морфолин

Also known as diethylene imidoxide, diethylene oximide, tetrahydro-1,4-oxazine, tetrahydro-p-oxazine

химическое соединение

In the Vinony graph

Within Vinony's link graph, морфолин is referenced by 69 other articles, and connects out to water, European Union and hydrogen.

It sits within the topics Amine solvents, Chembox having GHS data and ECHA InfoCard ID from Wikidata.

Its subject is documented across 27 Wikipedia language editions.

Chemical data

Formula: C4H9NO
Molecular weight: 87.12 g/mol
IUPAC name: morpholine
SMILES: C1COCCN1
InChIKey: YNAVUWVOSKDBBP-UHFFFAOYSA-N
XLogP: -0.9
Polar surface area: 21.3 Å²
H-bond donors: 1
H-bond acceptors: 2
Formal charge: 0

via PubChem

Drug data · ChEMBL

Molecule type: Small molecule

via ChEMBL · EBI

Wikidata facts

Has part: oxygen
Mass: 87.068
Autonomy: 290

Show 23 more facts

immediately dangerous to life or health: 4984
Commons category: Morpholine
ionization energy: 8.20
chemical formula: C₄H₉NO
NIOSH Pocket Guide ID: 0437
lower flammable limit: 1.8
upper flammable limit: 15.2
time-weighted average exposure limit: 70
short-term exposure limit: 105
pKa: 8.50
electric dipole moment: 1.55
canonical SMILES: C1COCCN1
has characteristic: hygroscopy
refractive index: 1.4548
dynamic viscosity: 0.627
smells of: ammonia
melting point: 23
partition coefficient water/octanol: -0.86
median lethal dose (LD50): 500
density: 1.007
boiling point: 264
vapor pressure: 51.7
flash point: 37

Sources (4)

via Wikidata · CC0

Article · Русский

Морфоли́н — гетероциклическое соединение (тетрагидрооксазин-1,4). Химическая формула HN(CH2CH2)2O. Ядовит. Используется в органическом синтезе как катализатор в качестве основания (акцептор протона), в частности, для получения геминальных дитиолов.

Abstract from DBpedia / Wikipedia · CC BY-SA