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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:
141-91-3
Molecular Weight:
115.17
Beilstein/REAXYS Number:
103036
EC Number:
205-509-3
MDL number:
MFCD00005973
UNSPSC Code:
12352100
PubChem Substance ID:
24847731
NACRES:
NA.22

Quality Level

100

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.

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Danger

Hazard Classifications

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

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

118.4 °F - closed cup

flash_point_c

48 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
03807EJ
07220JX
05127AW
06909CX

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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
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
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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