Academic literature on the topic 'Vanilline'
Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles
Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Vanilline.'
Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.
You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.
Journal articles on the topic "Vanilline"
Iskandar, Damayanti, and Susy Yunita Prabawati. "Synthesis of Compounds Acetyl Vanilat as Analgesic Compound Components." Jurnal ILMU DASAR 17, no. 2 (February 1, 2017): 73. http://dx.doi.org/10.19184/jid.v17i2.2683.
Full textChatonnet, Pascal, Jean-Noël Boidron, Denis Dubourdieu, and Monique Pons. "Evolution de certains composés volatils du bois de chêne au cours de son séchage premiers résultats." OENO One 28, no. 4 (December 31, 1994): 359. http://dx.doi.org/10.20870/oeno-one.1994.28.4.1720.
Full textKamaal, Saima, Md Serajul Haque Faizi, Arif Ali, Musheer Ahmad, Mayank Gupta, Necmi Dege, and Turganbay Iskenderov. "Crystal structure of 4-[(2-hydroxy-3-methoxybenzyl)amino]benzoic acid hemihydrate." Acta Crystallographica Section E Crystallographic Communications 75, no. 2 (January 8, 2019): 159–62. http://dx.doi.org/10.1107/s2056989018018455.
Full textOnozaki, Hiromichi, Hisaye Asai, Shinobu Isshiki, and Hideo Esaki. "Bacterial metabolism of vanillylamine and vanilline." Journal of Fermentation Technology 64, no. 5 (October 1986): 470. http://dx.doi.org/10.1016/0385-6380(86)90041-5.
Full textYue, Yongkang, Fangjun Huo, Caixia Yin, Jianbin Chao, Yongbin Zhang Yongbin Zhang, and Xing Wei. "An ICT based ultraselective and sensitive fluorescent probe for detection of HClO in living cells." RSC Advances 5, no. 95 (2015): 77670–72. http://dx.doi.org/10.1039/c5ra16097a.
Full textKim, Taehyeong, Heeseok Jeong, Suji Park, and Gyungmin Kim. "Anti-mold Activity of Vanillin and o-Vanillin for the Production of Anti-mold Wallpaper." Korean Science Education Society for the Gifted 15, no. 1 (April 30, 2023): 122–35. http://dx.doi.org/10.29306/jseg.2023.15.1.122.
Full textROSU, Tudor, Angela KRIZA, Viorel CARCU, and Anca NICOLAE. "TRANSITION METAL COMPLEXES OF THE FORMYL VANILLINE DERIVATIVES LIGAND FAMILY." SOUTHERN BRAZILIAN JOURNAL OF CHEMISTRY 5, no. 5 (December 20, 1997): 67–77. http://dx.doi.org/10.48141/sbjchem.v5.n5.1997.68_1997.pdf.
Full textKozlov, N. G., and L. I. Basalaeva. "Vanilline Alkanoates in the Synthesis of Hexahydrobenzacridine and Octahydroxanthene Derivatives." Russian Journal of General Chemistry 75, no. 4 (April 2005): 617–21. http://dx.doi.org/10.1007/s11176-005-0282-2.
Full textBöeseken, J., and J. Greup. "L'Oxydation de Quelques Dérivés de la Vanilline par L'acide Peracétique." Recueil des Travaux Chimiques des Pays-Bas 58, no. 6 (September 3, 2010): 528–37. http://dx.doi.org/10.1002/recl.19390580608.
Full textMonties, Bernard. "Composition chimique des bois de chêne: composés phénoliques, relations avec quelques propriétés physiques et chimiques susceptibles d'influencer la qualité des vins et des eaux-de-vie." OENO One 21, no. 3 (September 30, 1987): 169. http://dx.doi.org/10.20870/oeno-one.1987.21.3.1282.
Full textDissertations / Theses on the topic "Vanilline"
Lambert, Fanny. "Procédés de biosynthèse de composés phénoliques dérivés de la vanilline par bioconversion d'eugénol." Thesis, Strasbourg, 2013. http://www.theses.fr/2013STRAJ116.
