Category: 132-20-7

Wang, Zeyang; Lu, Song; Fu, Yan; Wang, Hui; Zhao, Guannan published an article in 2016, the title of the article was Sodium borohydride promotes drug molecules preparation.Name: N,N-Dimethyl-3-phenyl-3-(pyridin-2-yl)propan-1-amine maleate And the article contains the following content:

Sodium borohydride reduction is an excellent performance of “universal reducing agent”, which commonly used in a variety of reduction of organic functional groups, After the modified sodium borohydride reduction was greatly expanded in the field of application, can be used to restore the carboxylic acids, carboxylic acid esters, alcs., indole, enyne other substances, under certain reduction system, when compared with a sodium borohydride reduction good reduction On the other hand, due to the high amount of sodium borohydride hydrogen storage, mild reaction conditions, making it the people developed “green energy” hot hydrogen raw materials, and therefore there are many catalytic hydrogen production catalysts are finding out, it was discover the advantages of composite sodium borohydride hydrogen production The experimental process involved the reaction of N,N-Dimethyl-3-phenyl-3-(pyridin-2-yl)propan-1-amine maleate(cas: 132-20-7).Name: N,N-Dimethyl-3-phenyl-3-(pyridin-2-yl)propan-1-amine maleate

The Article related to sodium borohydride drug mol reduction, Placeholder for records without volume info and other aspects.Name: N,N-Dimethyl-3-phenyl-3-(pyridin-2-yl)propan-1-amine maleate

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Eltsova, Natalia O.; Budko, Elena V.; Yampolskii, Leonid M.; Kulikov, Alexander L. published an article in 2016, the title of the article was UPLC study of inter-component interaction in the system “naproxen – pheniramine maleate”.Computed Properties of 132-20-7 And the article contains the following content:

The anal. was performed for the two-component system “naproxen – pheniramine maleate” using the method UPLC. It is concluded that strengthening the destructive processes in the presence of pheniramine maleate with naproxen based on the chromatogram initial substances at influence of stress factors and identified degradation products. The experimental process involved the reaction of N,N-Dimethyl-3-phenyl-3-(pyridin-2-yl)propan-1-amine maleate(cas: 132-20-7).Computed Properties of 132-20-7

The Article related to naproxen pheniramine maleate inter component interaction uplc, Pharmaceuticals: Formulation and Compounding and other aspects.Computed Properties of 132-20-7

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Bukhari, Syed Majid Hanif; Khan, Samiullah; Rehanullah, Muhammad; Ranjha, Nazar Mohammad published an article in 2015, the title of the article was Synthesis and characterization of chemically cross-linked acrylic acid/gelatin hydrogels: effect of pH and composition on swelling and drug release.Category: pyridine-derivatives And the article contains the following content:

This present work was aimed at synthesizing pH-sensitive cross-linked AA/Gelatin hydrogels by free radical polymerization Ammonium persulfate and ethylene glycol dimethacrylate (EGDMA) were used as initiator and as crosslinking agent, resp. Different feed ratios of acrylic acid, gelatin, and EGDMA were used to investigate the effect of monomer, polymer, and degree of crosslinking on swelling and release pattern of the model drug.The swelling behavior of the hydrogel samples was studied in 0.05M USP phosphate buffer solutions of various pH values pH 1.2, pH 5.5, pH 6.5, and pH 7.5.The prepared samples were evaluated for porosity and sol-gel fraction anal. Pheniraminemaleate used for allergy treatment was loaded as model drug in selected samples. The release study of the drug was investigated in 0.05M USP phosphate buffer of varying pH values (1.2, 5.5, and 7.5) for 12 h. The release data was fitted to various kinetic models to study the release mechanism. Hydrogels were characterized by Fourier transformed IR (FTIR) spectroscopy which confirmed formation of structure. Surface morphol. of unloaded and loaded samples was studied by surface electron microscopy (SEM), which confirmed the distribution of model drug in the gel network. The experimental process involved the reaction of N,N-Dimethyl-3-phenyl-3-(pyridin-2-yl)propan-1-amine maleate(cas: 132-20-7).Category: pyridine-derivatives

The Article related to acrylic acid gelatin hydrogel drug delivery system, Pharmaceuticals: Formulation and Compounding and other aspects.Category: pyridine-derivatives

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

On March 31, 2010, Rajalakshmi, G.; Damodharan, N.; Chaudhary, Abhinav; Maheswara Reddy, D. published an article.COA of Formula: C20H24N2O4 The title of the article was Formulation and evaluation of Orodispersible tablets of Pheniramine maleate. And the article contained the following:

In the present study an attempt has been made to formulate Pheniramine maleate a selective H1 receptor antagonist into orodispersible tablet. The tablets were prepared by direct compression method using super disintegrants like croscarmellose sodium, crospovidone, sodium starch glycollate, low hydroxyl pr cellulose and pre gelatinized starch in different ratios. The blend was examined for various pre compression parameters. Tablets were evaluated by measuring hardness, friability, content uniformity, weight variation and drug release pattern. All the tablets met the pharmacopoeial requirements for phys. tests. Almost in all the formulations with increase in concentration of superdisintegrants, the drug release was rapid. Stability studies were also performed. Dissolution studies indicated that the tablets containing crospovidone and croscarmellose sodium showed rapid dissolution compared to other disintegrants releasing almost 100% of the drug in six minutes. The experimental process involved the reaction of N,N-Dimethyl-3-phenyl-3-(pyridin-2-yl)propan-1-amine maleate(cas: 132-20-7).COA of Formula: C20H24N2O4

The Article related to pheniramine maleate orodispersible tablet, Pharmaceuticals: Formulation and Compounding and other aspects.COA of Formula: C20H24N2O4

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Petkova, Valentina; Hadzhieva, Bozhidarka Radoslavova published an article in 2021, the title of the article was Pilot study of over-the-counter drugs applied among the pediatric population in Bulgaria.Application of 132-20-7 And the article contains the following content:

Herbal medicines have evolved through their traditional use in a specific or cultural context. The pharmacol. effects of herbal medicines are not due to their “natural” origin, but to the complex character of biol. active substances. Pediatricians have begun to integrate the use of complementary / alternative medical therapies with conventional health care. The first aim of the study was to make an anal. of over-the-counter (OTC) drugs (OTCDs) with a plant component. The secondary aim was to investigate OTCDs in terms of composition and nosol. for use by the pediatric population in Bulgaria. Registered OTC drugs with a herbal component for children are prescribed for the treatment of colds, pain, gastrointestinal diseases, mild sleep disorders, neurovegetative dystonias and kinetosis, urinary tract inflammation, liver disease, and are also applied topically to inflammation, trauma, urticaria and scars. The experimental process involved the reaction of N,N-Dimethyl-3-phenyl-3-(pyridin-2-yl)propan-1-amine maleate(cas: 132-20-7).Application of 132-20-7

The Article related to herbal medicine counter drug pediatric population pain gastrointestinal disease, Placeholder for records without volume info and other aspects.Application of 132-20-7

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Gasior, Justyna; Kawa-Rygielska, Joanna; Kucharska, Alicja Z. published an article in 2020, the title of the article was Carbohydrates profile, polyphenols content and antioxidative properties of beer worts produced with different dark malts varieties or roasted barley grains.Synthetic Route of 132-20-7 And the article contains the following content:

The aim of this study was to assess the possibility of shaping properties of beers at the stage of brewing wort production with the use of various types of special malts (chocolate pale, chocolate dark, wheat chocolate, brown barley) and roasted barley grains. The carbohydrate profile, polyphenols content, antioxidant capacity, 5-hydroxymethylfurfural content, and the browning index level were analyzed. Statistical anal. showed significant differences in the values of the examined features between the samples. The sugars whose content was most affected by the addition of special malts were maltose and dextrins. The polyphenol content in worts with 10% of additive was 176.02-397.03 mg GAE/L, ferric reducing antioxidant power (FRAP) 1.32-2.07 mmol TE/L, and capacity to reduction radical generated from 2,2′-Azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS•+) 1.46-2.70 mmol TE/L. Wort with 40% dark malt showed the highest content of polyphenolic compounds and antioxidant activity (FRAP and ABTS•+). The HMF content and the browning index value were higher for wort with the addition of darker-colored malts (EBC) and increased with increasing dark malt dose. The experimental process involved the reaction of N,N-Dimethyl-3-phenyl-3-(pyridin-2-yl)propan-1-amine maleate(cas: 132-20-7).Synthetic Route of 132-20-7

The Article related to carbohydrate polyphenol antioxidative beer wort malt barley grain, antioxidants, barley, beer, dark malt, malt, melanoidins, polyphenols, roasting, specialty malt, wort, Pharmaceuticals: Pharmacognostic Products and other aspects.Synthetic Route of 132-20-7

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

On August 31, 2010, Phatthiyaphaibun, K.; Som-Aum, W.; Srisa-ard, M.; Threeprom, J. published an article.Safety of N,N-Dimethyl-3-phenyl-3-(pyridin-2-yl)propan-1-amine maleate The title of the article was Chiral separation of pheniramine by capillary electrophoresis partial-filling technique using hydroxypropyl-β-cyclodextrin as chiral selector. And the article contained the following:

A simple capillary electrophoresis partial-filling technique for the enantioseparation of pheniramine is presented. Phosphate buffer and hydroxypropyl-β-cyclodextrin (HP-β-CD) were used as the electrolyte and chiral selector, resp. Several exptl. parameters such as HP-β-CD concentration, HP-β-CD plug length, CE temperature and applied voltage were studied. Under the selected conditions, pheniramine enantiomers can be separated within <14 min. The assay was validated for linearity (5.0 × 10-6 - 5.0 × 10-4 M; R2 = 0.9987), limit of detection (5.0 × 10-7 M), limit of quantitation (5.0 × 10-6 M), anal. precision (%RSD ≤ 9.8) and accuracy (%recovery = 101 ± 3). The proposed methodol. was then applied to the anal. of a com. available pharmaceutical eye drop preparation The results are in good agreement with that declared by the manufacturer. The proposed methodol. provides adequate results in terms of simplicity, cost, sample throughput, repeatability and accuracy for quality control of pheniramine enantiomers in pharmaceutical preparations The experimental process involved the reaction of N,N-Dimethyl-3-phenyl-3-(pyridin-2-yl)propan-1-amine maleate(cas: 132-20-7).Safety of N,N-Dimethyl-3-phenyl-3-(pyridin-2-yl)propan-1-amine maleate

The Article related to pheniramine enantiosepn capillary electrophoresis partial filling technique hydroxypropylcyclodextrin selector, Organic Analytical Chemistry: Separations and other aspects.Safety of N,N-Dimethyl-3-phenyl-3-(pyridin-2-yl)propan-1-amine maleate

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Petkova, Valentina; Hadzhieva, Bozhidarka Radoslavova published an article in 2021, the title of the article was Pilot study of over-the-counter drugs applied among the pediatric population in Bulgaria.Application of 132-20-7 And the article contains the following content:

Herbal medicines have evolved through their traditional use in a specific or cultural context. The pharmacol. effects of herbal medicines are not due to their “natural” origin, but to the complex character of biol. active substances. Pediatricians have begun to integrate the use of complementary / alternative medical therapies with conventional health care. The first aim of the study was to make an anal. of over-the-counter (OTC) drugs (OTCDs) with a plant component. The secondary aim was to investigate OTCDs in terms of composition and nosol. for use by the pediatric population in Bulgaria. Registered OTC drugs with a herbal component for children are prescribed for the treatment of colds, pain, gastrointestinal diseases, mild sleep disorders, neurovegetative dystonias and kinetosis, urinary tract inflammation, liver disease, and are also applied topically to inflammation, trauma, urticaria and scars. The experimental process involved the reaction of N,N-Dimethyl-3-phenyl-3-(pyridin-2-yl)propan-1-amine maleate(cas: 132-20-7).Application of 132-20-7

