bromide hydrate is utilized as a precursor for the synthesis of various yttrium compounds. It is instrumental in the production of materials with unique properties that are valuable in different industries.
Used in Organic Synthesis as a Catalyst:
In the realm of organic synthesis, yttrium(III) bromide hydrate is employed as a catalyst to facilitate specific chemical reactions, enhancing the efficiency and selectivity of the processes.
Used in Materials Science for Luminescent Materials and Phosphors:
Yttrium(III) bromide hydrate is used as a source of yttrium ions in the production of luminescent materials and phosphors. These materials are crucial in the development of technologies such as lighting, displays, and sensors that rely on the emission of light under certain conditions.
Used in Research and Development:
YTTRIUM(III) BROMIDE HYDRATE is also valuable in research and development settings, where it can be explored for new applications and properties, potentially leading to breakthroughs in various scientific and technological fields.

Check Digit Verification of cas no

The CAS Registry Mumber 13759-89-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,5 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13759-89:
(7*1)+(6*3)+(5*7)+(4*5)+(3*9)+(2*8)+(1*9)=132
132 % 10 = 2
So 13759-89-2 is a valid CAS Registry Number.
InChI:InChI=1/3BrH.Yb/h3*1H;/q;;;+3/p-3

13759-89-2 Well-known Company Product Price

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  • Alfa Aesar

  • (35748)  Ytterbium(III) bromide, ultra dry, 99.9% (REO)   

  • 13759-89-2

  • 1g

  • 2742.0CNY

  • Detail
  • Alfa Aesar

  • (35748)  Ytterbium(III) bromide, ultra dry, 99.9% (REO)   

  • 13759-89-2

  • 5g

  • 6946.0CNY

  • Detail
  • Aldrich

  • (451320)  Ytterbium(III)bromide  anhydrous, powder, 99.99% trace metals basis

  • 13759-89-2

  • 451320-1G

  • 1,250.73CNY

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13759-89-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name yttrium(3+),tribromide,hydrate

1.2 Other means of identification

Product number -
Other names ytterbium bromide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13759-89-2 SDS

13759-89-2Relevant articles and documents

Composition of saturated vapor over ytterbium bromides

Butman,Motalov,Sergeev,Kudin,Kraemer

, p. 751 - 759 (2011)

The vaporization process of ytterbium di- and tribromide was studied using high-temperature mass spectrometry over the temperature range of 850 to 1300 K. It was ascertained that, at the early vaporization stages, the vapor contained molecules YbBr3, YbBr2, YbBr, Br2, Yb 2Br2, Yb2Br3, Yb2Br 4, Yb2Br5, Yb2Br6, and atoms Yb and Br. The partial pressures of all components of saturated vapor were calculated. It was found that vapor composition reflected the course of the reactions of decomposition of tribromide and disproportionation of dibromide in the condensed phase. It was concluded that vaporization of di- and tribromide was incongruent at the initial stages; vaporization of both agents acquired a congruent character with the Yb: Br = 1.0: 1.9±0.2 ratio with time.

Structural characterization of methanol substituted lanthanum halides

Boyle, Timothy J.,Ottley, Leigh Anna M.,Alam, Todd M.,Rodriguez, Mark A.,Yang, Pin,Mcintyre, Sarah K.

, p. 1784 - 1795 (2010/07/03)

The first study into the alcohol solvation of lanthanum halide [LaX3] derivatives as a means to lower the processing temperature for the production of the LaBr3 scintillators was undertaken using methanol (MeOH). Initially the de-hydration of {[La(μ-Br)(H2O)7](Br)2}2 (1) was investigated through the simple room temperature dissolution of 1 in MeOH. The mixed solvate monomeric [La(H2O)7(MeOH)2](Br)3 (2) compound was isolated where the La metal center retains its original 9-coordination through the binding of two additional MeOH solvents but necessitates the transfer of the innersphere Br to the outersphere. In an attempt to in situ dry the reaction mixture of 1 in MeOH over CaH2, crystals of [Ca(MeOH)6](Br)2 (3) were isolated. Compound 1 dissolved in MeOH at reflux temperatures led to the isolation of an unusual arrangement identified as the salt derivative {[LaBr2.75·5.25(MeOH)]+0.25 [LaBr3.25·4.75(MeOH)]-0.25} (4). The fully substituted species was ultimately isolated through the dissolution of dried LaBr3 in MeOH forming the 8-coordinated [LaBr3(MeOH)5] (5) complex. It was determined that the concentration of the crystallization solution directed the structure isolated (4 concentrated; 5 dilute) The other LaX3 derivatives were isolated as [(MeOH)4(Cl)2La(μ-Cl)]2 (6) and [La(MeOH)9](I)3·MeOH (7). Beryllium Dome XRD analysis indicated that the bulk material for 5 appear to have multiple solvated species, 6 is consistent with the single crystal, and 7 was too broad to elucidate structural aspects. Multinuclear NMR (139La) indicated that these compounds do not retain their structure in MeOD. TGA/DTA data revealed that the de-solvation temperatures of the MeOH derivatives 4-6 were slightly higher in comparison to their hydrated counterparts.

Synthesis and crystal structure of (NH4)3Cu4Ho2Br13. Further bromides of the (NH4)3Cu4M2Br13 Type (M = Dy-Lu, Y) and on Rb3Cu4Ho2Br13

Wickleder, Mathias S.,Bohnsack, Andreas,Meyer, Gerd

, p. 675 - 678 (2008/10/09)

Single crystals of (NH4)3Cu4Ho2Br13 were obtained for the first time from the reaction of CuBr with HoBr3 which was contaminated with NH4Br: cubic, space group Pn3, Z = 2, a = 1101.71(5) pm. The crystal structure may be considered as a variant of the fluorite type according to [(HoBr6)4] [(NH4)6Cu4Br)2] ≡ Ca4F8. Pure products can be prepared from the binary halides in glass ampoules at 350°C. The bromides (NH4)3Cu4M2Br13 (M = Dy-Lu, Y) and Rb3Cu4Ho2Br13 are isotypic with (NH4)3Cu4Ho2Br13. Johann Ambrosius Barth 1996.

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