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126527

Sigma-Aldrich

2,6-Dimethylmorpholine

97%

Synonym(s):

2,6-Dimethylmorpholine

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About This Item

Empirical Formula (Hill Notation):
C6H13NO
CAS Number:
Molecular Weight:
115.17
Beilstein:
103036
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

refractive index

n20/D 1.446 (lit.)

bp

147 °C (lit.)

mp

−85 °C (lit.)

density

0.935 g/mL at 25 °C (lit.)

functional group

ether

SMILES string

CC1CNCC(C)O1

InChI

1S/C6H13NO/c1-5-3-7-4-6(2)8-5/h5-7H,3-4H2,1-2H3

InChI key

HNVIQLPOGUDBSU-UHFFFAOYSA-N

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Application

cis-2,6-Dimethylmorpholine (DMMP) has been used in the preparation of microporous material composed of hybrid T2 and T3 supertetrahedral clusters.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Flam. Liq. 3 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

118.4 °F - closed cup

Flash Point(C)

48 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Xiaohui Han et al.
Chemical communications (Cambridge, England), 50(7), 796-798 (2013-12-03)
Solvothermal reactions of S, Ga and Sn using cis-2,6-dimethylmorpholine (DMMP) as an organic template, in the presence of a trace amount of H2O at 180 °C, generated microporous [C6H14NO]14.4[Ga6.40Sn21.60S52O8] material composed of hybrid T2 and T3 supertetrahedral clusters with a
S S Mirvish et al.
Cancer research, 43(6), 2550-2554 (1983-06-01)
We reported previously that mice exposed to atmospheric NO2 contained a nitrosating agent (NSA) that reacted with morpholine in aqueous methanol homogenates of the mice to give N-nitrosomorpholine. We have now found that N-nitrosomorpholine was also produced by reacting morpholine
Natalia Szkaradek et al.
Anti-cancer agents in medicinal chemistry, 19(16), 1949-1965 (2019-04-06)
Natural plant metabolites and their semisynthetic derivatives have been used for years in cancer therapy. Xanthones are oxygenated heterocyclic compounds produced as secondary metabolites by higher plants, fungi or lichens. Xanthone core may serve as a template in the synthesis

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