Poly(2,6-dimethyl-1,4-phenylene oxide)

Product Information

Molecular Formula:
(C8H10O)x
Synonyms
2,6-dimethyl-phenohomopolymer; Phenol, 2,6-dimethyl-, homopolymer; Poly(2,6-xylenol); 2,6-Dimethylphenol polymer; 2,6-Xylenol polymer; 2,6-Dimethylphenylene oxide polymer
IUPAC Name
2,6-dimethylphenol
Canonical SMILES
CC1=C(C(=CC=C1)C)O
InChI
InChI=1S/C8H10O/c1-6-4-3-5-7(2)8(6)9/h3-5,9H,1-2H3
InChI Key
NXXYKOUNUYWIHA-UHFFFAOYSA-N
Boiling Point
397 °F at 760 mmHg
Melting Point
120 °F
Flash Point
165 °F
Density
1.06 g/mL at 25 °C(lit.)
Solubility
less than 1 mg/mL at 68 °F
Appearance
LEAVES OR NEEDLES FROM ALCOHOL
Application
Used as an intermediate in organic synthesis.
Storage
Store at room temperature
Refractive Index
n20/D 1.575
Tg
209°
LogP
log Kow= 2.36
Vapor Pressure
0.27 [mmHg]
Henry's Law Constant
6.7X10-6 atm-cu m/mol @ 25 °C
Decomposition
When heated to decomp, it emits acrid smoke and irritating fumes.
Dissociation Constants
pKa= 10.59 at 25 °C

Safety Information

Hazards
Harmless-use normal precautions
Handling
Exercise normal care

Computed Properties

XLogP3
2.4
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
0
Exact Mass
122.073164938 g/mol
Monoisotopic Mass
122.073164938 g/mol
Topological Polar Surface Area
20.2Ų
Heavy Atom Count
9
Formal Charge
0
Complexity
80.6
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-114106263-A Methacrylate functionalized polyphenyl ether and preparation method and application thereof 2021-12-29
CN-114181053-A Preparation method of diphenol monomer with lateral group containing trifluoromethyl and polyarylether polymer thereof 2021-12-29
CN-114015041-A Catalyst for synthesizing polyphenyl ether 2021-12-26
JP-2022037181-A A method for producing a chemically amplified photosensitive composition, a photosensitive dry film, and a method for producing a patterned resist film. 2021-12-22
CN-114057788-A Preparation method of high-purity 4, 4' -biphenol bis (di (2, 6-dimethylphenyl) phosphate) 2021-12-08
CN-114149683-A Polyphenyl ether and nylon composition and preparation method thereof 2021-12-08
CN-114085374-A Alkynyl-terminated polyphenyl ether and preparation method and application thereof 2021-12-07
CN-113912801-A Anhydrous phenolic resin binder for magnesia-calcium brick and preparation method thereof 2021-11-25
CN-113999353-A Castor oil-based hydroxyl acrylate emulsion and preparation method and application thereof 2021-11-16
CN-113956467-A Method for modifying double-end hydroxyl polyphenylene oxide 2021-10-29

Literatures

PMID Publication Date Title Journal
29658714 2018-05-21 Activation of TRPV3 by Wood Smoke Particles and Roles in Pneumotoxicity Chemical research in toxicology
22536123 2012-01-01 An efficient protocol for the synthesis of quinoxaline derivatives at room temperature using recyclable alumina-supported heteropolyoxometalates TheScientificWorldJournal
22064795 2011-10-01 Trichlorido-1κCl,2κCl-(2,6-dimethyl-phenolato-2κO)-μ-oxido-bis{1,2(η)-2,3,4,5-tetra-methyl-1-[4-(trimethyl-silyl)phen-yl]cyclo-penta-dien-yl}dititanium(IV) Acta crystallographica. Section E, Structure reports online
21696711 2011-09-27 Montmorillonite K-10 clay-catalyzed Ferrier rearrangement of 2-C-hydroxymethyl-d-glycals, 3,4,6-tri-O-alkyl-d-glycals, and 3,4-(dihydro-2H-pyran-5-yl)methanol: a few unexpected domino transformations Carbohydrate research
21624144 2011-05-31 Engineering Klebsiella sp. 601 multicopper oxidase enhances the catalytic efficiency towards phenolic substrates BMC biochemistry
21293815 2011-03-21 Anion exchange induced tunable catalysis properties of an uncommon butterfly-like tetranuclear copper(II) cluster and magnetic characterization Dalton transactions (Cambridge, England : 2003)
21081773 2011-02-01 The anticonvulsant effects of propofol and a propofol analog, 2,6-diisopropyl-4-(1-hydroxy-2,2,2-trifluoroethyl)phenol, in a 6 Hz partial seizure model Anesthesia and analgesia
21806452 2011-01-01 Oxidation of 2,6-dimethylaniline by the Fenton, electro-Fenton and photoelectro-Fenton processes Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering
21589102 2010-10-23 9-(2,6-Dimethyl-phen-oxy-carbon-yl)-10-methyl-acridinium trifluoro-methane-sulfonate Acta crystallographica. Section E, Structure reports online
20689870 2010-09-28 Gas-phase phenol methylation over Mg/Me/O (Me = Al, Cr, Fe) catalysts: mechanistic implications due to different acid-base and dehydrogenating properties Dalton transactions (Cambridge, England : 2003)
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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