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At least 19 recordsLinked to original sources
PubMed1988

The stability of uric acid in ammonium hydroxide.

We examined the stability of uric acid in dilute aqueous ammonium hydroxide solution by mass spectrometry. Uric acid decomposes in ammonium hydroxide even as dilute as 15 mmol/L when the mole ratio of ammonium hydroxide to uric acid is 50:1. There are at least four products of the decomposition, two of which have been identified as allantoin and urea. The slope of the decomposition curve indicates that uric acid is destroyed at an initial rate of 2-3% per hour. In ammonium hydroxide at a concentration of 1 mmol/L and a mole ratio of ammonium hydroxide to uric acid of less than or equal to 3.4, uric acid is not detectably decomposed. Evidently, any method for determination of uric acid that involves treating the analyte with ammonium hydroxide before analysis may destroy it. Therefore, a published method described as being "definitive" for uric acid (J Clin Chem Clin Biochem 1985; 23:129-35) could produce incorrect results because it involves storing the uric acid in 15 mmol/L ammonium hydroxide at a mole ratio of ammonium hydroxide to uric acid of greater than 120:1.

Ammonium Hydroxide↗
PubMed1997

Recovery of nucleic acids from immobilized biotin-streptavidin complexes using ammonium hydroxide and applications in MALDI-TOF mass spectrometry.

The effects of ammonium hydroxide treatment of complexes consisting of biotinylated nucleic acids and immobilized streptavidin were investigated. It was found that incubation of such complexes with ammonium hydroxide at room temperature leads to denaturation of double-stranded DNA molecules, liberating only the complementary nonbiotinylated strand, whereas incubation at elevated temperatures leads to an efficient dissociation of biotin-streptavidin complexes. The introduced procedure is especially suitable as a purification and conditioning format prior to matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometric analysis of DNA from complex enzymatic reactions. This is demonstrated by analysis of polymerase chain reaction (PCR) and sequencing products.

Ammonium Hydroxide↗
PubMed2001

Kinetics of phthalate reactions with ammonium hydroxide in aqueous matrix.

Common phthalate pollutants, such as dimethyl phthalate and diethyl phthalate found in aqueous environmental matrices react with ammonium hydroxide at ordinary temperatures exhibiting an overall reaction order in the range 1.3-1.4. While the reaction is of first order with respect to the phthalate, the order of reaction is fractional in ammonium hydroxide. The rate constants for the reactions of these two phthalates in alkaline waters at ambient temperatures are in the range 1.3 x 10(-4) and 8.5 x 10(-5) Lx/mol s. Under these conditions the estimated half-lives for dimethyl phthalate and diethyl phthalate at a concentration of each at 20 mg/L is 4.5 and 14 h, respectively. Other phthalates are expected to exhibit similar kinetics in their base hydrolysis with NH4OH. Thus, the presence of both the phthalate esters and ammonia or ammonium salts in the water under alkaline conditions may result in their self-removal by hydrolysis.

Ammonium Hydroxide↗
PubMed2002

Ion chromatographic analysis of anions in ammonium hydroxide, hydrofluoric acid, and slurries, used in semiconductor processing.

In this study, ion chromatography (IC) with suppressed conductivity detection was used for the determination of trace anions in 29% (w/w) ammonium hydroxide, 49% (w/w) hydrofluoric acid and slurries. For these samples, various sample pretreatment methods were applied to eliminate matrix interferences. For concentrated ammonium hydroxide, an on-line electrochemical neutralizer (SP10 AutoNeutralization module) was used to neutralize the base prior to the IC analysis. For concentrated hydrofluoric acid, a heart cutting technique with an ion-exclusion column was used to separate the anions of interest prior to an IC separation. A method was also developed to analyze chloride in silica slurries by IC.

Ammonium Hydroxide↗
PubMed1997

Liesegang Ring Type Structures and Bifurcation in Solid-Vapor and Liquid Phase Reactions between Cobalt Nitrate and Ammonium Hydroxide

New results on the reaction between (i) cobalt nitrate (A) and ammonium hydroxide (B) in gelatin and (ii) cobalt nitrate (solid) and ammonia vapor are reported. Spatial bifurcation of the blue wave into a number of normal Liesegang type bands is observed in a one-dimensional tube in gel media depending on the concentration of electrolytes and gel. Similar bifurcation is also observed when the reaction was carried out in gel media between two microslides. Results show that Ksp (solubility product), as envisaged in recent theories, plays a significant role in initiating bifurcation depending on K, the magnitude of the product of concentration of A and B, which determines the degree of supersaturation. The value of K at the instant of bifurcation, when (i) concentration of Co(NO3)2 is alone changed or when (ii) concentration of NH4OH alone is changed, is similar when uncertainties are taken into account. The bifurcation behavior when gel concentration is changed suggests that in case of high gel concentration pore size is affected, thereby influencing the diffusion of ions. The results satisfy the spacing law. The results further satisfy the relation d2 = m't + C' at any time t, where d is the distance between the lower front of the precipitate and the junction and m' and C' are constants, thereby suggesting that the role of diffusion is vital, as envisaged in various theories of the phenomenon. A colored banded structure separated by air gaps (vacant spaces) is formed when the solid cobalt nitrate reacts with ammonia vapor. This type of behavior has not been reported earlier. Initially, a single band is formed in a one-dimensional experiment, but in the course of time ( approximately 1 month) several bands are formed simultaneously. The diffusion kinetics in the initial stages of the solid-vapor reaction has been studied in a one-dimensional tube. The data obey the relation xi2 = kt, where xi is the thickness of the product layer at any time t and k is some constant. Similar studies were made on microslides which showed that during the reaction, a colored product is formed which undergoes change in the sequence pink --> blue --> brown. Results in the one-dimensional case support recent theories which postulate nucleation followed by aggregation. Copyright 1997Academic Press

Journal Article↗
PubMed1977

Rapid blister formation in human skin with ammonium hydroxide.

