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42582

Supelco

Ethyl 4-(dimethylamino)benzoate

Standard for quantitative NMR, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

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About This Item

Linear Formula:
(CH3)2NC6H4CO2C2H5
CAS Number:
Molecular Weight:
193.24
Beilstein/REAXYS Number:
2210233
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

Standard for quantitative NMR
certified reference material
TraceCERT®

Quality Level

description

qNMR Standard for organic solvents (~1.3; 3.0; 4.3; 6.7; 7.8 ppm)

product line

TraceCERT®

shelf life

limited shelf life, expiry date on the label

manufacturer/tradename

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

technique(s)

HPLC: suitable
gas chromatography (GC): suitable
qNMR: suitable

mp

63-66 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care
pharmaceutical

format

neat

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

InChI key

FZUGPQWGEGAKET-UHFFFAOYSA-N

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General description

Ethyl 4-(dimethylamino)benzoate can have the tendency to generate free radicals on illumination and hence it can find applications as an industrial photoinitiator for polymerization.
This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to primary material from an NMI, e.g. NIST or NMIJ.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com.

Check out our entire range of quantitative NMR standards (qNMR standards)

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Other Notes

Chemical Shift: ~1.3; 3.0; 4.3; 6.7; 7.8 ppm (chemical shifts may slightly vary depending on the experimental conditions)
suitable NMR solvents: MeOD, DMSO-d6, CDCl3

Recommended products

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Health hazardEnvironment

signalword

Danger

Hazard Classifications

Aquatic Chronic 2 - Repr. 1B

Storage Class

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

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Certificates of Analysis (COA)

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Sunscreen Photobiology: Molecular, Cellular and Physiological Aspects (2013)
Natasha Azzopardi et al.
Dental materials : official publication of the Academy of Dental Materials, 25(12), 1564-1568 (2009-08-28)
The purpose of this study was to investigate the effect of the resin matrix composition on the translucency of experimental dental composite resins. Three types of unfilled resin matrices (TEGDMA-, UDMA- and BisGMA-based) were formulated and light cured. In addition
A Peutzfeldt et al.
Acta odontologica Scandinavica, 47(4), 229-231 (1989-08-01)
The influence of the content of camphorquinone (CQ), amine (DABE), and inhibitor (MHQ) on the Wallace indentation hardness of light-curing polymers was investigated. The hardness was measured on disc-shaped specimens made from 50 bisphenol-A-glycidyl-dimethacrylate/triethyleneglycol-dimethacryla te-based monomers with various contents of
H Lygre et al.
Clinical oral investigations, 5(3), 167-171 (2001-10-20)
The possibility that 4-N,N-dimethyl amino benzoic acid ethylester (DMABEE), a leachable lipophilic component of dental fillings, could interact with biological membranes was investigated. Interaction of DMABEE with phospholipids was studied by two methods: First, by determining the surface pressure/molecular area
Mario Seiss et al.
Archives of toxicology, 83(12), 1109-1115 (2009-09-23)
This study investigated the leaching of ingredients from several commercial dental composite resins cured with LED, and immersed in methanol or water for 24 h, respectively. The composites used were: Admira Dentin (VOCO), Artemis Schmelz (Enamel) (Ivoclar Vivadent), Els extra

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