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520640

Sigma-Aldrich

Platinum(IV) chloride

≥99.9% trace metals basis

Synonyme(s) :

Platinum tetrachloride

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About This Item

Formule linéaire :
PtCl4
Numéro CAS:
13454-96-1
Poids moléculaire :
336.89
Numéro CE :
236-645-1
Numéro MDL:
MFCD00011182
Code UNSPSC :
12352302
ID de substance PubChem :
24874154
Nomenclature NACRES :
NA.23
Essai:
≥99.9% trace metals basis
Forme:
powder

Niveau de qualité

100

Essai

≥99.9% trace metals basis

Forme

powder

Composition

Pt, 55-58%

Pertinence de la réaction

reagent type: catalyst
core: platinum

Impuretés

≤1000.0 ppm Trace Metal Analysis

Pf

370 °C (dec.) (lit.)

Densité

4.303 g/mL at 25 °C (lit.)

Chaîne SMILES 

Cl[Pt](Cl)(Cl)Cl

InChI

1S/4ClH.Pt/h4*1H;/q;;;;+4/p-4

Clé InChI

FBEIPJNQGITEBL-UHFFFAOYSA-J

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Description générale

Platinum (IV)chloride is a weak Lewis acid used in surface modification, nanomaterialsynthesis, and catalysis.

Application

Platinum (IV) chloride can be used for the surfacemodification of crystalline and amorphous titania powders, to enhance theirphotocatalytic efficiency. Electronsinjected into the conduction band of titania due to visible light excitation ofplatinum (IV)chloride surface complex reduces oxygen to superoxide. The superoxide thusformed is responsible for the photodegradation reaction.

Platinumnanoparticles can be synthesized by reacting platinum (IV) chloride with Cyanobacteriumin an environmentally friendly method.

It can also be used as a dual catalyst forstereo- and regioselective glycosidations. Due to its ligand-bindingcapacity, platinum (IV) chloridehas an affinity for the glycosyl acceptor hydroxy group and forms the glycosidationproduct in β-configuration. It also enhances nucleophilicity differencesbetween hydroxy groups allowing regioselective glycosidation.

Pictogrammes

Skull and crossbonesHealth hazardCorrosion
GHS06,GHS08,GHS05

Mention d'avertissement

Danger

Mentions de danger

H301,H314,H317,H334

Classification des risques

Acute Tox. 3 Oral - Eye Dam. 1 - Resp. Sens. 1 - Skin Corr. 1B - Skin Sens. 1

Code de la classe de stockage

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

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

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Certificats d'analyse (COA)

Lot/Batch Number
MKCW8669
MKCT5394
MKCS3399
MKBV1421V
MKBB1279

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Maggy F Lengke et al.
Langmuir : the ACS journal of surfaces and colloids, 22(17), 7318-7323 (2006-08-09)
Interaction of cyanobacteria (Plectonema boryanum UTEX 485) with aqueous platinum(IV)-chloride (PtCl(4) degrees ) has been investigated at 25-100 degrees C for up to 28 days, and 180 degrees C for 1 day. The addition of PtCl(4) degrees to the cyanobacteria
W Macyk et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 7(9), 1862-1867 (2001-06-19)
Anatase, rutile, and amorphous titania powders were surface-modified by grinding with PtCl4 and H2[PtCl6]. Only the anatase modification afforded hybrid photocatalysts capable of degradation of 4-chlorophenol (4-CP) with visible light, with sufficient stability towards decomplexation. Grinding with K2[PtCl4] produced materials
Ivana Bednarova et al.
Neuro endocrinology letters, 33 Suppl 3, 107-112 (2013-01-29)
An enhanced worldwide application of platinum group elements (PGE), in particular platinum, has been observed during recent decades. An increased concentration of PGE was determined in collected samples of great amount of aqueous ecosystems.The aim was to compare phytotoxic effect
Lu Zhao et al.
Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences, 38(1), 59-66 (2009-03-03)
To construct a drug carrier and gene vector PEG-PEI-Pt. Polyethyleneglycol (PEG) was coupled to polyethylenimine (PEI 600) and platinum tetrachloride; PEG-PEI-Pt complex was formed in ethanol. The complex was characterized by XRD, UV-VIS and FT-IR and the DNA condensation was
B A Teicher et al.
Anticancer research, 13(5A), 1549-1556 (1993-09-01)
Since several anticancer drugs are known to become more cytotoxic to cells in an acidic milieu, we have attempted to utilize the carbonic anhydrase inhibitor, Acetazolamide, to acidify the blood and tumor of C3H mice bearing the FSaIIC fibrosarcoma in
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