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Catalog Number:
41403
CAS Number:
102096-60-6
( R -α-acryloyloxy-β,β-diméthyl-γ-butyrolactone
Purity:
≥ 94% (CG)
Synonym(s):
( Acrylate de R -4,4-diméthyl-2-oxotétrahydrofuran-3-yle
Documents
$283.93 /5G
Taille
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Informations sur le produit

(R)-a-Acryloyloxy-b,b-dimethyl-g-butyrolactone is a versatile compound known for its unique properties that make it valuable in various industrial applications. This compound, also recognized as (R)-Acryloyloxy-2,2-dimethyl-3-butyrolactone, features a reactive acryloyl group that allows for easy incorporation into polymerization processes. Its ability to undergo free radical polymerization makes it particularly useful in the production of specialty polymers and copolymers, which are essential in coatings, adhesives, and sealants. Researchers and industry professionals appreciate its role in enhancing the mechanical properties and thermal stability of materials, making it an ideal choice for high-performance applications.

Moreover, (R)-a-Acryloyloxy-b,b-dimethyl-g-butyrolactone is increasingly being explored in the field of biomedical applications, including drug delivery systems and tissue engineering. Its biocompatibility and ability to form hydrogels provide exciting opportunities for innovative solutions in healthcare. With its multifunctional characteristics, this compound stands out as a key ingredient for those looking to develop advanced materials that meet the demands of modern technology and industry.

Numéro CAS 
102096-60-6
Formule moléculaire
C9H12O4
Poids moléculaire 
184.19
Point de fusion 
7 - 8 °C
Indice de réfraction 
n20D 1.460
Informations générales
Numéro CAS 
102096-60-6
Formule moléculaire
C9H12O4
Poids moléculaire 
184.19
Point de fusion 
7 - 8 °C
Indice de réfraction 
n20D 1.460
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

(R)-a-Acryloyloxy-b,b-dimethyl-g-butyrolactone is widely utilized in research focused on

  • Polymer Chemistry: This compound serves as a monomer in the synthesis of specialty polymers, enhancing properties such as flexibility and durability in applications like coatings and adhesives.
  • Biomedical Applications: It is used in the development of drug delivery systems, where its biocompatibility and ability to form hydrogels can improve the release profiles of therapeutic agents.
  • Cosmetic Formulations: The compound is incorporated into skincare products for its film-forming abilities, providing a smooth application and enhancing moisture retention.
  • Surface Modification: It is employed in surface treatments to improve adhesion properties, making it valuable in industries such as automotive and electronics.
  • Research and Development: In academic and industrial research, it is used to explore new polymerization techniques and functional materials, contributing to advancements in material science.

Citations