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Glycidyl isopropyl ether

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Identification
Molecular formula
C6H12O2
CAS number
4016-14-2
IUPAC name
2-(isopropoxymethyl)oxirane
State
State

At room temperature, glycidyl isopropyl ether is in a liquid state. It maintains this state due to its relatively low melting point, making it suitable for various chemical applications that require a liquid reagent.

Melting point (Celsius)
-125.00
Melting point (Kelvin)
148.15
Boiling point (Celsius)
149.00
Boiling point (Kelvin)
422.15
General information
Molecular weight
116.16g/mol
Molar mass
116.1580g/mol
Density
0.9415g/cm3
Appearence

Glycidyl isopropyl ether appears as a clear, colorless liquid. It is typically free from any suspended particulate matter or sediments, which is indicative of its purity. This compound is often noted for its ether-like smell.

Comment on solubility

Solubility of 2-(isopropoxymethyl)oxirane

2-(isopropoxymethyl)oxirane, also known as a glycidyl ether, exhibits interesting solubility characteristics that make it notable in various applications. Understanding its solubility can provide insights into its behavior in different environments:

  • Solvent Compatibility: This compound is generally soluble in organic solvents such as ethers, alcohols, and hydrocarbons, while showing limited solubility in water due to its hydrophobic isopropoxy group.
  • Temperature Influence: Solubility can increase with temperature, which is a common trait among organic compounds. As temperature rises, the molecular motion enhances, facilitating better interactions with solvents.
  • Functional Group Impact: The presence of both an ether moiety and a cyclic structure influences solubility, making it more amenable to polar aprotic solvents.

In summary, the solubility of 2-(isopropoxymethyl)oxirane is influenced by its molecular structure, specific solvent properties, and environmental factors. Understanding these aspects is crucial for effectively utilizing this compound in various chemical processes.

Interesting facts

Interesting Facts about 2-(Isopropoxymethyl)oxirane

2-(Isopropoxymethyl)oxirane, commonly referred to in various chemical studies, is an intriguing compound with a unique structure and versatile applications. Here are some notable aspects of this compound:

  • Structure and Reactivity: As a member of the epoxide family, 2-(isopropoxymethyl)oxirane features a three-membered cyclic ether. This distinctive structure contributes to its high reactivity, making it an excellent candidate for various chemical transformations.
  • Synthesis: This compound can be synthesized through different routes, often involving the reaction of epichlorohydrin with isopropyl alcohol under acidic or basic conditions. This synthesis pathway showcases the compound's accessibility for further research and application.
  • Applications: The versatility of 2-(isopropoxymethyl)oxirane allows it to be utilized in several fields, including:
    • As an intermediate in the production of pharmaceuticals.
    • In the formulation of specialty coatings and adhesives.
    • In polymer chemistry for the development of new materials.
  • Toxicity and Safety: While exploring this compound, safety should be a priority. Epoxides, including 2-(isopropoxymethyl)oxirane, can be toxic and reactive, necessitating careful handling and adherence to safety protocols during experimentation.
  • Research Significance: Studies on this compound contribute to broader chemical knowledge, particularly in areas involving polymerization and ring-opening reactions. The ability to modify its structure opens the door to developing novel compounds with desirable properties.

In summary, 2-(isopropoxymethyl)oxirane showcases the intersection of reactivity and applications in modern chemistry. Whether for its structural nuances or its potential in industrial applications, this compound remains a point of interest for chemists and researchers alike.

Synonyms
Glycidyl isopropyl ether
4016-14-2
ISOPROPYL GLYCIDYL ETHER
2,3-Epoxypropyl isopropyl ether
(Isopropoxymethyl)oxirane
2-(Isopropoxymethyl)oxirane
3-Isopropyloxypropylene oxide
3-Isopropoxy-1,2-epoxypropane
Isopropyl epoxypropyl ether
Propane, 1,2-epoxy-3-isopropoxy-
NCI-C56439
1,2-Epoxy-3-isopropoxypropane
((1-Methylethoxy)methyl)oxirane
2,3-Epoxypropyl-isopropyl ether
NSC 4127
Oxirane, ((1-methylethoxy)methyl)-
Oxirane, [(1-methylethoxy)methyl]-
NSC 46562
CCRIS 2631
HSDB 4302
EINECS 223-672-9
Isopropyl glycidyl ether IGE
BRN 0103028
DTXSID6025480
AI3-52929
NSC-4127
NSC-46562
Oxirane, 2-((1-methylethoxy)methyl)-
DTXCID705480
1V3116630G
(ISOPROPYLOXYMETHYL)OXIRANE
2-[(1-methylethoxy)methyl]oxirane
ISOPROPYL GLYCIDYL ETHER [HSDB]
Oxirane, 2-[(1-methylethoxy)methyl]-
2-((1-METHYLETHOXY)METHYL)OXIRANE
Isopropoxymethyl oxirane
1,2Epoxy3isopropoxypropane
3Isopropoxy1,2epoxypropane
3Isopropyloxypropylene oxide
2,3Epoxypropylisopropyl ether
Propane, 1,2epoxy3isopropoxy
((1Methylethoxy)methyl)oxirane
2,3Epoxypropyl isopropyl ether
Isopropyl glycidyl ether (ACGIH:OSHA)
Oxirane, ((1-methylethoxy)methyl)-(9CI)
223-672-9
glycidylisopropylether
2-(propan-2-yloxymethyl)oxirane
2-[(propan-2-yloxy)methyl]oxirane
isopropylglycidyl ether
IGE
MFCD00005139
Glycidyl isopropyl ether purum
Propane,2-epoxy-3-isopropoxy-
WLN: T3OTJ B1OY1&1
UNII-1V3116630G
SCHEMBL39030
MLS002454412
2-(Isopropoxymethyl)oxirane #
Glycidyl isopropyl ether, 98%
CHEMBL1487011
1,2-Epoxy-3-iso-propoxypropane
NWLUZGJDEZBBRH-UHFFFAOYSA-
NSC4127
HMS3039F15
NSC46562
Tox21_200038
BBL027498
STK802341
AKOS000196880
AKOS017283448
NCGC00091815-01
NCGC00091815-02
NCGC00257592-01
FG166995
SMR001372011
SY051643
VS-08554
CAS-4016-14-2
DB-103806
GLYCIDYL ISOPROPYL ETHER, (+/-)-
G0255
NS00020644
EN300-22498
E78219
Glycidyl isopropyl ether, purum, >=98.0% (GC)
Q2803610
F0001-1133
Z147642824
InChI=1/C6H12O2/c1-5(2)7-3-6-4-8-6/h5-6H,3-4H2,1-2H3