D131806
3,4-Dimethoxybenzoic acid
≥99%
Synonym(s):
Veratric acid, 3,4-Dimethoxybenzoic acid
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About This Item
Linear Formula:
(CH3O)2C6H3CO2H
CAS Number:
Molecular Weight:
182.17
Beilstein/REAXYS Number:
518285
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
≥99%
form
powder
mp
179-182 °C (lit.)
SMILES string
COc1ccc(cc1OC)C(O)=O
InChI
1S/C9H10O4/c1-12-7-4-3-6(9(10)11)5-8(7)13-2/h3-5H,1-2H3,(H,10,11)
InChI key
DAUAQNGYDSHRET-UHFFFAOYSA-N
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Related Categories
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Murugesan Saravanakumar et al.
Journal of cardiovascular pharmacology, 59(6), 553-562 (2012-03-01)
Hypertension is associated with dyslipidemia, which is a significant risk factor for cardiovascular complications. This study was undertaken to investigate the effects of veratric acid (VA) on blood pressure, plasma, and tissue lipid profile in N-nitro-L-arginine methyl ester (L-NAME)-induced hypertensive
Stephen G Bell et al.
Molecular bioSystems, 6(1), 206-214 (2009-12-22)
CYP199A4 (RPB3613) from Rhodopseudomonas palustris HaA2 is a heme monooxygenase that catalyzes the hydroxylation of para-substituted benzoic acids. Monooxygenase activity of CYP199A4 can be reconstituted in a Class I electron transfer chain with an associated [2Fe-2S] ferredoxin, HaPux, (RPB3614) and
Marta Czarnecka et al.
Molecules (Basel, Switzerland), 23(8) (2018-08-15)
Phenolic acids and its methoxy derivatives are known to induce caspase-mediated apoptosis activity and exhibit cytotoxic effect towards various cancer cell lines. However, their low stability and poor bioavailability in the human organism extensively restrict the utility of this group
Pedro A R Fernandes et al.
Carbohydrate polymers, 223, 115132-115132 (2019-08-21)
In this work, polysaccharides extracted with hot water from apple pomace were isolated by C18 cartridge solid-phase extraction at pH 7 (Fr7). Dialysis (12-14 kDa) of this fraction allowed to obtain 17% (w/w) of polymeric material composed by 65% of polysaccharides
Gary Ward et al.
The Journal of biological chemistry, 278(41), 39726-39734 (2003-07-15)
The steady state kinetic parameters Km and kcat for the oxidation of phenolic substrates by lignin peroxidase correlated with the presteady state kinetic parameters Kd and k for the reaction of the enzyme intermediate compound II with the substrates, indicating
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