He, Xiao-Mei et al. published their research in Analytical and Bioanalytical Chemistry in 2016 | CAS: 122-18-9

N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.COA of Formula: C25H46ClN

Black phosphorus-assisted laser desorption ionization mass spectrometry for the determination of low-molecular-weight compounds in biofluids was written by He, Xiao-Mei;Ding, Jun;Yu, Lei;Hussain, Dilshad;Feng, Yu-Qi. And the article was included in Analytical and Bioanalytical Chemistry in 2016.COA of Formula: C25H46ClN The following contents are mentioned in the article:

Quant. anal. of small mols. by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) has been a challenging task due to matrix-derived interferences in low m/z region and poor reproducibility of MS signal response. The authors developed an approach by applying black phosphorus (BP) as a matrix-assisted laser desorption ionization (MALDI) matrix for the quant. anal. of small mols. for the first time. Black phosphorus-assisted laser desorption/ionization mass spectrometry (BP/ALDI-MS) showed clear background and exhibited superior detection sensitivity toward quaternary ammonium compounds compared to carbon-based materials. By combining stable isotope labeling (SIL) strategy with BP/ALDI-MS (SIL-BP/ALDI-MS), a variety of analytes labeled with quaternary ammonium group were sensitively detected. Moreover, the isotope-labeled forms of analytes also served as internal standards, which broadened the analyte coverage of BP/ALDI-MS and improved the reproducibility of MS signals. Based on these advantages, a reliable method for quant. anal. of aldehydes from complex biol. samples (saliva, urine, and serum) was successfully established. Good linearities were obtained for five aldehydes at 0.1-20.0 μM with correlation coefficients (R2) larger than 0.9928. The LODs are 20 to 100 nM. Reproducibility of the method was obtained with intra-day and inter-day relative standard deviations (RSDs) <10.4 %, and the recoveries in saliva samples ranged from 91.4 to 117.1%. Taken together, the proposed SIL-BP/ALDI-MS strategy proved to be a reliable tool for quant. anal. of aldehydes from complex samples. This study involved multiple reactions and reactants, such as N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9COA of Formula: C25H46ClN).

N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.COA of Formula: C25H46ClN

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Choi, Jong-Soon et al. published their research in Journal of Applied Phycology in 2020 | CAS: 122-18-9

N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Reference of 122-18-9

Efficient profiling of detergent-assisted membrane proteome in cyanobacteria was written by Choi, Jong-Soon;Park, Yun Hwan;Oh, Jeong Hyun;Kim, Sooyong;Kwon, Joseph;Choi, Yoon-E.. And the article was included in Journal of Applied Phycology in 2020.Reference of 122-18-9 The following contents are mentioned in the article:

Membrane proteins play key roles in cellular functions like transport of mols., perception of environmental cues, and signal transduction into the intracellular compartment. However, the profiling of membrane proteins is still a daunting task because of the hydrophobicity, restricting our knowledge of membrane proteins. Thus, we attempted to develop a novel detergent-based approach to uncover membrane proteins using cyanobacteria. We investigated the effect of five different detergents on the profiling of the cyanobacterial membrane proteome. The application of either amidosulfobetaine-14 (ASB14) or N-lauroylsarcosine (NL) doubled the number of the identified integral membrane proteins compared with the control. Extraction with ASB14 increased the number of transmembrane helixes over four times. The quant. index (mol%) of membrane proteins also increased from 13 to 22% when ASB14, NL, and benzyldimethyl-n-hexadecylammonium chloride (BAC) were used. ASB14 treatment was particularly useful for identifying membrane proteins with higher mol. weights (Mr), and the addition of BAC to the cyanobacterial membrane could identify the membrane proteins with acidic isoelec. points (pI). To validate the efficiency of the detergent-based proteomics, the functional membrane protein complexes involved in energy metabolism were selected as an example and shown to be successful with the combined data of ASB14, NL, and zwittergent 3-10 (ZW3-10). Taken together, we suggest that the use of a specific detergent and the subsequent combination of proteome data is critical for detailed profiling of cyanobacterial functional membrane proteins. This study involved multiple reactions and reactants, such as N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9Reference of 122-18-9).

