Determination of 1,1-Dimethylhydrazine by Reversed-Phase High-Performance Liquid Chromatography with Spectrophotometric Detection as a Derivative with 4-Nitrobenzaldehyde

A procedure was developed for the determination of 1,1-dimethylhydrazine by reversed-phase high-performance liquid chromatography with spectrophotometric detection and preliminary derivatization by the reaction with 4-nitrobenzaldehyde. Conditions were selected for the chromatographic separation and the detection of the peaks of the reagent and 4-nitrobenzaldehyde dimethylhydrazone. The optimum conditions were found for the derivatization of 1,1-dimethylhydrazine with 4-nitrobenzaldehyde. The determination limit of 1,1-dimethylhydrazine in aqueous solutions was 120 g/L (2 M/L).     

Spectrophotometric determination of hydrazine,methylhydrazine, and 1,1-dimethylhydrazine with preliminary derivatization by 5-nitro-2-furaldehyde

5-Nitro-2-furaldehyde, a new derivatizing agent for the spectrophotometric determination of hydrazine, methylhydrazine, and 1,1-dimethylhydrazine is proposed. It is characterized by high solubility in water and by a substantial difference in the positions of absorption bands of the formed colored derivatives. The kinetics of the reaction of analyte derivatization is studied, and reaction conditions (pH 5, concentration of derivatizing agent 2 mM, 60° C, duration 40 min) are optimized. The limits of detection are 5, 3, and 1.5 μg/L for hydrazine, methylhydrazine, and 1,1-dimetlhydrazine, respectively. A possibility of the spectrophotometric determination of analytes in their simultaneous presence using the Firordt method is shown. The developed approach is successfully applied to the analysis of polluted peat bog soil selected at a place of impact of the first step of a carrier rocket.     

Determination of hydrazine and 1,1-dimethylhydrazine as salicyldehyde derivates by liquid chromatography with electrochemical detection

Summary Determination of hydrazine and 1,1-dimethylhydrazine after derivatization with salicylaldehyde was done using high-performance liquid chromatography with electrochemical detection. The oxidation of the phenolic group of salicylaldazine (S-HY) and salicylaldehyde-1,1-dimethylhydrazone (S-UDMH) was optimized with respect to ionic strength, pH, and applied potential. Less than 5 ng of S-HY and S-UDMH could be detected. The detection limits for hydrazine and 1,1-dimethylhydrazine solutions were estimated to be 0.025 and 0.20 ppm, respectively.     

Highly sensitive determination of 1,1-dimethylhydrazine by high-performance liquid chromatography–tandem mass spectrometry with precolumn derivatization by phenylglyoxal

A new highly sensitive and rapid approach to the determination of 1,1-dimethylhydrazine in natural water is developed (determination range is 0.03–1 μg/L). It is based on the use of high-performance liquid chromatography–tandem mass spectrometry with precolumn derivatization by phenylglyoxal and does not require any preconcentration. Derivatization, chromatographic separation conditions, and tandem mass spectrometry detection parameters are chosen. Intra-day precision of the results of measurements of 1,1- dimethylhydrazine in natural water is 12–16%, and inter-day precision is 16–22%. The lowest limit of detection and the lowest limit of quantification are 0.010 μg/L and 0.030 μg/L, respectively.     

The use of glyoxal and glyoxylic acid to determine N- and N,N-alkyl-substituted hydrazines by liquid chromatography

Using chromatography and spectrophotometry, it has been shown that the reaction of 1,1-dimethylhydrazine (UDMH), methylhydrazine (MH), and 2-hydroxyethylhydrazine (HEH) with excess of glyoxal (Gl) and glyoxylic acid (GlA) in aqueous solutions yields corresponding monohydrazones as single derivatization products. The derivatization reaction occurs in a quantitative yield for 20 min at 25 or 40°C for Gl and GlA, respectively (pH 3.5). The electronic absorption spectra of the derivatives have maxima in the range of 275–305 nm. The conditions for the simultaneous determination of hydrazines in waters by reversed-phase HPLC coupled with UV detection in aqueous solutions with preliminary derivatization are proposed. The derivatives are separated on a Zorbax SB-C18 (150 × 4.6 mm) column with a mobile phase of 20 mM phosphate buffer solution (pH 3.5) and 2–5% acetonitrile. The detection limits are 0.25–0.5 or 0.4–0.7 μg/L for the derivative of Gl and GlA, respectively.     

