415367
N-Ethyl-p-toluenesulfonamide
98%
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About This Item
Formula condensata:
CH3C6H4SO2NHC2H5
Numero CAS:
Peso molecolare:
199.27
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
Prezzi e disponibilità al momento non sono disponibili
Prodotti consigliati
Saggio
98%
P. ebollizione
208 °C/745 mmHg (lit.)
Punto di fusione
63-65 °C (lit.)
Stringa SMILE
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
OHPZPBNDOVQJMH-UHFFFAOYSA-N
Descrizione generale
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]
Codice della classe di stoccaggio
13 - Non Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.
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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