scholarly journals Study on the Factors Influencing the Extraction of Chenodeoxycholic Acid from Duck Bile Paste by Calcium Salt Method

2018 ◽  
Vol 2018 ◽  
pp. 1-6 ◽  
Author(s):  
Xiangzheng Hu ◽  
Na Feng ◽  
Jiaqi Zhang

New extraction technology of chenodeoxycholic acid from duck bile paste by calcium salt was investigated. The optimum conditions of extraction were determined by orthogonal experimental design. The results indicated that influencing factors on the extraction efficiency of chenodeoxycholic acid were as follows: hydrogen peroxide, methyl alcohol, glacial acetic acid, and calcium chloride. The optimum extracting conditions of chenodeoxycholic acid were 1000 mL amount of methyl alcohol, 50 mL amount of hydrogen peroxide, 500 mL amount of 20% calcium chloride, and 600 mL amount of 60% glacial acetic acid for a quantity of duck paste. The yield of chenodeoxycholic acid was 30%.

1962 ◽  
Vol 8 (3) ◽  
pp. 296-301 ◽  
Author(s):  
Robert E Bowman ◽  
Richard C Wolf

Abstract An examination of the absorbance spectrum of the Zak cholesterol reaction, made with two brands of commercially available reagent-grade glacial acetic acid, showed not only the expected peak at 560 mµ, but an additional, higher peak at about 490 mµ. A specially purified glacial acetic acid did not show this 490 mµ peak. Conversely, increasing the ratio of color reagent to glacial acetic acid from 0.8 to 1.2 (v/v) greatly increased the height of the absorbance peak at 480 mµ and eliminated the 560 mµ peak. Under optimum conditions of time and color-reagent concentrations, the 480 mµ peak affords approximately double the sensitivity for cholesterol as compared to the 560 mµ peak. Finally, it was observed that the reported interference of bromide and iodide ions in the Zak reaction results almost entirely from an enhancement effect on the color by the cholesterol itself, and that the addition of about 100 µg. NaBr per milliliter of glacial acetic acid prior to reaction produced the full enhancement of 50 per cent greater color, and virtually eliminated interference at 560 mµ from additional amounts of bromide or iodide salts.


2003 ◽  
Vol 81 (2) ◽  
pp. 156-160 ◽  
Author(s):  
Tian Zhu ◽  
Hou-min Chang ◽  
John F Kadla

A new method for the preparation of peroxymonophosphoric acid (H3PO5) has been developed. It utilizes a biphasic solution to moderate the vigorous reaction between phosphorous pentoxide (P2O5) and hydrogen peroxide (H2O2). P2O5 is suspended in carbon tetrachloride (CCl4), and concentrated H2O2 is slowly added while being vigorously stirred at low temperature. Careful control of the reaction temperature through the slow addition of H2O2 is critical. Using typical preparation conditions (P2O5:H2O2 = 0.5:1, H2O2 70 wt %, 2°C, 120–180 min), ~70% of the H2O2 is effectively converted to H3PO5. Increasing the concentration of H2O2, as well as the mole ratio of P2O5:H2O2, leads to an even higher % conversion of H2O2 to H3PO5. The addition of glacial acetic acid to the P2O5:H2O2 suspension at the end of the 120–180 min reaction (P2O5:H2O2:CH3COOH = 0.5:1:0.3) leads to the formation of peracetic acid in addition to H3PO5, and to an overall increase in the conversion ratio of total peroxy acids based on H2O2 (>95%).Key words: peroxymonophosphoric acid, synthesis, stability, conversion ratio.


