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2-(2-{2-[2-(2-Methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethanol

Base Information Edit
  • Chemical Name:2-(2-{2-[2-(2-Methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethanol
  • CAS No.:23778-52-1
  • Molecular Formula:C11H24O6
  • Molecular Weight:252.308
  • Hs Code.:2909499000
  • European Community (EC) Number:245-874-6
  • DSSTox Substance ID:DTXSID8041371
  • Nikkaji Number:J97.012C
  • Wikidata:Q27093129
  • Metabolomics Workbench ID:146653
  • ChEMBL ID:CHEMBL1229767
  • Mol file:23778-52-1.mol
2-(2-{2-[2-(2-Methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethanol

Synonyms:23778-52-1;Pentaethylene glycol monomethyl ether;2,5,8,11,14-Pentaoxahexadecan-16-ol;m-PEG5-alcohol;mPEG5-OH;Methyl-PEG5-alcohol;3,6,9,12,15-Pentaoxahexadecanol;2-[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethoxy]ethanol;2-(2-{2-[2-(2-METHOXY-ETHOXY)-ETHOXY]-ETHOXY}-ETHOXY)-ETHANOL;Pentaethyleneglycol monomethyl ether;C11H24O6;3,6,9,12,15-Pentaoxahexadecan-1-ol;DTXSID8041371;EINECS 245-874-6;MFCD00045995;Pentaethylene glycol, monomethyl ether;1PG;PentaethyleneGlycolMonomethylEther;YSWG288;SCHEMBL145212;CHEMBL1229767;DTXCID6021371;BCP28370;Tox21_301472;3,6,9,12,15-pentaoxa-hexadecanol;AKOS015900975;DB02042;FS-5902;HY-W042713;s10616;NCGC00255633-01;3,6,9,12,15-Pentaoxahexadecane-1-ol;BP-22068;SY053760;16-Hexadecanol, 2,5,8,11,14-pentaoxa;CAS-23778-52-1;CS-0035716;FT-0638353;P1159;EN300-259923;A878145;J-523878;Q27093129

Suppliers and Price of 2-(2-{2-[2-(2-Methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethanol
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TCI Chemical
  • Pentaethylene Glycol Monomethyl Ether >96.0%(GC)
  • 5g
  • $ 521.00
  • TCI Chemical
  • Pentaethylene Glycol Monomethyl Ether >96.0%(GC)
  • 1g
  • $ 159.00
  • purepeg
  • Pentaethylene Glycol Monomethyl Ether min.97%
  • 5 g
  • $ 229.00
  • Crysdot
  • 2,5,8,11,14-Pentaoxahexadecan-16-ol 95%
  • 25g
  • $ 533.00
  • Crysdot
  • 2,5,8,11,14-Pentaoxahexadecan-16-ol 95%
  • 10g
  • $ 316.00
  • chempep
  • mPEG11-NH2 >=95%
  • 5g
  • $ 1388.00
  • chempep
  • mPEG5-OH >=95%
  • 5g
  • $ 320.00
  • chempep
  • mPEG5-OH >=95%
  • 25g
  • $ 720.00
  • chempep
  • mPEG11-NH2 >=95%
  • 1g
  • $ 555.00
  • Chem-Impex
  • Pentaethyleneglycolmonomethylether,≥96%(GC) ≥96%(GC)
  • 1G
  • $ 171.23
Total 54 raw suppliers
Chemical Property of 2-(2-{2-[2-(2-Methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethanol Edit
Chemical Property:
  • Vapor Pressure:1.06E-05mmHg at 25°C 
  • Refractive Index:1.441 
  • Boiling Point:332.3 °C at 760 mmHg 
  • PKA:14.36±0.10(Predicted) 
  • Flash Point:154.7 °C 
  • PSA:66.38000 
  • Density:1.053g/cm3 
  • LogP:-0.30850 
  • Storage Temp.:-20°C 
  • XLogP3:-1.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:14
  • Exact Mass:252.15728848
  • Heavy Atom Count:17
  • Complexity:133
Purity/Quality:

98%,99%, *data from raw suppliers

Pentaethylene Glycol Monomethyl Ether >96.0%(GC) *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Statements: 36/37/38 
  • Safety Statements: 26-36/37/39 
MSDS Files:

SDS file from LookChem

Useful:
  • Chemical Classes:Solvents -> Glycol Ethers (E Series)
  • Canonical SMILES:COCCOCCOCCOCCOCCO
  • Description m-PEG5-alcohol is a PEG linker containing a hydroxyl group. The hydroxyl group enables further derivatization or replacement with other reactive functional groups. The hydrophilic PEG spacer increases solubility in aqueous media.
  • Uses Applications may include: bioconjugation, drug delivery, PEG hydrogel, crosslinker, and surface functionalization
Technology Process of 2-(2-{2-[2-(2-Methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethanol

There total 24 articles about 2-(2-{2-[2-(2-Methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethanol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With sodium hydride; In tetrahydrofuran; at 80 ℃; for 15h; Inert atmosphere;
DOI:10.1021/acs.jmedchem.0c01153
Guidance literature:
With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 16h; Inert atmosphere;
DOI:10.1002/anie.202104233
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