N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Reference of 122-18-9

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Hatakeyama, Yoshikiyo et al. published their research in Journal of Physical Chemistry C in 2018 | CAS: 122-18-9

N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators. Organochlorine compounds are lipophylic, meaning they are more soluble in fat than in water. This gives them a high tenancy to accumulate in the food chain (biomagnification).SDS of cas: 122-18-9

Growth of gold nanorods synthesized by seed-mediated method: Tracking reaction by time-resolved x-ray absorption near-edge structure, small-angle x-ray scattering, and UV-visible spectroscopy was written by Hatakeyama, Yoshikiyo;Sasaki, Koh;Judai, Ken;Nishikawa, Keiko;Hino, Kazuyuki. And the article was included in Journal of Physical Chemistry C in 2018.SDS of cas: 122-18-9 The following contents are mentioned in the article:

Gold nanorods (GNRs) are attractive and important nanomaterials that show enormous promise for a wide range of applications. To investigate the formation process of GNRs generated by the seed-mediated method, we tracked the growth of GNRs with aspect ratios of 2 (GNR2s), 4 (GNR4s), and 6 (GNR6s) using time-resolved X-ray absorption near-edge structure (XANES). Moreover, for GNR6s, addnl. measurements by small-angle X-ray scattering and UV-visible spectroscopy were carried out for longer reaction times of up to 20 000 s. Cetyltrimethylammonium bromide (CTAB) was used as the surfactant in the generation of GNR2s and GNR4s, whereas benzyldimethylhexadecylammonium chloride (BDAC) and CTAB were used for GNR6s. The three anal. methods used provided consistent and compensatory results. It was found that GNR2s and GNR4s finish growing by 2000 s, consuming all the Au in the solutions, and that GNR6s keeps growing for more than 20 000 s by a different formation process. From these comprehensive results, it was revealed that severe competition for existence among the GNRs occurs in all solutions The seed particles added to the solutions of GNR2s and GNR4s start growing but the whole seed particles cannot mature into GNRs. Conversely, in the solution for GNR6s, some of the already-grown GNRs release Au atoms, allowing the growth of further GNRs, making the formation process slow, unique, and complex. The growth of GNR6s coordinated by CTAB and BDAC in appropriate proportions continues more than 20 000 s. In particular, back-and-forth growth of GNR6s is first observed by tracking the growth solution using time-resolved XANES. This study involved multiple reactions and reactants, such as N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9SDS of cas: 122-18-9).

N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators. Organochlorine compounds are lipophylic, meaning they are more soluble in fat than in water. This gives them a high tenancy to accumulate in the food chain (biomagnification).SDS of cas: 122-18-9

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Paijens, Claudia et al. published their research in Water, Air, & Soil Pollution in 2020 | CAS: 122-18-9

N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Electric Literature of C25H46ClN

Determination of 18 Biocides in Both the Dissolved and Particulate Fractions of Urban and Surface Waters by HPLC-MS/MS was written by Paijens, Claudia;Frere, Bertrand;Caupos, Emilie;Moilleron, Regis;Bressy, Adele. And the article was included in Water, Air, & Soil Pollution in 2020.Electric Literature of C25H46ClN The following contents are mentioned in the article:

A robust method is provided to analyze 18 hydrophilic and hydrophobic biocides in both dissolved and particulate fractions of five types of urban and surface waters using high-performance liquid chromatog. coupled to tandem mass spectrometry. The linearity, accuracy, and intermediate precision were validated. The target biocides were enriched by solid-phase extraction using Chromabond HR-X 200-mg cartridges and eluted with methanol, Et acetate, and dichloromethane. Suspended matter was extracted by microwave-assisted extraction in methanol and dichloromethane. Recoveries and variability (resp. > 75% and < 30% for most of the target biocides and matrixes) made it possible to quantify biocides at a trace level in all matrixes. Limits of quantification were in the range of nanograms per L in the dissolved fraction and in the range of nanograms per g of dry weight in the particulate fraction for most of the biocides and matrixes, and were generally lower than those reported in previous studies. The method was successfully applied to surface waters, treated and untreated wastewater, combined sewer overflows, and stormwater, providing unique data in these matrixes for some substances, in particular with respect to particle contamination. In urban waters, concentrations of most of the biocides ranged from 10 to 200 ng/L. Diuron, isothiazolinone, and benzalkonium concentrations could reach 0.9, 0.9, and 20μg/L resp. In rivers, most of the biocides were measured at less than 10 ng/L, but higher concentrations were observed for benzalkoniums (up to 200 ng/L) or after rain events, which indicates biocide transfer from urban surfaces into the aquatic environment during wet weather. This study involved multiple reactions and reactants, such as N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9Electric Literature of C25H46ClN).

