The Alkaloids of Senecio jacobaea L. III. The structure of Jaconecic Acid

1956 ◽  
Vol 9 (4) ◽  
pp. 521 ◽  
Author(s):  
RB Bradbury

Oxidation of jaconecic acid by nitric acid yields four acid products, which have been separated by a combination of partition chromatography on silica gel, and paper chromatography. Two of these fragments have been identified as αβ-dimethylmalic acid and oxalic acid, whilst the other two are dibasic acids having the formulae C9H14O6 and C9H12O7. These findings support the structure previously assigned to jaconecic acid.

Author(s):  
N.C. Lyon ◽  
W. C. Mueller

Schumacher and Halbsguth first demonstrated ectodesmata as pores or channels in the epidermal cell walls in haustoria of Cuscuta odorata L. by light microscopy in tissues fixed in a sublimate fixative (30% ethyl alcohol, 30 ml:glacial acetic acid, 10 ml: 65% nitric acid, 1 ml: 40% formaldehyde, 5 ml: oxalic acid, 2 g: mecuric chloride to saturation 2-3 g). Other workers have published electron micrographs of structures transversing the outer epidermal cell in thin sections of plant leaves that have been interpreted as ectodesmata. Such structures are evident following treatment with Hg++ or Ag+ salts and are only rarely observed by electron microscopy. If ectodesmata exist without such treatment, and are not artefacts, they would afford natural pathways of entry for applied foliar solutions and plant viruses.


1979 ◽  
Vol 44 (7) ◽  
pp. 2024-2031 ◽  
Author(s):  
František Vláčil ◽  
Huynh Dang Khanh

The dependence of the distribution ratio of the metal on the concentration of hydrochloric of nitric acid was examined for Fe, Co, Ni and Cu extraction with 0.05M solution of dibenzylsulfoxide in toluene. Iron is extracted considerably more than the other metals, and is better extracted from hydrochloric acid than from nitric acid. The separation factor αFe/M (for 8M-HCl) is of the order of 104; this is not sufficient for a separation of trace quantities of iron from Co, Ni and Cu, but even at lower concentrations of HCl (e.g., 5M) the values is high enough for extraction chromatographic separation. The composition of the iron solvate extracted from HCl or LiCl medium was determined to be HFeCl4.2 B (B = dibenzyl sulfoxide).


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Chuanbo Li ◽  
Yongzhi Ning ◽  
Taihong Yan ◽  
Weifang Zheng

Abstract The effects of feeding location, stirring speed and apparent average residence time on oxalate crystals size and distribution, tackiness of the product on the walls of reactor and stirring paddle were investigated in a vortex continuous precipitator at 45 °C. The results showed agglomeration happened during nucleation and crystals growth of U(IV) oxalate. Both local supersaturations and agglomeration maked the particles size distribution of U(IV) oxalate from 10–100 µm and the average sizes 35–45 µm. On the other hand, when the nucleation process were controlled to happen in the forced vortex zone, two feeding locations: (a) both oxalic acid and U(IV) nitrate solution into the forced vortex zone, (b) oxalic acid into the free vortex and U(IV) nitrate solution into the forced vortex, tackiness of the crystals on the wall of the precipitator could be effectively avoided.


Of the commoner mineral acids the chemical changes of Nitric Acid, from their evident complexity, have formed the subject of numerous memoirs, while those of sulphuric acid, from their assumed simplicity, have been to some degree neglected; on the other hand, the physical properties of the latter have been studied with considerable elaboration, while those of the former have been passed over, doubtless on account of the corrosive nature of the acid and the difficulty of preparing and preserving it in a reasonable degree of purity. Further, with certain exceptions, the alterations in physical properties induced by the products of reduction, be they nitrogen peroxide or nitrous acid, either singly or conjointly, have attracted but little attention, though it is a common matter of observation that the current intensity of a Grove’s or other cell containing nitric acid remains constant, even though the fuming acid, originally colourless or red, has become of a deep green tint. It is more than probable that of the factors of Ohm’s law, both the E. M. F. and internal resistance are continually varying. At the earliest stages of the enquiry it was found that the passage of a few bubbles of nitric oxide gas into a considerable volume of nitric acid produced an alteration of one percent, in the resistance, and the same result could be effected to a less degree by exposure to sunlight, and to a still less degree by exposure to artificial illumination. Therefore, we determined to investigate the alterations of conductivity produced by changes of concentration and temperature in samples of acid purified with necessary precautions, more especially as former workers upon the subject have either used samples of acid confessedly impure, or have been silent as to any method of purification, or have adopted no special care in dealing with a substance so susceptible of polarisation.


