Estimation of Pyridine Content of Pyridine-Acetic Acid Mixture Used in Riboflavin Determination

1944 ◽  
Vol 16 (9) ◽  
pp. 583-584
Author(s):  
J H. Lanning ◽  
C A. Roszmann
Keyword(s):  
Acetic Acid ◽  
Acid Mixture

Acetylation and Formylation of 3-Ferrocenylpyrroles

1999 ◽  
Vol 64 (1) ◽  
pp. 99-106
Author(s):  
Battsengel Gotov ◽  
Štefan Toma ◽  
Eva Solčániová
Keyword(s):  
Acetic Acid ◽  
Acetic Anhydride ◽  
Aluminum Chloride ◽  
Acetyl Chloride ◽  
Trifluoroacetic Anhydride ◽  
Acid Mixture ◽  
Chloride Method

Acetylations of 3-ferrocenyl-1-methylpyrrole as well as 3-cyano-4-ferrocenylpyrrole and 3-cyano-4-ferrocenyl-1-methylpyrrole were performed. The course of the acylation is highly dependent on the acylation agent, that is acetyl chloride/aluminum chloride (method A), trifluoroacetic anhydride-acetic acid mixture (method B) or acetic anhydride/Sc(OTf)3 (method C). Method A gives the acetylation on ferrocene moiety, method B affords the trifluoroacetylation on pyrrole moiety and method C affords pyrrole moiety acetylation. Vielsmeier-Haack formylation gives the products of substitution on pyrrole moiety.

Pyrimidine Derivatives and Related Compounds, V Synthesis of Some Isoxazolo [2,3-a] pyrimidines. A New Ring System

1977 ◽  
Vol 32 (3) ◽  
pp. 311-314 ◽  
Author(s):  
Mohamed Hilmy Elnagdi ◽  
Ezzat Mohamed Kandeel ◽  
Kamal Usef Sadek
Keyword(s):  
Acetic Acid ◽  
Hydrochloric Acid ◽  
Ethyl Acetoacetate ◽  
Pyrimidine Derivative ◽  
Ring System ◽  
The Other ◽  
Acid Mixture ◽  
Pyrimidine Derivatives ◽  
Benzoyl Isothiocyanates ◽  
Related Compounds

3-Amino-5-phenyl-4-phenylazoisoxazole (1) reacts with ethyl acetoacetate to yield the corresponding ethyl isoxazolylaminocrotonate derivative (2) which could be thermally cyclized into the isoxazolopyrimidine derivative (4). On the other hand, condensation of 1 with ethoxymethylenemalononitrile has resulted in the formation of the aminoethylene derivative (5).Compound 1 reacted with acrylonitrile to yield the isoxazolo[2,3-a]pyrimidine derivative (6). The latter was converted into the corresponding exo derivative (8) by the action of acetic acid-hydrochloric acid mixture.Compound 1 also reacted with methoxycarbonyl-, ethoxycarbomyl- and benzoyl isothiocyanates to yield the isoxazolylthioureas (10a, b) and (11), respectively. The reaction of 2 with acetic acid-hydrochloric acid and with phenylhydrazine is reported.

scholarly journals Chemicals with a natural reference for controlling water hyacinth, Eichhornia crassipes (Mart.) Solms

2015 ◽  
Vol 55 (3) ◽  
pp. 294-300 ◽  
Author(s):  
Tarek Abd El-Ghafar El-Shahawy
Keyword(s):  
Acetic Acid ◽  
Citric Acid ◽  
Formic Acid ◽  
Propionic Acid ◽  
Water Hyacinth ◽  
Eichhornia Crassipes ◽  
Effective Control ◽  
Acid Mixture ◽  
Aquatic Weeds ◽  
Herbicide Glyphosate

