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415367

Sigma-Aldrich

N-Ethyl-p-toluenesulfonamide

98%

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About This Item

Fórmula linear:
CH3C6H4SO2NHC2H5
Número CAS:
Peso molecular:
199.27
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:

Preço e disponibilidade não estão disponíveis no momento.

Ensaio

98%

p.e.

208 °C/745 mmHg (lit.)

pf

63-65 °C (lit.)

cadeia de caracteres 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

chave InChI

OHPZPBNDOVQJMH-UHFFFAOYSA-N

Descrição geral

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]

Código de classe de armazenamento

13 - Non Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves


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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
New Epoxide Resins by Reaction of Epichlorohydrin with Sulfonamides.
Cohen M.
Industrial & Engineering Chemistry Research, 47(10), 2095-2101 (1955)
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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