1973 ◽  
Vol 56 (6) ◽  
pp. 1475-1479 ◽  
Author(s):  
Ugo R Cieri

Abstract Sulfaquinoxaline is determined by its UV absorbance at about 358 nm, where the other 3 sulfonamides do not absorb. Sulfathiazole, sulfamerazine, and sulfamethazine are determined by a quantitative TLC procedure, based on the separation of the compounds on silica gel plates; the spots are extracted and the centrifuged extracts are analyzed spectro-photometrically. A method of calculating the total sulfonamide content, independent of the individual components, is also introduced.


1904 ◽  
Vol 24 ◽  
pp. 233-239 ◽  
Author(s):  
Hugh Marshall

When thio-urea is treated with suitable oxidising agents in presence of acids, salts are formed corresponding to the general formula (CSN2H4)2X2:—Of these salts the di-nitrate is very sparingly soluble, and is precipitated on the addition of nitric acid or a nitrate to solutions of the other salts. The salts, as a class, are not very stable, and their solutions decompose, especially on warming, with formation of sulphur, thio-urea, cyanamide, and free acid. A corresponding decomposition results immediately on the addition of alkali, and this constitutes a very characteristic reaction for these salts.


Author(s):  
Ihwan Rahmadi

Palm oil palm is one of the solid waste produced by oil palm plantations every harvest. Chemical analysis of palm oil palm oil pellets showed that there are components of cellulose, hemiscellulose, and lignin that show that palm oil pellets have the opportunity to be further processed into useful and economically valuable products. Palm waste contains cellulose by 34.89%, hemiscellulose by 27.14%, and lignin by 19.87%. The analysis conducted on raw materials includes the analysis of water content and cellulose levels of palm oil palm oil. 46.6% and cellulose levels of 29.2%. In this study quantitative analysis was conducted in the form of cellulose conversion and oxalic acid yield. The largest cellulose conversion was obtained at the use of 70% nitric acid concentration and 80 minutes reaction time of 58.56%.


1972 ◽  
Vol 55 (6) ◽  
pp. 1310-1315
Author(s):  
P R Beljaars ◽  
F H M Fabry ◽  
M M A Pickott ◽  
M J Peeters

Abstract Peanut butter extracts and samples spiked with 5-40 μg anatoxin B1/kg were analyzed, together with naturally contaminated peanut products, by 3 extraction procedures: the official Dutch method (KB), he Liem et al. method (methanol), and the IUPAC method. The last procedure was selected as a reference method, since it has international application. KB extracts were separated on silica gel G plates with a mixture of chloroform-acetone (90 + 10), whereas IUPAC extracts were separated similarly on MN-G-HR plates. Methanol extracts were resolved on silica gel II plates, using chloroform-trichloroethylene-n-amyl alcohol-formic acid (80 + 15 + 4 + 1) as the developing solvent. After development, plates were scanned with a reflectance flying-spot densitometer. With such techniques, average recoveries for spiked peanut butter extracts ranged from 99 to 105%, with variation values of 11-12%. Recovery values of 69% (KB method) and 84% (methanol and IUPAC methods) were obtained for spiked peanut butter samples. Coefficients of variation ranged from 13 to 15% for fluorodensitometric measurements. Innaturally contaminated peanuts and peanut products , precision values were 13.6% for fluorodensitometric measurements compared to 36% for visual estimations . Both the methanol and IUPAC methods yield extracts suitable for densitometric analysis after spotting on TLC plates; the analytical results obtained are comparable. Extracts from the KB method contained more interfering fluorescent material than the other 2 methods


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