Quantitative 1H Nuclear Magnetic Resonance Research Articles

Efficient and Selective Construction of 412 Metalla‐links Using Weak C−H⋅⋅⋅Halogen Interactions

AbstractThrough a coordination‐driven self‐assembly method, four metalla‐links and one tetranuclear monocycle were constructed with high selectivity and yield by adjusting the substituent species of the building blocks, as evidenced using X‐ray crystallographic analysis, electrospray ionization‐time‐of‐flight/mass spectrometry (ESI‐TOF/MS), elemental analysis and detailed solution‐state nuclear magnetic resonance (NMR) spectroscopy. Based on X‐ray crystallographic analysis and independent gradient model analysis, a significant factor leading to the formation of metalla‐links was the introduction of F, Cl, Br and I atoms, which generated additional weak C−H⋅⋅⋅X (X=F, Cl, Br and I) interactions. Furthermore, the dynamic conversion of metalla‐links to monocyclic rings in methanol solution was systematically investigated using quantitative 1H NMR techniques.

Efficient and Selective Construction of 41 2 Metalla-links Using Weak C-H⋅⋅⋅Halogen Interactions.

Through a coordination-driven self-assembly method, four metalla-links and one tetranuclear monocycle were constructed with high selectivity and yield by adjusting the substituent species of the building blocks, as evidenced using X-ray crystallographic analysis, electrospray ionization-time-of-flight/mass spectrometry (ESI-TOF/MS), elemental analysis and detailed solution-state nuclear magnetic resonance (NMR) spectroscopy. Based on X-ray crystallographic analysis and independent gradient model analysis, a significant factor leading to the formation of metalla-links was the introduction of F, Cl, Br and I atoms, which generated additional weak C-H⋅⋅⋅X (X=F, Cl, Br and I) interactions. Furthermore, the dynamic conversion of metalla-links to monocyclic rings in methanol solution was systematically investigated using quantitative 1H NMR techniques.

Implementation of analytical quality by design concepts for the optimization of quantitative 1H nuclear magnetic resonance (1H-qNMR) method for quantitation of novel anti-covid drugs (molnupiravir and favipiravir) in their pharmaceutical dosage forms

For the first time in the literature, the Analytical Quality by Design (AQbD) principles were applied to the development of a specific and simple quantitative proton nuclear magnetic resonance (1H-qNMR) method for quantitation of two antiviral drugs, molnupiravir (MOL) and favipiravir (FAV). This 1H-qNMR method was developed within the QbD framework, the new paradigm of quality recently outlined in the ICH Q14 guidelines. Basic principles of AQbD have been adapted starting with early risk assessment and identification of the analytical target profile (ATP), the analytical procedure attributes (APA) and the analytical procedure parameters (APPs). During the scouting phase, dimethyl sulfoxide-d6 (DMSO‑d6) was selected as the deuterated solvent and maleic acid as the internal standard. The quantitative determination was based on the selective proton signals from MOL's pyrimidine ring at 6.82 ppm (doublet) and FAV's hydroxyl group at 8.71 ppm (singlet), as well as a singlet signal from the IS at 6.24 ppm. A Box-Behnken Design was employed in response surface methodology to develop mathematical predictive models relating the APPs to the APAs followed by multicriteria- decision making with the aid of Derringer's desirability function. Finally, the method operable design regions (MODRs) were computed with the aid of Monte Carlo simulations and identified as the multidimensional combination of the APPs where the risk of failure to fulfill the requirements for the APAs was lower than 5 %. The most robust NMR conditions for MOL, with MODR intervals in brackets, were as follows: no. of scans of 72 (16–124.4), a relaxation delay of 19.8 s (1.2–40 s) and an acquisition time of 3.98 s (2.1–6 s). Similarly, for FAV NMR quantitation, the most robust conditions were found to be 72 scans (16–117.3), a relaxation delay of 19.8 s (1.4–40 s) and an acquisition time of 3.98 s (2.2–6 s). The developed method was validated in accordance with the recently endorsed ICH Q2R2 guidelines, and it exhibited detection limits of 1.04 and 0.88 mg mL−1, as well as quantitation limits of 3.45 and 2.95 mg mL−1 for MOL and FAV, respectively. The method was successfully applied to the analysis of the studied analytes in their pharmaceutical products, proving to be simple, fast, non-destructive, and accurate. Additionally, it can be considered an environmentally friendly alternative for quantitation and quality control analysis of pharmaceutical products.

