4-Oxopentanal

95%

  • Product Code: 82513
  CAS:    626-96-0
Molecular Weight: 100.12 g./mol Molecular Formula: C₅H₈O₂
EC Number: MDL Number: MFCD12545900
Melting Point: Boiling Point:
Density: Storage Condition: −20°C, inert gas
Product Description: 4-Oxopentanal is primarily used in organic synthesis as an intermediate for the production of various chemicals. It serves as a key building block in the manufacture of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) that require complex aldehyde and ketone functionalities. Additionally, it is utilized in the production of flavor and fragrance compounds, contributing to the creation of specific aroma profiles in food and cosmetic products. Its reactive carbonyl groups make it valuable in polymer chemistry, where it can be incorporated into resins and coatings to enhance their properties. Furthermore, 4-Oxopentanal is employed in research and development for exploring new chemical reactions and pathways, aiding in the advancement of synthetic methodologies.
Product Specification:
Test Specification
APPEARANCE liquid
PURITY 97.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.050 10-20 days $205.49
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4-Oxopentanal
4-Oxopentanal is primarily used in organic synthesis as an intermediate for the production of various chemicals. It serves as a key building block in the manufacture of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) that require complex aldehyde and ketone functionalities. Additionally, it is utilized in the production of flavor and fragrance compounds, contributing to the creation of specific aroma profiles in food and cosmetic products. Its reactive carbonyl groups make it valuable in polymer chemistry, where it can be incorporated into resins and coatings to enhance their properties. Furthermore, 4-Oxopentanal is employed in research and development for exploring new chemical reactions and pathways, aiding in the advancement of synthetic methodologies.
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