Cas no 5137-45-1 (Ethylene glycol ethyl methyl ether)
Ethylene glycol ethyl methyl ether Chemical and Physical Properties
Names and Identifiers
-
- Ethylene glycol ethyl methyl ether
- 1-Aethoxy-2-methoxy-aethan
- 1-ethoxy-2-methoxy-ethane
- 1-methoxy-2-ethoxyethane
- Aethylenglykol-methylaether-aethylaether
- Ethane,1-ethoxy-2-methoxy
- Ethylene glycol ethyl methyl ether,stab. with 0. BHT
- methyl ethyl cellosolve
- methylglycolmonoethylether
- monomethyl ether of ethyl glycol
- CAQYAZNFWDDMIT-UHFFFAOYSA-N
- SCHEMBL7415141
- 5137-45-1
- SCHEMBL12228
- 2,5-Dioxaheptane
- 1-Ethoxy-2-methoxyethane
- 500005-27-6
- EINECS 225-893-6
- FT-0635555
- DTXSID40964490
- NS00045456
- Ethane, 1-ethoxy-2-methoxy-
- MFCD00048580
- DB-051953
-
- MDL: MFCD00048580
- Inchi: 1S/C5H12O2/c1-3-7-5-4-6-2/h3-5H2,1-2H3
- InChI Key: CAQYAZNFWDDMIT-UHFFFAOYSA-N
- SMILES: O(CC)CCOC
Computed Properties
- Exact Mass: 104.08400
- Monoisotopic Mass: 104.084
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 7
- Rotatable Bond Count: 4
- Complexity: 29.3
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Surface Charge: 0
- XLogP3: 0.3
- Topological Polar Surface Area: 18.5
Experimental Properties
- Color/Form: colorless liquid
- Density: 0.850
- Boiling Point: 100-102°C
- Flash Point: 100-102°C
- Refractive Index: 1.3870
- Water Partition Coefficient: Fully miscible in water.
- PSA: 18.46000
- LogP: 0.66930
- Solubility: Uncertain
Ethylene glycol ethyl methyl ether Security Information
- Hazardous Material transportation number:UN 3271
- Safety Instruction: S23; S24/25
- HazardClass:3
- PackingGroup:II
- Packing Group:II
- Packing Group:II
Ethylene glycol ethyl methyl ether Customs Data
- HS CODE:2909199090
- Customs Data:
China Customs Code:
2909199090Overview:
2909199090. Other acyclic ethers and their halogenated derivatives(Including sulfonation,Nitrosative or nitrosative derivatives). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:5.5%. general tariff:30.0%
Declaration elements:
Product Name, component content, use to
Summary:
2909199090. other acyclic ethers and their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%
Ethylene glycol ethyl methyl ether Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| A FA AI SHA , SAI MO FEI SHI ER KE JI QI XIA GONG SI | B20819-10g |
Ethylene glycol ethyl methyl ether, 97%, stab. with 0.01% BHT |
5137-45-1 | stab. with 0.01% | 10g |
¥734.00 | 2023-03-15 | |
| A FA AI SHA , SAI MO FEI SHI ER KE JI QI XIA GONG SI | B20819-50g |
Ethylene glycol ethyl methyl ether, 97%, stab. with 0.01% BHT |
5137-45-1 | stab. with 0.01% | 50g |
¥2833.00 | 2023-03-15 | |
| abcr | AB126342-10 g |
Ethylene glycol ethyl methyl ether, 97%; . |
5137-45-1 | 97% | 10g |
€64.40 | 2023-05-10 | |
| abcr | AB126342-50 g |
Ethylene glycol ethyl methyl ether, 97%; . |
5137-45-1 | 97% | 50g |
€143.80 | 2023-05-10 | |
| SHENG KE LU SI SHENG WU JI SHU | sc-279153-10 g |
Ethylene glycol ethyl methyl ether, |
5137-45-1 | 10g |
¥639.00 | 2023-07-11 | ||
| SHENG KE LU SI SHENG WU JI SHU | sc-279153-10g |
Ethylene glycol ethyl methyl ether, |
5137-45-1 | 10g |
¥639.00 | 2023-09-05 | ||
| abcr | AB126342-10g |
Ethylene glycol ethyl methyl ether, 97%; . |
5137-45-1 | 97% | 10g |
€66.00 | 2025-02-21 | |
| abcr | AB126342-50g |
Ethylene glycol ethyl methyl ether, 97%; . |
5137-45-1 | 97% | 50g |
€148.60 | 2025-02-21 | |
| 1PlusChem | 1P003QZ5-5g |
ETHYLENE GLYCOL ETHYL METHYL ETHER |
5137-45-1 | 5g |
$66.00 | 2024-04-30 | ||
| 1PlusChem | 1P003QZ5-25g |
ETHYLENE GLYCOL ETHYL METHYL ETHER |
5137-45-1 | 25g |
$177.00 | 2024-04-30 |
Ethylene glycol ethyl methyl ether Related Literature
-
Yuankun Wang,Zhiming Li,Yunpeng Hou,Zhimeng Hao,Qiu Zhang,Youxuan Ni,Yong Lu,Zhenhua Yan,Kai Zhang,Qing Zhao,Fujun Li,Jun Chen Chem. Soc. Rev. 2023 52 2713
-
2. Thermodynamic functions of hydration of saturated uncharged organic compounds. Free energies, enthalpies and entropies at 25°CSergio Cabani,Paolo Gianni J. Chem. Soc. Faraday Trans. 1 1979 75 1184
Additional information on Ethylene glycol ethyl methyl ether
Ethylene glycol ethyl methyl ether (CAS No. 5137-45-1): A Comprehensive Overview
Ethylene glycol ethyl methyl ether, chemically identified by the CAS number 5137-45-1, is a significant compound in the realm of organic chemistry and industrial applications. This ether derivative, characterized by its unique molecular structure, has garnered attention due to its versatile properties and potential uses in various scientific and commercial domains.
