Results 131 to 140 of about 12,560 (208)

EFSA CEF Panel (EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids), 2015. Scientific Opinion on Flavouring Group Evaluation 213, Revision 2 (FGE.213Rev2): Consideration of genotoxic potential for α,β-unsaturated alicyclic ketones and precursors from chemical subgroup 2.7 of FGE.19. [PDF]

, 2015

core   +1 more source

Frontal Polymerization of Epoxy Resins: Kinetic Modeling, Rate Regulation and Curing Process Simulation for Space Manufacturing Applications. [PDF]

Polymers (Basel)
Wu H, Gu Y, Liu X, Xin C.
europepmc   +1 more source

Safety and efficacy of a feed additive consisting of an essential oil obtained from the flowering aerial parts of <i>Thymus vulgaris</i> L. and/or <i>Thymus zygis</i> L. (thyme oil) for use in all animal species (FEFANA asbl). [PDF]

EFSA J
EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP), Villa RE, Azimonti G, Bonos E, Christensen H, Durjava M, Dusemund B, Gehring R, Glandorf B, Kouba M, López-Alonso M, Marcon F, Nebbia C, Pechová A, Prieto-Maradona M, Röhe I, Theodoridou K, Bastos ML, Benfenati E, Brantom P, Chesson A, Schlatter J, Westendorf J, Manini P.   +23 more
europepmc   +1 more source

EFSA Panel on food contact materials, enzymes, flavourings and processing aids (CEF); Scientific Opinion on Flavouring Group Evaluation 74, Revision 1 (FGE.74Rev1): Consideration of Simple Aliphatic Sulphides and Thiols evaluated by the JECFA (53rd and 61st meeting) Structurally related to Aliphatic and Alicyclic Mono-, Di-, Tri-, and Polysulphides with or without Additional Oxygenated Functional Groups from Chemical Group 20 evaluated by EFSA in FGE.08Rev1 (2009) [PDF]

, 2011
Aeschbacher, Brams, Cox, Cox, Cramer, Dooley, Dorange, EC, EC, EC, EC, Eder, Eder, Hakura, JECFA, JECFA, JECFA, LaVoie, Lee, Marks, Morgareidge, Morgareidge, Morgareidge, Musk, Pence, Pennwalt Corporation, Pennwalt Corporation, SCF, Shellenberger, Stien, Watanabe, Watanabe, Wild, Zeiger   +33 more
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Constraining biorecalcitrance of carboxyl-rich alicyclic molecules in the ocean. [PDF]

Sci Adv
Cai R, Lechtenfeld OJ, Yan Z, Yi Y, Chen X, Zheng Q, Koch BP, Jiao N, He D.   +8 more
europepmc   +1 more source

Investigating the Stability of Individual Carboxylate-Rich Alicyclic Molecules Under Simulated Environmental Irradiation and Microbial Incubation Conditions. [PDF]

Environ Sci Technol
Craig AJ, Norouzi M, Löffler P, Lai FY, Mtibaà R, Breyer E, Baltar F, Moodie LWK, Hawkes JA.   +8 more
europepmc   +1 more source

The relation between bridgehead reactivity and electronic effects [PDF]

, 1990
Hadizamani, Katja, Langhals, Heinz
core   +1 more source

Comparative analysis of the properties of colorless and transparent polyimide nanocomposites with and without fluorine substitution. [PDF]

RSC Adv
Choi MY, Lim AR, Chang JH.
europepmc   +1 more source

Studies of alicyclic systems

, 2017
During the last decade the synthesis and spectroscopic characteristics of nitro compounds have aroused much interest. New synthetic methods have been developed, and the excellence of the nitro group as a chromophore in spectroscopy has been demonstrated.
openaire   +1 more source

Scientific Opinion on Flavouring Group Evaluation 212 Revision 3 (FGE.212Rev3): α,β-unsaturated alicyclic ketones and precursors from chemical subgroup 2.6 of FGE.19 [PDF]

, 2015

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