Grundinformationen
- CAS
931-36-2- Standard-SMILES
CCc1ncc(C)[nH]1- InChIKey
ULKLGIFJWFIQFF-UHFFFAOYSA-N- Summenformel
- C6H10N2
- Durchschnittliche Molmasse
- 110,16 g/mol
- Monoisotopische Masse
- 110,08439833
Überblick
5K8XI641G3 is a member of imidazoles.
Namen und Bezeichner
- Bevorzugter Name
- 2-Ethyl-4-methylimidazole
- IUPAC
- 2-ethyl-5-methyl-1H-imidazole
- Lokaler Name
- 2-Ethyl-4-methylimidazol
- Englischer Name
- 2-Ethyl-4-methylimidazole
- Summenformel
- C6H10N2
- Molmasse
- 110.16
Namen und Synonyme
2-Ethyl-4-methylimidazole931-36-22-Ethyl-4-methyl-1H-imidazole1H-Imidazole, 2-ethyl-4-methyl-4-Methyl-2-ethylimidazoleImidazole, 2-ethyl-4-methyl-1H-Imidazole, 2-ethyl-5-methyl-NSC 82315DTXSID90447445K8XI641G3EINECS 213-234-5Curezol 2E4MZ
Weitere Namen anzeigen
2E4MZ2E4MIEMI24Ethyl-4-MethyliMidazLABOTEST-BB LTBB0006892-ethyl-4-methyl-1h-imidazol2-Ethyl-5-methyl-1H-imidazole1H-Imidazole,2-ethyl-4-methyl-EMI-70
Epicure EMI 24Imicure EMI 24NSC-82315EMI 24DTXCID7024744EC 213-234-54Methyl2ethylimidazoleImidazole, 2ethyl4methyl
Datenbank-Bezeichner
- CAS
931-36-2- PubChem CID
- 70262
- DTXSID
DTXSID9044744
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 1,3
- Polarare Oberfläche (TPSA)
- 28,7 Ų
- H-Brücken-Donoren
- 1
- H-Brücken-Akzeptoren
- 1
- Frei drehbare Bindungen
- 1
- Schwere Atome
- 8
- Formalladung
- 0
- Komplexität
- 72,9
Experimentelle und physikochemische Eigenschaften
Chemical ClassesNitrogen Compounds -> Imidazoles
Solubility>16.5 [ug/mL] (The mean of the results at pH 7.4)
Physical Description
Liquid
Liquid; [Alfa Aesar MSDS]
Collision Cross Section121.2 Ų [M+H]+ [CCS Type: DT; Buffer gas: N2; Ionization: ESI+; Dataset: TOXCAST; Source Identifier: DTXSID9044744]
Physikochemische Eigenschaften
- Schmelzpunkt
- 47 · 47-54 °C (lit.)
- Siedepunkt
- 292 · 292-295 °C (lit.)
- Dichte
- 0.975 g/mL · 0.975 g/mL at 25 °C (lit.)
- Dampfdruck
- 0.028 Pa · 0.028Pa at 20℃
- Brechungsindex
- 20 · n20/D 1.5(lit.)
- Flammpunkt
- 280 °F · 280 °F
- storage temp.
- Inert atmosphere,Room Temperature
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 1.4% (7 of 488) of reports.
Danger
H302 (98.4%): Harmful if swallowed [Warning Acute toxicity, oral]
P261, P264, P264+P265, P270, P272, P280, P301+P317, P302+P352, P305+P354+P338, P317, P321, P330, P332+P317, P333+P317, P362+P364, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 488 reports by companies from 17 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Danger
Gefahrenhinweise
Regulatory Information
Chemical: 1H-Imidazole, 2-ethyl-4-methyl-
1H-Imidazole, 2-ethyl-5-methyl- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of 1H-Imidazole, 2-ethyl-5-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)
REACH registered substance: 2-ethyl-4-methylimidazole (EC: 213-234-5)
1H-Imidazole, 2-ethyl-4-methyl-: Does not have an individual approval but may be used under an appropriate group standard
Hazards SummaryCauses somnolence and convulsions in intraperitoneal lethal-dose studies of mice (LD50 = 250 mg/kg); [RTECS] An irritant that may cause serious eye injury; Harmful by ingestion; [Alfa Aesar MSDS] See 4-Methylimidazole.
Hazard Classes and CategoriesAcute Tox. 4 (98.4%)
Toxikologische Informationen
Adverse EffectsNeurotoxin - Other CNS neurotoxin
Chemie und Industrie
Verwendung und Herstellung
U.S. Production2023: <50,000 lb
Industry UsesIntermediate
General Manufacturing Information
All Other Basic Organic Chemical Manufacturing
1H-Imidazole, 2-ethyl-5-methyl-: ACTIVE
Anwendungen
Verwenden2-Ethyl-4-methylimidazole can be used as a:cross-linker for epoxy resins to synthesize network polymers with improved thermal resistance and physical properties.curing agent for polysiloxane episulfide resin (PSER).catalyst to promote curing of blends of hyperbranched aromatic epoxy polymer and bisphenol F diglycidyl ether.
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