Atropine/Hyoscyamine/Methenamine/Methylene Blue/Phenyl Salicylate/Benzoic Acid

2020 ◽  
Author(s):  
1970 ◽  
Vol 53 (4) ◽  
pp. 819-823
Author(s):  
Albert L Woodson

Abstract Methylene blue, methenamine, phenyl salicylate, benzoic acid, atropine sulfate, and hyoscyamine are separated by chromatographic procedures. Assays are described for each component. Phenyl salicylate, benzoic acid, atropine, and hyoscyamine are isolated by partitition chromatography on acid- and base-Celite columns. These isolated components are quantitated by ultraviolet spectrophotometry (phenyl salicylate and benzoic acid) and visible spectrophotometry (total alkaloids as atropine sulfate). Methenamine is separated and quantitated by GLC on a column of 6% Carbowax 20M on 80–100 mesh Gas Chrom Q. Methylene blue is quantitated by visible spectrophotometry without prior separation. The data obtained with a synthetic mixture and 3 commercial samples are presented.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Shan-Bao Qiao

Abstract A new Cu(II) complex, [Cu2(1,3-BMIB)(OBA)2] n (1) (1,3-BMIB = 1,3-bis(2-methyl-1H-imidazol-1-yl)benzene, H2OBA = 4,4′-oxybis(benzoic acid)) was hydrothermally synthesized and has been structurally characterized. Complex 1 possesses a 3D 2-fold interpenetrating framework based on [Cu(OBA)] n layers with a Schläfli symbol {412.63}. Complex 1 displays excellent photocatalytic properties in the degradation of methylene blue (MB) and rhodamine B (RhB).


2009 ◽  
Vol 163 (1) ◽  
pp. 363-369 ◽  
Author(s):  
G. Muthuraman ◽  
Tjoon Tow Teng ◽  
Cheu Peng Leh ◽  
I. Norli

2018 ◽  
Vol 47 (18) ◽  
pp. 6538-6548 ◽  
Author(s):  
Yongfang Yang ◽  
Zhanghao Niu ◽  
Hua Li ◽  
Yehui Ma ◽  
Yue Zhang ◽  
...  

A series of poly-vinyl benzoic acid (PVBA) and UiO-66 materials (PVBA-UiO-66) were prepared by a mixed-linker approach.


Author(s):  
B. J. Panessa ◽  
J. F. Gennaro

Tissue from the hood and sarcophagus regions were fixed in 6% glutaraldehyde in 1 M.cacodylate buffer and washed in buffer. Tissue for SEM was partially dried, attached to aluminium targets with silver conducting paint, carbon-gold coated(100-500Å), and examined in a Kent Cambridge Stereoscan S4. Tissue for the light microscope was post fixed in 1% aqueous OsO4, dehydrated in acetone (4°C), embedded in Epon 812 and sectioned at ½u on a Sorvall MT 2 ultramicrotome. Cross and longitudinal sections were cut and stained with PAS, 0.5% toluidine blue and 1% azure II-methylene blue. Measurements were made from both SEM and Light micrographs.The tissue had two structurally distinct surfaces, an outer surface with small (225-500 µ) pubescent hairs (12/mm2), numerous stoma (77/mm2), and nectar glands(8/mm2); and an inner surface with large (784-1000 µ)stiff hairs(4/mm2), fewer stoma (46/mm2) and larger, more complex glands(16/mm2), presumably of a digestive nature.


Author(s):  
W. E. Lee

An optical waveguide consists of a several-micron wide channel with a slightly different index of refraction than the host substrate; light can be trapped in the channel by total internal reflection.Optical waveguides can be formed from single-crystal LiNbO3 using the proton exhange technique. In this technique, polished specimens are masked with polycrystal1ine chromium in such a way as to leave 3-13 μm wide channels. These are held in benzoic acid at 249°C for 5 minutes allowing protons to exchange for lithium ions within the channels causing an increase in the refractive index of the channel and creating the waveguide. Unfortunately, optical measurements often reveal a loss in waveguiding ability up to several weeks after exchange.


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