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463779

Sigma-Aldrich

Ruthenium(III) chloride hydrate

99.98% trace metals basis

Synonym(s):

Trichlororuthenium hydrate, Ruthenium trichloride

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About This Item

Linear Formula:
RuCl3 · xH2O
CAS Number:
14898-67-0
Molecular Weight:
207.43 (anhydrous basis)
EC Number:
233-167-5
MDL number:
MFCD00149844
UNSPSC Code:
12352302
PubChem Substance ID:
24870096
NACRES:
NA.23

Quality Level

100

assay

99.98% trace metals basis

form

powder and chunks

reaction suitability

reagent type: catalyst
core: ruthenium

impurities

≤250.0 ppm Trace Metal Analysis

SMILES string

O.Cl[Ru](Cl)Cl

InChI

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

InChI key

BIXNGBXQRRXPLM-UHFFFAOYSA-K

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Application

Catalyzes the synthesis of 2-ethyl-3-methylquinolines from primary aromatic amines and triallylamine.
Used for the selective hydrogenation of unsaturated aldehydes.
Used with aluminum tri-sec-butoxide (201073) to prepare a nanoparticulate catalyst for acceptor-free dehydrogenation of alcohols to aldehydes and ketones.

Other Notes

soluble form

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible, corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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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Fujita, S.-I., et al.
J. Catal., 255, 95-95 (2004)
Won-Hee Kim et al.
Organic letters, 8(12), 2543-2545 (2006-06-02)
An efficient oxidant-free oxidation for a wide range of alcohols was achieved by a recyclable ruthenium catalyst. The catalyst was prepared from readily available reagents by a one-pot synthesis through nanoparticle generation and gelation. [structure: see text]
Cho, C.S. et al.
Tetrahedron Letters, 40, 1499-1499 (1999)
Yao Zhang et al.
European journal of medicinal chemistry, 86, 449-455 (2014-09-10)
Ruthenium-based anticancer complexes have become increasingly popular for study over the last two decades. Although ruthenium complexes are currently being investigated in clinical trials, there are still some difficulties with their delivery and associated side effects. Human serum albumin (HSA)-based
Huaiyi Huang et al.
Dalton transactions (Cambridge, England : 2003), 44(35), 15602-15610 (2015-08-08)
Ruthenium complexes have been considered as promising substitutes for cisplatin in cancer chemotherapy. However, novel ruthenium-based therapies are faced with some limitations, such as unimpressive cytotoxicity toward solid tumors. Herein, we designed and synthesized phenyl-substituted terpyridyl ruthenium(ii) complexes ([Ru(tpy)(bpy)Cl](+) (Ru1)
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