2-Ethoxyethyl ether - ≥98% , CAS No.112-36-7

CAS: 112-36-7 Cat. No.: E100702 Peso molecular: 162.23 Beilstein Registry Number: 1699259 Número EC: 203-963-7

GRADE & PURITY ≥98%

Synonyms

Diethyl ene glycol diethyl ether | diethoxydiglycol | MFCD00009254 | 1,1'-oxybis(2-ethoxyethane) | NCGC00255128-01 | HISOLVE EDE | Diethyldiethylene glycol | DIETHYLENE GLYCOL DIETHYL ETHER [HSDB] | 1,5-diethoxy-3-oxapentane | DEGDEE | AKOS015915322 | 1-E

Storage

Argon charged,Room temperature

Shipped In

Normal

Descripción general

Diethylene glycol diethyl ether is used as a solvent for reactions performed at higher temperatures. It is involved in the preparation of nitrocellulose, resins and adhesives. It is utilized as a scrubbing medium to absorb carbonyl sulfide (COS), an impurity in petroleum refineries.

Specifications

Sinónimos

Diethyl ene glycol diethyl ether | diethoxydiglycol | MFCD00009254 | 1, 1'-oxybis(2-ethoxyethane) | NCGC00255128-01 | HISOLVE EDE | Diethyldiethylene glycol | DIETHYLENE GLYCOL DIETHYL ETHER [HSDB] | 1, 5-diethoxy-3-oxapentane | DEGDEE | AKOS015915322 | 1-E

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 508812673
• Sonrisas canónicas: CCOCCOCCOCC
• IUPAC Name: 1-ethoxy-2-(2-ethoxyethoxy)ethane
• InChIKey: RRQYJINTUHWNHW-UHFFFAOYSA-N
• INCHI: 1S/C8H18O3/c1-3-9-5-7-11-8-6-10-4-2/h3-8H2,1-2H3
• Isómeros SMILES: CCOCCOCCOCC
• WGK Alemania: 2
• RTECS: KN3160000
• Número ONU: 1993
• Grupo de embalaje: I
• Peso molecular: 162.23
• Beilstein: 1699259
• Reaxy-Rn: 1699259
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1699259&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Clase Organooxygen compounds
      • Subclass Ethers

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: Organooxygen compounds
• Subclass: Ethers
• Intermediate Tree Nodes: Not available
• Direct Parent: Dialkyl ethers
• Alternative Parents: Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Dialkyl ether - Hydrocarbon derivative - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as dialkyl ethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are alkyl groups.
• External Descriptors: polyether

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Solubilidad: Miscible with hydrocarbons, ethanol, ethyl ether and organic solvents. Immiscible with water.
• Sensibilidad: Air sensitive
• Índice de refracción: 1.4115
• Punto de inflamación (°F): 159.8 ℉
• Punto de inflamación (°C): 71℃
• Punto de ebullición (°C): 188°C
• Punto de fusión (°C): -44°C(lit.)
• Peso molecular: 162.230 g/mol
• XLogP3: 0.400
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 8
• Exact Mass: 162.126 Da
• Monoisotopic Mass: 162.126 Da
• Topological Polar Surface Area: 27.700 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 58.400
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Shumin Hong, Ting Li, Min Xiao, Teerawat Sema, Hongxia Gao, Zhiwu Liang.  (2023)  A low energy-consuming phase change absorbent of MAE/DGM/H2O for CO2 capture.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.148079]

2. Yan Li, Ying Dai, Wei Dai, Feiqiang He, Zhuyao Li, Xing Zhong, Qinqin Tao.  (2023)  Bifunctional solid-state ionic liquid supported amidoxime chitosan adsorbents for Th(IV) and U(VI): Enhanced adsorption capacity from the synergistic effect.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:38096930] [10.1016/j.ijbiomac.2023.128708]

3. Zetian Zhang, Hao Liu, Tiandu Dong, Yingjiao Deng, Yunxi Li, Chuanrui Lu, Wendi Jia, Zihan Meng, Mingzheng Zhou, Haolin Tang.  (2023)  Phosphonate poly(vinylbenzyl chloride)-Modified Sulfonated poly(aryl ether nitrile) for Blend Proton Exchange Membranes: Enhanced Mechanical and Electrochemical Properties.  Polymers,  15  (15): (3203).  [PMID:37571097] [10.3390/polym15153203]

4. Yanqun Yang, Yipeng Huang, Zhuqiang Wu, Rui Shi, Zhengyi Chen, Guihua Ruan.  (2022)  Porous capillary monolithic column coupled with ultrahigh performance liquid chromatography-tandem mass spectrometry for fast and effective separation and determination of estrogens.  ANALYTICA CHIMICA ACTA,      [PMID:36089309] [10.1016/j.aca.2022.340270]

5. Qianchun Zhang, Xiaolan Zhang, Bingnian Yang, Shan Liu, Ming Wen, Linchun Bao, Li Jiang.  (2021)  Development of a highly efficient in-tube solid-phase microextraction system coupled with UHPLC-MS/MS for analyzing trace hydroxyl polycyclic aromatic hydrocarbons in biological samples.  JOURNAL OF SEPARATION SCIENCE,  45  (4): (919-928).  [PMID:34923746] [10.1002/jssc.202100751]

6. Wei Wang, Zhi Yun, Zhigang Tang, Xia Gui.  (2015)  Solubilities of CO2 in some glycol ethers under high pressure by experimental determination and correlation.  CHINESE JOURNAL OF CHEMICAL ENGINEERING,      [PMID:] [10.1016/j.cjche.2015.08.007]

7. Runfen Zheng, Lixin Wei, Yuxin Bai, Jianfei Man, Jian Ye, Huiping Zhang, Yihan Wang.  (2025)  CO2 Capture Performance of the DEGDEE-AEEA-AMP Ternary Phase-Change Absorbent.  ENERGY & FUELS,      [PMID:] [10.1021/acs.energyfuels.5c00759]

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