Curing of paints by exposure to UV radiations is emerging as one of the best film forming technique as an alternative to traditional solvent borne oxidative and thermal curing coatings. The composition and chemistry of UV curable coatings and role of multifunctional and monofunctional monomers, oligomers, and photoinitiators have been discussed. The limitations imposed by thermodynamic equilibrium and tendency for acrylic double bond polymerizations during synthesis of multifunctional acrylates have been presented. Aim of present investigation was thus to explore the reaction variables associated with synthesis of multifunctional acrylates. Zirconium oxychloride was evaluated as catalyst against regular acid functional catalyst. The catalyzed synthesis of glyceryl acrylate and neopentyl glycol acrylate was conducted by variation of following reaction parameters: two different reactant molar ratios- 1:4 and 1:6; catalyst usage in % by moles on polyol- 2.5, 5.0 and 7.5 and two different reaction temperatures- 45 and 75 0C. The reaction was monitored by determination of acid value and hydroxy value at regular intervals, besides TLC, HPLC, and FTIR analysis of intermediates and products. On the basis of determination of reaction progress over 1-60 hrs, the esterification reaction was observed to follow 2nd order kinetics with rate constant varying from 1*10-4 to 7*10-4. The thermal and catalytic components of second order rate constant and energy of activation were also determined. Uses of these kinetic and thermodynamic parameters in design of reactor for manufacture of multifunctional acrylate ester have been presented. The synthesized multifunctional acrylates were used to formulate and apply UV curable clear coat followed by determination of curing characteristics and mechanical properties of cured film. The overall curing rates less than 05 min. were easily attained indicating economical viability of radiation curable system due to faster production schedules, {"references":["Dan Sweet wood and Michael Kelly, www.PCIMAG.com, , Nov. 2007,\npp.78-80.","K. Lawson, RadTech. Rep., 12 (1), 1998, pp. 25.","Wang Qingfeng and Wenfang Shi, \"Growth and Use of Radiation\nCuring in China\", JCT CoatingTech., pp. 48- 54, Oct 2005. Available\n:http://www.coatingstech.org","Vincent D. McGinniss, \"Radiation Curing\", in Kirk Othmer\nEncyclopedia of Chemical Technology, 4th Ed., Vol. 20, Wiley-\nInterscience, New York, ,1996, pp. 830-859.","Belfield, K. D., J. V. Crivello, Eds., ÔÇÿPhotoinitiated Polymerisation-,\nACS Symp. Ser. 847, American Chemical Society, Washington DC,\n2003.","Koleske, J. V., ÔÇÿRadiation Curing of Coatings-, ASTM International,\nWest Conshocken, PA 2002.","P.K.T. Oldring,, Ed., ÔÇÿChemistry and Technology of Formulating UV\nCure Coatings-, Inks and Paints,- Vol. 1-5, SITA Technology, London,\n1991-94.","Christian Decker and Khalil Mousssa, \"Recent advances in UV Curing\nChemistry\", J. Coat Technol., 65(819), pp.49-57,1993.","W. A. Green, \"Photoinitiators Old and New Food for thought\", Surface\nCoating International, 90 (02), pp. 69-75, 2007.\n[10] V. D. McGinniss, Org. Coatings Plast. Chem. 39, 1978, pp. 529-537.\n[11] G. C. Derringer, J. Quality Tech., 12 (4), 1980, pp. 214-219.\n[12] Classification System of the Environmental Protection Agency (EPA),\ntital 40, code of federal regulations, part 162.10H.\n[13] Hoyle Charles E., James F. Kinstle, Ed. ÔÇÿRadiation Curing of Polymeric\nMaterials, American Chemical Society, Washington DC, 1989, pp.1-16.\n[14] Chattopadhya D. K., S. S. Pande, K. V. S. N. Raju, \"Thermal and\nmechanical properties of epoxy acrylate /methacrylates UV cured\ncoatings\", Progress in Organic Coatings, 54, pp.10-19, 2005.\n[15] R Golden, J. Coat. Technol., 69(871), p. 83, 1997.\n[16] Takashi Ohara, Takahisa Sato, Noboru Shimizu, Gunter Prescher,\nHelmut Schwind, Otto Weiberg, Ullaman-s Encyclopedia of Industrial\nChemistry, Vol. A1, VCH 1985, pp. 161-172.\n[17] Franciscus J. M. Derks, Michae A. C. Van Dijck, \"Process for the\npreraration of esters of (metha) acrylic acid\", US Patent 6838515 B2,\nJan., 04, 2005.\n[18] EP 054105 A1 assigned to Vianova, 1982.\n[19] EP 0933353 A1 assigned to BASF, 1999.\n[20] F. G. Martin, G. Nestel , J. Schroder, \"Method for producing (meth)\nacrylic acid esters\", US Patent 20040030179 A1, Feb. 12, 2004.\n[21] Levenspiel Octave, \"Chemical Reaction Engineering\", 3rd Ed., John\nWiley and Sons, Singapore, 1999, p. 43.\n[22] Hong-Bin Sun, Ruimao Hua & Yingwa Yin, \"ZrOCl2:8H2O: An\nefficient, Cheap and Reusable Catalyst for the Esterification of Acrylic\nacid and other Carboxylic Acids with equimolar amounts of Alcohols\"\nMolecules, 11, pp. 263-271, 2006. Available: http://www.mdpi.org"]}