137448
2-Methyl-2-oxazoline
98%
Synonym(s):
2-Methyloxazoline
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About This Item
Empirical Formula (Hill Notation):
C4H7NO
CAS Number:
Molecular Weight:
85.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
214-316-3
Beilstein/REAXYS Number:
104227
MDL number:
Assay:
98%
Form:
liquid
InChI key
GUXJXWKCUUWCLX-UHFFFAOYSA-N
InChI
1S/C4H7NO/c1-4-5-2-3-6-4/h2-3H2,1H3
SMILES string
CC1=NCCO1
assay
98%
form
liquid
Quality Level
bp
109.5-110.5 °C (lit.)
density
1.005 g/mL at 25 °C (lit.)
Related Categories
General description
2-Methyl-2-oxazoline undergoes polymerization with 2-butyl-2-oxazoline to form poly(2-oxazoline) block copolymer. It undergoes cationic ring-opening polymerization with 2-(dec-9-enyl)-2-oxazoline to yield copoly(2-oxazoline)s.
Application
2-Methyl-2-oxazoline was used in cationic polymerization of a series of linear 2-alkyl-2-oxazolines under microwave irradiation.
signalword
Danger
hcodes
pcodes
Hazard Classifications
Flam. Liq. 2
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
68.0 °F - closed cup
flash_point_c
20 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Yunjiao Che et al.
Soft matter, 16(29), 6733-6742 (2020-06-27)
We report a novel double cross-linked hydrogel system based on polyacrylamide and poly(2-methyl-2-oxazoline) (PMOXA) network chains, as well as on supramolecular host-guest interactions with on-demand tailored mechanical properties. Well-defined vinyl-bearing PMOXA macromonomers, functionalized with either β-cyclodextrin units (β-CD-PMOXA) or adamantane
Giulia Morgese et al.
ACS nano, 11(3), 2794-2804 (2017-03-09)
Osteoarthritis leads to an alteration in the composition of the synovial fluid, which is associated with an increase in friction and the progressive and irreversible destruction of the articular cartilage. In order to tackle this degenerative disease, there has been
Microwave-assisted synthesis and properties of a series of poly (2-alkyl-2-oxazoline) s.
Hoogenboom R, et al.
Designed Monomers and Polymers, 8(6), 659-671 (2005)
Pavel Sťahel et al.
Polymers, 11(12) (2019-12-18)
Polyoxazolines are a new promising class of polymers for biomedical applications. Antibiofouling polyoxazoline coatings can suppress bacterial colonization of medical devices, which can cause infections to patients. However, the creation of oxazoline-based films using conventional methods is difficult. This study
Ke Mao et al.
Talanta, 168, 230-239 (2017-04-11)
In this work, a one-step coating procedure by a simple annealing protocol of poly (2-methyl-2-oxazoline)-random-glycidyl methacrylate (PMOXA-r-GMA) copolymer was used to yield covalent and cross-linked PMOXA-based antifouling coating on a fused-silica capillary inner surface, which was used to determine the
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