2013 ◽  
Vol 2 (3) ◽  
pp. 33-39 ◽  
Author(s):  
M Roganda L Lumban Gaol ◽  
Roganda Sitorus ◽  
Yanthi S ◽  
Indra Surya ◽  
Renita Manurung

Utilization of empty fruit bunches of oil palm in Indonesia is still very low, so it should be developed further. One of them by researching the manufacture of cellulose acetate from oil palm empty fruit bunches. The process used in this study is the cellanase with α-cellulose materials. Stages reaction is activation, acetylation, hydrolysis, neutralization and drying. Activation in thethree-neck flask with the addition of 50 ml of glacial acetic acid and stirredfor 3 hour,then added 15 ml of acetic acid anhydride as acetylation agent. Acetylation performed with the variation of time, 2, 2.5, 3, 3.5 hours.  In the hydrolysis step, add 2 ml of water and5 ml of glacial acetic acid. The reaction lasted for 30 minutes, then added 1 g of sodium acetate for neutralization, neutralization lasts for 5 minutes.  Then do the washing up to the smell of acetic acid is lost, and the last stage is the drying is done with a temperature below 50 oC.  The resulting products are then analyzed the degree of substitution, melting point, and then carried out FTIR analysis.  The results obtained when the optimum conditions for the acetylation reaction is 2.5 - 3 hours.


ACS Omega ◽  
2020 ◽  
Vol 5 (12) ◽  
pp. 6389-6394
Author(s):  
Yingjie Zhang ◽  
Guanqun Gong ◽  
Honglei Zheng ◽  
Xin Yuan ◽  
Liangwei Xu

1959 ◽  
Vol 37 (2) ◽  
pp. 366-369 ◽  
Author(s):  
Paul E. Gagnon ◽  
Brian T. Newbold

A series of dihalogenated and five tetrachloroazobenzenes were oxidized to the corresponding azoxy compounds by means of 30% hydrogen peroxide in glacial acetic acid, the reaction being carried out at about 60–70 °C, for 24 hoursAs expected, the yields, in general, obtained from azobenzenes containing substituents in the 2,2′-positions were lower than those from compounds having substituents in the 3,3′- and 4,4′-positions, which gave very good results.


2008 ◽  
Vol 5 (s1) ◽  
pp. 1063-1068 ◽  
Author(s):  
Yogesh Dixit ◽  
Rahul Dixit ◽  
Naveen Gautam ◽  
D. C. Gautam

The present communication deals with the synthesis of a series of fluorinated 10H-phenothiazines. 10H-phenothiazines is prepared by Smiles rearrangement of substituted 2-foramido-2´-nitrodiphenylsulfide. Substituted 2-foramido-2´-nitrodiphenylsulfide were obtained by the reaction of 2-amino-3-fluorobenzenethiol witho-halonitrobenzenes followed by formylation and 1-nitro/1-halo-10H-phenothiazines have been prepared by the reaction of substituted 2-aminobenzenethiols with reactiveo-halonitrobenzene containing a nitro group or halogen atom ato-position to the reactive halogen atom directly yielded 1-nitro/1-halo-10H-phenothiazines in situ. 10H-phenothiazine sulfone derivatives have been synthesized by the oxidation of 10H-phenothiazines by 30% hydrogen peroxide in glacial acetic acid. The structure of the synthesized compounds has been characterized by spectroscopic data and elemental analysis. Antimicrobial studies of the synthesized compounds have also been included.


Author(s):  
Ferra Naidir ◽  
Robiah Yunus ◽  
Irmawati Ramli ◽  
Tinia I. Mohd. Ghazi

To improve the oxidative stability of the palm oil-based biolubricant, the fatty acid double bonds in palm oil-based trimethylolpropane ester (TMP ester) was converted into an oxirane ring via an in-situ epoxidation method. The epoxidized TMP ester was produced from a reaction between TMP ester and peracetic acid which was prepared in-situ by reacting glacial acetic acid with hydrogen peroxide in the presence of concentrated sulphuric acid. The response surface methodology was applied using a central composite design technique to optimize the conditions of the epoxidation reaction to produce the epoxidized TMP ester. The effects of four independent variables namely concentration of acetic acid (0-2 mol), concentration of hydrogen peroxide (1.5-9.5 mol), temperature of reaction (30-110°C) and reaction time (0.5-26.5 h) on the three dependent variables; percentage of oxirane oxygen, iodine value, and hydroxyl value were studied. A second-order polynomial multiple regression model was employed to predict the three dependent variables under optimum conditions of 0.59 mol of glacial acetic acid, 7.5 mol of hydrogen peroxide concentration, at temperature of 50°C and reaction times of 7 h. The optimum values of percentage of oxirane oxygen, iodine value, and hydroxyl value were 4.01%, 1.94%, and 0.43% respectively. The analysis of variance yielded a high coefficient of determination value of 0.9395-0.9880, hence indicating the fitness of the second-order regression model to the experimental data.


