Morpholine

Morpholine
Names
Preferred IUPAC name
Morpholine
Other names
Diethylenimide oxide
1,4-Oxazinane
Tetrahydro-1,4-oxazine
Diethylene imidoxide
Diethylene oximide
Tetrahydro-p-oxazine
Identifiers
3D model (JSmol)
102549
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.003.469
EC Number
  • 203-815-1
1803
KEGG
RTECS number
  • QD6475000
UNII
UN number 2054
  • InChI=1S/C4H9NO/c1-3-6-4-2-5-1/h5H,1-4H2 Y
    Key: YNAVUWVOSKDBBP-UHFFFAOYSA-N Y
  • InChI=1/C4H9NO/c1-3-6-4-2-5-1/h5H,1-4H2
    Key: YNAVUWVOSKDBBP-UHFFFAOYAU
  • C1CNCCO1
Properties
C4H9NO
Molar mass 87.122 g·mol−1
Appearance Colorless liquid
Odor Weak ammonia-like or fish-like
Density 1.007 g/cm3
Melting point −5 °C (23 °F; 268 K)
Boiling point 129 °C (264 °F; 402 K)
miscible
Vapor pressure 6 mmHg (20 °C)
Acidity (pKa) 8.36 (of conjugate acid)
−55.0·10−6 cm3/mol
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Flammable, Corrosive
GHS labelling:
Danger
H226, H302, H312, H314, H332
P210, P233, P240, P241, P242, P243, P260, P261, P264, P270, P271, P280, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P312, P304+P340, P305+P351+P338, P310, P312, P321, P322, P330, P363, P370+P378, P403+P235, P405, P501
NFPA 704 (fire diamond)
3
3
0
Flash point 31 °C (88 °F; 304 K)
275 °C (527 °F; 548 K)
Explosive limits 1.4%–11.2%
Lethal dose or concentration (LD, LC):
1220 mg/kg (mammal, oral)
525 mg/kg (mouse, oral)
1050 mg/kg (rat, oral)
365 ppm (mouse, 2 hr)
NIOSH (US health exposure limits):
PEL (Permissible)
TWA 20 ppm (70 mg/m3) [skin]
REL (Recommended)
TWA 20 ppm (70 mg/m3) ST 30 ppm (105 mg/m3) [skin]
IDLH (Immediate danger)
1400 ppm
Safety data sheet (SDS) hazard.com
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

Morpholine is an organic chemical compound having the chemical formula O(CH2CH2)2NH. This heterocycle features both amine and ether functional groups. Because of the amine, morpholine is a base; its conjugate acid is called morpholinium. For example, treating morpholine with hydrochloric acid generates the salt morpholinium chloride. It is a colorless liquid with a weak, ammonia- or fish-like odor. The naming of morpholine is attributed to Ludwig Knorr, who incorrectly believed it to be part of the structure of morphine.