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Malonic acid

Malonic acid is a dicarboxylic acid with the chemical formula CH2(COOH)2.
It is a colorless, crystalline solid that is soluble in water and organic solvents.
Malonic acid is an important intermediate in organic synthesis and is commonly used in the preparation of various pharmaceutical and chemical compounds.
It plays a role in the citric acid cycle and is involved in various metabolic pathways.
Malonic acid and its derivatives have a wide range of applications, including in the production of plastics, dyes, and agricultural chemicals.
Reasearch on malonic acid can be facilitated through the use of PubCompare.ai, an AI-driven platform that helps identify the best protocols and products for your needs, while ensuring reproducibility and accuracy in your work.

Most cited protocols related to «Malonic acid»

Fecal SCFA content was determined by gas chromatography. Chromatographic
analysis was carried out using a Shimadzu GC14-A system with a flame ionization
detector (FID) (Shimadzu Corp, Kyoto, Japan). Fused silica capillary columns 30m
× 0.25 mm coated with 0.25um film thickness were used (Nukol™
for the volatile acids and SPB™-1000 for the nonvolatile acids (Supelco
Analytical, Bellefonte, PA). Nitrogen was used as the carrier gas. The oven
temperature was 170°C and the FID and injection port was set to
225°C. The injected sample volume was 2 µL and the run time for
each analysis was 10 minutes. The chromatograms and data integration was carried
out using a Shimadzu C-R5A Chromatopac. A volatile acid mix containing 10 mM of
acetic, propionic, isobutyric, butyric, isovaleric, valeric, isocaproic,
caproic, and heptanoic acids was used (Matreya, Pleasant Gap, PA). A
non-volatile acid mix containing 10 mM of pyruvic and lactic and 5 mM of
oxalacetic, oxalic, methy malonic, malonic, fumaric, and succinic was used
(Matreya, Pleasant Gap, PA). A standard stock solution containing 1%
2-methyl pentanoic acid (Sigma-Aldrich, St. Louis, MO) was prepared as an
internal standard control for the volatile acid extractions. A standard stock
solution containing 50 mM benzoic acid (Sigma-Aldrich, St. Louis, MO) was
prepared as an internal standard control for the non-volatile acid
extractions.
Samples were kept frozen at −80°C until analysis. The
samples were removed from the freezer and 1,200µL of water was added to
each thawed sample. The samples were vortexed for 1 minute until the material
was homogenized. The pH of the suspension was adjusted to 2–3 by adding
50 µL of 50% sulfuric acid. The acidified samples were kept at
room temperature for 5 minutes and vortexed briefly every minute. The samples
were centrifuged for 10 minutes at 5,000g. 500 µL of the clear
supernatant was transferred into two tubes for further processing. For the
volatile extraction 50 µL of the internal standard (1% 2-methyl
pentanoic acid solution) and 500 µL of ethyl ether anhydrous were added.
The tubes were vortexed for 30 seconds and then centrifuged at 5,000g for 10
minutes. 1 µL of the upper ether layer was injected into the
chromatogram for analysis. For the nonvolatile extraction 50 µL of the
internal standard (50 mM benzoic acid solution) and 500 µL of boron
trifluoride-methanol solution (Sigma-Aldrich St. Louis, MO) were added to each
tube. These tubes were incubated overnight at room temperature. 1 mL of water
and 500 µL of chloroform were added to each tube. The tubes were
vortexed for 30 seconds and then centrifuged at 5,000g for 10 minutes. 1
µL of the lower chloroform layer was injected into the chromatogram for
analysis. 500 µL of each standard mix was used and the extracts prepared
as described for the samples. The retention times and peak heights of the acids
in the standard mix were used as references for the sample unknowns. These acids
were identified by their specific retention times and the concentrations
determined and expressed as mM concentrations per gram of sample.
Publication 2013
Acids Benzoic Acid Capillaries Chloroform Ethers Feces ferrous fumarate Freezing Gas Chromatography Heptanoic Acids Methanol Neoplasm Metastasis Nitrogen Retention (Psychology) Silicon Dioxide Sulfuric Acids valeric acid
Respiration was measured simultaneously in 10 respiration chambers (O2k; Oroboros Oxygraph-2k, Innsbruck, Austria), one O2k with two chambers for each of the following temperatures: 4, 25, 30, 37, and 40 °C. Permeabilized fibers (0.7–1.3 mg at 25 to 40 °C and 7–8 mg at 4 °C) were used in each chamber containing 2 ml of MiR05. Respiratory flux was expressed per mg wet weight of fibers. Instrumental and chemical oxygen background fluxes were calibrated as a function of oxygen concentration and subtracted from the total volume-specific oxygen flux (Datlab software, Oroboros Instruments)55 (link), 82 (link), 86 (link). An oxygen regime of 500 to >200 µM was maintained at 30 to 40 °C, but up to 700 and 900 µM at 25 and 4 °C, to avoid artificial oxygen diffusion limitation of flux86 (link), 87 (link). In the first substrate-uncoupler-inhibitor titration protocol (SUIT 1), the following final concentrations were added sequentially: P (5 mM), M (5 mM), G (10 mM), ADP (1 mM), cytochrome c (10 μM), S (10 mM), FCCP (carbonyl cyanide p-trifluoromethoxyphenylhydrazone; optimum concentration, 0.125 to 0.375 μM), rotenone (Rot; 0.5 μM), antimycin