Tetraethyleneglycol monomethyl ether - ≥98% , CAS No.23783-42-8

CAS: 23783-42-8 Cat. No.: T122020 Molecular Weight: 208.25 EC Number: 245-883-5 PubChem CID: 90263

GRADE & PURITY ≥98%

Synonyms

5S,6S-epoxy-15R-hydroxy-ETE | CAS-23783-42-8 | 3,6,9,12-Tetraoxatridecan-1-ol | AS-18227 | C9H20O5 | EN300-1428641 | Glycinamidehydrochloride | 2-(2-(2-(2-methoxyethoxy)-ethoxy)-ethoxy)-ethanol | Q27095147 | DB04332 | BP-22067 | tetraethylene glycol mono

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Synonyms

5S, 6S-epoxy-15R-hydroxy-ETE | CAS-23783-42-8 | 3, 6, 9, 12-Tetraoxatridecan-1-ol | AS-18227 | C9H20O5 | EN300-1428641 | Glycinamidehydrochloride | 2-(2-(2-(2-methoxyethoxy)-ethoxy)-ethoxy)-ethanol | Q27095147 | DB04332 | BP-22067 | tetraethylene glycol mono

Specifications & Purity

≥98%

Storage

Store at 2-8°C

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 504756022
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504756022
• Canonical Smiles: COCCOCCOCCOCCO
• IUPAC Name: 2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethanol
• InChIKey: ZNYRFEPBTVGZDN-UHFFFAOYSA-N
• INCHI: 1S/C9H20O5/c1-11-4-5-13-8-9-14-7-6-12-3-2-10/h10H,2-9H2,1H3
• Isomeric SMILES: COCCOCCOCCOCCO
• WGK Germany: 1
• PubChem CID: 90263
• Molecular Weight: 208.25
• Reaxy-Rn: 1904942

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Class Organooxygen compounds
      • Subclass Ethers
        • Level5 Dialkyl ethers
          • Level6 Polyethylene glycols

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Class: Organooxygen compounds
• Subclass: Ethers
• Intermediate Tree Nodes: Dialkyl ethers
• Direct Parent: Polyethylene glycols
• Alternative Parents: Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Polyethylene glycol - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as polyethylene glycols. These are oligomers or polymers of ethylene oxide, with the general formula (C2H4O)n (with n>=3).
• External Descriptors: Not available

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

Chemical and Physical Properties

• Solubility: Water solubility 999,999c.
• Refractive Index: 1.445
• Flash Point(°F): 235.4 °F
• Flash Point(°C): 113 °C
• Boil Point(°C): 125°C/1mmHg
• Molecular Weight: 208.250 g/mol
• XLogP3: -1.000
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 11
• Exact Mass: 208.131 Da
• Monoisotopic Mass: 208.131 Da
• Topological Polar Surface Area: 57.200 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 99.200
• 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

References

1. Yang Tang, Song-Qing Zhao, Na Liu, Zong-Quan Wu.  (2018)  Facile synthesis of stereoregular helical poly(phenyl isocyanide)s and poly(3-hexylthiophene)-block-poly(phenyl isocyanide) copolymer using chiral π-allylnickel complexes as initiators.  POLYMER,      [PMID:] [10.1016/j.polymer.2018.03.024]

2. Liheng Feng, Lixia Guo, Xiaoju Wang.  (2016)  Preparation, properties and applications in cell imaging and ions detection of conjugated polymer nanoparticles with alcoxyl bonding fluorene core.  BIOSENSORS & BIOELECTRONICS,      [PMID:27598853] [10.1016/j.bios.2016.08.114]

3. Zhihuang Zhang, Yan Peng, Liyan Qiu.  (2024)  Rigid nanoparticles for efficient tumor immunotherapy through mechanical force mediated reprogramming of tumor-associated macrophages.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.152129]