N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Electric Literature of C25H46ClN

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Gutierrez-Sanchez, Oriol et al. published their research in ACS Applied Materials & Interfaces in 2021 | CAS: 122-18-9

N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Computed Properties of C25H46ClN

Effects of Benzyl-Functionalized Cationic Surfactants on the Inhibition of the Hydrogen Evolution Reaction in CO2 Reduction Systems was written by Gutierrez-Sanchez, Oriol;Daems, Nick;Bulut, Metin;Pant, Deepak;Breugelmans, Tom. And the article was included in ACS Applied Materials & Interfaces in 2021.Computed Properties of C25H46ClN The following contents are mentioned in the article:

Cationic surfactants, mainly hexadecyl cetrimonium bromide (CTAB), are widely used in electrocatalysis to affect the selectivity of the reaction, specifically to inhibit the hydrogen evolution reaction (HER) in CO2 reduction (CO2R) systems. However, little research has been done on the modification of the functional groups present in such surfactants in order to promote this HER-inhibiting effect. In this work, the effectiveness of CTAB was promoted by substituting a Me group of the quaternary amine for a benzyl group. This cationic s heptadecyl trimethylammonium and octadecyl trimethylammonium, urfactant, cetalkonium chloride (CKC), increased the hydrophobicity of the surface of the electrode, promoting the HER inhibition and the CO2R when HCO3 is used as a carbon source, which allows combining capture and conversion in one and the same medium, making it industrially highly attractive. By performing a detailed electrochem. characterization, we proved that the benzyl group formed an enhanced hydrophobic layer on the surface of the electrode in addition to the alkyl chain of the surfactant, showing higher effectiveness compared to CTAB. In fact, the Faradaic efficiency of the CO2R increased from 39 to 66% in saturated HCO3 electrolytes by using CKC instead of CTAB as the HER inhibitor. This opens up a wide range of avenues for research on the application of surfactants in the field of electrocatalysis, because, as proven, a selective modification of it can tune the selectivity of the reaction, adding a new variable in the design of an efficient carbon capture and utilization system. This study involved multiple reactions and reactants, such as N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9Computed Properties of C25H46ClN).

N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Computed Properties of C25H46ClN

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Di Ianni, Emilio et al. published their research in Nanotoxicology in 2020 | CAS: 122-18-9

N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. Organochlorines stimulate the central nervous system and cause convulsions, tremor, nausea, and mental confusion. Examples are dichlorodiphenyltrichloroethane (DDT), chlordane, lindane, endosulfan, and dieldrin. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Safety of N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride

Organomodified nanoclays induce less inflammation, acute phase response, and genotoxicity than pristine nanoclays in mice lungs was written by Di Ianni, Emilio;Moeller, Peter;Mortensen, Alicja;Szarek, Jozef;Clausen, Per Axel;Saber, Anne Thoustrup;Vogel, Ulla;Jacobsen, Nicklas Raun. And the article was included in Nanotoxicology in 2020.Safety of N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride The following contents are mentioned in the article:

Surface modification by different quaternary ammonium compounds (QAC) makes nanoclays more compatible with various polymeric matrixes, thereby expanding their potential applications. The growing industrial use of nanoclays could potentially pose a health risk for workers. Here, we assessed how surface modification of nanoclays modulates their pulmonary toxicity. An in vitro screening of the unmodified nanoclay Bentonite (montmorillonite) and four organomodified nanoclays (ONC); coated with various QAC, including benzalkonium chloride (BAC), guided the selection of the materials for the in vivo study. Mice were exposed via a single intratracheal instillation to 18, 54, and 162 μg of unmodified Bentonite or dialkyldimethyl-ammonium-coated ONC (NanofilSE3000), or to 6, 18, and 54 μg of a BAC-coated ONC (Nanofil9), and followed for one, 3, or 28 days. All materials induced dose- and time-dependent responses in the exposed mice. However, all doses of Bentonite induced larger, but reversible, inflammation (BAL neutrophils) and acute phase response (Saa3 gene expression in lung) than the two ONC. Similarly, highest levels of DNA strand breaks were found in BAL cells of mice exposed to Bentonite 1 day post-exposure. A significant increase of DNA strand breaks was detected also for NanofilSE3000, 3 days post-exposure. Only mice exposed to Bentonite showed increased Tgf-β gene expression in lung, biomarker of pro-fibrotic processes and hepatic extravasation, 3 days post-exposure. This study indicates that Bentonite treatment with some QAC changes main phys.-chem. properties, including shape and surface area, and may decrease their pulmonary toxicity in exposed mice. This study involved multiple reactions and reactants, such as N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9Safety of N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride).

