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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
HOC6H3(OCH3)CH2CO2H
CAS 번호:
Molecular Weight:
182.17
NACRES:
NA.47
PubChem Substance ID:
UNSPSC Code:
12171500
EC Number:
206-176-7
MDL number:
Beilstein/REAXYS Number:
2213447
제품 이름
Homovanillic acid, Fluorimetric reagent
assay
>99% (TLC)
form
powder
InChI key
QRMZSPFSDQBLIX-UHFFFAOYSA-N
InChI
1S/C9H10O4/c1-13-8-4-6(5-9(11)12)2-3-7(8)10/h2-4,10H,5H2,1H3,(H,11,12)
SMILES string
COc1cc(CC(O)=O)ccc1O
technique(s)
titration: suitable
color
white to off-white
mp
142-145 °C (lit.)
solubility
ethanol: 50 mg/mL, colorless to light yellow
application(s)
diagnostic assay manufacturing
hematology
histology
storage temp.
room temp
Quality Level
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Application
Homovanillic acid has been used as a standard in HPLC analysis.
Biochem/physiol Actions
Metabolite of dihydroxyphenylacetic acid (DOPAC) by catechol O-methyltransferase; reagent for the fluorimetric determination of glucose oxidase and other oxidative enzymes.
저장 등급
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Tashjian AH and Armstrong EJ
Principles of Pharmacology: The Pathophysiologic Basis of Drug Therapy (2011)
Practical Fluorescence (1990)
Exercise induces behavioral recovery and attenuates neurochemical deficits in rodent models of Parkinson's disease.
Tillerson JL
Neuroscience, 119, 899-899 (2003)
Forced nonuse in unilateral parkinsonian rats exacerbates injury.
Tillerson JL
The Journal of Neuroscience, 22, 6790-6790 (2002)
Michèl A Willemsen et al.
Brain : a journal of neurology, 133(Pt 6), 1810-1822 (2010-05-01)
Tyrosine hydroxylase deficiency is an autosomal recessive disorder resulting from cerebral catecholamine deficiency. Tyrosine hydroxylase deficiency has been reported in fewer than 40 patients worldwide. To recapitulate all available evidence on clinical phenotypes and rational diagnostic and therapeutic approaches for
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