Propyl Ether - ≥98%(GC) , CAS No.111-43-3

CAS: 111-43-3 Cat. No.: P160596 Peso molecular: 102.18 Beilstein Registry Number: 1731310 Número EC: 203-869-6 PubChem CID: 8114

GRADE & PURITY ≥98%(GC)

Synonyms

MFCD00009376 | PROPYL ETHER [HSDB] | Di-n-propyl ether | AKOS005258382 | LS-13215 | NCGC00248266-01 | 1,1'-oxydipropane | 1-Propoxypropane | 1,1'-OXYBIS(PROPANE) | Dipropyl ether, >=99% | (n-C3H7)2O | Dipropyl oxide | J-640290 | DTXSID8042343 | 1,1'-Oxybi

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

Descripción general

application：

Dipropyl ether was used to study the low proton-transporting ability of a water molecule in the excited-state proton transfer (ESPT) of a 7-azaindole (7AI) moiety.

Specifications

Sinónimos

MFCD00009376 | PROPYL ETHER [HSDB] | Di-n-propyl ether | AKOS005258382 | LS-13215 | NCGC00248266-01 | 1, 1'-oxydipropane | 1-Propoxypropane | 1, 1'-OXYBIS(PROPANE) | Dipropyl ether, >=99% | (n-C3H7)2O | Dipropyl oxide | J-640290 | DTXSID8042343 | 1, 1'-Oxybi

Especificaciones y pureza

≥98%(GC)

Condiciones de almacenamiento de almacenamiento

Room temperature, Argon charged

Enviado en

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Pureza

≥98%(GC)

Nombres e identificadores

• Pubchem Sid: 504751585
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504751585
• Sonrisas canónicas: CCCOCCC
• IUPAC Name: 1-propoxypropane
• InChIKey: POLCUAVZOMRGSN-UHFFFAOYSA-N
• INCHI: 1S/C6H14O/c1-3-5-7-6-4-2/h3-6H2,1-2H3
• Isómeros SMILES: CCCOCCC
• WGK Alemania: 1
• RTECS: UJ5125000
• PubChem CID: 8114
• Número ONU: 2384
• Grupo de embalaje: II
• Peso molecular: 102.18
• Beilstein: 1731310
• Reaxy-Rn: 1731312

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: a small molecule

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: It is slightly soluble in water 3 g/L (20°C), soluble in alcohol and ether.
• Índice de refracción: 1.38
• Punto de inflamación (°F): -18.4 °F
• Punto de inflamación (°C): 21°C(lit.)
• Punto de ebullición (°C): 90°C
• Punto de fusión (°C): -123 °C
• Peso molecular: 102.170 g/mol
• XLogP3: 2.000
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 102.104 Da
• Monoisotopic Mass: 102.104 Da
• Topological Polar Surface Area: 9.200 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 23.400
• 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. Li Zhihao, Jia Chunmei, Wan Zhi, Xue Jiayi, Cao Junchao, Zhang Meng, Li Can, Shen Jianghua, Zhang Chao, Li Zhen.  (2023)  Hyperbranched polymer functionalized flexible perovskite solar cells with mechanical robustness and reduced lead leakage.  Nature Communications,  14  (1): (1-12).  [PMID:37833324] [10.1038/s41467-023-41931-1]

2. Xirui Kong, Yichen Kong, Yayun Zheng, Lang He, Du Wang, Yan Zhao.  (2022)  Hydrofluoroether Diluted Dual-Salts-Based Electrolytes for Lithium-Sulfur Batteries with Enhanced Lithium Anode Protection.  Small,  18  (52): (2205017).  [PMID:36354183] [10.1002/smll.202205017]

3. Xirui Kong, Yichen Kong, Xiaobin Liao, Sheng Liu, Yan Zhao.  (2022)  A novel mixed ether-based electrolyte for lithium–sulfur batteries with Li anode protection by dual salts.  Sustainable Energy & Fuels,  6  (15): (3658-3668).  [PMID:] [10.1039/D2SE00647B]

4. Zhao Chang-Xin, Li Zheng, Chen Bin, Chen Fu, Wang Chunsheng.  (2025)  Self-adaptive electrolytes for fast-charging batteries.  Nature Energy,      [PMID:] [10.1038/s41560-025-01801-0]