Hexaethylene Glycol Monomethyl Ether CAS 23601-40-3

Introduction:Basic information about Hexaethylene Glycol Monomethyl Ether CAS 23601-40-3, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Hexaethylene Glycol Monomethyl Ether Basic information

Product Name:Hexaethylene Glycol Monomethyl Ether
Synonyms:HEXAETHYLENE GLYCOL MONOMETHYL ETHER;2,5,8,11,14,17-hexaoxanonadecan-19-ol;2-[2-[2-[2-[2-(2-Methoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethanol;3,6,9,12,15,18-Hexaoxanonadecane-1-ol;MPEG6-OH;MPEG-6;m-PEG6-alcohol;Methyl-PEG6-alcohol
CAS:23601-40-3
MF:C13H28O7
MW:296.36
EINECS:245-775-8
Product Categories:Ethylene Glycols & Monofunctional Ethylene Glycols;Monofunctional Ethylene Glycols;PEG-COOH;peg
Mol File:23601-40-3.mol

Hexaethylene Glycol Monomethyl Ether Chemical Properties

Boiling point 167 °C / 1mmHg
density 1,08 g/cm3
refractive index 1.4510-1.4550
storage temp. -20°C
form clear liquid
pka14.36±0.10(Predicted)
color Colorless to Light yellow to Light orange
InChIInChI=1S/C13H28O7/c1-15-4-5-17-8-9-19-12-13-20-11-10-18-7-6-16-3-2-14/h14H,2-13H2,1H3
InChIKeyFHHGCKHKTAJLOM-UHFFFAOYSA-N
SMILESC(O)COCCOCCOCCOCCOCCOC
CAS DataBase Reference23601-40-3
EPA Substance Registry System2,5,8,11,14,17-Hexaoxanonadecan-19-ol (23601-40-3)

Safety Information

WGK Germany WGK 3
TSCA TSCA listed
HS Code 29094990
Storage Class10 - Combustible liquids

Hexaethylene Glycol Monomethyl Ether Usage And Synthesis

Descriptionm-PEG6-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.
UsesApplications may include: bioconjugation, drug delivery, PEG hydrogel, crosslinker, and surface functionalization
DefinitionChEBI: Hexaethylene glycol monomethyl ether is a hydroxypolyether. It is functionally related to a hexaethylene glycol.
reaction suitabilityreagent type: cross-linking reagent
Synthesis

62921-74-8

112-27-6

23601-40-3

Under stirring conditions, 2-(2-(2-methoxyethoxy)ethoxy)ethyl 4-methylbenzenesulfonate (1.0 g, 3.14 mmol) was slowly added to triethylene glycol (2.10 mL, 15.7 mmol). Subsequently, potassium hydroxide (510 mg, 9.42 mmol) was ground into a fine powder and added to the reaction system. The reaction mixture was refluxed at 100 °C for 12 hours. After completion of the reaction, the reaction mixture was diluted with deionized water (50 mL) and extracted with dichloromethane. The organic phases were combined, dried with anhydrous sodium sulfate and concentrated under reduced pressure to afford 2,5,8,11,14,17-hexaoxanonadecan-19-ol as a yellow oil in 69% yield.

IC 50PEGs
References[1] Journal of Organic Chemistry, 2006, vol. 71, # 20, p. 7499 - 7508
[2] Organic Letters, 2004, vol. 6, # 4, p. 469 - 472
[3] Patent: WO2015/143185, 2015, A1. Location in patent: Paragraph 00819
[4] Patent: WO2016/40891, 2016, A2. Location in patent: Paragraph 00316
[5] Bulletin of the Korean Chemical Society, 2011, vol. 32, # 7, p. 2193 - 2198

Hexaethylene Glycol Monomethyl Ether Preparation Products And Raw materials

Raw materialsTHP-PEG4-->Hexaethylene glycol-->2-(2-(2-Methoxyethoxy)ethoxy)ethyl 4-Methylbenzenesulfonate-->2,5,8,11,14,17,20-Heptaoxaheneicosane, 1-phenyl--->Methyl-PEG3-MS-->N-Hydroxysuccinimide-->Methanol-->Diethylene glycol monomethyl ether-->TRIETHYLENE GLYCOL MONOMETHYL ETHER-->Dimethyl sulfate
Preparation ProductsmPEG6-CH2COOH-->2,5,8,11,14,17-Hexaoxanonadecan-19-ol, methanesulfonate-->2,5,8,11,14,17-Hexaoxanonadecan-19-amine
HEXAETHYLENE GLYCOL MONOHEXADECYL ETHER CAS 5168-91-2
HEXAETHYLENE GLYCOL MONOOCTYL ETHER CAS 4440-54-4
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