POLY[(O-CRESYL GLYCIDYL ETHER)-CO-FORMALDEHYDE]
POLY[(O-CRESYL GLYCIDYL ETHER)-CO-FORMALDEHYDE] Basic information
- Product Name:
- POLY[(O-CRESYL GLYCIDYL ETHER)-CO-FORMALDEHYDE]
- Synonyms:
-
- Epichlorohydrin,o-cresol,formaldehydepolymer
- Ortho-Cresol Novolac Epoxy Resins
- Formaldehyde, polymer with 2-(chloromethyl)oxirane and 2-methylphenol
- 2-(chloromethyl)oxirane,formaldehyde,2-methylphenol
- POLY[(O-CRESYL GLYCIDYL ETHER)-CO-FORMALDEHYDE]
- Poly[(o-cresyl glycidyl ether)-co-formaldehyde] average Mn ~1,080
- Formaldehyde,polymerwith(chloromethyl)oxiraneand2-methylphenol
- o-Cresol,1-chloro-2,3-epoxypropane,formaldehydepolymer
- CAS:
- 29690-82-2
- MF:
- C33H42O9X2
- MW:
- 582.68
- Product Categories:
-
- Formaldehyde Copolymers and Epoxies
- Polymer Science
- Polymers
- Engineering Polymers
- Mol File:
- 29690-82-2.mol
POLY[(O-CRESYL GLYCIDYL ETHER)-CO-FORMALDEHYDE] Chemical Properties
- Melting point:
- 70-75 °C(lit.)
- Density
- 1.12 g/mL at 25 °C(lit.)
- Flash point:
- >230 °F
- EPA Substance Registry System
- Epichlorohydrin, o-cresol, formaldehyde polymer (29690-82-2)
MSDS
- Language:English Provider:SigmaAldrich
POLY[(O-CRESYL GLYCIDYL ETHER)-CO-FORMALDEHYDE] Usage And Synthesis
Chemical Properties
Hazardous polymerization can occur with aliphatic amines in quantities greater than 1 lb.
Uses
The epoxy novolac resins are
used and cured in ways similar to the resins based on the
diglycidyl ether of bisphenol A. These resins differ from
bisphenol A epoxy resins in that whereas a bisphenol A
polymeric chain can contain a maximum of two epoxide
group regardless of chain length, cresolic and phenolic
novolacs can contain an epoxide group for each phenol or
cresol molecule incorporated in the chain.
Because of their high functionality, epoxy novolac resins,
when cured, produce tightly cross-linked systems with improved high-temperature performance, chemical resistance,
and adhesion over the resins based on the diglycidyl
ether of bisphenol A. The thermal stability of epoxy novolac
resins has made them useful for structural and electrical
laminates and as coatings and castings for elevated temperature
service. Owing to the chemical resistance of these resins,
they are used for lining storage tanks, pumps, and other
process equipment as well as for corrosion-resistant coatings.
Uses
For high temperature adhesives, coatings, electrical and laminating products.
Production Methods
The term novolac refers to the reaction products of phenolic compounds and formaldehyde. Glycidation of the phenolic hydroxyl groups by epichlorohydrin under conditions similar to those used for forming the diglycidyl ether of bisphenol A produces the corresponding epoxy novolac resins. The average n in the above formula varies from 0.2 to 1.8, depending on the ultimate use of the resin.
POLY[(O-CRESYL GLYCIDYL ETHER)-CO-FORMALDEHYDE]Supplier
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- xg01_gj@163.com
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POLY[(O-CRESYL GLYCIDYL ETHER)-CO-FORMALDEHYDE](29690-82-2)Related Product Information
- Epichlorohydrin
- Formaldehyde, polymer with (chloromethyl)oxirane and phenol
- EPOXYNOVOLACRESINS(CRESOLIC)
- bis(2,3-epoxypropyl) cyclohex-4-ene-1,2-dicarboxylate
- BIS(3,4-EPOXYCYCLOHEXYLMETHYL) ADIPATE
- 4,5-epoxytetrahydrophthalic acid diglycidylester
- Resin epoxy
- 3,4-Epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate
- Cresyl glycidyl ether
- POLY[(O-CRESYL GLYCIDYL ETHER)-CO-FORMALDEHYDE]
- POLY[(O-CRESYL GLYCIDYL ETHER)-CO-FORMALDEHYDE]