Identification | More | [Name]
TETRAETHYLENEGLYCOL MONOMETHYL ETHER | [CAS]
23783-42-8 | [Synonyms]
2,5,8,11-TETRAOXATRIDECAN-13-OL METHYL TETRAGLYCOL TETRAETHYLENEGLYCOL MONOMETHYL ETHER 3,6,9,12-Tetraoxatridecan-1-ol tetraethylenemonomethylether 3,6,9,12-tetraoxatridecanol 3,6,9,12-tetraoxotridecanol TETRAETHYLENEGLYCOLMETHYLETHER Tetraethyleneglycol monomethyl ether (m-PEG-4-OH) | [EINECS(EC#)]
245-883-5 | [Molecular Formula]
C9H20O5 | [MDL Number]
MFCD00041756 | [Molecular Weight]
208.25 | [MOL File]
23783-42-8.mol |
Chemical Properties | Back Directory | [Appearance]
CLEAR COLOURLESS TO VERY SLIGHTLY YELLOW LIQUID | [Boiling point ]
158-160 °C (5 mmHg) | [density ]
1.045 g/mL at 25 °C | [vapor pressure ]
0.1Pa at 20℃ | [refractive index ]
1.444-1.446
| [Fp ]
>110°C | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
Soluble in DMSO | [form ]
Liquid | [pka]
14.36±0.10(Predicted) | [color ]
Clear colorless to very slightly yellow | [Water Solubility ]
Water solubility 999,999c. | [α-end]
methoxy | [Ω-end]
hydroxyl | [InChIKey]
ZNYRFEPBTVGZDN-UHFFFAOYSA-N | [LogP]
-1.5 at 20℃ | [CAS DataBase Reference]
23783-42-8(CAS DataBase Reference) | [EPA Substance Registry System]
2,5,8,11-Tetraoxatridecan-13-ol (23783-42-8) |
Safety Data | Back Directory | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
1 | [TSCA ]
Yes | [HS Code ]
29094990 |
Hazard Information | Back Directory | [Description]
m-PEG4-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. | [Chemical Properties]
CLEAR COLOURLESS TO VERY SLIGHTLY YELLOW LIQUID | [Uses]
2,5,8,11-Tetraoxatridecan-13-o1, can be used in the synthesis of various chemicla compounds. It is also a monofunctional PEG that can be used in polymer science. | [Definition]
ChEBI: 5S,6S-epoxy-15R-hydroxy-ETE is a poly(ethylene glycol). | [Synthesis]
General procedure: Tetraethylene glycol monomethyl ether was synthesized from the compound (CAS: 727986-31-4). This was done as follows: to a solution of 2-(2,5,8,11-tetraoxatridecan-13-yloxy)tetrahydro-2H-pyran (280 mg, 0.96 mmol) in methanol (5 mL) was added pyridinium salt of p-toluenesulfonate (PPTS, 24 mg, 0.096 mmol) at 0 °C. The reaction mixture was slowly warmed from 0 °C to room temperature and stirred for 16 hours. Upon completion of the reaction, the solvent was removed by concentration under reduced pressure to give the crude product. Subsequently, the crude product was purified using silica gel column chromatography with an eluent of 5% methanol/dichloromethane (v/v), resulting in the target compound 5-2A (180 mg, 0.87 mmol, 90% yield) as a pale yellow liquid. | [IC 50]
PEGs | [References]
[1] Patent: WO2016/154241, 2016, A1. Location in patent: Paragraph 328; 331 [2] Macromolecules, 2004, vol. 37, # 14, p. 5133 - 5135 |
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