Medusheva, E. O.’s team published research in Fibre Chemistry in 41 | CAS: 38146-42-8

Fibre Chemistry published new progress about 38146-42-8. 38146-42-8 belongs to chlorides-buliding-blocks, auxiliary class Achiral Phase-Transfer Catalysts, name is N1,N10-Bis(2-((2-isopropyl-5-methylcyclohexyl)oxy)-2-oxoethyl)-N1,N1,N10,N10-tetramethyldecane-1,10-diaminium chloride, and the molecular formula is C38H74Cl2N2O4, Synthetic Route of 38146-42-8.

Medusheva, E. O. published the artcilePossibilities of molecular modeling of cellulose in fabrication of therapeutically active textile materials, Synthetic Route of 38146-42-8, the publication is Fibre Chemistry (2009), 41(1), 34-37, database is CAplus.

Highly effective means of stopping capillary-parenchymatous bleeding – one of the main causes of death in people from 1 to 34 years of age in traffic accidents – were developed. Biol. active wound dressings that reduce purulent-necrotic wound cleansing time by 3 times, healing time by 2.5 times, and hospital stays by 6 times were developed.

Fibre Chemistry published new progress about 38146-42-8. 38146-42-8 belongs to chlorides-buliding-blocks, auxiliary class Achiral Phase-Transfer Catalysts, name is N1,N10-Bis(2-((2-isopropyl-5-methylcyclohexyl)oxy)-2-oxoethyl)-N1,N1,N10,N10-tetramethyldecane-1,10-diaminium chloride, and the molecular formula is C38H74Cl2N2O4, Synthetic Route of 38146-42-8.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Blazhevs’kii, M. E.’s team published research in Farmatsevtichnii Zhurnal (Kiev) in | CAS: 38146-42-8

Farmatsevtichnii Zhurnal (Kiev) published new progress about 38146-42-8. 38146-42-8 belongs to chlorides-buliding-blocks, auxiliary class Achiral Phase-Transfer Catalysts, name is N1,N10-Bis(2-((2-isopropyl-5-methylcyclohexyl)oxy)-2-oxoethyl)-N1,N1,N10,N10-tetramethyldecane-1,10-diaminium chloride, and the molecular formula is C38H74Cl2N2O4, COA of Formula: C38H74Cl2N2O4.

Blazhevs’kii, M. E. published the artcileA spectrophotometric assay for kinetic determination of cholinesterase inhibitors using p-phenetidine oxidation, COA of Formula: C38H74Cl2N2O4, the publication is Farmatsevtichnii Zhurnal (Kiev) (2004), 52-58, database is CAplus.

An assay for detecting cholinesterase inhibitors using p-phenetidine oxidation is described. The high-sensitivity spectrophotometric assay is developed for quant. determination of quaternary ammonium salts, phenothiazine derivatives, phosphonous acid derivatives and some alkaloids. In the concentration range of the analyte 6·10-19-6·10-5 M the relative error does not exceed ±11%.

Farmatsevtichnii Zhurnal (Kiev) published new progress about 38146-42-8. 38146-42-8 belongs to chlorides-buliding-blocks, auxiliary class Achiral Phase-Transfer Catalysts, name is N1,N10-Bis(2-((2-isopropyl-5-methylcyclohexyl)oxy)-2-oxoethyl)-N1,N1,N10,N10-tetramethyldecane-1,10-diaminium chloride, and the molecular formula is C38H74Cl2N2O4, COA of Formula: C38H74Cl2N2O4.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Nagiev, Kh. D.’s team published research in Zavodskaya Laboratoriya, Diagnostika Materialov in 69 | CAS: 38146-42-8

Zavodskaya Laboratoriya, Diagnostika Materialov published new progress about 38146-42-8. 38146-42-8 belongs to chlorides-buliding-blocks, auxiliary class Achiral Phase-Transfer Catalysts, name is N1,N10-Bis(2-((2-isopropyl-5-methylcyclohexyl)oxy)-2-oxoethyl)-N1,N1,N10,N10-tetramethyldecane-1,10-diaminium chloride, and the molecular formula is C38H74Cl2N2O4, Related Products of chlorides-buliding-blocks.

