Interesting facts
Exploring 2-(Dodecoxymethyl)oxirane
2-(Dodecoxymethyl)oxirane, commonly known as a specific type of oxirane compound, presents a fascinating area of study for chemists. This compound falls under the class of epoxides, characterized by its unique three-membered cyclic ether structure.
Key Characteristics
- Structure: The presence of an oxirane group indicates high reactivity, which is often utilized in various chemical reactions, including ring-opening and polymerization.
- Applications: It is known for its role in synthesizing complex molecules, making it valuable in pharmaceutical and polymer chemistry.
- Properties: The long dodecyl chain enhances its hydrophobic properties, which can be beneficial in creating surfactants and emulsifiers.
Interesting Insights
Chemists and researchers often explore 2-(dodecoxymethyl)oxirane because of its remarkable potential in industry and academia. Some things to consider include:
- Reactivity: The epoxide ring can be opened by various nucleophiles, leading to diverse synthetic pathways.
- Biological Impact: Studies show that certain oxirane compounds possess antimicrobial properties, which can be pivotal in developing new antibiotics.
- Environmental Considerations: Understanding its behavior in different environments is crucial, as long-chain alkyl compounds may affect ecosystems.
As a versatile compound, 2-(dodecoxymethyl)oxirane continues to draw attention in research. The balance of its chemical behavior and practical applications makes it a valuable focal point for scientific inquiry.
Synonyms
Lauryl glycidyl ether
2461-18-9
DODECYL GLYCIDYL ETHER
Glycidyl Lauryl Ether
N-Dodecyl glycidyl ether
Oxirane, 2-[(dodecyloxy)methyl]-
Ether, dodecyl 2,3-epoxypropyl
((Dodecyloxy)methyl)oxirane
Oxirane, ((dodecyloxy)methyl)-
Propane, 1-(dodecyloxy)-2,3-epoxy-
CCRIS 2635
HSDB 5462
[(Dodecyloxy)methyl]oxirane
EINECS 219-554-1
glycidyl dodecyl ether
DTXSID0025494
Oxirane, [(dodecyloxy)methyl]-
Oxirane, 2-((dodecyloxy)methyl)-
DENACOL EX 192
DTXCID605494
GLYCIDYL N-DODECYL ETHER
84653J97E3
DODECYL ALCOHOL GLYCIDYL ETHER
DODECYL 2,3-EPOXYPROPYL ETHER
1,2-EPOXY-3-(DODECYLOXY)PROPANE
nDodecyl glycidyl ether
1Dodecyl glycidyl ether
Ether, dodecyl 2,3epoxypropyl
Oxirane, ((dodecyloxy)methyl)
Propane, 1(dodecyloxy)2,3epoxy
219-554-1
2-(dodecoxymethyl)oxirane
2-[(Dodecyloxy)methyl]oxirane
laurylglycidylether
2-((Dodecyloxy)methyl)oxirane
dodecylglycidyl ether
1-Dodecyl glycidyl ether
UNII-84653J97E3
C12Ge cpd
DSSTox_CID_5494
DSSTox_RID_78656
DSSTox_GSID_28774
SCHEMBL15970
CHEMBL1574716
2-[(Dodecyloxy)methyl]oxirane #
Tox21_200787
Tox21_303452
[(DODECYLOXY)METHYL] OXIRANE
MFCD00022344
STL453740
AKOS024332807
1-DODECYL GLYCIDYL ETHER [HSDB]
NCGC00091870-01
NCGC00091870-02
NCGC00257384-01
NCGC00258341-01
AS-60945
CAS-2461-18-9
CAS-68609-97-2
CS-0320613
G0448
NS00020611
T72150
Q27269499
Solubility of 2-(dodecoxymethyl)oxirane
2-(Dodecoxymethyl)oxirane is a compound of particular interest when examining its solubility characteristics. Solubility can be influenced by various factors, such as the structure of the molecule, temperature, and the type of solvent used. Generally, the solubility of organic compounds can be summarized by the phrase "like dissolves like," which indicates that polar substances tend to dissolve well in polar solvents, while non-polar substances prefer non-polar solvents.
In the case of 2-(dodecoxymethyl)oxirane, several points can be made regarding its solubility:
In summary, while 2-(dodecoxymethyl)oxirane may not readily dissolve in polar solvents like water, it should show favorable solubility in non-polar organic solvents. Understanding the solubility aspects of this compound is essential for applications in various chemical processes and formulations.