Hippuric acid 98% | Sigma-Aldrich

Properties

Related Categories	Amino Acid Derivatives, Bioactive Small Molecules, Cell Biology, Chemical Biology, Chemical Synthesis, Glycine, H, Nutrition Research, Peptide Chemistry, Phytochemicals by Plant (Food/Spice/Herb), Vaccinium macrocarpon (Cranberry) More...
assay	98%
mp	187-191 °C(lit.)
Gene Information	rat ... Akr1b1(24192)

Description

Packaging

100, 500 g in poly bottle

5 g in glass bottle

Application

Hippuric acid can be used to study cell biology, chemical biology, bioactive small molecules, amino acid derivatives, peptide synthesis, chemical synthesis and nutrition. Hippuric acid has been used to inform the metabolism and urinary excretion of procyanidins.

Price and Availability

Suggested Laboratory Gloves

This substance has been tested against several types of hand protection for CE compliance. Click below to find the recommended gloves for handling this product.

for splash & immersion protection

Related Papers

Consumption of Hibiscus sabdariffa L. aqueous extract and its impact on systemic antioxidant potential in healthy subjects Frank, T., et al. J. Sci. Food Agric. 92(10), 2207-18, (2012)

Documents

Certificate of Analysis

Certificate of Origin

Safety Information

Symbol	GHS05, GHS07
Signal word	Danger
Hazard statements	H302-H315-H318-H335
Precautionary statements	P261-P280-P305 + P351 + P338
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes (Europe)	Xn
Risk Statements (Europe)	22-37/38-41
Safety Statements (Europe)	26-39
WGK Germany	3
RTECS	MR8150000

Technical information & documentation associated with this product is available in the Safety & Documentation tab.

Papers

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Consumption of Hibiscus sabdariffa L. aqueous extract and its impact on systemic antioxidant potential in healthy subjects Frank, T., et al. J. Sci. Food Agric. 92(10), 2207-18, (2012)

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Protein-bound uremic toxins in hemodialysis patients measured by liquid chromatography/tandem mass spectrometry and their effects on endothelial ROS production Itoh, Y., et al. Anal. Bioanal. Chem 403(7), 1841-50, (2012)

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Urinary excretion and metabolism of procyanidins in pigs Rzeppa, S., et al. Mol. Nutr. Food. Res. 56, 653-65, (2012)

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Structural variation governs substrate specificity for organic anion transporter (OAT) homologs. Potential remote sensing by OAT family members. Gregory Kaler et al J. Biol. Chem. 282, 23841-53, (2007)

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Crystal structure of the Homo sapiens kynureninase-3-hydroxyhippuric acid inhibitor complex: insights into the molecular basis of kynureninase substrate specificity. Santiago Lima et al J. Med. Chem. 52, 389-96, (2009)

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Molecular modifications on carboxylic acid derivatives as potent histone deacetylase inhibitors: Activity and docking studies. Gamze Bora-Tatar et al Bioorg. Med. Chem. 17, 5219-28, (2009)

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Elucidation of common pharmacophores from analysis of targeted metabolites transported by the multispecific drug transporter-Organic anion transporter1 (Oat1). Valentina L Kouznetsova et al Bioorg. Med. Chem. 19, 3320-40, (2011)

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Merck 14,4716

Beil. 9,IV,778

Fieser 1,432

FT-IR 2 (2), 3010:D / FT-IR 1 (2), 376:D / FT-NMR 1 (2), 1405:A / IR-Spectra (3), 1082:G / IR-Spectra (2), 945:B / NMR-Reference 2 (2), 353:C / RegBook 1 (2), 2025:K / Sigma FT-IR 1 (1), 179:D / Structure Index 1, 323:C:4

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Hippuric acid

98%

Properties

Description

Packaging

Application

Price and Availability

Suggested Laboratory Gloves

Related Papers

Documents

Safety Information

Papers

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