Nagiev, Kh. D. published the artcilePhotometric determination of Mo(VI) by pyrogallol derivatives in the presence of a third component, Related Products of chlorides-buliding-blocks, the publication is Zavodskaya Laboratoriya, Diagnostika Materialov (2003), 69(10), 15-19, database is CAplus.

The complex formation of Mo(VI) with pyrogallol derivatives in the presence of a 3rd component is studied photometrically. Amines, especially ethylenediamine, and benzidine, and surfactants, especially cetylpyridinium chloride, and decametoxin, were used as 3rd components. The optimal requirements for binary Mo(VI) complex formations and their basic spectro-photometric parameters were determined The method is applied to determine micro quantities of molybdenum in tap water, soil of the Apsheron peninsula and in different kinds of steels.

Zavodskaya Laboratoriya, Diagnostika Materialov published new progress about 38146-42-8. 38146-42-8 belongs to chlorides-buliding-blocks, auxiliary class Achiral Phase-Transfer Catalysts, name is N1,N10-Bis(2-((2-isopropyl-5-methylcyclohexyl)oxy)-2-oxoethyl)-N1,N1,N10,N10-tetramethyldecane-1,10-diaminium chloride, and the molecular formula is C38H74Cl2N2O4, Related Products of chlorides-buliding-blocks.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Kucherenko, Ludmila’s team published research in ScienceRise: Pharmaceutical Science in | CAS: 38146-42-8

ScienceRise: Pharmaceutical Science published new progress about 38146-42-8. 38146-42-8 belongs to chlorides-buliding-blocks, auxiliary class Achiral Phase-Transfer Catalysts, name is N1,N10-Bis(2-((2-isopropyl-5-methylcyclohexyl)oxy)-2-oxoethyl)-N1,N1,N10,N10-tetramethyldecane-1,10-diaminium chloride, and the molecular formula is C38H74Cl2N2O4, COA of Formula: C38H74Cl2N2O4.

Kucherenko, Ludmila published the artcileTheoretical study of the possibility of decamethoxin complexes with thiotriazoline to be formed, COA of Formula: C38H74Cl2N2O4, the publication is ScienceRise: Pharmaceutical Science (2021), 37-42, database is CAplus.

Over the last decade, much attention has been paid to the prevention and treatment of chronic diseases of the oral mucosa. This is primarily due to the increase in the number of patients who seek dental care for diseases of the oral muco-sa (DOM). Currently, due to the lack of special epidemiol. studies, information on the pathol. of the oral mucosa in the literature is almost non-existent. The etiol. and pathogenesis have not been definitively elucidated. It is established that a significant role in the pathogenesis of chronic inflammatory processes belongs to the state of the microbiocenosis of the oral mucosa. One of the most striking examples of domestic drugs of the antioxidant group is thiotriazoline, developed by the staff of the NGO ‘Pharmatron’, as well as specialists of the Department of Pharmaceutical Chem. of Zaporozhye State Medical University under the leadership of professor Mazur I. This drug has an antioxidant and membrane-stabilizing effect. The combined use of several drugs can be complicated by the formation of their supramol. complexes. Therefore, before the introduction of several substances in it is necessary to model the possibility of intermol. interactions between them. For this purpose, methods of quantum chem. are used. We examined the structures and energy characteristics of the complexes, formed thiotriazoline and decamethoxin, also carried out anal. and established at what temperature the formation of a substance from two active components was possible. As a result, the probability of the formation of intermol. hydrogen bonds is reduced, which is very well seen in the trend of interactions between acid and morpholine. Quantum chem. study of a two-component system consisting of thiotriazoline and decamethoxine showed that the most energetically advantageous three-component complexes have a sufficiently low interaction energy of thiotriazoline and decamethoxine. In addition, the data that are provided in the anal. of the tree diagram suggest that in the technol. process in the manufacture of dosage forms, it is advisable to use a temperature not higher than 115°C.