N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. Organochlorines stimulate the central nervous system and cause convulsions, tremor, nausea, and mental confusion. Examples are dichlorodiphenyltrichloroethane (DDT), chlordane, lindane, endosulfan, and dieldrin. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Safety of N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Fernandes, Susana et al. published their research in Food Research International in 2020 | CAS: 122-18-9

N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.Computed Properties of C25H46ClN

Antimicrobial activity of glycolic acid and glyoxal against Bacillus cereus and Pseudomonas fluorescens was written by Fernandes, Susana;Gomes, Ines B.;Simoes, Manuel. And the article was included in Food Research International in 2020.Computed Properties of C25H46ClN The following contents are mentioned in the article:

The development of effective disinfection strategies, including the search for new active biocides, is a priority research for the food industry. Glycolic acid (GA) and glyoxal (GO) are two glycolysis byproducts approved as biocides for surface disinfection, whose antimicrobial action remains to be understood. This study focused on the understanding of the antimicrobial activity of GA and GO against two foodborne pathogens, Bacillus cereus and Pseudomonas fluorescens. Benzalkonium chloride (BAC) and peracetic acid (PAA) were used as reference biocides for comparison. The influence of biocide concentration and exposure time on the antimicrobial activity of the selected biocides was evaluated based on the European Standard EN 1276. The mode of action of each biocide was characterized based on their effects on the cell envelope and cell replication. According to the Chick-Watson model, all biocides interacted chem. with cell targets of both bacteria, except GO that only stablished physicochem. interactions with P. fluorescens. The survival curves revealed that high concentrations of biocide induced readily effects on cell culturability. The susceptibility profile of P. fluorescens was constant over time. In general, B. cereus increased tolerance to BAC and became more susceptible to cumulative damages of GA. Overall, this study demonstrates that the biocidal activity was species-, dose- and time-dependent. GA, similarly to BAC, was a membrane-active and oxidant agent. GO had no effect on the bacterial surface as well as PAA. GO was mainly categorized as a cell replication inhibitor. For the first time, the antimicrobial activity of GA and GO were characterized revealing their potential for rational combination with other biocides commonly used in the food industry. This study involved multiple reactions and reactants, such as N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9Computed Properties of C25H46ClN).

N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.Computed Properties of C25H46ClN

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Silva Thomsen, Lars Bjoern et al. published their research in Water Research in 2020 | CAS: 122-18-9

N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Recommanded Product: N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride

Hydrothermal liquefaction of sewage sludge; energy considerations and fate of micropollutants during pilot scale processing was written by Silva Thomsen, Lars Bjoern;Carvalho, Pedro N.;dos Passos, Juliano Souza;Anastasakis, Konstantinos;Bester, Kai;Biller, Patrick. And the article was included in Water Research in 2020.Recommanded Product: N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride The following contents are mentioned in the article:

The beneficial use of sewage sludge for valorization of carbon and nutrients is of increasing interest while micropollutants in sludge are of concern to the environment and human health. This study investigates the hydrothermal liquefaction (HTL) of sewage sludge in a continuous flow pilot scale reactor at conditions expected to reflect future industrial installations. The processing is evaluated in terms of energy efficiency, bio-crude yields and quality. The raw sludge and post-HTL process water and solid residues were analyzed extensively for micropollutants via HPLC-MS/MS for target pharmaceuticals including antibiotics, blood pressure medicine, antidepressants, analgesics, x-ray contrast media, angiotensin II receptor blockers, immunosuppressant drugs and biocides including triazines, triazoles, carbamates, a carboxamide, an organophosphate and a cationic surfactant. The results show that a pos. energy return on investment was achieved for all three HTL processing temperatures of 300, 325 and 350°C with the most beneficial temperature identified as 325°C. The anal. of the HTL byproducts, process water and solids, indicates that HTL is indeed a suitable technol. for the destruction of micropollutants. However, due to the large matrix effect of the HTL process water it can only be stated with certainty that 9 out of 30 pharmaceuticals and 5 out of 7 biocides products were destroyed successfully (over 98% removal). One compound, the antidepressant citalopram, was shown to be moderately recalcitrant at 300°C with 87% removal and was only destroyed at temperatures≥325°C (>99% removal). Overall, the results suggest that HTL is a suitable technol. for energy efficient and value added sewage sludge treatment enabling destruction of micropollutants. This study involved multiple reactions and reactants, such as N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9Recommanded Product: N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride).

