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Merck
CN

55520

3-Hydroxymandelic acid

≥97.0% (T)

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About This Item

Empirical Formula (Hill Notation):
C8H8O4
CAS Number:
Molecular Weight:
168.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
241-182-3
Beilstein/REAXYS Number:
2365378
MDL number:
Assay:
≥97.0% (T)
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InChI key

OLSDAJRAVOVKLG-UHFFFAOYSA-N

InChI

1S/C8H8O4/c9-6-3-1-2-5(4-6)7(10)8(11)12/h1-4,7,9-10H,(H,11,12)

SMILES string

OC(C(O)=O)c1cccc(O)c1

assay

≥97.0% (T)

mp

128-132 °C

functional group

carboxylic acid, hydroxyl

Quality Level

General description

3-Hydroxymandelic acid is a hydroxy acid derivative. Chiral separation of 3-hydroxymandelic acid has been achieved by ligand-exchange capillary electrochromatography.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Excretion of m-hydroxymandelic acid in human urine.
B A Davis et al.
Journal of chromatography, 222(2), 271-275 (1981-02-13)
J R Crowley et al.
Clinica chimica acta; international journal of clinical chemistry, 109(2), 125-131 (1981-01-22)
o-Hydroxymandelic acid (OHMA), m-hydroxymandelic acid (MHMA) and p-hydroxymandelic acid (PHMA) were measured in the urine of 42 normotensive and 54 hypertensive patients. Patients having high urinary MHMA levels were all found to be ingesting medications containing m-synephrine (phenylephrine). These patients
Role of the charge in continuous beds in the chiral separation of hydroxy acids by ligand-exchange capillary electrochromatography.
Lecnik O, et al.
Electrophoresis, 24(17), 2983-2985 (2003)
K Gumbhir et al.
Journal of pharmaceutical and biomedical analysis, 12(7), 943-949 (1994-07-01)
An LC method for the analysis of m-hydroxymandelic acid (MHMA) and m-hydroxyphenylglycol (MHPG) and their conjugates in human plasma was developed and validated. The method for the quantitation involved extraction of acidified plasma (subject to hydrolysis with beta-glucuronidase for 120
J R Crowley et al.
Biomedical mass spectrometry, 9(4), 146-152 (1982-04-01)
m-Hydroxyphenylglycol (MHPG) has been identified in mammalian urine by gas chromatography mass spectrometry selected ion monitoring. (2H0) MHPG and (2H5) MHPG were synthesized for use as authentic sample and internal standard, respectively. After acid hydrolysis or treatment with sulfatase, the

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