Accurate Determination of Trace Water in Organic Solution by Quantitative Nuclear Magnetic Resonance.

A new method accompanied by a derived equation for accurate determination of trace water was developed by using quantitative 1H nuclear magnetic resonance (qNMR) spectroscopy. Given that the response for each chemically distinct moiety is uniformly proportional to the number of the corresponding resonant nuclei within the analyte, it is practicable to directly quantify the water content via its proton number using qNMR. In this study, three water standards with known water contents (e.g., 10.02, 1.006, and 0.103 mg/g), which were accurately determined by a well-established Coulometric Karl Fischer (CKF) titration method, were measured by using the developed qNMR method. An excellent agreement between the results from these two methods was obtained. Then, the water content of Sudan I was determined by high-field NMR (HF-NMR) spectroscopy, and the water contents of acetone and bioethanol were measured by low-field NMR (LF-NMR) spectroscopy. These results were compared with the water content measured by the CKF method to confirm the applicability of the established qNMR method. The developed method can eliminate the influences of environmental humidity and background water in the solvent; subsequently, the results calculated by the derived equation were comparable to the nominal values. Under the optimal conditions, the limit of quantitation of this method was as low as 6.7 μg. The recommended sample sizes for practical samples with various water contents (e.g., 10.02, 1.006, and 0.103 mg/g) were determined to be 5, 50, and 60 mg, respectively, which are much smaller than those required for the CKF method. The new method has a static and stable process without any side reactions, and the traceability to the SI unit can be directly achieved through the NMR internal standard. This method overcomes the limitations of the CKF method, especially for measuring methanol-insoluble substances.

Quantitative 1H Nuclear Magnetic Resonance (qNMR) of Aromatic Amino Acids for Protein Quantification.

Hydrolysis of protein samples into amino acids facilitates the use of NMR spectroscopy for protein and peptide quantification. Different conditions have been tested for quantifying aromatic amino acids and proteins. The pH-dependent signal shifts in the aromatic region of amino acid samples were examined. A pH of 12 was found to minimize signal overlap of the four aromatic amino acids. Several aromatic compounds, such as terephthalic acid, sulfoisophthalic acid, and benzene tricarboxylic acid, were applied as internal standards. The quantification of amino acids from an amino acid standard was performed. Using the first two suggested internal standards, recovery was ~97% for histidine, phenylalanine, and tyrosine at a concentration of approximately 1 mM in solution. Acidic hydrolysis of a certified reference material (CRM) of bovine serum albumin (BSA) and subsequent quantification of Phe and Tyr yielded recoveries of 98% ± 2% and 88% ± 4%, respectively, at a protein concentration of 16 g/L or 250 µM.

Quantitative NMR spectroscopy reveals solvent effects in the photochemical degradation of thymoquinone

Thymoquinone, a monoterpene natural product isolated from Nigella sativa, has demonstrated potent antioxidant, cytotoxic, anticancer, and anti-inflammatory activity, making it a compound of great therapeutic potential and scientific interest. However, as a photochemically labile compound that can dimerize or decompose into other compounds upon irradiation, its clinical administration and synthetic modifications are greatly limited by its instability in the presence of light. Therefore, it is crucial to have a reliable way to quantify decreases in thymoquinone concentration as an indicator of photodegradation to provide insight into the chemical use of the compound. Here, we employed quantitative 1H nuclear magnetic resonance (NMR) spectroscopy as well as computational time-dependent density functional theory (TD-DFT) calculations to identify the effect of solvation on the photochemical degradation of thymoquinone under ultraviolet light (UV). We found that the rate of photochemical degradation of thymoquinone is highly solvent dependent, and that greatest photodegradation occurs in chloroform. The results presented here are informative for future solvent selection related to the isolation and experimental usage of the compound in solution.

