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934550

Sigma-Aldrich

Silyl-ether based ROMP monomer

iPrSi

Synonyma:

2,2-Bis(1-methylethyl)-1,3-dioxa-2-silacyclohept-5-ene

Přihlásitk zobrazení cen stanovených pro organizaci a smluvních cen


About This Item

Empirický vzorec (Hillův zápis):
C11H22O2Si
Číslo CAS:
Molekulová hmotnost:
214.38
MDL number:
UNSPSC Code:
12162002
NACRES:
NA.21

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

InChI

1S/C11H22O2Si/c1-10(2)14(11(3)4)12-8-6-5-7-9-13-14/h5-6,10-11H,7-9H2,1-4H3/b6-5-

Inchi Key

YBYQYMPJHKPHMH-WAYWQWQTSA-N

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

Č. produktu
Popis
Stanovení ceny

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Navštívit knihovnu dokumentů

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
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

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