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Technology Process of Dodecanamide, N,N-1,2-ethanediylbis-

Dodecanamide, N,N-1,2-ethanediylbis-

Base Information
  • Chemical Name:Dodecanamide, N,N-1,2-ethanediylbis-
  • CAS No.:29690-82-2
  • Molecular Formula:C11H15ClO3
  • Molecular Weight:230.69
  • Hs Code.:
  • European Community (EC) Number:608-398-3,810-249-4
  • Mol file:29690-82-2.mol
Dodecanamide, N,N-1,2-ethanediylbis-

Synonyms:Dodecanamide, N,N-1,2-ethanediylbis-;29690-82-2;68609-31-4;Poly[(o-cresyl glycidyl ether)-co-formaldehyde];2-(chloromethyl)oxirane;formaldehyde;2-methylphenol;SCHEMBL1066364;AKOS015912629;AS-81875;(C7-H8-O.C3-H5-Cl-O.C-H2-O)x-

Suppliers and Price of Dodecanamide, N,N-1,2-ethanediylbis-
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Sigma-Aldrich
  • Poly[(o-cresyl glycidyl ether)-co-formaldehyde] average Mn ~1,080
  • 100g
  • $ 47.70
  • Sigma-Aldrich
  • Poly[(o-cresyl glycidyl ether)-co-formaldehyde] average Mn ~870
  • 100g
  • $ 47.70
  • American Custom Chemicals Corporation
  • POLY[(O-CRESYL GLYCIDYL ETHER)-CO-FORMALDEHYDE] 95.00%
  • 5MG
  • $ 496.66
Total 43 raw suppliers
Chemical Property of Dodecanamide, N,N-1,2-ethanediylbis-
Chemical Property:
  • Vapor Pressure:0.379mmHg at 25°C 
  • Melting Point:70-75 °C(lit.)  
  • Boiling Point:191 °C at 760 mmHg 
  • Flash Point:81.1 °C 
  • PSA：49.83000 
  • Density:1.12 g/mL at 25 °C(lit.)  
  • LogP:2.77560 
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:1
  • Exact Mass:230.0709720
  • Heavy Atom Count:15
  • Complexity:111
Purity/Quality:

98%,99%, *data from raw suppliers

Poly[(o-cresyl glycidyl ether)-co-formaldehyde] average Mn ~1,080 *data from reagent suppliers

Safty Information:
  • Pictogram(s): Xi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Chemical Classes:UVCB,Plastics & Rubber -> Polymers
  • Canonical SMILES:CC1=CC=CC=C1O.C=O.C1C(O1)CCl
  • 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. For high temperature adhesives, coatings, electrical and laminating products.
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