AbstractLife cannot exist without water. Appropriate management of water, from the water’s source to its utilization, is necessary to sustain life. Aquatic weeds pose a serious threat to aquatic environments and related eco-environments. Short- and long-term planning to control aquatic weeds is extremely important. Water hyacinth,Eichhornia crassipes(Mart.) Solms, is one of the world’s worst pests with a bad reputation as an invasive weed. In this study we are seeking the possibility of using certain chemicals with a natural background, for controlling water hyacinth since there is a delicate balance that needs to be taken into account when using herbicides in water. Five compounds, namely: acetic acid, citric acid, formic acid, and propionic acid, in three concentrations (10, 15, and 20%) were applied (i.e. as a foliar application under wire-house conditions) and compared with the use of the herbicide glyphosate (1.8 kg ∙ ha−1). All of the five compounds performed well in the control of the water hyacinth. As expected, the efficacy increased as the concentration was increased from 10 to 20%. With formic and propionic acids, the plants died earlier than when the other acids or the herbicide glyphosate, were used. Acetic acid came after formic and propionic acids in terms of efficacy. Citric acid ranked last. Formic acid/propionic acid mixtures showed superior activity in suppressing water hyacinth growth especially at the rate of (8 : 2) at the different examined concentrations (3 or 5 or 10%) compared to the formic acid/acetic acid mixtures. Using the formic acid/propionic acid mixture (8 : 2; at 3%) in the open field, provided good control and confirmed the viability of these chemicals in the effective control of water hyacinth. Eventually, these chemical treatments could be used on water for controlling water hyacinth. In the future, these chemicals could probably replace the traditional herbicides widely used in this regard. These chemicals are perceived as environmentally benign for their rapid degradation to carbon dioxide and water. For maximum efficiency thorough coverage especially in bright sunlight is essential.

Urea supplementation of two forms of barley for intensively fed Friesian bulls

1984 ◽  
Vol 1984 ◽  
pp. 118-118
Author(s):  
I.E. Edwards ◽  
J.H. Topps ◽  
G.F.M Paterson
Keyword(s):  
Acetic Acid ◽  
Acid Mixture ◽  
Rumen Degradation

Previous work has shown that treating moist grain with ‘Farmline’, a formalin acetic acid mixture, affords some protection of protein and perhaps starch from rumen degradation. A comparison with and without ‘Farmline’ treatment investigated the protection afforded to dried barley.

Determination of the Iodine Value of Oils and Fats: Summary of Collaborative Study

1994 ◽  
Vol 77 (3) ◽  
pp. 674-676 ◽  
Author(s):  
David Firestone
Keyword(s):  
Acetic Acid ◽  
Iodine Value ◽  
Collaborative Study ◽  
Solvent Mixture ◽  
Acid Mixture ◽  
Collaborative Studies ◽  
Wide Range ◽  
Aoac Method ◽  
Iodine Values

Abstract Two collaborative studies were conducted using the Wijs method for determining the iodine value in a wide range of vegetable and animal oils and fats. The results obtained when using carbon tetrachlo-ride were compared to those obtained when using a substitute solvent mixture of cyclohexane and glacial acetic acid. The values reported for the iodine values indicate that the cyclohexane and acetic acid mixture can be used in place of carbon tetrachloride without loss of precision. The method has been adopted first action by AOAC INTERNATIONAL as an IUPAC/AOCS/AOAC method.

APPLICATION OF THE COATED CHARCOAL SEPARATION METHOD TO THE RADIOIMMUNOASSAY OF PLASMA CORTICOTROPHIN

1968 ◽  
Vol 41 (4) ◽  
pp. 499-508 ◽  
Author(s):  
R. A. DONALD
Keyword(s):  
Acetic Acid ◽  
Sensitivity And Specificity ◽  
Silicic Acid ◽  
Activated Charcoal ◽  
Acid Mixture ◽  
Factors Affecting ◽  
Reaction Proceeds ◽  
Subsequent Elution ◽  
Antigen Antibody ◽  
Radioimmunoassay Method

SUMMARY A radioimmunoassay method for plasma corticotrophin (ACTH) is described. ACTH is extracted from plasma by adsorption to silicic acid powder and subsequent elution by an acetone—acetic acid mixture. ACTH antiserum and 131I-labelled ACTH are added and the antigen-antibody reaction proceeds for 3 days. Activated charcoal coated with plasma is used to separate antibody-bound and unbound ACTH. Factors affecting the accuracy, sensitivity, and specificity of the assay have been assessed.

Can Nitroalkanes be Obtained Directly from Alcohols and Sodium Nitrite in Acetic Acid - Hydrochloric Acid Mixture?

Synlett ◽  
2001 ◽  
Vol 2001 (07) ◽  
pp. 1121-1122 ◽  
Author(s):  
Mieczysław Mąkosza ◽  
Michał Barbasiewicz ◽  
Krzysztof Wojciechowski
Keyword(s):  
Acetic Acid ◽  
Hydrochloric Acid ◽  
Sodium Nitrite ◽  
Acid Mixture
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