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Merck

E24905

Sigma-Aldrich

Ethyl-4-(dimethylamino)benzoat

≥99%

Synonym(e):

Parbenate

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About This Item

Lineare Formel:
(CH3)2NC6H4CO2C2H5
CAS-Nummer:
Molekulargewicht:
193.24
Beilstein:
2210233
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352103
PubChem Substanz-ID:
NACRES:
NA.23

Assay

≥99%

mp (Schmelzpunkt)

63-66 °C (lit.)

SMILES String

CCOC(=O)c1ccc(cc1)N(C)C

InChI

1S/C11H15NO2/c1-4-14-11(13)9-5-7-10(8-6-9)12(2)3/h5-8H,4H2,1-3H3

InChIKey

FZUGPQWGEGAKET-UHFFFAOYSA-N

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Allgemeine Beschreibung

Ethyl 4-(dimethylamino)benzoate (Et-PABA) is a hydrophilic polymer, which can also be used as a derivate of 4-aminobenzoate. It is majorly used as a photo-initiator with a strong estrogenic activity, which finds application as an ultraviolet filter in sunscreens.
Ethyl 4-(dimethylamino)benzoate is a photoinitiator in visible light system.

Anwendung

Can be used as a photoinititator in cell encapsulation applications.
Et-PABA is used as a co-initiator with camphorquinone (CQ) to form a self-adhesive composite for the fabrication of photosensitizers in dental materials.

Piktogramme

Health hazardEnvironment

Signalwort

Danger

H-Sätze

Gefahreneinstufungen

Aquatic Chronic 2 - Repr. 1B

Lagerklassenschlüssel

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)


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Die Dokumentenbibliothek aufrufen

S J Bryant et al.
Journal of biomaterials science. Polymer edition, 11(5), 439-457 (2000-07-15)
This work investigates the cytocompatibility of several photoinitiating systems for potential cell encapsulation applications. Both UV and visible light initiating schemes were examined. The UV photoinitiators included 2,2-dimethoxy-2-phenylacetophenone (Irgacure 651), 1-hydroxycyclohexyl phenyl ketone (Irgacure 184), 2-methyl-1-[4-(methylthio) phenyl]-2-(4-morpholinyl)-1-propanone (Irgacure 907), and
Effect of photoinitiator combinations on hardness, depth of cure, and color of model resin composites.
Salgado VE, et al.
Journal of Esthetic and Restorative Dentistry : Official Publication of the American Academy of Esthetic Dentistry ... [Et al.], 27, S41-S48 (2015)
Fabrício Aulo Ogliari et al.
Journal of dentistry, 35(7), 583-587 (2007-06-02)
The aim of this study was to evaluate the influence of an onium salt in the polymerization kinetics of a dental adhesive model resin. A monomer mixture, based on Bis-GMA, TEGDMA and HEMA, was used as a model dental adhesive
Effect of adhesive-monomers and photoinitiator on C=C conversion and color stability of model self-adhesive flowable composites.
Monteiro AA, et al.
International Journal of Adhesion and Adhesives, 87, 119-123 (2018)
Magali Dewaele et al.
Dental materials : official publication of the Academy of Dental Materials, 25(12), 1576-1584 (2009-09-15)
The purpose of this study was to investigate the effect of light-curing protocol on degree of conversion (DC), volume contraction (C), elastic modulus (E), and glass transition temperature (T(g)) as measured on a model polymer. It was a further aim

Artikel

With dentists placing nearly 100 million dental fillings into patients′ teeth annually in the U.S. alone, polymeric composite restoratives account for a very large share of the biomaterials market.

Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..

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