The Article related to herbal medicine counter drug pediatric population pain gastrointestinal disease, Placeholder for records without volume info and other aspects.Application of 132-20-7

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

On March 31, 2010, Rajalakshmi, G.; Damodharan, N.; Chaudhary, Abhinav; Maheswara Reddy, D. published an article.COA of Formula: C20H24N2O4 The title of the article was Formulation and evaluation of Orodispersible tablets of Pheniramine maleate. And the article contained the following:

In the present study an attempt has been made to formulate Pheniramine maleate a selective H1 receptor antagonist into orodispersible tablet. The tablets were prepared by direct compression method using super disintegrants like croscarmellose sodium, crospovidone, sodium starch glycollate, low hydroxyl pr cellulose and pre gelatinized starch in different ratios. The blend was examined for various pre compression parameters. Tablets were evaluated by measuring hardness, friability, content uniformity, weight variation and drug release pattern. All the tablets met the pharmacopoeial requirements for phys. tests. Almost in all the formulations with increase in concentration of superdisintegrants, the drug release was rapid. Stability studies were also performed. Dissolution studies indicated that the tablets containing crospovidone and croscarmellose sodium showed rapid dissolution compared to other disintegrants releasing almost 100% of the drug in six minutes. The experimental process involved the reaction of N,N-Dimethyl-3-phenyl-3-(pyridin-2-yl)propan-1-amine maleate(cas: 132-20-7).COA of Formula: C20H24N2O4

The Article related to pheniramine maleate orodispersible tablet, Pharmaceuticals: Formulation and Compounding and other aspects.COA of Formula: C20H24N2O4

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Bukhari, Syed Majid Hanif; Khan, Samiullah; Rehanullah, Muhammad; Ranjha, Nazar Mohammad published an article in 2015, the title of the article was Synthesis and characterization of chemically cross-linked acrylic acid/gelatin hydrogels: effect of pH and composition on swelling and drug release.Category: pyridine-derivatives And the article contains the following content:

This present work was aimed at synthesizing pH-sensitive cross-linked AA/Gelatin hydrogels by free radical polymerization Ammonium persulfate and ethylene glycol dimethacrylate (EGDMA) were used as initiator and as crosslinking agent, resp. Different feed ratios of acrylic acid, gelatin, and EGDMA were used to investigate the effect of monomer, polymer, and degree of crosslinking on swelling and release pattern of the model drug.The swelling behavior of the hydrogel samples was studied in 0.05M USP phosphate buffer solutions of various pH values pH 1.2, pH 5.5, pH 6.5, and pH 7.5.The prepared samples were evaluated for porosity and sol-gel fraction anal. Pheniraminemaleate used for allergy treatment was loaded as model drug in selected samples. The release study of the drug was investigated in 0.05M USP phosphate buffer of varying pH values (1.2, 5.5, and 7.5) for 12 h. The release data was fitted to various kinetic models to study the release mechanism. Hydrogels were characterized by Fourier transformed IR (FTIR) spectroscopy which confirmed formation of structure. Surface morphol. of unloaded and loaded samples was studied by surface electron microscopy (SEM), which confirmed the distribution of model drug in the gel network. The experimental process involved the reaction of N,N-Dimethyl-3-phenyl-3-(pyridin-2-yl)propan-1-amine maleate(cas: 132-20-7).Category: pyridine-derivatives

The Article related to acrylic acid gelatin hydrogel drug delivery system, Pharmaceuticals: Formulation and Compounding and other aspects.Category: pyridine-derivatives

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem