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W288918 Aldrich

3-Phenylpropionic acid

99%, FG

Synonym: 3-Phenylpropionic acid, Benzylacetic acid, Hydrocinnamic acid

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Properties

Related Categories Alphabetical Listings, Flavors and Fragrances, Halal Certified Products, Kosher Certified Products, O - Z,
biological source   synthetic
grade   FG
  Halal
  Kosher
  NI
reg. compliance   FDA 21 CFR (172.515)
  EU Regulation 1334/2008 & 872/2012
assay   99%
bp   280 °C(lit.)
mp   45-48 °C(lit.)
density   1.071 g/mL at 25 °C(lit.)
Organoleptic   rose; sweet
food allergen   no known allergens

Description

Packaging

1 kg in glass bottle

10 kg in fiber drum

100 g in glass bottle

Other Notes

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Price and Availability

Additional Products to Explore

Benzoic acid

ACS reagent, ≥99.5%

Safety & Documentation

Safety Information

WGK Germany 
3
RTECS 
DA8600000
Flash Point(F) 
235.4 °F
Flash Point(C) 
113 °C

Protocols & Articles

Articles

Understanding the Complexities of Kosher Ingredients

Dr. Luke Grocholl, Quality Assurance Supervisor, Sigma-Aldrich Flavors & Fragrances and Rabbi Gershon Segal
Keywords: Fermentation, Food & Beverage, Safety industry

Peer-Reviewed Papers

References

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Plasma carotenoids, retinol, and tocopherols and the risk of prostate cancer in the European Prospective Investigation into Cancer and Nutrition study. Key TJ, Appleby PN, Allen NE, et al. Am. J. Clin. Nutr. 86(3), 672-81, (2007)

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Human fecal water inhibits COX-2 in colonic HT-29 cells: role of phenolic compounds. Karlsson PC, Huss U, Jenner A, et al. J. Nutr. 135(10), 2343-9, (2005)

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A metabolite profiling approach to identify biomarkers of flavonoid intake in humans. Loke, W.M., et al. J. Nucl. Med. 139, 2309-14, (2009)

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Activation of remote meta-C-H bonds assisted by an end-on template Leow, D.; Li, G.; Mei, T-S.; Yu, J-Q. Nature 7404th ed., 486, 518-522, (2012)

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Ligand-enabled reactivity and selectivity in a synthetically versatile aryl C-H olefination. Wang DH, Engle KM, Shi BF, et al. Science 327(5963), 315-9, (2010)

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Metabolomic profiles delineate potential role for sarcosine in prostate cancer progression. Sreekumar A, Poisson LM, Rajendiran TM, et al. Nature 457(7231), 910-4, (2009)

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Biological activity of phenylpropionic acid isolated from a terrestrial Streptomycetes. Narayana KJ, Prabhakar P, Vijayalakshmi M, et al. Pol. J. Microbiol. 56(3), 191-7, (2007)

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Janus PEG-based dendrimers for use in combination therapy: controlled multi-drug loading and sequential release. Acton AL, Fante C, Flatley B, et al. Biomacromolecules 14(2), 564-74, (2013)

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Monolignol pathway 4-coumaric acid:coenzyme A ligases in Populus trichocarpa: novel specificity, metabolic regulation, and simulation of coenzyme A ligation fluxes. Chen HC, Song J, Williams CM, et al. Plant Physiol. 161(3), 1501-16, (2013)

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Lipophilic phenolic antioxidants: correlation between antioxidant profile, partition coefficients and redox properties. Fernanda M F Roleira et al Bioorg. Med. Chem. 18, 5816-25, (2010)

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Selenium and selenomethionine levels in prostate cancer patients. Nyman DW, Suzanne Stratton M, Kopplin MJ, et al. Cancer Detect. Prev. 28(1), 8-16, (2004)

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Directed functionalization of C-H bonds: now also meta selective. Truong T and Daugulis O Angew. Chem. Int. Ed. Engl. 51(47), 11677-9, (2012)

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HCl-induced inflammatory mediators in cat esophageal mucosa and inflammatory mediators in esophageal circular muscle in an in vitro model of esophagitis. Cheng L, Cao W, Fiocchi C, et al. Am. J. Physiol. Gastrointest. Liver Physiol. 290(6), G1307-17, (2006)

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Distinct substrate specificities and unusual substrate flexibilities of two hydroxycinnamoyltransferases, rosmarinic acid synthase and hydroxycinnamoyl-CoA:shikimate hydroxycinnamoyl-transferase, from Coleus blumei Benth. Sander M and Petersen M Planta 233(6), 1157-71, (2011)

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Complex formation of uranium(VI) with L-phenylalanine and 3-phenylpropionic acid studied by attenuated total reflection Fourier transform infrared spectroscopy. Barkleit A, Foerstendorf H, Heim K, et al. Appl. Spectrosc. 62(7), 798-802, (2008)

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Protective effects of 4-phenylbutyrate derivatives on the neuronal cell death and endoplasmic reticulum stress. Mimori S, Okuma Y, Kaneko M, et al. Biol. Pharm. Bull. 35(1), 84-90, (2012)

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Metabolism of [(14)C]omapatrilat, a sulfhydryl-containing vasopeptidase inhibitor in humans. Iyer RA, Mitroka J, Malhotra B, et al. Drug Metab. Dispos. 29(1), 60-9, (2001)

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Comparative biotransformation of radiolabeled [(14)C]omapatrilat and stable-labeled [(13)C(2)]omapatrilat after oral administration to rats, dogs, and humans. Iyer RA, Malhotra B, Khan S, et al. Drug Metab. Dispos. 31(1), 67-75, (2003)

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Antimicrobial potential of 3-hydroxy-2-methylene-3-phenylpropionic acid derivatives. Singh SA and Bhat SV Acta. Pharm. 61(4), 447-55, (2011)

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Study on bioactive compounds from Streptomyces sp. ANU 6277. Narayana KJ, Prabhakar P, Vijayalakshmi M, et al. Pol. J. Microbiol. 57(1), 35-9, (2008)

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High-performance functional ecopolymers based on flora and fauna. Kaneko T Chem. Rec. 7(4), 210-9, (2007)

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3-phenylpropionate catabolism and the Escherichia coli oxidative stress response. Turlin E, Sismeiro O, Le Caer JP, et al. Res. Microbiol. 156(3), 312-21, (2005)

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Isolation and characterization of antifungal substances from Burkholderia sp. culture broth. Mao S, Lee SJ, Hwangbo H, et al. Curr. Microbiol. 53(5), 358-64, (2006)

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Dynamical dimer structure and liquid structure of fatty acids in their binary liquid mixture: dodecanoic and 3-phenylpropionic acids system. Iwahashi M, Takebayashi S, Umehara A, et al. Chem. Phys. Lipids 129(2), 195-208, (2004)

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Production of 4-ethylphenol from 4-hydroxycinnamic acid by Lactobacillus sp. isolated from a swine waste lagoon. Kridelbaugh D, Hughes S, Allen T, et al. J. Appl. Microbiol. 109(1), 190-8, (2010)

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Physico-chemical studies of new luminescent chemosensor for Cu2+. Jayabharathi J, Thanikachalam V, Vennila M, et al. Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 96, 677-83, (2012)

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Development of a simple system for dehydrocondensation using solid-phase adsorption of a water-soluble dehydrocondensing reagent (DMT-MM). Watanabe Y, Fuji T, Hioki K, et al. Chem. Pharm. Bull. 52(10), 1223-6, (2004)

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Urinary unconjugated 5 alpha-androstane-3 alpha, 17 beta-diol in patients with prostatic tumours. Puah CM, Williams G, and Ghanadian R Urol. Res. 10(2), 81-4, (1982)

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Merck 14,4784

Beil. 9,III,2382

Arctander, 2579 / Corp MSDS 1, 1893:C / Corp MSDS 1 (1), 1893:C / FT-IR 2 (2), 2576:D / FT-IR 1 (2), 139:C / FT-NMR 1 (2), 985:A / Fenaroli / IR-Spectra (3), 931:D / IR-Spectra (2), 815:C / NMR-Reference 2 (2), 135:B / RegBook 1 (2), 1741:O / RegBook 79 (2), 1741:O / Sigma FT-IR 1 (2), 618:A / Structure Index 1, 278:D:3

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