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About This Item
Linear Formula:
HOC6H4CH2CO2H
CAS Number:
Molecular Weight:
152.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-684-4
Beilstein/REAXYS Number:
2086506
MDL number:
Product Name
3-Hydroxyphenylacetic acid, ≥99%
InChI
1S/C8H8O3/c9-7-3-1-2-6(4-7)5-8(10)11/h1-4,9H,5H2,(H,10,11)
InChI key
FVMDYYGIDFPZAX-UHFFFAOYSA-N
SMILES string
OC(=O)Cc1cccc(O)c1
assay
≥99%
mp
129-133 °C (lit.)
Quality Level
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Related Categories
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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P S McQuade et al.
Progress in neuro-psychopharmacology & biological psychiatry, 7(4-6), 755-759 (1983-01-01)
The administration of deuterated beta-phenylethylamine to mice causes increased concentrations of deuterated para-hydroxyphenylacetic acid and meta-hydroxyphenylacetic acid within the caudate nuclei two hours after injection. Deuterated m-HPAA concentrations remain elevated at 4 hours. This suggests that high concentrations of PE
Hanne Winning et al.
The Analyst, 134(11), 2344-2351 (2009-10-20)
The metabolome following intake of onion by-products is evaluated. Thirty-two rats were fed a diet containing an onion by-product or one of the two derived onion by-product fractions: an ethanol extract and the residue. A 24 hour urine sample was
Xin Fang et al.
Frontiers in microbiology, 9, 2559-2559 (2018-11-15)
Dysbiosis of the gut microbiome, including elevated abundance of putative leading bacterial triggers such as E. coli in inflammatory bowel disease (IBD) patients, is of great interest. To date, most E. coli studies in IBD patients are focused on clinical
Doris M Jacobs et al.
Journal of agricultural and food chemistry, 60(12), 3078-3085 (2012-03-01)
Red wine and grape polyphenols are considered to promote cardiovascular health and are involved in multiple biological functions. Their overall impact on the human metabolome is not known. Therefore, exogenous and endogenous metabolic effects were determined in fasting plasma and
P S McQuade et al.
Progress in neuro-psychopharmacology & biological psychiatry, 8(4-6), 705-709 (1984-01-01)
Para-tyramine administration decreased the release of dopamine as indicated by the decline in 3-MT concentrations, increased HVA concentrations at 30 and 60 min and decreased DA concentrations at the same times. DOPAC concentrations declined after 60 min. Meta-tyramine reduced the
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