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716391

Sigma-Aldrich

3-Hydroxy-4-methoxyphenylacetic acid

97%

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About This Item

Fórmula empírica (notación de Hill):
C9H10O4
Número de CAS:
1131-94-8
Peso molecular:
182.17
MDL number:
MFCD00016829
UNSPSC Code:
12352100
PubChem Substance ID:
329763388
NACRES:
NA.22

Quality Level

100

assay

97%

form

solid

mp

127-132 °C

SMILES string

COc1ccc(CC(O)=O)cc1O

InChI

1S/C9H10O4/c1-13-8-3-2-6(4-7(8)10)5-9(11)12/h2-4,10H,5H2,1H3,(H,11,12)

InChI key

BWXLCOBSWMQCGP-UHFFFAOYSA-N

Categorías relacionadas

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificados de análisis (COA)

Lot/Batch Number
MKBC4860V
MKBC4860

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M K Sim et al.
Clinical and experimental hypertension. Part A, Theory and practice, 12(3), 343-353 (1990-01-01)
The levels of dopamine and its metabolites in the adenohypophysis of the normo- and hypertensive rats were determined. Dopamine was present as the free and sulfate-conjugated form in the adenohypophysis of the spontaneously hypertensive rat (SHR), Wistar Kyoto (WKY) and
J Chauhan et al.
Journal of chromatography, 183(4), 391-401 (1980-10-10)
The determination of urinary homovanillic, isohomovanillic and vanillylmandelic acids as their trifluoroacetylhexafluoroisopropyl ester derivatives by glass capillary gas-liquid chromatography has been studied. It was shown that even with high column efficiencies a single peak-single compound relationship could not be assumed
F A Muskiet et al.
Clinical chemistry, 25(10), 1708-1713 (1979-10-01)
We describe the determination of the 4-O-methylated catecholamine metabolites 4-methoxy-3-hydroxyphenylacetic acid (iso-HVA), 4-methoxy-3-hydroxyphenylmandelic acid (iso-VMA) and 4-methoxy-3-hydroxyphenylethylene glycol (iso-MOPEG) in urine with use of mass fragmentography and deuterated internal standards. Normal values, expressed in terms of creatinine, are given as
T Oishi et al.
Journal of neural transmission, 53(2-3), 101-108 (1982-01-01)
The injection of reserpine [2.5 mg/kg, intraperitoneally (i.p.)] increased brain concentration of tyrosine and of the major catecholamine metabolites, 3-methoxy-4-hydroxy-phenylethylene--glycol-sulfate (MHPG-SO4) in the rat. In reserpine-treated animals, tyrosine administration (200 mg/kg, i.p.) caused further increases in brain tyrosine, DOPAC, and
Violetta Mohos et al.
International journal of molecular sciences, 20(11) (2019-06-05)
Quercetin is an abundant flavonoid in nature and is used in several dietary supplements. Although quercetin is extensively metabolized by human enzymes and the colonic microflora, we have only few data regarding the pharmacokinetic interactions of its metabolites. Therefore, we
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