Allyloxypolyethyleneglycol

Product Information

Molecular Formula:
C3H5O.(C2H4O)n.H
Molecular Weight:
102.13
Description
Allyloxypolyethyleneglycol can alter drug solubility and improve drug bioavailability beyond traditional drug delivery systems. This bioactive compound has demonstrated versatility, becoming an indispensable tool in the fight against cancer, cardiovascular disease, and infectious diseases. With its unique properties, the incorporation of Allyloxypolyethyleneglycol into pharmaceutical formulations can enhance therapeutic effects.
Synonyms
Allyloxypolyethyleneglycol; Monoallylether ethoxylate EO 9 + EO 10
IUPAC Name
2-prop-2-enoxyethanol
Canonical SMILES
C=CCOCCO
InChI
InChI=1S/C5H10O2/c1-2-4-7-5-3-6/h2,6H,1,3-5H2
InChI Key
GCYHRYNSUGLLMA-UHFFFAOYSA-N
Melting Point
20-25°C
Flash Point
>150°C (>300°F)
Purity
0.98
Density
0.762g/cm3
Storage
Store at 4 degrees celsius
Refractive Index
1.465

Safety Information

Hazards
Irritant

Computed Properties

XLogP3
-0.1
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
4
Exact Mass
102.068079557 g/mol
Monoisotopic Mass
102.068079557 g/mol
Topological Polar Surface Area
29.5Ų
Heavy Atom Count
7
Formal Charge
0
Complexity
43.3
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114163913-A Preparation method of polyurethane-cured silver-doped fluorine-containing antibacterial anticorrosive paint and coating 2022-01-18
CN-114133532-A Fluorine-containing polyacrylate modified polyurethane elastomer and preparation method thereof 2021-12-16
JP-2022023921-A Ink and inkjet recording method 2021-10-27
CN-113788924-A Polyurethane elastomer and preparation method thereof 2021-10-25
CN-113943237-A Chain extender and preparation method and application thereof 2021-10-25
CN-113683780-A Antiserum and low-cytotoxicity polyamino acid gene delivery carrier material with membrane penetrating activity and nucleus positioning function 2021-09-15
CN-113735892-A Synthesis method of amino alkyl silane 2021-09-07
CN-113752651-A Composite material for manufacturing heat vulcanized silica gel heater and preparation method thereof 2021-09-06
CN-113717641-A Biocompatible membranes and uses thereof 2021-09-02
CN-113605114-A Scarf and processing technology thereof 2021-09-01

Literatures

PMID Publication Date Title Journal
22225480 2012-02-07 Influence of mesoporosity on lithium-ion storage capacity and rate performance of nanostructured TiO2(B) Langmuir : the ACS journal of surfaces and colloids
20502649 2010-03-15 Synthesis of bis(3-{[2-(allyloxy)ethoxy]methyl}-2,4,6-trimethylbenzoyl)(phenyl)phosphine oxide - a tailor-made photoinitiator for dental adhesives Beilstein journal of organic chemistry
19198434 2008-10-01 Use of pluronic F108 as a cosurfactant in a synthesis of mesoporous silica microspheres with bimodal pore size distribution Journal of nanoscience and nanotechnology
5852 1976-03-01 Vagal reflexes in the bronchoconstriction occurring after induced intravascular platelet aggregation Acta physiologica Scandinavica
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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