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3-METHYL-2,4-PENTANEDIONE

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3-METHYL-2,4-PENTANEDIONE Basic information

Product Name:
3-METHYL-2,4-PENTANEDIONE
Synonyms:
  • 3-METHYL-2,4-PENTANEDIONE
  • 3-METHYLPENTANE-2,4-DIONE
  • 3-ACETYLBUTAN-2-ONE
  • 3-ACETYL-2-BUTANONE
  • 1,1-DIACETYLETHANE
  • METHYLACETYLACETONE
  • 3-methyl-2,4-pentanedione,mixtureoftautomers
  • 3-Methyl-2,4-Pentanedione,>95%
CAS:
815-57-6
MF:
C6H10O2
MW:
114.14
EINECS:
212-420-3
Product Categories:
  • Synthetic Organic Chemistry
  • C3 to C6
  • Miscellaneous
  • Environmentally-friendly Oxidation
  • Carbonyl Compounds
  • Ketones
  • Ligands (Environmentally-friendly Oxidation)
Mol File:
815-57-6.mol
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3-METHYL-2,4-PENTANEDIONE Chemical Properties

Melting point:
-7.75°C (estimate)
Boiling point:
172-174 °C(lit.)
Density 
0.981 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.442(lit.)
Flash point:
134 °F
storage temp. 
Inert atmosphere,2-8°C
pka
pK1:10.87 (25°C)
form 
clear liquid
color 
Light yellow to Yellow to Green
Water Solubility 
Soluble in water.
BRN 
635909
LogP
0.623 (est)
CAS DataBase Reference
815-57-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
RIDADR 
UN 1224 3/PG 3
WGK Germany 
3
HS Code 
2914.19.0000
HazardClass 
3
PackingGroup 
III

MSDS

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3-METHYL-2,4-PENTANEDIONE Usage And Synthesis

Chemical Properties

clear colourless to yellow liquid

Uses

3-Methyl-2,4-pentanedione involves in asymmetric substitution of 1,3-diphenyl-2-propenyl acetate catalyzed by amphiphilic resin-supported monodentate phosphine ligands can occur.

Synthesis Reference(s)

Chemistry Letters, 8, p. 45, 1979
Journal of the American Chemical Society, 90, p. 2421, 1968 DOI: 10.1021/ja01011a039
Organic Syntheses, Coll. Vol. 5, p. 785, 1973

General Description

Peroxynitrite promoted aerobic oxidation of 3-methyl-2,4-pentanedione has been reported. The kinetics of the reaction of OH radicals with 3-methyl-2,4-pentanedione has been investigated in the gas-phase using a pulsed laser photolysis-laser induced fluorescence technique. 3-methyl-2,4-pentanedione participates in asymmetric substitution of 1,3-diphenyl-2-propenyl acetate catalyzed by amphiphilic resin-supported monodentate phosphine ligands.

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