Establishment of SI-traceable purity assessment of Fumonisin B1 using a combination of quantitative 1H NMR and mass balance

The accurate purity assessment of Fumonisin B1 (FB1) is of great challenge due to the lack of inherent chromophore, which is important for the development of FB1 certified reference material. In this study, differential scanning calorimetry (DSC), mass balance and quantitative 1H nuclear magnetic resonance (qH NMR) methods were developed and validated for international system of unit (SI) traceable purity assessment of in-house prepared FB1. The thermodynamic analysis showed no typical melting peak was observed for FB1, indicating DSC was not applicable for purity assessment of FB1. A high-performance liquid chromatography coupled with corona charged aerosol detector (HPLC-CAD) method was developed and an isocratic elution procedure was optimized for the chromatographic purity analysis of FB1. The linear range of optimized HPLC-CAD method could not cover the concentration range of FB1 and the structure-related impurity in the raw material, which was identified to be partial hydrolyzed FB1 (pHFB1). The correction factor used to correct the chromatographic purity obtained by area normalization method was approximately 0.2 %. Moisture (0.30 %) and pHFB1 (0.48 %) were the main impurities according to the mass balance analysis. A mixture of dimethyl sulfoxide-d6 and trifluoroacetic acid-d was confirmed to be a suitable deuterated solvent for accurate qH NMR analysis of FB1. The purity obtained by mass balance (99.13 % with uncertainty of 0.06 %) and qH NMR (99.12 % with uncertainty of 0.28 %) showed good consistency and equivalent precision. These methods are expected to be applicable to development of FB1 certified reference material with metrological traceability to the SI unit to ensure comparable and reliable detection results.

Boosting Electrocatalytic CO 2 Reduction with Conjugated Bimetallic Co/Zn Polyphthalocyanine Frameworks

Boosting Electrocatalytic CO ₂ Reduction with Conjugated Bimetallic Co/Zn Polyphthalocyanine Frameworks

Quantitative 1H-NMR analysis reveals steric and electronic effects on the substrate specificity of benzoate dioxygenase in Ralstonia eutropha B9.

The cis-dihydroxylation of arenes by Rieske dearomatizing dioxygenases (RDDs) represents a powerful tool for the production of chiral precursors in organic synthesis. Here, the substrate specificity of the RDD benzoate dioxygenase (BZDO) in Ralstonia eutropha B9 whole cells was explored using quantitative 1H nuclear magnetic resonance spectroscopy (q1H-NMR). The specific activity, specific carbon uptake, and regioselectivity of the dihydroxylation reaction were evaluated in resting cell cultures for a panel of 17 monosubstituted benzoates. Two new substrates of this dioxygenase system were identified (2-methyl- and 3-methoxybenzoic acid) and the corresponding cis-diol metabolites were characterized. Higher activities were observed for benzoates with smaller substituents, predominantly at the 3-position. Elevated activities were also observed in substrates bearing greater partial charge at the C-2 position of the benzoate ring. The regioselectivity of the reaction was directly measured using q1H-NMR and found to have positive correlation with increasing substituent size. These results widen the pool of cis-diol metabolites available for synthetic applications and offer a window into the substrate traits that govern specificity for BZDO.

Neopentyl Esters as Robust Linkers for Introducing Functionality to Bis-MPA Dendrimers

A series of neopentyl carboxylic acids bearing functionality amenable to click chemistry were prepared and then appended to high-generation bis-MPA dendrons via fluoride-promoted esterification. The nucleophilic stability of neopentyl and non-neopentyl dendrons in acidic to basic phosphate buffers was compared by monitoring degradation via quantitative 1H nuclear magnetic resonance (NMR). The neopentyl periphery dendrons were found to be highly resistant to hydrolysis under all experimental conditions. The neopentyl groups also did not impede click functionalization onto the dendrons.

Altered amino acid metabolism between coronary heart disease patients with and without type 2 diabetes by quantitative 1H NMR based metabolomics

Coronary heart disease (CHD) is a multifactorial disease associated with complicated altered metabolic pathways, especially when it occurs with type 2 diabetes (T2D). Identification of metabolic changes could provide further understanding of the underlying pathological link between with CHD and T2D. In this study, 61 controls, 30 consecutive patients with only T2D, 188 with confirmed CHD among which 50 also having T2D were enrolled. Quantitative 1H nuclear magnetic resonance (1H NMR) based metabonomic approach was used to obtain the plasma metabolic profiles of the study samples. Multivariate principal component analysis and orthogonal partial least-squares discriminant analysis (OPLS-DA) were used to evaluate the differences of metabolites. Compared with controls, there were significant differences in CHD patient with T2D groups including BCAAs (isoleucine, leucine, and valine) and phenylalanine by using quantitative metabolomic profiling (all p < 0.05). With OPLS-DA, the results showed that, compared to CHD patients without T2D, there had higher levels of metabolites for leucine, valine, fumarate, tyrosine, and phenylalanine in the plasma of CHD patients with T2D. Moreover, the CHD patients with T2D showed modified phenylalanine, tyrosine and tryptophan biosynthesis, valine, leucine and isoleucine biosynthesis and degradation compared with CHD patients without T2D. By 1H NMR based quantitative metabolomic method, our findings suggest that T2D has important effects on BCAAs and AAAs metabolism in CHD patients indicating altered cardiac energy metabolism and activated signaling pathway could be potential targets for therapy in CHD disease combined with T2D.

