HO-PEG5-OH - CAS 4792-15-8
Catalog: |
BB026426 |
Product Name: |
HO-PEG5-OH |
CAS: |
4792-15-8 |
Synonyms: |
2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethanol; 2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethanol |
IUPAC Name: | 2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethanol |
Description: | Pentaethylene Glycol (CAS# 4792-15-8) is part of a group of compounds called polyethylene glycols (PEGs), which are major byproducts of non-ionic surfactants biodegradation. Pentaethylene glycol is a useful synthetic intermediate, and is used as a reagent to synthesize macrocyclic oligoesters through lipase-catalysis. |
Molecular Weight: | 238.28 |
Molecular Formula: | C10H22O6 |
Canonical SMILES: | C(COCCOCCOCCOCCO)O |
InChI: | InChI=1S/C10H22O6/c11-1-3-13-5-7-15-9-10-16-8-6-14-4-2-12/h11-12H,1-10H2 |
InChI Key: | JLFNLZLINWHATN-UHFFFAOYSA-N |
Boiling Point: | 185-340 °C (2 torr) |
Purity: | >98% |
Density: | 1.12 g/cm3 |
Appearance: | Colorless Liquid |
Storage: | Pure form, -20°C, 3 years; 4°C, 2 years; In solvent, -80°C, 6 months; -20°C, 1 month |
MDL: | MFCD00002878 |
LogP: | -0.96260 |
GHS Hazard Statement: | H315 (97.18%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-113480453-A | Synthesis method of NH2-PEG5-NHBoc | 20210809 |
CN-113514444-A | Method for rapidly detecting aging degree of lubricating oil by fluorescence | 20210714 |
CN-113509439-A | Application of self-emulsifying delivery system in preparation of oral medicine for treating lymphatic metastasis tumor | 20210712 |
CN-113456588-A | Abiraterone acetate solid self-microemulsion and preparation method thereof | 20210705 |
CN-113304109-A | A flavone acetylsalicylate solid lipid nanoparticle dispersion and its preparation method | 20210608 |
PMID | Publication Date | Title | Journal |
22876958 | 20121101 | Synthesis and biological evaluation of chalcone derivatives (mini review) | Mini reviews in medicinal chemistry |
22266531 | 20121001 | Bacterial cellulose membranes applied in topical and transdermal delivery of lidocaine hydrochloride and ibuprofen: in vitro diffusion studies | International journal of pharmaceutics |
22746271 | 20120901 | Design porosity osmotic tablet for delivering low and pH-dependent soluble drug using an artificial neural network | Current drug delivery |
22344922 | 20120326 | Oligoethylene glycols as highly efficient mutifunctional promoters for nucleophilic-substitution reactions | Chemistry (Weinheim an der Bergstrasse, Germany) |
22250701 | 20120214 | Experimental study on dynamic interfacial tension with mixture of SDS-PEG as surfactants in a coflowing microfluidic device | Langmuir : the ACS journal of surfaces and colloids |
Complexity: | 108 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 238.14163842 |
Formal Charge: | 0 |
Heavy Atom Count: | 16 |
Hydrogen Bond Acceptor Count: | 6 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 238.14163842 |
Rotatable Bond Count: | 13 |
Topological Polar Surface Area: | 77.4 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | -1.7 |
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