The topical application to human skin of a 1:1 aqueous solution of ammonium hydroxide in a well drilled into a plastic block will provoke an intra-epidermal blister in an average time of about 13 min. The blister roof can be used for physico-chemical analyses of the horny layer while the base is suitable for studies of wound healing, bacterial infections, etc. The minimal blistering time (MBT) increases directly as the number of cell layers of the stratum corneum and ranges from 3 to 57 min in different regions and persons. The intensity of the dermatitis provoked by a 24 h exposure to sodium lauryl sulphate is strongly correlated with the MBT. The latter is therefore a reliable measure of cutaneous irritability. The blisters are virtually painless. The inflammatory reaction clinically and histologically is slight. Healing is rapid without scarring.

Adolescent↗
PubMed1995

Ethylenediaminetetraacetic acid in ammonium hydroxide for reducing decalcification time.

Ethylenediaminetetraacetic acid (EDTA) solution is used to decalcify bone specimens for histological examination. Sodium hydroxide (NaOH) has been used to dissolve EDTA and to bring EDTA solutions to neutral pH. This solution, however, requires several weeks to decalcify bone specimens. We investigated a new decalcification fluid using concentrated ammonium hydroxide (NH4OH) to dissolve EDTA and to adjust the pH to neutral. Decalcification was performed using a magnetic stirrer with and without vacuum, or with a sonic cleaner. Decalcification end point was confirmed using both the weight loss and X-ray methods. After decalcification, specimens were processed through paraffin and sections were stained with hematoxylin and eosin. Decalcification employing NH4OH required an average of six days. Light microscopy indicated good retention of cellular detail.

Ammonium Hydroxide↗
PubMed2002

Ammonium hydroxide hydrolysis: a valuable support in the MALDI-TOF mass spectrometry analysis of Lipid A fatty acid distribution.

Lipid A is the lipophilic moiety of lipopolysaccharides (LPSs), the major components of the external membrane of almost all gram-negative bacteria. It is responsible for the toxicity of LPS and has a heterogeneous structure composed of a bis-phosphorylated glucosamine disaccharide backbone that is acylated at the positions 2, 3 of the GlcN I (proximal) and GlcN II (distal) residue with O- and N-linked 3-hydroxy fatty acids (primary substitution). These fatty acids are further acylated by means of their 3-hydroxy groups (secondary substitution). The toxicity of Lipid A is dependent on its primary structure; the number, the length, and the distribution of the fatty acids on the disaccharide backbone strongly influence the endotoxic activity. In this paper a general and easy methodology to obtain secondary fatty acid distribution, which is one of the most difficult issues in the structural determination of Lipid A, is proposed. The method combines ammonium hydroxide hydrolysis and matrix assisted laser desorption ionization (MALDI)-mass spectrometry analysis and has been successfully proven with five different Lipid A species. The procedure exploits the lower stability under mild alkaline conditions of acyl and acyloxyacyl esters with respect to that of the acyl and acyloxyacyl amides. The partially degraded Lipid A species obtained are analyzed by MALDI-MS. The generality of this approach was tested on five Lipid As, namely those arising from Escherichia coli, Klebsiella pneumoniae, Klebsiella oxytoca, Pseudomonas reactans, and Burkholderia caryophylli.

Ammonium Hydroxide↗
PubMed1984

Electrothermal atomic absorption determination of aluminum in tissues dissolved in tetramethyl ammonium hydroxide.

In this rapid, precise method for the accurate determination of aluminum in biological tissue, the only preparative step required is the dissolution of the sample in hot aqueous tetramethyl ammonium hydroxide, followed by dilution with ethanol. Aluminum is measured by electrothermal (graphite furnace) atomic absorption spectroscopy, with direct reference to aqueous standards. The CVs for the method within-day and day-to-day are 3.0% and 6.8%, respectively. Analytical recovery of added aluminum is 86 to 108%, and matrix effects are minimal. Measurement of aluminum in tissue from normal laboratory rats and rats injected with aluminum gave values close to those found by an acid digestion method, but higher than those obtained by extraction with a saturated solution of ethylenediaminetetraacetate.

Aluminum↗
PubMed1999

Electrostatic ion chromatography of polarizable anions in saline waters with N-[2-[acetyl(3-sulfopropyl)amino]ethyl]-N,N-dimethyldodecanaminium hydroxide (ammonium sulfobetaine-1) as the stationary phase and a dilute electrolytic solution as the mobile phase.

A new type of zwitterionic surfactant, N-{2-[acetyl(3-sulfopropyl)amino]ethyl}-N,N-dimethyldodecanaminium hydroxide (ammonium sulfobetaine-1), with a greater distance between the two charged groups, was used as the stationary phase for electrostatic ion chromatography (EIC) of polarizable anions (e.g., thiocyanate, iodide and nitrate) in saline water samples. The targeted species (polarizable anions) were baseline separated using this type of zwitterionic surfactant as the stationary phase, but the highly polarizable species (iodide and thiocyanate) were eluted faster (compared with the results obtained using N-dodecyl-N,N-dimethyl-3-ammonio-1-propanesulfonate, C12N3S, with a shorter distance between the two charged groups, as the stationary phase). In other words, the extent of binding of the highly polarizable anion (iodide and thiocyanate) was found to be smaller when using ammonium sulfobetaine-1 as the stationary phase. This provides a rapid but effective method for the analysis of highly polarizable anions in saline water samples. The results for the successful detection of iodide in seawater demonstrates the usefulness of this new type of zwitterionic surfactants for EIC.

Betaine↗