Moderate Salinity Stress Affects Expression of Main Sugar Metabolism and Transport Genes and Soluble Carbohydrate Content in Ripe Fig Fruits (Ficus carica L. cv. Dottato).

Fig trees (Ficus carica L.) are commonly grown in the Mediterranean area, where salinity is an increasing problem in coastal areas. Young, fruiting plants of cv. Dottato were subjected to moderate salt stress (100 mM NaCl added to irrigation water) for 48 days before fruit sampling. To clarify the effect of salinity stress, we investigated changes in the transcription of the main sugar metabolism-related genes involved in the synthesis, accumulation and transport of soluble carbohydrates in ripe fruits by quantitative real-time PCR as well as the content of soluble sugars by quantitative 1H nuclear magnetic resonance spectroscopy. A general increase in the transcript levels of genes involved in the transport of soluble carbohydrates was observed. Alkaline-neutral and Acid Invertases transcripts, related to the synthesis of glucose and fructose, were up-regulated in ripe fruits of NaCl-stressed plants without a change in the content of D-glucose and D-fructose. The increases in sucrose and D-sorbitol contents were likely the result of the up-regulation of the transcription of Sucrose-Synthase- and Sorbitol-Dehydrogenase-encoding genes.

Ambient-Pressured Acid-Catalysed Ethylene Glycol Organosolv Process: Liquefaction Structure-Activity Relationships from Model Cellulose-Lignin Mixtures to Lignocellulosic Wood Biomass.

Raising the awareness of carbon dioxide emissions, climate global warming and fossil fuel depletion has renewed the transition towards a circular economy approach, starting by addressing active bio-economic precepts that all portion amounts of wood are valorised as products. This is accomplished by minimizing residues formed (preferably no waste materials), maximizing reaction productivity yields, and optimising catalysed chemical by-products. Within framework structure determination, the present work aims at drawing a parallel between the characterisation of cellulose–lignin mixture (derived system model) liquefaction and real conversion process in the acidified ethylene glycol at moderate process conditions, i.e., 150 °C, ambient atmospheric pressure and potential bio-based solvent, for 4 h. Extended-processing liquid phase is characterized considering catalyst-transformed reactant species being produced, mainly recovered lignin-based polymer, by quantitative 31P, 13C and 1H nuclear magnetic resonance (NMR) spectroscopy, as well as the size exclusion- (SEC) or high performance liquid chromatography (HPLC) separation for higher or lower molecular weight compound compositions, respectively. Such mechanistic pathway analytics help to understand the steps in mild organosolv biopolymer fractionation, which is one of the key industrial barriers preventing a more widespread manufacturing of the biomass-derived (hydroxyl, carbonyl or carboxyl) aromatic monomers or oligomers for polycarbonates, polyesters, polyamides, polyurethanes and (epoxy) resins.

Sensomics-Assisted Flavor Decoding of Dairy Model Systems and Flavor Reconstitution Experiments.

The whole sensometabolome of a typical dairy milk dessert was decoded to potentially serve as a blueprint for further flavor optimization steps of functional fat-reduced food. By applying the sensomics approach, a wide range of different dairy volatiles, semi and nonvolatiles, were analyzed by ultrahigh-performance liquid chromatography tandem mass spectrometry with or without derivatization presteps. While for volatile sulfur compounds with low odor thresholds, headspace solid-phase microextraction gas chromatography was established, abundant carbohydrates and organic acids were quantified by quantitative 1H nuclear magnetic resonance spectroscopy. Validated quantitation, sensory reconstitution, and omission studies highlighted eight flavor-active compounds, namely, diacetyl, δ-tetra-, δ-hexa-, and δ-octadecalactone, sucrose, galactose, lactic acid, and citric acid as indispensable for flavor recombination. Furthermore, eight odorants (acetaldehyde, acetic acid, butyric acid, methanethiol, phenylacetic acid, dimethyl sulfide, acetoin, and hexanoic acid), all with odor activity values >1, additionally contributed to the overall flavor blueprint. Within this work, a dairy flavor analytical toolbox covering four different high-throughput methods could successfully be established showing potential for industrial applications.