N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Recommanded Product: N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Molla, Mohammad Robel et al. published their research in Journal of Surfactants and Detergents in 2018 | CAS: 122-18-9

N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.Name: N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride

Conductometric Probe Analysis of the Effect of Benzyldimethylhexadecylammonium Chloride on the Micellization Behavior of Dodecyltrimethylammonium Bromide in Aqueous/Urea Solution: Investigation of Concentration and Temperature Effect was written by Molla, Mohammad Robel;Rana, Shahed;Abdul Rub, Malik;Ahmed, Anwar;Hoque, Anamul Md.. And the article was included in Journal of Surfactants and Detergents in 2018.Name: N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride The following contents are mentioned in the article:

Surfactant mixtures are used in many different industrial formulations. In this study, the mixed micelle formation behavior of 2 different cationic surfactants, namely dodecyltrimethylammonium bromide (DTAB) and benzyldimethylhexadecylammonium chloride (BDHAC), in the absence and presence of urea at various temperatures (298.15-318.15 K) was studied using the conductometric method. The attractive interaction between DTAB and BDHAC was estimated from the values of critical micelle concentration (CMC) and the CMC for ideal mixing (CMCid). Urea increases the CMC value as a result of the enrichment in the surface charge of the micelles/mixed micelles. The values of micellar mole fraction (X1Rub [Rubingh], X1M [Motomura], X1Rod [Rodenas]) and ideal micellar (X1id) of surfactant BDHAC were obtained by different models and are shown to exhibit the high contribution or effective involvement of BDHAC in mixed micelles and increase with increasing BDHAC mole fraction (a1). Activity coefficients (f1 and f2) were also evaluated from the relevant formula given in the literature. The neg. values of the interaction parameters (β) show the attractive interaction among the studied components. Excess Gibbs free energy ([Δ]Gex) of micellization revealed that the stability of mixed micelles is higher in aqueous solution than in urea solution The thermodn. parameters, namely the Gibbs free energy change, enthalpy change, and entropy change ([Δ]Gom, ΔHom, and [Δ]Som, resp.), were also calculated from the conventional standard equations. This study involved multiple reactions and reactants, such as N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9Name: N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride).

N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.Name: N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Groothuis, Floris A. et al. published their research in Chemical Research in Toxicology in 2019 | CAS: 122-18-9

N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Quality Control of N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride

Influence of in Vitro Assay Setup on the Apparent Cytotoxic Potency of Benzalkonium Chlorides was written by Groothuis, Floris A.;Timmer, Niels;Opsahl, Eystein;Nicol, Beate;Droge, Steven T. J.;Blaauboer, Bas J.;Kramer, Nynke I.. And the article was included in Chemical Research in Toxicology in 2019.Quality Control of N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride The following contents are mentioned in the article:

The nominal concentration is generally used to express concentration-effect relationships in in vitro toxicity assays. However, the nominal concentration does not necessarily represent the exposure concentration responsible for the observed effect. Surfactants accumulate at interphases and likely sorb to in vitro system components such as serum protein and well plate plastic. The extent of sorption and the consequences of this sorption on in vitro readouts is largely unknown for these chems. The aim of this study was to demonstrate the effect of sorption to in vitro components on the observed cytotoxic potency of benzalkonium chlorides (BAC) varying in alkyl chain length (6-18 carbon atoms, C6-18) in a basal cytotoxicity assay with the rainbow trout gill cell line (RTgill-W1). Cells were exposed for 48h in 96-well plates to increasing concentration of BACs in exposure medium containing 0, 60 μM Bovine Serum Albumin (BSA) or 10% fetal bovine serum (FBS). Before and after exposure, BAC concentrations in exposure medium were anal. determined Based on freely dissolved concentrations at the end of the exposure, median effect concentrations (EC50) decreased with increasing alkyl chain length up to 14 carbons. For BAC with alkyl chains of twelve or more carbons, EC50s based on measured concentrations after exposure in supplement-free medium were up to 25-times lower than EC50 calculated using nominal concentrations When BSA or FBS was added to the medium, a decrease in cytotoxic potency of up to 22 times was observed for BAC with alkyl chains of eight or more carbons. The results of this study emphasize the importance of expressing the in vitro readouts as a function of a dose metric that is least influenced by assay setup to compare assay sensitivities and chem. potencies. This study involved multiple reactions and reactants, such as N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9Quality Control of N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride).

N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Quality Control of N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics