934550
Silyl-ether based ROMP monomer
iPrSi
Synonym(s):
2,2-Bis(1-methylethyl)-1,3-dioxa-2-silacyclohept-5-ene
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C11H22O2Si
CAS Number:
Molecular Weight:
214.38
MDL number:
UNSPSC Code:
12162002
NACRES:
NA.21
Recommended Products
Assay
≥98%
Quality Level
form
liquid
composition
iPrSi
color
colorless to pale yellow
storage temp.
2-8°C
SMILES string
CC(C)[Si]1(C(C)C)OC/C=C\CCO1
General description
Ring opening metathesis polymerization (ROMP) monomers are attractive building block for advanced polymeric materials in the biomedical field. 2,2-Bis(1-methylethyl)-1,3-dioxa-2-silacyclohept-5-ene , or the silyl ether based ROMP monomer iPrSi, is a bifunctional cyclic olefin that can be used to synthesize a variety of marcomolecules and polymers with diverse compositions and complex structures. iPrSi can copolymerize with a variety of norbornene derivatives including small molecules and macromolecules, enabling the formation of backbone-degradable copolymers that can be used in a variety of biomedical applications. The ROMP polymerization method is superior as it permits the tailorability of the resulting polymer material.
Application
Synthesis of advanced polymeric materials for biomedical applications including:
- drug delivery
- molecular imaging
- self assembly
- hydrogels
- medical device coatings
- stimuli responsive material
Features and Benefits
- Copolymerize efficiency with a wide variety of norbornene-based (macro)monomers
- Controlled ROMP polymerization
- Silyl ether substitute can be tuned to control degradation
related product
Product No.
Description
Pricing
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Choose from one of the most recent versions:
Certificates of Analysis (COA)
Lot/Batch Number
Don't see the Right Version?
If you require a particular version, you can look up a specific certificate by the Lot or Batch number.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Banruo Huang et al.
Journal of the American Chemical Society, 143(43), 17920-17925 (2021-10-23)
Materials capable of degradation upon exposure to light hold promise in a diverse range of applications including biomedical devices and smart coatings. Despite the rapid access to macromolecules with diverse compositions and architectures enabled by ring-opening metathesis polymerization (ROMP), a
Scott C Radzinski et al.
Macromolecular rapid communications, 37(7), 616-621 (2016-02-06)
Bottlebrush polymers are synthesized using a tandem ring-opening polymerization (ROP) and ring-opening metathesis polymerization (ROMP) strategy. For the first time, ROP and ROMP are conducted sequentially in the same pot to yield well-defined bottlebrush polymers with molecular weights in excess
Peyton Shieh et al.
Nature chemistry, 11(12), 1124-1132 (2019-10-30)
Ring-opening metathesis polymerization of norbornene-based (macro)monomers is a powerful approach for the synthesis of macromolecules with diverse compositions and complex architectures. Nevertheless, a fundamental limitation of polymers prepared by this strategy is their lack of facile degradability, limiting their utility
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service