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Glycidyl allyl ether

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Identification
Molecular formula
C6H10O2
CAS number
106-92-3
IUPAC name
2-(allyloxymethyl)oxirane
State
State

At room temperature, glycidyl allyl ether is a liquid.

Melting point (Celsius)
-108.00
Melting point (Kelvin)
165.15
Boiling point (Celsius)
172.00
Boiling point (Kelvin)
445.15
General information
Molecular weight
114.14g/mol
Molar mass
114.1420g/mol
Density
0.9589g/cm3
Appearence

Glycidyl allyl ether typically appears as a clear, colorless liquid. It has a distinct, ether-like odor.

Comment on solubility

Solubility of 2-(allyloxymethyl)oxirane

The solubility characteristics of 2-(allyloxymethyl)oxirane are quite intriguing due to its unique structure. This compound, an epoxide, typically exhibits the following solubility properties:

  • Polar solvents: 2-(allyloxymethyl)oxirane is generally soluble in polar solvents such as water, methanol, and ethanol. This is primarily due to its ability to form hydrogen bonds, facilitating a greater interaction with polar environments.
  • Non-polar solvents: Conversely, this compound shows limited solubility in non-polar solvents such as hexane or toluene. The absence of significant polarity means that these solvents cannot adequately disrupt the intermolecular forces within the structure of the compound.
  • Temperature effects: The solubility of 2-(allyloxymethyl)oxirane can also be influenced by temperature. Generally, increasing the temperature enhances solubility in polar solvents, making it a crucial factor during practical applications.

It is essential to consider these factors when working with 2-(allyloxymethyl)oxirane in various chemical processes. As emphasized by the principle of “like dissolves like”, understanding the solubility of this compound is key to effectively utilizing it in research and industry.

Interesting facts

Interesting Facts about 2-(Allyloxymethyl)oxirane

2-(Allyloxymethyl)oxirane, commonly known as an epoxide, is a fascinating compound with unique properties and applications. As a building block in organic synthesis, this compound showcases the remarkable versatility of epoxides in various chemical reactions. Here are some engaging insights:

  • Structural Significance: The epoxide group features a three-membered ring that includes an oxygen and two carbon atoms, leading to high ring strain. This makes epoxides like 2-(Allyloxymethyl)oxirane highly reactive, allowing them to participate in nucleophilic reactions.
  • Versatile Reagent: It serves as an essential reagent in the synthesis of various organic compounds. Its unique structure allows for the creation of complex molecules, making it a valuable tool in both academic research and industrial applications.
  • Fine Chemical Intermediates: 2-(Allyloxymethyl)oxirane can be used as an intermediate in producing pharmaceuticals and agrochemicals. Its application in synthesizing larger molecules helps accelerate the development of new drugs.
  • Polymer Chemistry: This compound can be utilized in polymerization processes. Its ability to react with various nucleophiles allows for the design of new materials with desirable properties, such as increased durability and flexibility.
  • Environmental Impacts: While useful in many applications, it’s essential for chemists to assess the environmental and health impacts of such compounds. Continuous research is necessary to find greener and safer alternatives for its applications.

In conclusion, 2-(Allyloxymethyl)oxirane stands out not only for its structural characteristics but also for its significance in the field of organic chemistry. As scientists and students explore its potential, they contribute to the evolving world of chemical compounds and their myriad applications.

Synonyms
ALLYL GLYCIDYL ETHER
106-92-3
Glycidyl allyl ether
Oxirane, [(2-propenyloxy)methyl]-
Allyl 2,3-epoxypropyl ether
Allylglycidaether
Allil-glicidil-etere
1,2-Epoxy-3-allyloxypropane
1-Allyloxy-2,3-epoxypropane
Denacol EX 111
Propane, 1-(allyloxy)-2,3-epoxy-
1-Allyloxy-2,3-epoxypropan
Ether, allyl 2,3-epoxypropyl
Oxyde d'allyle et de glycidyle
1-Allilossi-2,3 epossipropano
1-Allyloxy-2,3-epoxy-propaan
2-(prop-2-enoxymethyl)oxirane
1-(Allyloxy)-2,3-epoxypropane
Allylglycidaether [German]
NCI-C56666
NSC 18596
M 560
CCRIS 2375
HSDB 505
Allil-glicidil-etere [Italian]
2,3-Epoxypropyl-1-allyl ether
Ageflex AGE
Sipomer AGE
Allylglycide ether
allylglycidyl ether
Oxirane, ((2-propenyloxy)methyl)-
EINECS 203-442-4
UN2219
1-Allyloxy-2,3-epoxypropan [German]
1-Allyloxy-2,3-epoxy-propaan [Dutch]
BRN 0105871
[(2-Propenyloxy)methyl]oxirane
Oxyde d'allyle et de glycidyle [French]
1-Allilossi-2,3 epossipropano [Italian]
DTXSID9039232
UNII-HDC0791894
AI3-37791
NSC-631
2-Allyloxymethyl-oxirane
NSC-18596
HDC0791894
1-Allyl-2,3-epoxypropane
DTXCID6046
2-[(Allyloxy)methyl]oxirane
Oxirane, 2-((2-propen-1-yloxy)methyl)-
AGE
((ALLYLOXY)METHYL)OXIRANE
[(2-Propenyloxy)methyl] oxirane
EC 203-442-4
5-17-03-00012 (Beilstein Handbook Reference)
ALLYL GLYCIDYL ETHER [HSDB]
Ether,3-epoxypropyl
(+/-)-ALLYL GLYCIDYL ETHER
UN 2219
Oxirane, 2-[(2-propen-1-yloxy)methyl]-
WLN: T3OTJ B1O2U1
((2-propenyloxy)methyl)oxirane
[(ALLYLOXY)METHYL]OXIRANE
ALLYLGLYCIDAETHER (GERMAN)
Oxirane,[(2-propenyloxy)methyl]-
2-((ALLYLOXY)METHYL)OXIRANE
ALLIL-GLICIDIL-ETERE (ITALIAN)
((2-PROPENYLOXY)METHYL) OXIRANE
PAGE 10
1-ALLYLOXY-2,3-EPOXYPROPAN (GERMAN)
1-ALLYLOXY-2,3-EPOXY-PROPAAN (DUTCH)
1-ALLILOSSI-2,3 EPOSSIPROPANO (ITALIAN)
OXYDE D'ALLYLE ET DE GLYCIDYLE (FRENCH)
MFCD00005143
1Allyloxy2,3epoxypropane
2-(allyloxymethyl)oxirane
Allyl glycidyl ether, 99%
SCHEMBL15162
Allyl glycidyl ether, >=99%
NSC631
ALLYL OXIRANEMETHYL ETHER
2-[(Allyloxy)methyl]oxirane #
CHEMBL1528174
GLYCIDYL 2-PROPENYL ETHER
(R)-2-[(Allyloxy)methyl]oxirane
(+-)-ALLYL GLYCIDYL ETHER
NSC18596
Allyl glycidyl ether (ACGIH:OSHA)
Tox21_200389
Allyl 2,3-epoxypropyl ether; 98%
AKOS015901458
(.+-.)-ALLYL GLYCIDYL ETHER
2-((2-Propen-1-yloxy)methyl)oxirane
AT32916
NCGC00091526-01
NCGC00091526-02
NCGC00257943-01
90907-93-0
CAS-106-92-3
SY391580
Propane, 1-(allyloxy)-2,3-epoxy-(8CI)
A0221
NS00002883
Allyl glycidyl ether [UN2219] [Flammable liquid]
Q2467070
F1995-0410
95043-56-4