Full textOur aim was to develop a process for the biosynthesis of vanillin derivatives from eugenol.Vanillyl alcohol oxidase isolated from Peniciiiium simplissicimum, catalyzes the hydroxylation of eugenolinto coniferyl alcohol. In this study, two strains expressing the biocatalyst were constructed: a yeast,Saccharomyces cerevisiae, and a bacteria; Streptomyces setonii.It has been demonstrated that the wild strain Saccharomyces cerevisiae can bioconvert coniferyl alcohol, most probably due to its dehydrogenase activity. Strain 93645, genetically modified to expressvanillyl-alcohol oxidase, enabled us to optimize an industrial scale process for the production of natural ferulic acid.Streptomyces setonii strain ATCC 39116 was also genetically engineered to over-express VAO. Abioconversion process was developed leading to a coniferyl alcohol concentration of 15 g/1 coniferyl alcohol. The impact of several parameters; such as temperature, substrate addition mode and pH, werealso explored to improve the bioconversion reaction of coniferyl alcohol to vanillin. The amounts of product resulting from bacterial biosynthesis were however too low for implementation of an industrial process
Rabe, Ravelona Manda. "Hydrolyse enzymatique en solution hydroalcoolique de la gousse verte de vanille en vue de l’obtention de l’arôme naturel de vanille." Compiègne, 2006. http://www.theses.fr/2006COMP1652.
Full textAims of traditional procedures for curing vanilla consist of drying the bean and hydrolyzing vanilla aroma precursors. Inconvenient of those procedures is its relatively long duration being able to go in 8 months and poor yield of transformation per hydrolysis of aroma precursors. Aims of this study consist to optimize the production of vanilla extract by improving content of principal compounds (vanillin, vanillic acid, parahydroxybenzaldehyd, parahydroxybenzoic acid) and by reducing the time of obtaining extract. The method used is based on making macerate ground of green beans into hydrolalchoolic solution and by bringing enzymatic preparation source of β-glucosidase activity. Result of this study is the diminution of time procedure to 15 days for obtaining vanilla extract and increase of vanillin content to 2,7 g / 100 g of equivalent cured bean to compare with 1,8-2 g of vanillin obtained with traditional procedure
Fache, Maxence. "Fonctionnalisation et polymérisation de dérivés phénoliques naturels : Vers des matériaux aromatiques biosourcés Vanillin, a key-intermediate of biobased polymers Vanillin, a promising biobased building-block for monomer synthesis Biobased epoxy thermosets from vanillin-derived oligomers Amine hardeners and epoxy cross-linker from aromatic renewable resources Epoxy thermosets from model mixtures of the lignin-tovanillin process." Thesis, Montpellier, Ecole nationale supérieure de chimie, 2015. http://www.theses.fr/2015ENCM0014.
Full textThe background of this work is the synthesis of bio-based polymers, a very active area of research. Epoxy thermosets were chosen as target because of the double problematic of bisphenol A substitution and of renewable resources use. Thus, the aim of this work is to prepare bio-based epoxy thermosets and to evaluate their potential as substitutes of current formulations. In order to display good thermo-mechanical properties, these polymers have to be prepared from renewable aromatics. Indeed, aromatic cycles bring rigidity and thermal stability to the network. Vanillin is one of the only aromatic molecules available from biomass at an industrial scale. It is obtained from the alkaline oxidative depolymerization of lignin. Recently, the preparation of renewable polymers from vanillin has been intensively explored; a review on this subject was compiled. Vanillin served as a building-block to prepare a platform of derivatives bearing various functions. Di-amine, di-epoxy, or di-(cyclic carbonate) monomers – among others – were synthesized. The di-epoxy monomers prepared were cross-linked with a common amine hardener and the polymers obtained were characterized. Their thermo-mechanical properties were linked to the monomers structure. These potentially bio-based epoxy thermosets have properties comparable to the bisphenol A-based reference. In order to tune these properties, vanillin-based epoxy oligomers were synthesized by the same method as the one used industrially. The properties of these oligomers and of the thermosets prepared from them could indeed be modulated. Other means of controlling the properties were tested, like the preparation and polymerization of new bio-based amine hardeners, or of a vanillin-based, tri-functional epoxy monomer. The thermoset prepared from this last compound displayed better properties than the bisphenol A-based reference. Finally, a work more centered on the resource was performed. Mixtures of phenolic compounds modelling the products of the lignin-to-vanillin process were prepared. The use of such mixtures instead of pure vanillin could be advantageous both from an economic and an ecologic point of view. These mixtures were glycidylated, polymerized, and the materials obtained were characterized. The excellent properties displayed by these materials allow a potential integration of this strategy in a bio-refinery
Brunelliere, Jérôme. "Caractérisation des voies métaboliques d'une souche de Streptomyces impliquée dans la production de vanilline." Clermont-Ferrand 2, 2009. http://www.theses.fr/2009CLF21947.