A (Ama; 2.5 μM), malonic acid (Mna; 5 mM), ascorbate (As; 0.5 mM) and TMPD (N,N,N’,N’-tetramethyl-p-phenylenediamine; 2 mM). In SUIT 2 addition of P and G were inversed (Fig. 1b). An increase of respiration due to cytochrome c addition after ADP was observed at 30 to 40 °C, with cytochrome c control factors (change of respiration divided by cytochrome c stimulated respiration)19 in the range of 0.05 to 0.15, with higher values of 0.11 to 0.20 at 25 °C. At 4 °C, N-OXPHOS capacity showed a trend to decline during the experiment particularly with PM, and no stimulation could be observed with cytochrome c. Thus the integrity of the outer mitochondrial membrane in mouse heart permeabilized fibers was comparable to rat heart fibers studied at 30 °C88 (link). Residual oxygen consumption (ROX), evaluated after inhibition of CI, CII and CIII with Rot, Mna and Ama was a small fraction (0.01 to 0.02) of NS-ETS capacity at 25 to 40 °C, but increased to 0.04 to 0.10 at 4 °C. Nevertheless, correction of fluxes in all respiratory states for ROX was significant, particularly in the resting state of LEAK respiration, when ROX was as high as 0.12 to 0.32 of total oxygen consumption in the N-LEAK state at 25 to 40 °C.
Apparent CIV excess capacities were determined by azide titrations of CIV activity and of NS-ETS capacity at 4, 25, 30, 37, and 40 °C. Threshold plots of relative respiration rate against the fraction of inhibited CIV activity at the same azide concentration were made as previously described57 (link), 89 (link). Azide titrations were performed at optimum uncoupler concentration supporting maximum flux, preventing the effect of inhibition of ATP synthase90 (link) and eliminating any contribution of the phosphorylation system to flux control. The following azide concentrations were used [mM]: 0.02, 0.04, 0.06, 0.16, 0.26, 0.36, 2.9, 5.4, 10.4 between 25 and 40 °C, and 0.004, 0.008, 0.012, 0.032, 0.052, 0.072, 0.092, 0.11, 0.21, 0.31, 2.8, 5.3, 10.3 at 4 °C (not all points visible in Fig. 5 due to overlap).
The contents of the chambers were removed at the end of each experimental run and the chamber was rinsed twice with 500 μl of respiration medium. The fibers were homogenized for 2 × 30 s with an Ultra-Turrax homogenizer at maximum speed and immediately frozen in liquid nitrogen and stored at −80 °C for subsequent measurement of citrate synthase at 30 °C91 (link).
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Publication 2017
The bacterial strains grown in triplicate in 10 ml NBRIP broth supplemented with 0.5% tricalcium phosphate (TCP), Mussoorie rock phosphate (MRP), Udaipur rock phosphate (URP) and North Carolina rock phosphate (NCRP) at 28°C for 5 days at 180 rpm in a refrigerated incubator shaker (Innova Model 4230, New Brunswick Scientific, USA) were centrifuged at 10,000 rpm for 10 min. and passed through 0.22 μm nylon filter. Quantitative estimation of P-liberated from inorganic phosphates was done using vanado-molybdate method as described earlier [8 (link)]. Detection and quantification of organic acids was done on Waters 996 High Performance Liquid Chromatogram (HPLC) equipped with PDA detector, Waters 717 plus autosampler, Waters 600 controller, Waters™ pump, Waters inline degasser AF, and Lichrosphere RP-18 column 250 mm × 4.6 mm and 5 μm particle size (Merck, Germany). The mobile phase was 0.1% ortho-phosphoric acid (Merck, Germany) in the gradient of flow rate as given in Table 1. Eluates were detected at λ 210 nm and identified by retention time and co-chromatography by spiking the sample with the authentic organic acids. The organic acids were quantified by reference to the peak areas obtained for the authentic standards for gluconic acid (Sigma-Aldrich, USA), 2-ketogluconic acid (Sigma, USA), and lactic acid, oxalic acid, malic acid, succinic acid, formic acid, citric acid, malonic acid, propionic acid and tartaric acid (Supelco, USA). Each replicate was analyzed in a single run on HPLC for 76 samples for the four phosphate substrates. The values were presented as the mean of three replicates.
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Publication 2009
2-ketogluconate Acids Bacteria Chromatography Citric Acid DNA Replication formic acid gluconic acid Lactic Acid malic acid malonic acid molybdate Nylons Oxalic Acids Phosphates Phosphoric Acids propionic acid Retention (Psychology) Strains Succinic Acid tartaric acid tricalcium phosphate
Arsenic species, including trivalent and pentavalent forms of 2 and 1, were analyzed by high-pressure liquid chromatography (HPLC) (Series 2000; PerkinElmer, Waltham, MA, USA) coupled to inductively coupled plasma mass spectrometry (ICP-MS) (ELAN DRC-e; PerkinElmer), as described previously,3 ,5 (link) with minor modifications. Briefly, arsenic species in samples were separated by HPLC on a BioBasic 18 LC column (250 mm × 4.6 mm, 5 μm, 300 Å) (Thermo Fisher Scientific) using a mobile phase consisting of 3 mM malonic acid and 5% MeOH (v/v) (pH 5.6 adjusted with tetrabutylammonium hydroxide) with a flow rate of 1 mL min−1 at 25 °C. Arsenic was monitored by ICP-MS. Arsenic species were determined from the HPLC retention time of known standards (Figures 1 and 2).
Publication 2020
Arsenic High-Performance Liquid Chromatographies malonic acid Mass Spectrometry Plasma Retention (Psychology) tetrabutylammonium hydroxide