The molecular formula of ethylene glycol ethyl methyl ether is C?H??O, reflecting its composition of four carbon atoms, ten hydrogen atoms, and one oxygen atom. This structure imparts upon it a distinct set of chemical and physical properties that make it valuable in multiple contexts. As an isomer of butanone oxime, it shares some structural similarities but exhibits different reactivity and functionality.
In recent years, the study of ethers has seen considerable advancements, particularly in their role as solvents and intermediates in chemical synthesis. Ethylene glycol ethyl methyl ether has been explored for its ability to dissolve a wide range of organic compounds, making it a candidate for use in pharmaceutical formulations and laboratory research. Its low toxicity profile compared to other solvents has further enhanced its appeal in these applications.
One of the most intriguing aspects of ethylene glycol ethyl methyl ether is its potential application in the development of novel materials. Researchers have been investigating its use as a precursor for polymers and coatings that exhibit enhanced durability and chemical resistance. These properties make it particularly useful in environments where exposure to harsh chemicals is a concern.
The compound's role in pharmaceutical research is also noteworthy. Its solvent properties have been leveraged in the synthesis of complex molecules, including active pharmaceutical ingredients (APIs). Studies have shown that it can facilitate reactions that would otherwise be inefficient or impossible with other solvents. This capability is crucial in the pursuit of new drug candidates and improvements to existing medications.
Moreover, ethylene glycol ethyl methyl ether has found utility in the field of analytical chemistry. Its ability to act as a mobile phase in gas chromatography (GC) has enabled more precise separation and identification of organic compounds. This application is particularly valuable in environmental monitoring and forensic analysis, where the detection of trace substances is often required.
The industrial use of this compound extends to the production of specialty chemicals. It serves as a building block for more complex molecules, contributing to the synthesis of agrochemicals, fragrances, and other fine chemicals. Its versatility makes it a preferred choice for manufacturers seeking efficient and cost-effective synthetic routes.
In terms of safety and handling, ethylene glycol ethyl methyl ether is generally considered to be non-hazardous under normal conditions. However, like all chemical compounds, it requires proper handling procedures to ensure safe usage. Proper ventilation, personal protective equipment (PPE), and adherence to safety protocols are essential when working with this substance.
The environmental impact of using ethylene glycol ethyl methyl ether has also been a subject of interest. Research indicates that it biodegrades relatively quickly under natural conditions, minimizing long-term environmental persistence. This characteristic aligns with the growing emphasis on sustainable chemistry practices, where minimizing ecological footprints is paramount.
Future research directions for this compound are promising. Scientists are exploring its potential as a green solvent alternative, particularly in processes where traditional solvents pose environmental or health risks. Additionally, its role in catalytic systems is being investigated to improve reaction efficiencies and selectivities.
The integration of computational methods into the study of ethylene glycol ethyl methyl ether has also opened new avenues for discovery. Molecular modeling techniques allow researchers to predict properties and reactivities with high accuracy, accelerating the development of new applications without extensive experimental trials.
In conclusion, ethylene glycol ethyl methyl ether (CAS No. 5137-45-1) stands out as a multifaceted compound with significant implications across various sectors. Its unique properties make it indispensable in pharmaceuticals, materials science, analytical chemistry, and industrial manufacturing. As research continues to uncover new applications and refine existing ones, this compound will undoubtedly remain at the forefront of chemical innovation.
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