Full textOdoux, Eric. "Contribution à l'étude de l'hydrolyse de la glucovanilline en vanilline dans la "gousse" du vanillier (vanilla planifolia G. Jackson)." Montpellier 2, 2004. http://www.theses.fr/2004MON20057.
Full textFoyer, Gabriel. "Synthèse de résines phénoliques bio-sourcées sans formaldéhyde pour l’industrie aérospatiale." Thesis, Montpellier, Ecole nationale supérieure de chimie, 2015. http://www.theses.fr/2015ENCM0021/document.
Full textResol-type phenolic resins present applicative and thermal properties suitable for applications such as composite manufacture in aeropatial industry. Especially, resols can be polymerized stage-wise and present after curing high char yield properties. However, those resins are typically synthesized from formaldehyde and phenol. Those precursors are both classified as Carcinogenic Mutagenic Reprotoxic (CMR), respectively 1B and 2, and are petrobased. Because of this classification and of the fossil feedstock depletion, SAFRAN-Herakles wants to substitute formaldehyde by non-toxic and biobased aldehyde precursors. Aromatic aldehyde precursors such as 4-hydroxybenzaldehyde, vanillin and syringaldehyde are interestingly non-toxic and can be produced from the cheap and abundant lignins. Nevertheless, we have shown that those precursors are not reactive in resol synthesis conditions. Also, we have shown that difunctional and reactive aromatic aldehyde precursors are suitable for the synthesis of high char yield resins. Then, we have designed two functionalization methods to turn the biobased aldehyde precursors into difunctional and reactive ones. Finally, those precursors have been used for the synthesis of biobased resols without formaldehyde. Those new resins can be polymerized stage-wise and present higher char yield properties than the current formophenolic resins. Hence, those new biobased aldehyde precursors represent promising alternatives to formaldehyde for the synthesis of resols with target properties for aerospatial industry applications
Abdennadher, Mohamed-Naceur. "Valorisation de la lignine organocell par le système oxydant ozone-forane 113." Toulouse, INPT, 1987. http://www.theses.fr/1987INPT002G.
Full textPuzio, Kinga. "Towards controlled release of Vanillin and bio-sensing of Adenosine monophosphate using molecularly imprinted polymers." Thesis, Orléans, 2012. http://www.theses.fr/2012ORLE2075.
Full textThis thesis report presents the exploration of molecularly imprinted polymers (MIP) for the application in controlled release and targeting antivirus and anticancer drugs. The first part of this study describes the imprinting of vanillin as a monolith. Several strategies were studied: non-covalent, covalent and semi-covalent. The composition of the MIP prepared in each approach was optimized to obtain the best properties and performance. The affinity, selectivity and capacity of MIP were determined. MIPs were evaluated in solid-phase extraction (SPE) of structural analogues in natural samples (vanilla extract, wine). We also present the study of the exploration of spherical beads as potential tools for the controlled release of vanillin. These studies concern the characteristics of uptake and release of the molecule of interest in the aqueous medium on functionalised microspheres supplied by Merck ESTAPOR Microspheres®. The second part of this thesis is devoted to studies on the evaluation of MIP of adenosine 5'-monophosphate (AMP). The polymer was prepared in non-covalent approach and efficiency of binding was characterised using frontal analysis (FA). FA is a useful technique that allows discriminate specific and nonspecific interactions and to understand the binding mechanisms in specific cavities
JAWAD, MOHAMED ADEL. "Etude electrochimique de la vanilline et de constituants alimentaires dans les produits lactes." Nantes, 1991. http://www.theses.fr/1991NANT2015.
Full textGuiraud, Pascale. "Métabolisation de l'acide vanillique par les micromycètes : relation avec la production de phénoloxydases extracellulaires." Université Joseph Fourier (Grenoble), 1991. http://www.theses.fr/1991GRE18002.
Full textBooks on the topic "Vanilline"
Tercier, Nicole Stäuble. Vanille, safran. Genève: Conservatoire et jardin botaniques de Genève, 1992.
Find full textHandbook of vanilla science and technology. Chichester, West Sussex: Wiley-Blackwell, 2011.
Find full textPan, Ruqiu. Effect of iron on reactivity of vanillin in wine models. St. Catharines, Ont: Brock University, Dept. of Chemistry, 2004.
Find full textMuszer, Dariusz. Die Freiheit riecht nach Vanille: Roman. München: A1 Verlag, 1999.
Find full textWilhelm Haarmann auf den Spuren der Vanille: Forscher, Unternehmer und Pionier der Riechstoffe. Holzminden: Verlag Jörg Mitzkat, 2012.
Find full textBarret, Jacquelin. Résultats campagne 1993 de préparation de vanille. [Mamoudzou]: Collectivité territoriale de Mayotte, Direction de l'agriculture et de la forêt, 1993.
Find full textBook chapters on the topic "Vanilline"
Bährle-Rapp, Marina. "Vanillin." In Springer Lexikon Kosmetik und Körperpflege, 578. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_10953.
Full textWang, Xiao-Bo, Li-Da Du, Shu-Mei Wang, and Guan-Hua Du. "Vanillin." In Natural Small Molecule Drugs from Plants, 343–46. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-8022-7_57.
Full textBährle-Rapp, Marina. "Ethyl Vanillin." In Springer Lexikon Kosmetik und Körperpflege, 194. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_3798.
Full textLabuda, Ivica. "Biotechnology of Vanillin: Vanillin from Microbial Sources." In Handbook of Vanilla Science and Technology, 299–331. Oxford, UK: Wiley-Blackwell, 2010. http://dx.doi.org/10.1002/9781444329353.ch19.
Full textHavkin-Frenkel, Daphna, Andrzej Podstolski, Ewa Witkowska, Piotr Molecki, and Monika Mikolajczyk. "Vanillin Biosynthetic Pathways." In Plant Cell and Tissue Culture for the Production of Food Ingredients, 35–43. Boston, MA: Springer US, 1999. http://dx.doi.org/10.1007/978-1-4615-4753-2_4.
Full textBährle-Rapp, Marina. "Vanille." In Springer Lexikon Kosmetik und Körperpflege, 578. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_10952.
Full textHavkin-Frenkel, Daphna, and Faith C. Belanger. "Biotechnological production of vanillin." In Biotechnology in Flavor Production, 165–92. Chichester, UK: John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781118354056.ch5.
Full textKhoyratty, Shahnoo, Rob Verpoorte, and Hippolyte Kodja. "Vanillin: Biosynthesis, Biotechnology, and Bioproduction." In Reference Series in Phytochemistry, 341–58. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-38392-3_14.
Full textKhoyratty, Shahnoo, Rob Verpoorte, and Hippolyte Kodja. "Vanillin: Biosynthesis, Biotechnology, and Bioproduction." In Reference Series in Phytochemistry, 1–18. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-11257-8_14-1.
Full textKhoyratty, Shahnoo, Rob Verpoorte, and Hippolyte Kodja. "Vanillin: Biosynthesis, Biotechnology, and Bioproduction." In Reference Series in Phytochemistry, 1–18. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-11257-8_14-2.
Full textConference papers on the topic "Vanilline"
Kashimura, Keiichiro, Chen Qu, Tomohiko Mitani, Naoki Shinohara, and Takashi Watanabe. "Microwave frequency dependence of thermal distribution in the production of vanillin and vanillic acid from lignocellulosic biomass." In 2016 Progress in Electromagnetic Research Symposium (PIERS). IEEE, 2016. http://dx.doi.org/10.1109/piers.2016.7735582.
Full textEltayeb, M. "Preparation and characterization of nanoparticles for encapsulation and delivery vehicles." In Advanced Topics in Mechanics of Materials, Structures and Construction. Materials Research Forum LLC, 2023. http://dx.doi.org/10.21741/9781644902592-18.
