Michler's ketone

98%

  • Product Code: 126899
  Alias:    Michler's ketone; 4,4'-bis(N,N-dimethylamino)benzophenone, Michler's ketone, tetramethyl-Michler's ketone
  CAS:    90-94-8
Molecular Weight: 268.35 g./mol Molecular Formula: C₁₇H₂₀N₂O
EC Number: 202-027-5 MDL Number: MFCD00008312
Melting Point: 174 -176 °C(lit.) Boiling Point: 360 °C
Density: Storage Condition: room temperature, sealed
Product Description: Michler's ketone is primarily used as an intermediate in the synthesis of dyes and pigments, particularly in the production of triarylmethane dyes. These dyes are widely employed in the textile, paper, and leather industries for coloring purposes. Additionally, it serves as a photosensitizer in photopolymerization processes, where it aids in the initiation of polymerization reactions under light exposure. In research, Michler's ketone is utilized as a reagent in organic synthesis and as a model compound in studies related to photochemistry and electron transfer reactions. Its ability to act as a UV absorber also makes it valuable in certain applications requiring light stabilization.
Product Specification:
Test Specification
Melting Point 168-176
Purity (%) 97.5-102.5
Appearance Light Yellow Or Grey To Amber To Dark Green Powder To Crystal
Infrared Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
25.000 10-20 days €8.71
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100.000 10-20 days €23.48
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500.000 10-20 days €69.91
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2500.000 10-20 days €263.56
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Michler's ketone
Michler's ketone is primarily used as an intermediate in the synthesis of dyes and pigments, particularly in the production of triarylmethane dyes. These dyes are widely employed in the textile, paper, and leather industries for coloring purposes. Additionally, it serves as a photosensitizer in photopolymerization processes, where it aids in the initiation of polymerization reactions under light exposure. In research, Michler's ketone is utilized as a reagent in organic synthesis and as a model compound in studies related to photochemistry and electron transfer reactions. Its ability to act as a UV absorber also makes it valuable in certain applications requiring light stabilization.
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