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CS-W001157 4
Total: USD 88.00

4-(Oxiran-2-ylmethoxy)butyl acrylate

  • CAS No. 119692-59-0

  • Cat. No. CS-0069855
  • Molecule weight200.23
  • Purity≥98%
  • MDL No.MFCD30474906

*For research and further manufacturing use only, not for direct human use.

4-(Oxiran-2-ylmethoxy)butyl acrylate|CS-0069855

Structure of 119692-59-0

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General Information

  • CAS No. 119692-59-0
  • Cat. No. CS-0069855
  • Purity ≥98%
  • MDL No. MFCD30474906
  • Storage 4°C, stored under nitrogen, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₁₆O₄
  • Molecular Weight 200.23
  • Synonym(s) 2-Propenoic acid, 4-(oxiranylmethoxy)butyl ester
  • SMILES C=CC(OCCCCOCC1CO1)=O

Description

4-(Oxiran-2-ylmethoxy)butyl acrylate features a reactive epoxide group flanked by a hydrophilic ether linkage and an acrylate terminus, enabling orthogonal functionalization in polymer synthesis. This trifunctional architecture supports efficient coupling with nucleophilic sites while maintaining compatibility with radical polymerization. The pendant oxirane facilitates post-polymerization modification under mild conditions, offering precise control over surface functionality and network architecture.

Application

4-(Oxiran-2-ylmethoxy)butyl acrylate serves as a versatile bifunctional monomer, enabling controlled polymerization through its acrylate group while the epoxide functionality facilitates post-polymerization modification. The oxirane ring undergoes selective ring-opening with nucleophiles, allowing for grafting of polar or bioactive moieties. Its bench-stable nature and compatibility with common reaction conditions make it ideal for synthesizing functionalized polymers in biomedical and materials applications.

Safety Information

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GHS Pictogram :
GHS No : GHS07,GHS08,GHS09
Signal Word : Danger
UN#: 3082
Class : 9
Packing Group : Ⅲ
Hazard Statements : H227-H315-H319-H372-H410
Precautionary Statements : P210-P260-P264-P270-P273-P280-P302+P352-P362+P364-P370+P378-P391-P403-P501

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Computational Chemistry Data

  • TPSA   48.06
  • LogP   0.9112
  • H_Acceptors   4
  • H_Donors   0
  • Rotatable_Bonds   8

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