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Publication 2014
Acids Argon arsenate Arsenic arsenite Brain Cacodylic Acid Capcell Cells Cyclonic Storms dimethylarsine Embryo Fetus Freezing High-Performance Liquid Chromatographies malonic acid Methanol monomethylarsonic acid Nebulizers Oxides Plasma Retention (Psychology) Tissues

Most recents protocols related to «Malonic acid»

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Example 16

A solution of Varenicline free base (20.0 g) in methylene dichloride (100 ml) was stirred with the aqueous solution of Malonic acid (11.82 g, 1.2 eq in 100 ml of water). The aqueous layer containing Varenicline malonate was stirred with methylene dichloride to remove the nitrosamine impurity by solvent extraction. Thereafter, follow the general procedure for the isolation of Varenicline base from the aqueous layer. Yield: 13.6 g

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Patent 2024
isolation malonate malonic acid Methylene Chloride Nitrosamines Solvents Varenicline
4,4′-Bi­pyridine (91.54 mg) and malonic acid (51.50 mg) were dissolved in 8 ml EtOH:DMSO solution (1:1 v/v ratio) and left for slow evaporation (at room temperature, in a vial covered with a parafilm with a few needle-size holes in it) to yield colourless, needle crystals.
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Publication 2024
Not available on PMC !
The amount of lipid peroxidation products, mainly malonic dialdehyde, reacting with 2-thiobarbituric acid was analysed by homogenising the shoots in a reaction medium containing 0.25% 2-thiobarbituric acid in 10% trichloroacetic acid. The homogenate was placed in tubes covered with foil lids and boiled for 30 minutes in a water bath. After cooling, the samples were centrifuged at 10000 g for 15 minutes. The supernatantʼs absorbance was measured at 532 nm, malonic dialdehydeʼs maximum light absorption, and at 600 nm to correct for non-specific light absorption (Kolupaev et al., 2021) (link).
Publication 2024
Whole blood was collected in non-fasted state by dried blood sampling (DBS), a biosampling method where capillary blood was obtained by a fingerprick using a disposable lancet. Complete DBS cards were allowed to dry overnight (maximum 12 h) in a room without light exposure, before being stored in a sealed aluminium bag with a desiccant pack at -20 degrees Celsius (°C) until analysis. Methylmalonic acid (MMA) was analyzed from the whole blood (VITAS™ Analytical Services, Norway). A sufficient volume of blood for analysis of MMA was available for 65 participants. MMA was extracted from 8 mm DBS punches using an isotope dilution GC-MS assay. Four punches were eluted in an aqueous alkaline solution containing stable isotope-labelled MMA prior to derivatization using propyl chloroformate. The liquid extraction of derivatized MMA was performed before injection into the GC-MS system. The GC-MS system utilized was an Agilent 6890 GC (Agilent Technologies, Palo Alto, CA, USA) equipped with an Agilent 5973 N mass-selective detector operated in EI-SIM mode. Separation was performed on a Zebron ZB-AAA GC column supplied by Phenomenex Inc (Torrance, CA, USA) and quantification was performed against a 5-point standard curve prepared from standards with known concentrations.
Haemoglobin (Hb) was measured from the same finger prick as the whole blood for DBS, using Hemocue® HB801 Analyzer and Microcuvettes (Sweden). In total 164 participants provided blood for analysis of Hb.
Publication 2024