2017 ◽  
Vol Volume-1 (Issue-6) ◽  
pp. 1271-1275
Author(s):  
Bach Trong Phuc ◽  
Vu Van Hai ◽  
Nguyen Thi Hien | Nguyen Thanh Liem ◽  

1934 ◽  
Vol 7 (3) ◽  
pp. 454-461
Author(s):  
G. F. Bloomfield ◽  
E. H. Farmer

Abstract Mair and Todd (J. Chem. Soc., 1932,, 386), in extending the earlier work of Robertson and Mair (J. Soc. Chem. Ind., 46, 41T (1927)), studied the interaction of a chloroform solution of purified rubber with concentrated hydrogen peroxide (100 vols.) dissolved in glacial acetic acid; by this means they obtained a non-acidic substance of the empirical formula C50H92O16, which was unsaturated toward bromine and permanganate, and was considered to have all its oxygen present in the form of hydroxyl groups. Other workers have reported that when peracetic acid dissolved in glacial acetic acid is used in place of the hydrogen peroxide—acetic acid mixture, the products of reaction are acetylated derivatives of rubber (British Patent 369,716). These acetylated derivatives are stated to be obtainable either from solid rubber or from solutions of rubber, but no evidence as to their constitution has been advanced. Now the oxidative degradation of rubber is of considerable interest from two points of view: first, with regard to the light which it may throw on the size, structure, homogeneity, and normality of chemical behavior of the molecules of rubber; and, second, with regard to its efficacy as a means of transforming rubber into derivatives of similar or smaller molecular weight, capable of useful application in industry. The very careful work of Mair and Todd has gone far to show that hydrogen peroxide under the conditions of their experiments attacks the unsaturated centers of the rubber molecule and effects more or less complete hydroxylation of the carbon chain; at the same time it brings about a considerable degree of degradation of the molecule. The product of Mair and Todd, however, is produced under rather restricted conditions of reaction and the reagents employed are costly; consequently the extent to which the character of the product can be modified (i. e., by controlling the degree of degradation, hydroxylation, and acetylation) is left undetermined, and the possibility of producing useful materials at a reasonably low cost by modifying the conditions of reaction and the form of reactants is left unexplored. On the other hand, the employment of peracetic acid as an oxidizing agent, though offering a theoretically elegant way of effecting hydroxylation or acetoxylation at the unsaturated centers of the rubber molecule, is not without drawbacks: the preparation of the reagent is expensive and on a large scale dangerous; moreover, in spite of the fact that it is claimed to be employable either with solutions of rubber or with solid rubber, its reaction with rubber is so vigorous that the prospect of exercising any effective control over the extent of degradation or degree of hydroxylation (acetoxylation) is greatly diminished.


1927 ◽  
Vol 23 (4) ◽  
pp. 465-465
Author(s):  
К. Usami

The author suggests the following method: take 5.0 of the test feces by eye, thoroughly grind it in a porcelain mortar with excess acetone and filter it, and the feces remaining on the filter is washed with acetone until almost discolored liquid flows out; after the acetone is squeezed with a pestle as much as possible, the feces is removed from the filter into another porcelain mortar, grinded with 20 cc. c. of a mixture of alcohol and glacial acetic acid (1 c. c. of acid to 1 c. c. of absol. alcohol), is filtered again, and 1 c. c. of the filtrate is poured into a mixture consisting of 1 c. of Leukomethyl-violett'a or Leukofuchsin with 2 drops of 3% hydrogen peroxide.


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