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The structural properties of a noncentrosymmetric polymorph of 4-aminobenzoic acid
Acta Crystallographica Section C Structural Chemistry, 2014The crystal structure of a polymorph of 4-aminobenzoic acid (PABA), C7H7NO2, at 100 K is noncentrosymmetric, as opposed to centrosymmetric in the structures of the other known polymorphs. The two crystallographically independent PABA molecules form pseudocentrosymmetric O—H...O hydrogen-bonded dimers that are further linked by N—H...O hydrogen bonds ...
El-Eulmi Bendeif+3 more
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Screening for cocrystals of succinic acid and 4-aminobenzoic acid
CrystEngComm, 2012The ability of the pharmaceutically acceptable cocrystallising agents, succinic acid and 4-aminobenzoic acid, to form cocrystals with ten small organic molecules with hydrogen bonding acceptors but no donors, was investigated by grinding, hot-stage microscopy and solution based crystallisation experiments. The reproducible results obtained by different
Nizar Issa+6 more
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Physical Chemistry, Chemical Physics - PCCP, 2020
4-Aminobenzoic acid (PABA) is one of the earliest patented and most commonly used sunscreen components. There is however a long-lasting controversy on its photo-protective efficacy owing to the lack of information on its protolytic equilibrium and photo ...
C. Chan+7 more
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4-Aminobenzoic acid (PABA) is one of the earliest patented and most commonly used sunscreen components. There is however a long-lasting controversy on its photo-protective efficacy owing to the lack of information on its protolytic equilibrium and photo ...
C. Chan+7 more
semanticscholar +1 more source
Journal of the American Society for Mass Spectrometry, 2020
The most basic site of 4-aminobenzoic acid in aqueous solution is the amino nitrogen while the carbonyl oxygen is calculated to be the most basic site in the gas phase.
Rashmi Kumar, H. Kenttämaa
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The most basic site of 4-aminobenzoic acid in aqueous solution is the amino nitrogen while the carbonyl oxygen is calculated to be the most basic site in the gas phase.
Rashmi Kumar, H. Kenttämaa
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The synthesis of 2‐mercapto‐4‐aminobenzoic acid
Recueil des Travaux Chimiques des Pays-Bas, 1951AbstractThe synthesis of 2‐mercapto‐4‐aminobenzoic acid, a compound which is the sulphur analogue of p‐amino‐salicylic acid (2‐hydroxy‐4‐aminobenzoic acid), is described.
W. van Der Lugt+2 more
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Isoniazid and 4-aminobenzoic acid in the treatment of murine tuberculosis
Experientia, 1961Bei der Mausetuberkulose war die kombinierte Therapie von Isoniazid mit 4-Aminobenzoesaure (PABA) (3 mg/Tag/Tier) wirksamer als diejenige von Isoniazid allein. Bei niedrigerer PABA-Dosis wurde der Synergismus nicht nachgewiesen.
Z. Šimáně+3 more
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Growth and characterization of an adduct 4-aminobenzoic acid with nicotinic acid
Journal of Crystal Growth, 2011Abstract Synthesis, crystal growth of an adduct 2:1 4-aminobenzoic acid–nicotinic acid (AMN) and characterization are reported. The crystallographic data of the title compound are obtained from single crystal X-ray diffraction technique. The optical absorbance spectrum from 200 to 2250 nm shows the cutoff occurs at 490 nm.
T.S. Shyju+3 more
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Decarboxylation of substituted 4‐aminobenzoic acids in acidic aqueous solution
Recueil des Travaux Chimiques des Pays-Bas, 1967AbstractRates of decarboxylation have been determined of the following substituted 4‐aminobenzoic acids 2‐H‐, 2‐CH3‐, 2‐Cl‐, 2‐Br‐, 2‐NO2‐, 2‐OH‐, 2‐OCH3‐, 3‐Br‐, 2,6‐(CH3)2‐, 2,6‐(C2H5)2‐, 2,6‐Cl2‐ and 2,6‐Br2‐ in aqueous hydrochloric acid solution (pH ranging from about 0 to about 2), at 50° and an ionic strength of 0.1 (except for the lowest pH ...
R. F. Rekker+2 more
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On the mechanism of increasing the tuberculostatic activity of isoniazid in the presence of 4-aminobenzoic acid [PDF]
4-Acetaminobenzoesaure hatin vitro im Unterschied zu 4-Aminobenzoesaure, keinen gunstigen Einfluss auf die antituberkulotische Wirkung von Isoniazid. Bei den StammenMycobacterium 607 und H37Rv wurde jedoch chromatographisch keine Bildung acetylierter 4-Aminobenzoesaure nachgewiesen.
P. Kraus, R. Urbančík, Z. Šimáně
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Archiv der Pharmazie, 1988
AbstractWir danken Herrn Prof. Dr. G. Zinner, Institut für Pharm. Chemie der Techn. Universität Braunschweig, für die Elementaranalyse. Herrn L. Schulte danken wir für seine gewissenhafte Mitarbeit.
Grigat H, Büsing G
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AbstractWir danken Herrn Prof. Dr. G. Zinner, Institut für Pharm. Chemie der Techn. Universität Braunschweig, für die Elementaranalyse. Herrn L. Schulte danken wir für seine gewissenhafte Mitarbeit.
Grigat H, Büsing G
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