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Fragrance material review on benzyl formate.
McGinty D, Letizia CS, Api AM. McGinty D, et al. Food Chem Toxicol. 2012 Sep;50 Suppl 2:S402-6. doi: 10.1016/j.fct.2012.02.062. Epub 2012 Mar 3. Food Chem Toxicol. 2012. PMID: 22406578 Review.
A toxicologic and dermatologic review of benzyl formate when used as a fragrance ingredient is presented. Benzyl formate is a member of the fragrance structural group Aryl Alkyl Alcohol Simple Acid Esters (AAASAE). ...This review contains a detailed su …
A toxicologic and dermatologic review of benzyl formate when used as a fragrance ingredient is presented. Benzyl for …
RIFM fragrance ingredient safety assessment, benzyl formate, CAS Registry Number 104-57-4.
Api AM, Belsito D, Botelho D, Browne D, Bruze M, Burton GA Jr, Buschmann J, Dagli ML, Date M, Dekant W, Deodhar C, Francis M, Fryer AD, Joshi K, La Cava S, Lapczynski A, Liebler DC, O'Brien D, Parakhia R, Patel A, Penning TM, Ritacco G, Romine J, Salvito D, Schultz TW, Sipes IG, Thakkar Y, Theophilus EH, Tiethof AK, Tokura Y, Tsang S, Wahler J. Api AM, et al. Food Chem Toxicol. 2018 May;115 Suppl 1:S173-S182. doi: 10.1016/j.fct.2018.01.007. Epub 2018 Jan 6. Food Chem Toxicol. 2018. PMID: 29317331 Review. No abstract available.
Photochemical degradation of fragrance ingredient benzyl formate in water: Mechanism and toxicity assessment.
Wu J, Gao Y, Qin Y, Li G, An T. Wu J, et al. Ecotoxicol Environ Saf. 2021 Mar 15;211:111950. doi: 10.1016/j.ecoenv.2021.111950. Epub 2021 Jan 25. Ecotoxicol Environ Saf. 2021. PMID: 33493723 Free article.
To understand transformation mechanisms and toxicity evolution of benzyl formate (BF) in environment, its photochemical degradation in water was thoroughly studied herein. ...
To understand transformation mechanisms and toxicity evolution of benzyl formate (BF) in environment, its photochemical degrad …
Biological Activity of Picrorhiza kurroa: A Source of Potential Antimicrobial Compounds against Yersinia enterocolitica.
Thapa A, Kaushik R, Arora S, Jaglan S, Jaswal V, Yadav VK, Singh M, Bains A, Chawla P, Khan A, Fogarasi M, Fogarasi S. Thapa A, et al. Int J Mol Sci. 2022 Nov 15;23(22):14090. doi: 10.3390/ijms232214090. Int J Mol Sci. 2022. PMID: 36430568 Free PMC article.
Potential bioactive compounds from P. kurroa were identified using LC-MS, namely, cerberidol, annonidine A, benzyl formate, picroside-1, and furcatoside A. P. kurroa showed effective antimicrobial potential in skim milk at different pH, acidity, and water activity l …
Potential bioactive compounds from P. kurroa were identified using LC-MS, namely, cerberidol, annonidine A, benzyl formate, pi …
Chemo-Enzymatic Synthesis of Poly(4-piperidine lactone- b-ω-pentadecalactone) Block Copolymers as Biomaterials with Antibacterial Properties.
Xiao Y, Pan J, Wang D, Heise A, Lang M. Xiao Y, et al. Biomacromolecules. 2018 Jul 9;19(7):2673-2681. doi: 10.1021/acs.biomac.8b00296. Epub 2018 May 4. Biomacromolecules. 2018. PMID: 29698599
Herein, we demonstrated a chemo-enzymatic ring opening polymerization (ROP) approach for block copolyester, that is, poly(4-benzyl formate piperidine lactone- b-omega-pentadecalactone) (PNPIL- b-PPDL), in a one-pot two-step process. ...
Herein, we demonstrated a chemo-enzymatic ring opening polymerization (ROP) approach for block copolyester, that is, poly(4-benzyl …
Nickel Nanoparticles Immobilized over Mesoporous SBA-15 for Efficient Carbonylative Coupling Reactions Utilizing CO2: A Spotlight.
Chongdar S, Bhattacharjee S, Azad S, Samui S, Dutta S, Bal R, Bhaumik A. Chongdar S, et al. ACS Appl Mater Interfaces. 2021 Sep 1;13(34):40157-40171. doi: 10.1021/acsami.1c09942. Epub 2021 Aug 20. ACS Appl Mater Interfaces. 2021. PMID: 34415715
Ecofriendly routes for the synthesis of carbamates and carbonylative coupling products such as benzyl formate derivatives are very demanding for both academia and industries. ...
Ecofriendly routes for the synthesis of carbamates and carbonylative coupling products such as benzyl formate derivatives are …
Measuring and Predicting the Extraction Behavior of Biogenic Formic Acid in Biphasic Aqueous/Organic Reaction Mixtures.
Veith H, Voges M, Held C, Albert J. Veith H, et al. ACS Omega. 2017 Dec 14;2(12):8982-8989. doi: 10.1021/acsomega.7b01588. eCollection 2017 Dec 31. ACS Omega. 2017. PMID: 31457422 Free PMC article.
Extraction solvents discussed in this work are 1-butanol, 1-pentanol, 1-hexanol, 1-heptanol, 1-octanol, 1-decanol, ethyl n-butyl ether, diisopropyl ether, di-n-butyl ether, benzyl formate, and heptyl formate. The considered temperature ranged from 273 to 363 K under …
Extraction solvents discussed in this work are 1-butanol, 1-pentanol, 1-hexanol, 1-heptanol, 1-octanol, 1-decanol, ethyl n-butyl ether, diis …