Direct determination of hydrazine,methylhydrazine, and 1,1-dimethylhydrazine by zwitterionic hydrophilic interaction liquid chromatography with amperometric detection

A promising alternative to ion-chromatographic methods currently used for the direct determination of hydrazines is provided by hydrophilic interaction liquid chromatography (HILIC). In this work, we propose a method for the simultaneous determination of hydrazine, methylhydrazine and 1,1-dimethylhydrazine in natural waters and soils based on a combination of chromatographic separation on a zwitterionic sulfobetaine stationary phase (Nucleodur HILIC) in the HILIC mode with amperometric detection.

Effects of different factors on the retention of analytes were studied and the optimum conditions of analysis were found. We recommend a mixture of acetonitrile with an aqueous phosphate buffer solution of pH 2.5 (78:22 v/v) with an ionic strength of 20 mM as a mobile phase. Detection in the direct current mode was performed at a working electrode potential of 1.1 V.

The advantages of the method are the high efficiency of separation, rapidity, high sensitivity and a wide dynamic range of analyte concentrations, covering four orders of magnitude. The attained LOD values for analytes lie in the range 0.07–0.13 μg L^–1, which is two orders of magnitude lower than those in currently used methods of ion chromatography with electrochemical and mass spectrometric detection.

The method was validated on samples of natural waters of different origin using the added–found technique. It was found that the error of analysis did not exceed 10% for river and ground waters and increased to 20–30% for peat bog surface waters.

The possibility of application of the developed method to the analysis of soils was shown on samples of peat bog soils selected at places of impact of the first steps of carrier rockets and polluted by rocket fuel based on 1,1-dimethylhydrazine.     

The determination of hydrazine and 1,1-dimethylhydrazine,separately or in mixtures,by high-pressure liquid chromatography

A rapid, sensitive liquid chromatographic method for the determination of hydrazine and 1,1-dimethylhydrazine, separately or in mixtures of varying proportions, is described. The procedure involves salicylaldehyde derivative formation followed by chromatography on a reversed phase (octadecylsilane) column with acetonitrile (52%)—0.14 M potassium dihydrogenphosphate (48%) as a mobile phase and u.v. (254 nm) detection. This system is sensitive to 2 μg ml^-1 of hydrazine and 5 μg ml^-1 of 1,1-dimethylhydrazine and has a relative standard deviation of less than 1%. Monomethylhydrazine forms an unstable salicylaldehyde hydrazone; although it cannot be determined, it can be detected (sensitivity 5 μg ml^-1 ) and does not interfere with quantitative measurement of either hydrazine or 1,1-dimethylhydrazine.     

A sensitive chromatographic determination of hydrazines by naphthalene-2,3-dialdehyde derivatization

A new high-performance liquid chromatography (HPLC) method for the sensitive simultaneous determination of hydrazine (Hy), monomethylhydrazine (MMH) and 1,1-dimethylhydrazine (UDMH) based upon the derivatization of hydrazines with naphthalene-2,3-dialdehyde and the separation of the derivatives on Zorbax Eclipse AAA column in a single chromatographic run under acidic conditions (pH 2.4) was developed. Hydrazine and monomethylhydrazine derivatives were found to be strongly fluorescent at λ_ex?=?273?nm, λ_em?=?500?nm. It was shown that UDMH derivative can be detected as non-fluorescent hydrazone at 290?nm by UV-detection. Limits of detection were 0.05?µg?·?L^?1 for Hy and MMH, and 1?µg?·?L^?1 for UDMH for the injection volume of 100?µL. The method was validated for water sample analysis. It proved to be selective, accurate and precise with the supplementary advantage of the simple and rapid sample preparation.     

Determination of hydrazines by chip electrophoresis with contactless conductivity detection

In this report, a new approach for the fast determination of hydrazine compounds (hy) in complex matrices is presented. The experimental protocol is based on poly(methylmethacrylate) (PMMA) microchip separations with contactless conductivity detection using a compact portable device, which integrates all separation and detection components. Three hy (hydrozine (Hy), methylhydrazine (MH), and 1,1-dimethylhydrazine (UDMH)) were separated within < 30 s at a separation voltage of 3.8 kV using a L(-)-histidine/2-(N-morpholinoethanesulfonic acid) (His/MES) buffer (25:50 mM, pH 5.87). The contactless conductivity detection enables detection limits for Hy, MH, and UDMH of 11.9, 35.5, and 337.8 ng/mL, respectively, with linear concentration dependence up to 10 μg/mL. In complex matrices such as soil samples or river water, interferences were eliminated by implementing ultrasound-assisted headspace single-drop microextraction of hy under strongly alkaline conditions, using an aqueous drop of His/MES buffer as the extractant phase. The incorporation of this miniaturized sample preparation step led to improved limits of detection for Hy, MH, and UDMH of 6.5, 15.3, and 11.4 ng/mL, respectively. The overall protocol demonstrates a promising approach for interfacing chip electrophoresis with real-world applications.     

Ion chromatography as a tool for the investigation of unsymmetrical hydrazine degradation in soils

A new procedure for the determination of 1,1-dimethylhydrazine (UDMH) in soil samples was developed. This involves the distillation of UDMH from an alkaline suspension of soil and ion chromatographic analysis of the distillate. The separation was performed on a silica cation-exchanger column with ammonium acetate buffer solution as mobile phase and amperometric detection at +1.2?V. Hydrazine (Hy) and methylhydrazine (MH), which are decomposition products of UDMH, can be determined simultaneously. The limits of detection in aqueous solutions were 0.2, 0.5 and 1?µg?L^?1 for Hy, MH and UDMH, respectively. The developed technique was used for investigating the behaviour of UDMH in spills of rocket fuels on soils. It was found that the addition of 4?kg?m^?2 UDMH resulted in a 0.02% residue one year after the soil treatment. The vertical migration of UDMH in soil was less than 50?cm.     

Sorption-chromatographic determination of hydrazine and its substituted derivatives in air

Working conditions were found for the chemisorption preconcentration of hydrazine, phenylhydrazine, and 1,1-dimethylhydrazine from air with tubes containing silica gel with immobilized 4-chloro-5,7-dinitrobenzofurazan and the subsequent determination by high-performance liquid chromatography with diode array detection. A recovery of 98% (hydrazine), 90% (phenylhydrazine), and 97% (1,1-dimethylhydrazine) is attained at a thickness of the sorbent layer of 2 cm, an aspiration rate of 0.2–0.8 L/min, and a volume of aspirated air of 10 L. Silica gel with a particle size of 0.1–0.3 mm impregnated with 4-chloro-5,7-dinitrobenzofurazan (2 wt %) was used as the sorbent. The detection limits of compounds without regard for preconcentration after their desorption are 0.01 (hydrazine), 0.017 (1,1-dimethylhydrazine), and 0.015 mg/m³ (phenylhydrazine).     

Electrically driven microseparation methods for pesticides and metabolites: VI. Surfactant-mediated electrokinetic capillary chromatography of aniline pesticidic metabolites derivatized with 9-fluoroenylmethyl chloroformate and their detection by laser-induced fluorescence

In this report, we describe a surfactant-mediated electrokinetic capillary chromatography (SM-EKC) system for the separation of 9-fluoroenylmethyl chloroformate (FMOC)-derivatized anilines by capillary electrophoresis (CE). The SM-EKC system consisted of dioctyl sulfosuccinate (DOSS)/acetonitrile mixtures and was suited for the CE separation of the relatively hydrophobic FMOC-aniline analytes and other neutral compounds, e.g. alkylphenyl ketones. While the organic modifier acetonitrile (ACN) allowed the solubilization of the hydrophobic solutes and maintained the DOSS surfactant in its monomeric form by inhibiting micellization, the DOSS surfactant associated with the FMOC anilines to a varying degree thus leading to their differential migration and separation. Under these conditions, the FMOC-anilines were readily detected at the 10(-6) M level by UV at 214 nm and at the 10(-8) M level by laser-induced fluorescence (LIF) using a solid-state UV laser operating at 266 nm line as the excitation wavelength. The FMOC precolumn derivatization was also readily performed in lake water spiked with anilines at near the limit of detection (LOD) level. The lake water matrix showed no significant effects on the extent of derivatization at the LOD level as well as on the detection of the analytes due to the selectivity of the FMOC derivatization. The derivatization and detection of spiked lake water necessitated only the removal of microparticles by microfiltration prior to derivatization and detection.     

Electrically driven microseparation methods for pesticides and metabolites: V. Micellar electrokinetic capillary chromatography of aniline pesticidic metabolites derivatized with fluorescein isothiocyanate and their detection in real water at low levels by laser-induced fluorescence

Anilines are important pollutants occurring in the environment as industrial discharges as well as the transformation products (i.e., metabolites) of a wide variety of commonly used pesticides. In this report, we describe the precolumn derivatization of anilines with fluorescein isothiocyanate (FITC) and their subsequent separation and detection by capillary electrophoresis-laser induced fluorescence (CE-LIF) detection. The FITC-aniline derivatives were readily detected at the 10(-10) M level. This limit of detection (LOD) was achieved in the presence of glycosidic surfactants complexed with borate at alkaline pH yielding the so-called in situ charged micelles. The glycosidic surfactants evaluated were n-octyl- and n-nonylglucopyranoside. Furthermore, and under optimum conditions, the FITC precolumn derivatization of the anilines was performed in real water (e.g., tap and lake water) spiked with anilines at the LOD level. The water matrices showed marginal effects on the extent of derivatization at the LOD level, and the possible interferents in the water samples did not affect the FITC-solute signal due to the selectivity of the derivatization and detection schemes. Besides filtration from microparticles, the real water samples did not necessitate extensive sample cleanup prior to derivatization.     

Chromogenic Reaction of 1,1-Dimethylhydrazine with Aryltetrazolium Salts

The reactions of 1,1-dimethylhydrazine with 2,3,5-triphenyl-2Н-tetrazolium and 2,5-diphenyl-3-(4-nitrophenyl)-2Н-tetrazolium chlorides in a solution and on a cellulose carrier have been studied by means of spectrophotometry and chromato–mass spectrometry to develop new chromogenic indicators for detection of 1,1-dimethylhydrazine. 1,3,5-Triphenylformazan and 1,3-diphenyl-5-(4-nitrophenyl)formazan are formed in these reactions, respectively; deep red shifts have been observed. Other products of these reactions result from oligomerization and addition of short-living 1,1-dimethylhydrazyl and tetrazolium radicals.     

Gas-chromatographic determination of 1,1-dimethylhydrazine in water

A gas-chromatographic procedure for the determination of 1,1-dimethylhydrazine in water was developed on the basis of its reaction with 4-nitrobenzaldehyde yielding the corresponding hydrazone, the extraction of the latter from water with an organic solvent, its subsequent preconcentration by evaporation, and the determination on a gas chromatograph with a nitrogen-phosphorus detector. The determination limit of 1,1-dimethylhydrazine is 0.03 μg/L. The relative error of the determination is no larger than 22% in the concentration range 0.06–0.60 μg/L and 33% at a level of 0.03 μg/L.     

Analysis of glycoproteins, glycopeptides and glycoprotein-derived oligosaccharides by high-performance capillary electrophoresis

Recent developments in the analysis of glycoproteins by high-performance capillary electrophoresis are reviewed, with emphasis on their carbohydrate chains. Glycoforms of glycoproteins were directly separated from each other by careful optimization of the analytical conditions. Glycopeptides in tryptic digests were separated and the peptides carrying glycosylation sites were differentiated from others. Released oligosaccharide chains were separated at a low wavelength. Precolumn derivatization by various methods extended the utility of both the absorption at a low wavelength. Precolumn derivatization by various methods extended the utility of both the separation mode and detection technique. Dual mode analysis after derivatization permitted reliable identification and quantification without references.     

Spectrophotometric determination of hydrazine and 1,1-dimethylhydrazine,separately or in admixture

A rapid, sensitive spectrophotometric method for the determination of hydrazine and 1,1-dimethylhydrazine, separately or in mixtures of varying proportions, is described. The analysis is based on the well-known reaction of these compounds with salicylaldehyde to form, in the case of hydrazine, a symmetrical azine, or with 1,l-dimethylhydrazine, a hydrazone. Absorbance measurements were made in the ultraviolet at wavelengths characteristic of the derivatives and of salicylaldehyde; the results were calculated by means of simultaneous equations. The procedure is sensitive to concentrations of hydrazine as low as 0.3 μg/ml and of 1,1-dimethylhydrazine as low as 0.25 μg/ml. This corresponds to initial sample solutions having a concentration of 3.0 mg of hydrazine and 1.25 mg of 1,1-dimethyl hydrazine per ml.     

1-Formyl-2,2-dimethylhydrazine as a new decomposition product of 1,1-dimethylhydrazine

A new decomposition product of 1,1-dimethylhydrazine (UDMH), 1-formyl-2,2-dimethylhydrazine (FDMH), was found in water and soil samples. The formation of FDMH was confirmed by LC-MS and NMR studies. The possibility of FDMH conversion to initial UDMH by alkaline hydrolysis was shown.     

Simultaneous determination of 1,1-dimethylhydrazine and products of its oxidative transformations by liquid chromatography–tandem mass spectrometry

A liquid chromatography–tandem mass spectrometry method is proposed for the simultaneous determination of 1,1-dimethylhydrazine, methylhydrazine, N,N-dimethylformamide, 1-methyl-1H-1,2,4-triazole, dimethylguanidine, N-nitrosodimethylamine and 1,1,4,4-tetramethyltetrazene, important rocket fuel pollutants of soils. Chromatographic separation was conducted according to previously published results in an isocratic mode on an analytical column with a Nucleosil-100–5SA sulfo-cation-exchanger. The mobile phase composition was optimised in order to achieve effective separation of all analytes and provide high sensitivity of mass spectrometric detection – an ammonium acetate buffer solution (50 mM, pH 5.4) containing methanol (25%) was used. Detection was performed in the positive electrospray ionisation mode with multiple reaction monitoring (MRM). The parameters of ion source, ion optics, the inlet potentials of the quadrupoles and the collision energy for the detection of the found product ions were optimised. Calibration dependences for all compounds are linear in wide concentration ranges, covering 3–4 orders of magnitude. The detection limits vary from 40 pg mL^?1 for dimethylguanidine to 18 ng mL^?1 for methylhydrazine. No significant matrix effects were observed in the analysis of acid peaty soil extracts. The method was validated and successfully used to analyse a real soil sample collected at the place of impact of the first stage of a carrier rocket.     

A general approach for the quantitative analysis of bisphosphonates in human serum and urine by high-performance liquid chromatography/tandem mass spectrometry

Bisphosphonates are extremely hydrophilic and structurally similar to many endogenous phosphorylated compounds, making their selective extraction from serum or urine very challenging. Many bisphosphonates lack strong chromophores for sensitive UV or fluorescence detection. We report here the first general approach to enable sensitive and selective quantitation of N-containing bisphosphonates by liquid chromatography/tandem mass spectrometry (LC/MS/MS) following derivatization with diazomethane. The novelty of the strategy lies in performing the derivatization on silica-based anion-exchange sorbents as an integrated step in the sample purification by solid-phase extraction (SPE). The 'on-cartridge' reaction with diazomethane not only led to higher efficiency of derivatization, but also enabled a more discriminatory recovery of the drug's derivatives. The derivatized bisphosphonates demonstrated improved chromatographic separation and increased sensitivity of the detection. The general applicability of the approach was demonstrated by validation of bioanalytical methods for risedronate and alendronate in human serum and urine. Sensitivity was achieved at the pg/mL level with merely 100-200 microL of sample.