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Neopentyl glycol (IUPAC name: 2,2-dimethylpropane-1,3-diol) is an organic chemical compound. It is used in the synthesis of polyesters , paints , lubricants , and plasticizers . When used in the manufacture of polyesters, it enhances the stability of the product towards heat, light, and water.
Neopentyl glycol diglycidyl ether (NPGDGE) is an organic chemical in the glycidyl ether family. It is aliphatic and a colorless liquid. It has the formula C 11 H 20 O 4 and the CAS registry number of 17557-23-2. [2] It has two oxirane groups per molecule. [3] Its principle use is in modifying epoxy resins. [4] It is REACH registered. [5]
surfactant used as a detergent and emulsifier propane: propane CH 3 CH 2 CH 3: propellant (pressurized dispenser) paraben: preservative peg-20: a variety of Polyethylene glycol: often used as an ointment base polymethyl methacrylate (PMMA) [7] (C 5 O 2 H 8) n: palmitic acid: CH 3 (CH 2) 14 COOH paraffinum liquidum: petrolatum: C 15 H 15 N ...
Dibromo neopentyl glycol diglycidyl ether is a brominated version of neopentyl glycol diglycidyl ether. It is an aliphatic organic chemical in the glycidyl ether family that is used in epoxy resin formulations. It has the molecular formula C 11 H 18 Br 2 O 4
Typical components for these resins are poly carboxylic and polyhydroxyl components. The more commonly used polyacids are phthalic, isophthalic, terephthalic and adipic acid. Phthalic and trimellitic anhydrides may also be used. Polyols tend to be neopentyl glycol, 1,6-hexanediol and trimethylolpropane. To make them waterborne organic acids or ...
Almost everything is used. Even so, the Swartzes’ financial situation feels precarious. They draw $3,890 a month from Social Security, along with $240 a month from two small pensions.
Turn off the TV and phone. “All screens should be turned off at least one hour before bedtime,” says Dasgupta. “The blue light emitted by screens can interfere with melatonin production ...
Pentaerythritol was first reported in 1891 by German chemist Bernhard Tollens and his student P. Wigand. [5] It may be prepared via a base-catalyzed multiple-addition reaction between acetaldehyde and 3 equivalents of formaldehyde to give pentaerythrose (CAS: 3818-32-4), followed by a Cannizzaro reaction with a fourth equivalent of formaldehyde to give the final product plus formate ion.