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Publication 2024

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Malonic acid is a dicarboxylic acid with the chemical formula CH2(COOH)2. It is a white, crystalline solid that is soluble in water and organic solvents. Malonic acid is used as a laboratory reagent and in the synthesis of various organic compounds.
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Citric acid is a commonly used chemical compound in laboratory settings. It is a weak organic acid that can be found naturally in citrus fruits. Citric acid has a wide range of applications in various laboratory procedures and analyses.
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Succinic acid is a laboratory chemical used as a reagent in various scientific applications. It is a dicarboxylic acid with the chemical formula C₄H₆O₄. Succinic acid is a naturally occurring substance found in many organisms and is commonly used in the production of pharmaceuticals, food additives, and other chemical compounds.
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Fumaric acid is a dicarboxylic acid found naturally in many plant and animal tissues. It is a white, crystalline solid that is used as a food additive and in various industrial applications.
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Pyridine is a colorless, flammable liquid used as a solvent and as an intermediate in the production of various organic compounds. It has a distinctive pungent odor. Pyridine is commonly employed in chemical synthesis, pharmaceuticals, and the production of other industrial chemicals.
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Oxalic acid is a chemical compound with the formula H2C2O4. It is a colorless crystalline solid that is highly soluble in water. Oxalic acid is commonly used in various industrial and laboratory applications.
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DPPH is a chemical compound used as a free radical scavenger in various analytical techniques. It is commonly used to assess the antioxidant activity of substances. The core function of DPPH is to serve as a stable free radical that can be reduced, resulting in a color change that can be measured spectrophotometrically.
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Glutaric acid is a dicarboxylic acid used as a laboratory reagent. It is a colorless, crystalline solid with the chemical formula C5H8O4.
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Hydrochloric acid is a commonly used laboratory reagent. It is a clear, colorless, and highly corrosive liquid with a pungent odor. Hydrochloric acid is an aqueous solution of hydrogen chloride gas.
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Formic acid is a colorless, pungent-smelling liquid chemical compound. It is the simplest carboxylic acid, with the chemical formula HCOOH. Formic acid is widely used in various industrial and laboratory applications.

More about "Malonic acid"

Malonic acid, also known as propanedioic acid, is a dicarboxylic acid with the chemical formula CH2(COOH)2.
It is a colorless, crystalline solid that is soluble in water and organic solvents.
Malonic acid is an important intermediate in organic synthesis and is commonly used in the preparation of various pharmaceutical and chemical compounds.
It plays a role in the citric acid cycle, also known as the Krebs cycle, and is involved in various metabolic pathways.
Malonic acid and its derivatives have a wide range of applications, including in the production of plastics, dyes, and agricultural chemicals.
Malonate, the conjugate base of malonic acid, is an inhibitor of the enzyme succinate dehydrogenase, which is a key component of the citric acid cycle.
This inhibition can lead to the accumulation of succinic acid, another dicarboxylic acid, as well as fumaric acid and other intermediates.
Malonic acid is also related to other carboxylic acids, such as oxalic acid, glutaric acid, and formic acid, which can have similar or related functions in organic synthesis and metabolism.
Reasearch on malonic acid can be facilitated through the use of PubCompare.ai, an AI-driven platform that helps identify the best protocols and products for your needs, while ensuring reproducibility and accuracy in your work.
Discover the power of PubCompare.ai, the leading AI-driven platform for reproducible and accurate protocols, and explore a wealth of information on malonic acid and related compounds.