2-Hydroxyhippuric acid

95%

Reagent Code: #195939
label
Alias O-hydroxymauric acid; 2-hydroxybenzolaminoacetic acid; o-Hydroxyhippuric acid; 2-Hydroxyhippuric acid
fingerprint
CAS Number 487-54-7

science Other reagents with same CAS 487-54-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 195.17 g/mol
Formula C₉H₉NO₄
badge Registry Numbers
EC Number 207-661-6
MDL Number MFCD00002695
thermostat Physical Properties
Melting Point 167-169 °C (lit.)
Boiling Point 331.83°C
inventory_2 Storage & Handling
Density 1.3544g/cm3
Storage 2-8°C

description Product Description

2-Hydroxyhippuric acid, also known as salicyluric acid, is used as a biomarker in metabolomics research, particularly for assessing exposure to salicylic acid or phenolic compounds from dietary sources such as fruits, coffee, and plants. It is a metabolite formed through glycine conjugation of salicylic acid and is primarily excreted in urine, aiding in the evaluation of health status, antioxidant intake, and metabolic processes. Additionally, it serves as an indicator in microbiome studies, as it is produced by gut microbiota during the breakdown of phenolic acids.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,200.00
inventory 1g
10-20 days ฿3,500.00
inventory 5g
10-20 days ฿17,360.00

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2-Hydroxyhippuric acid
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2-Hydroxyhippuric acid, also known as salicyluric acid, is used as a biomarker in metabolomics research, particularly for assessing exposure to salicylic acid or phenolic compounds from dietary sources such as fruits, coffee, and plants. It is a metabolite formed through glycine conjugation of salicylic acid and is primarily excreted in urine, aiding in the evaluation of health status, antioxidant intake, and metabolic processes. Additionally, it serves as an indicator in microbiome studies, as it is pro

2-Hydroxyhippuric acid, also known as salicyluric acid, is used as a biomarker in metabolomics research, particularly for assessing exposure to salicylic acid or phenolic compounds from dietary sources such as fruits, coffee, and plants. It is a metabolite formed through glycine conjugation of salicylic acid and is primarily excreted in urine, aiding in the evaluation of health status, antioxidant intake, and metabolic processes. Additionally, it serves as an indicator in microbiome studies, as it is produced by gut microbiota during the breakdown of phenolic acids.

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