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Platinum bis(acetylacetonate)

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Platinum bis(acetylacetonate) Basic information

Product Name:
Platinum bis(acetylacetonate)
Synonyms:
  • 4-pentanedionato-o,o’)-bis((sp-4-1)-platinu
  • Bis(2,4-pentanedionato-O,O')platinum
  • 2,4-Pentanedione platinum(II) derivative, Pt(acac)2
  • Platinum(II) acetylacetonate,2,4-Pentanedione platinum(II) derivative, Pt(acac)2
  • Platinum(Ⅱ) 2,4-pentanedionate, Pt 48.0% min
  • PlatinuM(Ⅱ) 2,4-pentanedionate
  • PlatinuM(II) acetylacetonate,98% Pt(CH3COCHCOCH3)2
  • Acetylacetone Platinum(II) Salt Platinum(II) Acetylacetonate
CAS:
15170-57-7
MF:
C10H14O4Pt
MW:
393.29
EINECS:
239-223-5
Product Categories:
  • chemical reaction,pharm,electronic,materials
  • Synthetic Organic Chemistry
  • Catalysts for Organic Synthesis
  • Classes of Metal Compounds
  • Homogeneous Catalysts
  • Transition Metal Compounds
  • Metal Complexes
  • Pt (Platinum) Compounds
Mol File:
15170-57-7.mol
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Platinum bis(acetylacetonate) Chemical Properties

Melting point:
249-252 °C(lit.)
Flash point:
170°C
storage temp. 
Store below +30°C.
solubility 
soluble in Acetone
form 
Powder
color 
Yellow to yellow-green
Specific Gravity
2.336
Water Solubility 
insoluble
Sublimation 
170 ºC
BRN 
4136189
NIST Chemistry Reference
Platinum bis(acetylacetonate)(15170-57-7)
EPA Substance Registry System
Platinum, bis(2,4-pentanedionato-.kappa.O,.kappa.O')-, (SP-4-1)- (15170-57-7)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
20/21/22-36/37/38-63
Safety Statements 
26-36/37/39
WGK Germany 
3
10
TSCA 
Yes
HS Code 
3815 90 90
Toxicity
LD50 orally in Rabbit: > 500 mg/kg

MSDS

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Platinum bis(acetylacetonate) Usage And Synthesis

Chemical Properties

yellow to yellow-green powder

Uses

Used for photoactivated hydrosilylation reactions between vinyl and silane groups; in the deposition of platinum metal and in the preparation of platinum nanotubes. Precursor for FePt superlattice magnetic nanoparticles.

Purification Methods

It crystallises from *C6H6 as yellow crystals and is dried in air or in a vacuum desiccator. [Werner Chem Ber 34 2584 1901, Fernelius & Bryant Inorg Synth V 105 1957, Beilstein 1 H 783, 1 IV 3678.]

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