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Ethyl 4-(dimethylamino)benzoate

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

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About This Item

Formule linéaire :
(CH3)2NC6H4CO2C2H5
Numéro CAS:
Poids moléculaire :
193.24
Beilstein:
2210233
Numéro CE :
Numéro MDL:
Code UNSPSC:
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

Standard for quantitative NMR
certified reference material
TraceCERT®

Niveau de qualité

Description

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

Gamme de produits

TraceCERT®

Durée de conservation

limited shelf life, expiry date on the label

Fabricant/nom de marque

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Technique(s)

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

Pf

63-66 °C (lit.)

Application(s)

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

Format

neat

Chaîne SMILES 

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

Clé InChI

FZUGPQWGEGAKET-UHFFFAOYSA-N

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Description générale

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.

Autres remarques

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

Produits recommandés

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.

Informations légales

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

Pictogrammes

Health hazardEnvironment

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Aquatic Chronic 2 - Repr. 1B

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Sunscreen Photobiology: Molecular, Cellular and Physiological Aspects (2013)
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
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
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
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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