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685364

Sigma-Aldrich

Tetrakis[triphenylphosphine]palladium(0), ChemDose™ Tablets

Loading: 2μmol per tablet

Synonyme(s) :

ChemDose™, Tetrakis(triphenylphosphine)palladium(0) impregnated tablets, Palladium-tetrakis(triphenylphosphine) impregnated tablets

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About This Item

Formule linéaire :
Pd[(C6H5)3P]4
Numéro CAS:
14221-01-3
Poids moléculaire :
1155.56
Numéro MDL:
MFCD00010012
Code UNSPSC :
12352200
ID de substance PubChem :
329760964
Le tarif et la disponibilité ne sont pas disponibles actuellement.

Forme

tablet

Matrice

Magnesium aluminometasilicate base material

Température de stockage

2-8°C

Chaîne SMILES 

[Pd].c1ccc(cc1)P(c2ccccc2)c3ccccc3.c4ccc(cc4)P(c5ccccc5)c6ccccc6.c7ccc(cc7)P(c8ccccc8)c9ccccc9.c%10ccc(cc%10)P(c%11ccccc%11)c%12ccccc%12

InChI

1S/4C18H15P.Pd/c4*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;/h4*1-15H;

Clé InChI

NFHFRUOZVGFOOS-UHFFFAOYSA-N

Informations légales

ChemDose is a trademark of Reaxa Ltd.

Pictogrammes

Health hazard
GHS08

Mention d'avertissement

Warning

Mentions de danger

H351

Classification des risques

Carc. 2

Code de la classe de stockage

13 - Non Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

Listes réglementaires

Les listes réglementaires sont principalement fournies pour les produits chimiques. Seules des informations limitées peuvent être fournies ici pour les produits non chimiques. L'absence d'indication signifie qu'aucun des composants n'est répertorié. Il incombe à l'utilisateur de s'assurer de l'utilisation sûre et légale du produit.

EU REACH Annex XVII (Restriction List)

CAS No.

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Certificats d'analyse (COA)

Lot/Batch Number
07103DH
02126TH

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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

Wenhan Zhang et al.
Angewandte Chemie (International ed. in English), 53(34), 8980-8984 (2014-07-01)
tert-Butoxyacetylene is shown to undergo Sonogashira coupling with aryl iodides to yield aryl-substituted tert-butyl ynol ethers. These intermediates participate in a [1,5]-hydride shift, which results in the extrusion of isobutylene and the generation of aryl ketenes. The ketenes are trapped
Chanchal Chakraborty et al.
ACS applied materials & interfaces, 7(34), 19034-19042 (2015-08-19)
A platinum(II)-based, luminescent, metallo-supramolecular polymer (PolyPtL1) having an inherent dipole moment was synthesized via complexation of Pt(II) ions with an asymmetric ligand L1, containing terpyridyl and pyridyl moieties. The synthesized ligand and polymer were well characterized by various NMR techniques
Debabrata Jana et al.
Organic & biomolecular chemistry, 13(43), 10663-10674 (2015-09-09)
Four pyrene-vinyl-tetraphenylethylene based conjugated materials were synthesized and characterized by FT-IR, NMR, and mass spectroscopy. The photophysical (including absorption, fluorescence, and fluorescence lifetime) and aggregation properties in tetrahydrofuran were investigated. The photophysical and aggregation behavior depends on the spacer, substituent
Shouchun Yin et al.
Soft matter, 11(22), 4424-4429 (2015-05-01)
In this paper, a pyrene moiety is incorporated into a bolaamphiphile to form a novel molecule denoted PRB. Above the critical micelle concentration, PRB forms nanodisks in the aqueous solution. The addition of acetate ions induces a morphological change in
Haiyin Li et al.
Macromolecular bioscience, 14(10), 1361-1367 (2014-06-14)
Phospholipid monomer and aggregation-induced emission (AIE) dye-based dimers are incorporated via reversible addition-fragmentation transfer polymerization to afford cross-linked zwitterionic fluorescent copolymers. Such copolymers are prone to self-assembly into fluorescent polymeric nanoparticles (FPNs) in physiological solution due to their amphiphilic nature.

Questions

1–7 of 7 Questions  

  1. Can I use ChemDose® tablets in a microwave or pressure vessel?

    1 answer

    1. Absolutely. Please see the Technical Information for Download section (below) for additional examples of cross-coupling reactions involving the use of microwaves.

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  2. What is the pH stability of the ChemDose® tablets?

    1 answer

    1. The ChemDose® tablets are mildly basic and will dissolve in the presence of mineral acids.

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  3. Can I use ChemDose® tablets in any solvent?

    1 answer

    1. Yes, including aqueous solvents.

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  4. Do the ChemDose® tablets disintegrate during the course of the reaction?

    1 answer

    1. They are normally recovered intact, however, they may disintegrate somewhat in aqueous reactions. Any disintegrated tablets can be removed from the reaction via filtration.

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  5. What is the Department of Transportation shipping information for this product?

    1 answer

    1. Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.

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  6. How should I store ChemDose® tablets?

    1 answer

    1. As with most catalysts and ligands, as a general precaution it is best to store them in a refrigerator and/or under an inert atmosphere to maintain activity. Some catalysts, such as Pd(dppf)Cl2·CH2Cl2, are more robust and can be handled in air without issue. Please refer to the ChemDose® label for specific handling of a given catalyst, ligand, or reagent.

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  7. How should I dispose of spent ChemDose® tablets?

    1 answer

    1. They should be treated as solid waste, contaminated with reaction species. The matrix is non-toxic and environmentally benign.

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