Improving the Phloroglucinolysis Protocol and Characterization of Sagrantino Wines Proanthocyanidins.

Proanthocyanidins are key metabolites that explain wine sensorial character (bitterness and astringency) and red wine color changes during aging. Therefore, a fast and accurate method to evaluate the degree of polymerization and the structural composition of the polymeric proanthocyanidins is a crucial analytical tool. Phloroglucinolysis is the most used method for this analysis but, unfortunately, the phloroglucinol adducts of the monomeric flavan-3-ols are not commercially available, making the results less accurate. The aim of this work was the isolation by semi-preparative high performance liquid chromatography (HPLC) of these non-commercial compounds and their use for the development of an accurate UHPLC-MS/MS protocol. The purity of each adduct was established via quantitative 1H-nuclear magnetic resonance (NMR) measurements with 3-trimethylsilyl-propionic-d4 acid sodium salt as the calibration standard. The developed method was applied to evaluate the proanthocyanidins profile of Sagrantino di Montefalco wines in comparison to other well-known tannic wines. Commercial, 6–8 years old Sagrantino wines were demonstrated to be very rich in epicatechin type B procyanidins, to have low galloylation %, and to have a high mean degree of polymerization of the proanthocyanidins with respect to the other analyzed wines.

No-D quantitative 1H Nuclear Magnetic Resonance spectroscopy method for the determination of ethanol in distilled spirits

Quantitative NMR (qNMR) is an emerging analytical method that is recommended for food samples because of its simple and rapid analysis. Commonly prepared in deuterated solvents, the use of a non-deuterated solvent (no-D) for routine analysis was explored in this study. The amount of ethanol was determined in distilled spirits using Varian 500 MHz NMR spectrometer. Ethanol standards and samples were prepared in deionized water with acetonitrile as the internal standard. Using the optimized acquisition parameters, the 1H NMR spectra of the standards and samples were obtained. The ethanol content of distilled spirit samples obtained from no-D qNMR experiments was validated using GC-FID and the results obtained were not significantly different (p > 0.05) using ANOVA. The developed and validated no-D qNMR method was fast, simple, accurate, non-destructive, and provides an alternative technique for the analysis of ethanol in distilled spirits.

Accurate and Precise External Calibration Enhances the Versatility of Quantitative NMR (qNMR)

Quantitative 1H nuclear magnetic resonance (qHNMR) is a highly regarded analytical methodology for purity determination as it balances metrological rigor, practicality, and versatility well. While ideal for intrinsically mass-limited samples, external calibration (EC) qHNMR is overshadowed by the prevalence of internal calibration and perceived rather than real practical limitations. To overcome this hurdle, this study applied the principle of reciprocity, certified reference materials (caffeine as analyte, dimethyl sulfone as calibrant), and a systematic evaluation of data acquisition workflows to extract key factors for the achievement of accuracy and precision in EC-qHNMR. Automatic calibration of the 90° pulse width (90 PW) formed the foundation for the principle of reciprocity and used optimized nutation experiments, showing good agreement with values derived from manual high-precision measurement of 360 PW. Employing the automatic 90 PW calibration, EC-qHNMR with automatic vs manual tuning and matching (T&M) yielded the certified purity value within 1% error. The timing of T&M (before vs after shimming) turned out to be critically important: sufficient time is required to achieve full-temperature equilibrium relative to thermal gradients in the air inside the probe and the sample. Achievable accuracy across different NMR solvents varies with differences in thermal conductivity and leads to 2% or greater errors. With matching solvents, the demonstrated accuracy of ∼1.0% underscores the feasibility of EC-qHNMR as a highly practical research tool.

13C-Satellite Decoupling Strategies for Improving Accuracy in Quantitative Nuclear Magnetic Resonance.

Quantitative 1H nuclear magnetic resonance (qHNMR) with an appropriate internal standard is a well-established quantitation method for assigning purity to organic molecules. For accurate measurements, the premise of qHNMR relies on the careful selection of integrals, for both the analyte and the standard, in such a way that the selected integrals are free from interferences. The 13C-satellite signals of adjacent integrals, low-level impurities, and tautomer signals are among the common integral interferences that are typically encountered. One of the simplest ways to identify and avoid these interferences is to decouple the 13C-satellites. Two decoupling schemes were explored to illustrate the benefits of 13C-decoupling for qHNMR or qH{13C}NMR: GARP and bilevel adiabatic broadband decoupling. Unwanted sample heating and nuclear Overhauser effect (NOE) enhancements are the two main drawbacks of decoupling schemes. We show that with careful optimization of acquisition parameters and decoupling power, no excessive sample heating occurred during acquisition at 400 MHz. At 900 MHz, only bilevel adiabatic decoupling could be safely implemented. Furthermore, any undesirable NOE enhancements were completely avoided if acquisition was executed with an inverse-gated pulse sequence. We explored and confirmed the benefits of qH{13C}NMR through the quantitation of a diverse set of compounds, namely, small molecules (dimethyl terephthalate and zearalenone), a 13C-labeled compound (13C6-ochratoxin A), and an octapeptide (angiotensin II). Statistical comparisons confirmed that qH{13C}NMR produced comparable data to qHNMR. However, with qH{13C}NMR data providing added clarity about the presence of overlapping 13C-satellites, impurities, and tautomers, it has an edge over qHNMR for accurate measurements.

A validated 1H-NMR method for quantitative analysis of DOTAP lipid in nanoliposomes containing soluble Leishmania antigen

Leishmaniasis is a serious health problem that needs a suitable vaccine delivery system to control the disease. Cationic lipids such as 1, 2-dioleoyl-3-trimethylammonium-propane (DOTAP) have been widely used in nanoliposomes’ formulation to deliver antigen and adjuvant at the same time to induce protection against Leishmaniasis. Therefore, it is necessary to accurately quantify DOTAP concentration in the formulation and biological materials. Due to the poor UV absorbance of DOTAP, the use of the conventional HPLC-UV method was impossible. Currently, an evaporative light scattering detector (ELSD) or MS/MS detector in conjunction with HPLC is used to quantify DOTAP. These methods have several disadvantages, including time- consuming during extraction procedure and decrease or/and even remove some components of the formulation. According to the advantages of the quantitative 1H Nuclear Magnetic Resonance (1H-NMR) spectroscopic method, a free extraction approach was developed to the assay of DOTAP in nanoliposomes containing Leishmania antigens. This method was carried out based on the relative ratio of signal integration of DOTAP [CH2 (CH2−CH = CH−CH2)] in δ 2 ppm to a definite amount of an internal standard called dimethyl sulfone (DMSO2). The q1H-NMR method showed good precision (intra-day RSD = 1.8 % and inter-day RSD = 2.5 %), linearity (in the ranges of 1.3–7.8 mg. mL−1 with correlation coefficients at 1), repeatability (RSD ≤ 2.39 %), and stability (RSD ≤ 2.32 %) for the quantification of the DOTAP without any extraction method. Considering all the experiments conducted in this study, NMR can be a feasible alternative to other traditional techniques for the simultaneous quantification of lipids in liposome formulations.

Accurate determination of highly volatile chloroethylene by quantitative 1H-NMR

In Japan, chloroethylene is a regulated substance under the soil contamination countermeasures act since 2017, due to the presence of chloroethylene in soil leachate and groundwater. As a consequence, chloroethylene concentrations must be accurately determined to ensure the safety of drinking water, chloroethylene standard solutions with reliable concentrations had not been available because chloroethylene is difficult to handle due to its boiling point of − 13 °C. Here, we developed a quantitative 1H nuclear magnetic resonance (1H-qNMR) method to measure chloroethylene concentration in a standard solution in CD3OD. Sampling temperature must be between − 80 °C and − 21 °C, and the NMR tube headspace volume ratio must be lower than 23% to reduce the volatilization of chloroethylene. We used the signal of CD2HOD present in the standard solution as an internal standard because chloroethylene was volatilized during the addition of another internal standard. The chloroethylene concentration in the standard solution was accurately determined as 117.7 ± 1.4 mg kg−1.