Basic information Safety Supplier Related

2-METHYL-2-OXAZOLINE

Basic information Safety Supplier Related

2-METHYL-2-OXAZOLINE Basic information

Product Name:
2-METHYL-2-OXAZOLINE
Synonyms:
  • 2-Methyl-2-oxazoline, 99% 100GR
  • 4,5-Dihydro-2-methyl-1,3-oxazole
  • 2-Methyl-2-oxazoline 98%
  • NSC 43141
  • 4,5-Dihydro-2-methyloxazole
  • 2-Methyl-2-oxazoline,99%
  • 2-Methyl-4,5-dihydro-1,3-oxazole
  • 2-Methyloxazoline
CAS:
1120-64-5
MF:
C4H7NO
MW:
85.1
EINECS:
214-316-3
Product Categories:
  • Oxazolines/Oxazolidines
  • Building Blocks
  • Heterocyclic Building Blocks
Mol File:
1120-64-5.mol
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2-METHYL-2-OXAZOLINE Chemical Properties

Boiling point:
109.5-110.5 °C(lit.)
Density 
1.005 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.434(lit.)
Flash point:
68 °F
storage temp. 
Sealed in dry,Room Temperature
form 
Liquid
pka
5.77±0.50(Predicted)
Specific Gravity
1.01
color 
Clear colorless to very faint yellow
Water Solubility 
Soluble in water (7051 mg/L at 25°C).
BRN 
104227
LogP
0.058 (est)
CAS DataBase Reference
1120-64-5(CAS DataBase Reference)
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Safety Information

Hazard Codes 
F
Risk Statements 
11
Safety Statements 
23-24/25
RIDADR 
UN 1993 3/PG 2
WGK Germany 
3
HazardClass 
3
PackingGroup 
II
HS Code 
29339900

MSDS

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2-METHYL-2-OXAZOLINE Usage And Synthesis

Chemical Properties

CLEAR COLOURLESS TO VERY FAINT YELLOW LIQUID

Uses

2-Methyl-2-oxazoline is used in cationic polymerization of a series of linear 2-alkyl-2-oxazolines under microwave irradiation. It 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. It react with N'-phenyl-benzohydrazonoyl chloride to get 4-(2-hydroxyethyl)-5-methyl-1,3-diphenyl-1,2,4-triazol-4-ium chloride.

Definition

ChEBI: A 5-membered heterocyclic compound, which is substituted in the 2-position with a methyl group and which is often used as a monomer in polymerisation reactions.

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.

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