Grundinformationen
- Standard-SMILES
CCNCc1cccnc1- InChIKey
SGROJTFSHJVVSF-UHFFFAOYSA-N- Summenformel
- C8H12N2
- Durchschnittliche Molmasse
- 136,19 g/mol
- Monoisotopische Masse
- 136,10004838
Namen und Bezeichner
- Bevorzugter Name
- Ethyl[(pyridin-3-yl)methyl]amine
- IUPAC
- N-(pyridin-3-ylmethyl)ethanamine
- Englischer Name
- N-(Pyridin-3-ylmethyl)ethylamine
- Summenformel
- C8H12N2
- Molmasse
- 136.19
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
3000-75-7- PubChem CID
- 4716480
- DTXSID
DTXSID20405876- ChEMBL
CHEMBL2286832- EC Number
- 682-067-1
- Nikkaji
- J508.050I
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 0,8
- Polarare Oberfläche (TPSA)
- 24,9 Ų
- H-Brücken-Donoren
- 1
- H-Brücken-Akzeptoren
- 2
- Frei drehbare Bindungen
- 3
- Schwere Atome
- 10
- Formalladung
- 0
- Komplexität
- 83,3
Experimentelle und physikochemische Eigenschaften
Physikochemische Eigenschaften
- Siedepunkt
- 217.5 · 217.5±15.0 °C(Predicted)
- Dichte
- 0.967 · 0.967±0.06 g/cm3(Predicted)
- storage temp.
- 2 · under inert gas (nitrogen or Argon) at 2–8 °C
- Löslichkeit
- Chloroform (Slightly), Methanol (Slightly)
- Aggregatzustand
- Oil
- pka
- 8.66 · 8.66±0.10(Predicted)
- Farbe
- Clear Yellow
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Danger
H302 (37.5%): Harmful if swallowed [Warning Acute toxicity, oral]
P260, P261, P264, P264+P265, P270, P271, P272, P280, P301+P317, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P351+P338, P305+P354+P338, P316, P319, P321, P330, P332+P317, P333+P317, P337+P317, P362+P364, P363, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 8 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Gefahrenhinweise
Sicherheitsdaten
- ridadr
- UN3259
- hs_code
- 2921490090
- hazard_class
- 8
- packing_group
- III
Chemie und Industrie
Anwendungen
VerwendenN-(Pyridin-3-ylmethyl)ethanamine is used as a reagent in organic synthesis, in particular, that of bis-nicotine derivatives which act as inhibitors of cholinesterases and β-amyloid aggregation. It is also used in the synthesis of [11C]EMPA which acts as a potential PET tracer for orexin 2 receptors. N-(Pyridin-3-ylmethyl)ethanamine is also a nicotinic analog.
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