Full textThaweboon, Sroisiri, Ratchaporn Srichan, Supaporn Mala, and Boonyanit Thaweboon. "The Development of Artificial Saliva with Oral Wound Healing Property." In 2023 7th International Conference on Nanomaterials and Biomaterials & 2023 5th Asia Conference on Material and Manufacturing Technology. Switzerland: Trans Tech Publications Ltd, 2024. http://dx.doi.org/10.4028/p-wc6acn.
Full textJeremić, Svetlana, Nenad Janković, Jelena Đorović Jovanović, and Zoran Marković. "The assessment of the antioxidant capacity of the selected vanillin-based pyrido-dipyrimidines using DPPH assay: in silico approach." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.613j.
Full textCox, Ashley, Kathleen Brown, and Monica Valentovic. "Effects of the E-liquid Flavoring Agents Vanillin and Ethyl Vanillin in Human Proximal Tubule Epithelial Cells." In ASPET 2023 Annual Meeting Abstracts. American Society for Pharmacology and Experimental Therapeutics, 2023. http://dx.doi.org/10.1124/jpet.122.219880.
Full textRetnosari, Rini, Ihsan B. Rachman, Sutrisno Sutrisno, Meyga E. F. Sari, Dedek Sukarianingsih, and Yaya Rukayadi. "The antibacterial activity of vanillin derivative compounds." In 4TH INTERNATIONAL SEMINAR ON CHEMISTRY. AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0051523.
Full textMarković, Violeta R., Jovana M. Muškinja, and Tamara Lj Todorović. "Synthesis and antioxidant activity of novel vanillin-based ferrocenyl chalcones." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.547m.
Full textViseshsin, Napat, Pimwalun Sukhitkul, Rangsalid Panyadee, Chularat Sakdaronnarong, and Pattaraporn Posoknistakul. "Study of vanillin formation under oxygen delignification process." In 2018 IEEE 5th International Conference on Engineering Technologies and Applied Sciences (ICETAS). IEEE, 2018. http://dx.doi.org/10.1109/icetas.2018.8629121.
Full textRahayu, Reni, Muhammad A. Aziz, Mohammad Holil, and Mardi Santoso. "Synthesis of new vanillin derivatives from natural eugenol." In 4TH INTERNATIONAL SEMINAR ON CHEMISTRY. AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0051751.
Full textRajesh, T. S. F., A. S. Mideen, J. Karthikeyan, and A. MuthuKrishnan. "Inhibition effect of the corrosion of mild steel in acidic solutions by Vanillin-4-methylthio semicarbazone and Vanillin-4-ethylthiosemi-carbazone." In International Conference on Frontiers in Automobile and Mechanical Engineering (FAME 2010). IEEE, 2010. http://dx.doi.org/10.1109/fame.2010.5714842.
Full textReports on the topic "Vanilline"
Beckham, Gregg. Catalytic Depolymerization and Upgrading of Lignin for Vanillin Production: Cooperative Research and Development Final Report, CRADA Number CRD-14-545. Office of Scientific and Technical Information (OSTI), March 2017. http://dx.doi.org/10.2172/1350019.
Full textAggarwal, R. L., L. W. Farrar, B. G. Saar, T. H. Jeys, and R. B. Goodman. Measurement of the Absolute Raman Cross Sections of Diethyl Phthalate, Dimethyl Phthalate, Ethyl Cinnamate, Propylene Carbonate, Tripropyl Phosphate, 1,3-Cyclohexanedione, 3'-Aminoacetophenone, 3'-Hydroxyacetophenone, Diethyl Acetamidomalonate, Isovanillin, Lactide, Meldrum's Acid, p-Tolyl Sulfoxide, and Vanillin. Fort Belvoir, VA: Defense Technical Information Center, September 2013. http://dx.doi.org/10.21236/ada591110.
Full textPichersky, Eran, Alexander Vainstein, and Natalia Dudareva. Scent biosynthesis in petunia flowers under normal and adverse environmental conditions. United States Department of Agriculture, January 2014. http://dx.doi.org/10.32747/2014.7699859.bard.
Full textStruthers, Kim. Natural resource conditions at Fort Pulaski National Monument: Findings and management considerations for selected resources. National Park Service, December 2023. http://dx.doi.org/10.36967/2300064.
Full text