ScienceRise: Pharmaceutical Science published new progress about 38146-42-8. 38146-42-8 belongs to chlorides-buliding-blocks, auxiliary class Achiral Phase-Transfer Catalysts, name is N1,N10-Bis(2-((2-isopropyl-5-methylcyclohexyl)oxy)-2-oxoethyl)-N1,N1,N10,N10-tetramethyldecane-1,10-diaminium chloride, and the molecular formula is C38H74Cl2N2O4, COA of Formula: C38H74Cl2N2O4.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Kosevich, Marina V.’s team published research in Rapid Communications in Mass Spectrometry in 21 | CAS: 38146-42-8

Rapid Communications in Mass Spectrometry published new progress about 38146-42-8. 38146-42-8 belongs to chlorides-buliding-blocks, auxiliary class Achiral Phase-Transfer Catalysts, name is N1,N10-Bis(2-((2-isopropyl-5-methylcyclohexyl)oxy)-2-oxoethyl)-N1,N1,N10,N10-tetramethyldecane-1,10-diaminium chloride, and the molecular formula is C38H74Cl2N2O4, SDS of cas: 38146-42-8.

Kosevich, Marina V. published the artcileIs there a ‘matrix suppression effect’ under fast-atom bombardment liquid secondary ion mass spectrometry of ionic surfactants in glycerol?, SDS of cas: 38146-42-8, the publication is Rapid Communications in Mass Spectrometry (2007), 21(4), 466-478, database is CAplus.

Some features of a ‘matrix suppression effect’ caused by ionic surface-active compounds under fast-atom bombardment (FAB) liquid secondary ion mass spectrometry (LSIMS) are being revised. It is shown that abundant transfer of the glycerol matrix mols. to the gas phase does occur under FAB-LSIMS of ionic surfactants, contrary to popular belief. This process can be obscure because of the dependence of the charge state of the glycerol-containing cluster ions on the type of ionic surfactant. It is revealed that, while glycerol matrix signals are really completely suppressed in the pos. ion mass spectra of cationic surfactants (decamethoxinum, aethonium), abundant deprotonated glycerol and glycerol-anion clusters are recorded in the neg. ion mode. In the case of an anionic surfactant (sodium dodecyl sulfate), on the contrary, glycerol is completely suppressed in the neg. ion mode, but is present in the protonated and cationized forms in the pos. ion mass spectra. It is suggested that such patterns of pos. and neg. ion FAB-LSIMS spectra of ionic surfactants solutions reflect the structure and composition of the elec. double layer formed at the vacuum-liquid interface by organic cations or anions and their counterions. Processes leading to the formation of the glycerol-containing ions preferentially of pos. or neg. charge are discussed. The most obvious of them is efficient binding of glycerol to inorganic counterions of the salts Cl or Na+, which is confirmed by data from quantum chem. calculations The high content of the counterions and relatively small content of glycerol in the sputtered zone may be responsible for the charge-selective suppression of neat glycerol clusters of opposite charge to the counterions. In the case of a mixture of cationic and anionic surfactants the substitution of inorganic counterions by organic ones was observed The dependence of the exchange rate in the surface layer is not a linear function of the bulk solution concentration, and an effect of abrupt recharging of the surface can be registered. No both pos. or neg. charged pure glycerol and glycerol-inorganic counterion clusters are recorded for the mixture Correlations between the mass spectrometric observations and some phenomena of surface and colloid chem. and physics are discussed.

Rapid Communications in Mass Spectrometry published new progress about 38146-42-8. 38146-42-8 belongs to chlorides-buliding-blocks, auxiliary class Achiral Phase-Transfer Catalysts, name is N1,N10-Bis(2-((2-isopropyl-5-methylcyclohexyl)oxy)-2-oxoethyl)-N1,N1,N10,N10-tetramethyldecane-1,10-diaminium chloride, and the molecular formula is C38H74Cl2N2O4, SDS of cas: 38146-42-8.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics