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Toutes les photos(1)

Principaux documents

415367

Sigma-Aldrich

N-Ethyl-p-toluenesulfonamide

98%

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About This Item

Formule linéaire :
CH3C6H4SO2NHC2H5
Numéro CAS:
Poids moléculaire :
199.27
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :

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Essai

98%

pb

208 °C/745 mmHg (lit.)

Pf

63-65 °C (lit.)

Chaîne SMILES 

CCNS(=O)(=O)c1ccc(C)cc1

InChI

1S/C9H13NO2S/c1-3-10-13(11,12)9-6-4-8(2)5-7-9/h4-7,10H,3H2,1-2H3

Clé InChI

OHPZPBNDOVQJMH-UHFFFAOYSA-N

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Cet article
HPA058272HPA057442HPA016643
conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

biological source

rabbit

biological source

rabbit

biological source

rabbit

biological source

rabbit

product line

Prestige Antibodies® Powered by Atlas Antibodies

product line

Prestige Antibodies® Powered by Atlas Antibodies

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Prestige Antibodies® Powered by Atlas Antibodies

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Prestige Antibodies® Powered by Atlas Antibodies

UniProt accession no.

Q6IF82

UniProt accession no.

O95047

UniProt accession no.

Q8N0Y3

UniProt accession no.

Q8NGZ2

Description générale

N-Ethyl-p-toluenesulfonamide is an herbicide. It is an organic contaminant present in the river Rhine.[1] N-Ethyl-p-toluenesulfonamide/ N-bromo succinimmide (NBS) along with N-methyl-p-toluenesulfonamide/NBS serves as nitrogen/halogen resources during the synthesis of vicinal haloamino ketone derivatives.[2] Reaction of epichlorohydrin with bisphenol is useful for the industrial preparation of epoxide resins.[3]

Code de la classe de stockage

13 - Non Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves


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Consulter la Bibliothèque de documents

New Epoxide Resins by Reaction of Epichlorohydrin with Sulfonamides.
Cohen M.
Industrial & Engineering Chemistry Research, 47(10), 2095-2101 (1955)
G M Alink et al.
Mutation research, 631(2), 93-100 (2007-06-15)
Surface water used for drinking-water preparation requires continuous monitoring for the presence of toxic compounds. For monitoring of genotoxic compounds fish models have been developed, such as the Eastern mudminnow (Umbra pygmaea L.) because of its clearly visible 22 meta-centric
Hao Sun et al.
Chemical biology & drug design, 75(3), 269-276 (2010-03-25)
The combinations of N-methyl-p-toluenesulfonamide/NBS and N-ethyl-p-toluenesulfonamide/NBS were found to be good nitrogen/halogen resources for the aminohalogenation of alpha,beta-unsaturated ketones in the presence of Ni(OAc)(2) as the catalyst for the synthesis of vicinal haloamino ketone derivatives. The introduction of N-alkyl groups
L Kanerva et al.
Acta dermato-venereologica, 73(2), 126-129 (1993-04-01)
Dental personnel are exposed to many sensitizing compounds at work and often develop multiple delayed allergies. Here we report on a dentist who got sensitized to several products that have not, or only seldom, caused sensitization earlier. These products were:
Ingun Skjevrak et al.
Food additives and contaminants, 22(10), 1012-1022 (2005-10-18)
A procedure used by the Norwegian Food Safety Authority for surveillance of contaminants from plastic food contact materials (polyolefin drinking bottles, water boilers, polyamide cooking utensils and plastic multi-layer materials) is described. It is based on gas chromatographic-mass spectrometric (GC/MS)

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