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Merck
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Documenti

901185

Sigma-Aldrich

3,3′-Diethoxypropyl methacrylate

≥98.0%, contains ≤100 ppm MEHQ as inhibitor

Sinonimo/i:

3,3-Diethoxypropyl 2-methylprop-2-enoate, DEPMA, Diethoxypropyl methacrylate

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About This Item

Formula empirica (notazione di Hill):
C11H20O4
Numero CAS:
95984-01-3
Peso molecolare:
216.27
Numero MDL:
MFCD31657490
Codice UNSPSC:
12162002
NACRES:
NA.23

Saggio

≥98.0%

Forma fisica

liquid

contiene

≤100 ppm MEHQ as inhibitor

Colore

colorless to pale yellow

Condizioni di spedizione

wet ice

Temperatura di conservazione

−20°C

InChI

1S/C11H20O4/c1-5-13-10(14-6-2)7-8-15-11(12)9(3)4/h10H,3,5-8H2,1-2,4H3
CPARKAXEDHCHNX-UHFFFAOYSA-N

Applicazioni

3,3′-Diethoxypropyl methacrylate is a methacrylate monomer used in the synthesis of the pH-responsive polymer poly(3,3′-diethoxypropyl methacrylate) (PDEPMA). PDEPMA contains acetal groups, which upon exposure to acid in solution hydrolyze to form aldehyde groups that can be further reacted via chemical conjugation with biomolecules or other small molecules. Due to their responsive nature and well-controlled deprotection reactions, these materials have been used in a wide variety of biomedical applications such as surface patterning for sensors, the synthesis of polymer-biomolecule conjugates, and drug delivery applications.

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319

Classi di pericolo

Eye Irrit. 2 - Skin Irrit. 2

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

161.6 °F

Punto d’infiammabilità (°C)

72 °C

Certificati d'analisi (COA)

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Jungyeon Hwang et al.
Journal of controlled release : official journal of the Controlled Release Society, 122(3), 279-286 (2007-06-30)
Polymers with reactive side chains and narrow molecular weight distributions were synthesized by reversible addition-fragmentation chain transfer (RAFT) polymerization, and the potential to utilize these polymers to prepare drug carriers was demonstrated. p-Nitrophenyl methacrylate (NPMA) and diethoxypropyl methacrylate (DEPMA) were
Karen L Christman et al.
Langmuir : the ACS journal of surfaces and colloids, 21(18), 8389-8393 (2005-08-24)
Protein and peptide microarrays are popular candidates for medical diagnostics because of the possibility for high sensitivity and simultaneous marker screening. To realize the potential of these arrays, new strategies for ligand patterning are needed. We report a method for
The emergence of oxime click chemistry and its utility in polymer science.
Collins J, et al.
Polym. Chem., 7, 3812-3826 (2016)
Anja S Goldmann et al.
Macromolecular rapid communications, 34(10), 810-849 (2013-04-30)
The establishment of advanced living/controlled polymerization protocols allows for engineering synthetic polymers in a precise fashion. Combining advanced living/controlled polymerization techniques with highly efficient coupling chemistries facilitates quantitative, modular, and orthogonal functionalization of synthetic polymer strands at their chain termini

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