N-Ethyl-p-toluenesulfonamide
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Grundinformationen
- CAS
1321-54-6- Standard-SMILES
CCNS(=O)(=O)c1ccc(C)cc1- InChIKey
OHPZPBNDOVQJMH-UHFFFAOYSA-N- Summenformel
- C9H13NO2S
- Durchschnittliche Molmasse
- 199,27 g/mol
- Monoisotopische Masse
- 199,06669966
Überblick
Platelets (from dilute alcohol or ligroin) or off-white solid. (NTP, 1992)
Namen und Bezeichner
- Bevorzugter Name
- N-Ethyl-p-toluenesulfonamide
- IUPAC
- N-ethyl-4-methylbenzenesulfonamide
- Englischer Name
- Ethyl-p-toluenesulfonamide
- Summenformel
- C9H13NO2S
- Molmasse
- 199.273
Namen und Synonyme
N-ETHYL-P-TOLUENESULFONAMIDEN-Ethyl-4-methylbenzenesulfonamideN-Ethyl-p-tolylsulfonamideBenzenesulfonamide, N-ethyl-4-methyl-N-Ethyl-4-toluenesulfonamideEthyl tosylamidep-Tolueneethylsulfonamideethyl-p-toluenesulfonamideN-Ethyltoluene-4-sulphonamideNSC 68803DTXSID5025310CCRIS 6037
Weitere Namen anzeigen
N-Ethylp-toluene Sulfonamide(N-PTSA)Ethyl-p-toluenesulfonamide ISO 9001：2015 REACH
N-Ethyl-4-methyl benzenesulfonamideEINECS 201-275-1992S798SJBNSC-68803DTXCID4053104-Toluenesulfonamide, N-ethyl-ETHYL P-TOLUENESULFONAMIDEOHPZPBNDOVQJMH-UHFFFAOYSA-
Datenbank-Bezeichner
- CAS
1321-54-6、80-39-7- PubChem CID
- 6637
- DTXSID
DTXSID5025310- ChEMBL
CHEMBL1492809- UNII
- 992S798SJB
- EC Number
- 201-275-1
- Nikkaji
- J45.867H
Eigenschaften
Berechnete StruktureigenschaftenWird ergänzt
- XLogP
- 1,6
- Polarare Oberfläche (TPSA)
- 54,6 Ų
- H-Brücken-Donoren
- 1
- H-Brücken-Akzeptoren
- 3
- Frei drehbare Bindungen
- 3
- Schwere Atome
- 13
- Formalladung
- 0
- Komplexität
- 235
Experimentelle und physikochemische Eigenschaften
Chemical ClassesNitrogen Compounds -> Sulfonamides
CosmeticsPlasticiser; Film forming
Solubilityless than 1 mg/mL at 70 °F (NTP, 1992)
Melting Point147 °F (NTP, 1992)
Food Contact Substances
FCS -> FDA Inventory of Food Contact Substances Listed in 21 CFR
FCS -> FDA Inventory of Food Contact Substances Listed in 21 CFR
FCS -> FDA Inventory of Food Contact Substances Listed in 21 CFR
FCS -> FDA Inventory of Effective Food Contact Substance (FCS) Notifications
Physical Description
Platelets (from dilute alcohol or ligroin) or off-white solid. (NTP, 1992)
Liquid
Solid; [CAMEO]
Sicherheit und Regulatorisches
Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.
GHS-Klassifizierung
GHS Classification
This chemical does not meet GHS hazard criteria for 22.6% (19 of 84) of reports.
Warning
H315 (72.6%): Causes skin irritation [Warning Skin corrosion/irritation]
P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 84 reports by companies from 8 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Gefahrenhinweise
Regulatory Information
Chemical: Benzenesulfonamide, N-ethyl-4-methyl-
Benzenesulfonamide, N-ethyl-4-methyl- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Benzenesulfonamide, N-ethyl-4-methyl- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)
Benzenesulfonamide, N-ethyl-4-methyl-: Does not have an individual approval but may be used as a component in a product covered by a group standard. It is not approved for use as a chemical in its own right.
Fire HazardsFlash point data for this chemical are not available; however, it is probably combustible. (NTP, 1992)
Hazards SummaryA skin and strong eye irritant; [Sigma-Aldrich MSDS] See Toluenesulfonamide.
Reactive GroupAmines, Phosphines, and Pyridines
Reactivity Profile
An amide. Organic amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).
Chemie und Industrie
Verwendung und Herstellung
UsesPermitted for use as an inert ingredient in non-food pesticide products; [EPA]
U.S. Production2023: 183,987 lb
Industry UsesPlasticizer
Household ProductsInformation on 4 consumer products that contain Ethyl tosylamide in the following categories is provided:
Use ClassificationCosmetics -> Plasticiser; Film forming
General Manufacturing Information
Printing Ink Manufacturing
Benzenesulfonamide, N-ethyl-4-methyl-: ACTIVE
Zugehörige Reaktionen
13
Notizen zur Verbindung
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