methylol

meth·y·lol

(meth'ĭ-lol),
Hydroxymethyl; the moiety, -CH2OH.

meth·y·lol

(meth'i-lol)
Hydroxymethyl; the radical, -CH2OH.
References in periodicals archive ?
To this aqueous solution of methylol melamine, 1 mole of FA was added followed by addition of maleic anhydride as catalyst and finally polymerized for another 45 min.
5% Cytec Acrylate (IBOA) acrylate monomer Tri propylene Difunctional 10% Cytec Glycol Di acrylate monomer Acrylate (TPGDA) Tri Methylol Trifunctional 20% Cytec Propane Tri acrylate monomer Acrylate (TMPTA) Di Pentafunctional 12.
3 to 3 parts by weight of partial condensate of hexamethylol melamine pentamethyl ether or partial condensate of hexa methoxy methylol melamine, and (D) organic acid cobalt, based on 100 parts by weight of a rubber component; wherein the cobalt content in the organic acid cobalt (D) is 0.
Formaldehyde reacts with 6- or 8-position on the 5,7-dihydroxy flavonoids forming a methylol derivative that attaches to another 6- or 8-position on following flavonoid and so on.
Tenders are invited for Supply Of Tri Methylol Propane Tri Oleate To Sbu Greases And Lubricants Kolkata Plant
The resin spectrum is dominated by the methylol species (2.
Phenols condense initially with formaldehyde at pH either acid or alkaline, to form a methylol phenol or phenolic alcohol, and then, dimethylol phenol.
Random pre-polymers of phenol/formaldehyde are prepared by reacting phenol on the ortho and para positions in the boxing ring with bifunctional formaldehyde, where the bases catalyzed reaction produce a mixture of methylol phenols where the composition of the mixture can be varied by altering the phenol to formaldehyde ratio Inorganic catalysts such as copper halides are known to catalyze phenol polymerization in the presence of molecular oxygen [17].
The solubility of methylol urea in water was obtained by mixing 1 ml of the resin with 5ml of distilled water at room temperature (30[degrees]C).
Initial reactions take place to form various methylol derivatives (-C[H.
Ab-initio calculations of vibrational frequencies enabled confident assignment of bands to monitor the consumption of methylol groups (C[H.
13] nuclear magnetic resonance (NMR) spec troscopy show several peaks in the C-Br region of both resoles suggesting primary bonds between the para-bromophenol and phenol methylol groups for these systems.