Carboxylic acids tests

Table 11. Photophysical and photochemical properties of sulfur-containing carboxylic acids tested as electron donors is 4-carboxybenzophenone-sensitized polymerization.

Keywords spice-aromatic plants, essential oils, antioxidant activity, aldehyde/carboxylic acid test, capillary gas chromatography. 

Indeed, hydrochloric acid failed to catalyze formation of l-deoxy-l-/ -tolylamino-D-finctose from A- -tolyl-D-glucosylamine in methanol at 100 °C, while all carboxylic acids tested gave 8-40% yields of the Amadori rearrangement product, and even better yields were provided by the respective carboxylate potassium salts." ... 

The S. chrysormllus enzyme displays dififerent activities in the presence of a number of different benzene carboxylic acids tested as substrates (Table 2). The value of the equilibrium constant of the adenylate formation reaction, was increased when substituents such as an amino-, hydroxyl-, or methyl-groups in the 4-position were present, compared with benzoic acid alone. The same substituents in the 3-position resulted in a less pronounced response of the enzyme, whereas substituents in the Z-position were... 

Dimethy thiazolidine-4-carboxylic acid test solution (Uo). Add 500 p.1 of concentrated... 

Dimethylthiazolidine-4-carboxylic acid test solution (Ud). Add 500 pi of concentrated hydrochloric acid to 500 mg of D-5,5-dimethylthiazolidine-4-carboxylic acid and make up to 10 ml with isopropanol. 

Figure 157. Ad values for the amides of the /3-chiral carboxylic acids tested with PGME.

Sodium benzoate,—Burns with great difficulty, and after prolonged heating leaves a white infusible residue of NajCOj. Scrape this residue into a test-tube, and test for carbonate in the usual way. Typical of alkali salts of carboxylic acids. 

Take two test-tubes A and B in A place about 5 ml. of neutralised tartaric acid solution and in B place 5 ml. of distilled water. To each solution add 3-4 drops of ferric chloride solution. Place a piece of white paper under the tubes, look down their length and note that A is definitely yellow compared with the control tube B. This yellow colour is given by a-hydroxy-carboxylic-acids, lactic acid, tartaric acid, citric acid. 

Aqueous solutions give with ferric chloride the characteristic reactions of the neutral salt of the acid (p. 348). Identify the carboxylic acids by the tests already given (Section 14, p. 347), or by the preparation of one of the crystalline derivatives below. 

Solubility in sodium carbonate solution. See Section 5 (p. 330), and also Test 2 for carboxylic acids (p. 347). 

Test a small quantity of the aqueous solution or extract of the carboxylic acid with litmus or with Universal indicator paper. 

Methylation with diazomethane may be carried out as follows (FUME CUPBOARD )-. Dissolve 2-3 g. of the compound (say, a phenol or a carboxylic acid) in a little anhydrous ether or absolute methanol, cool in ice, and add the ethereal solution of diazomethane in small portions until gas evolution ceases and the solution acquires a pale yellow colour. Test the coloured solution for the presence of excess of diazomethane by removing a few drops into a test-tube and introducing a glass rod moistened with glacial acetic acid immediate evolution of gas should... 

These equations tell us that the reverse process proton transfer from acids to bicarbon ate to form carbon dioxide will be favorable when of the acid exceeds 4 3 X 10 (pK, < 6 4) Among compounds containing carbon hydrogen and oxygen only car boxylic acids are acidic enough to meet this requirement They dissolve m aqueous sodium bicarbonate with the evolution of carbon dioxide This behavior is the basis of a qualitative test for carboxylic acids... 

One of the most sensitive tests of the dependence of chemical reactivity on the size of the reacting molecules is the comparison of the rates of reaction for compounds which are members of a homologous series with different chain lengths. Studies by Flory and others on the rates of esterification and saponification of esters were the first investigations conducted to clarify the dependence of reactivity on molecular size. The rate constants for these reactions are observed to converge quite rapidly to a constant value which is independent of molecular size, after an initial dependence on molecular size for small molecules. The effect is reminiscent of the discussion on the uniqueness of end groups in connection with Example 1.1. In the esterification of carboxylic acids, for example, the rate constants are different for acetic, propionic, and butyric acids, but constant for carboxyUc acids with 4-18 carbon atoms. This observation on nonpolymeric compounds has been generalized to apply to polymerization reactions as well. The latter are subject to several complications which are not involved in the study of simple model compounds, but when these complications are properly considered, the independence of reactivity on molecular size has been repeatedly verified. 

Reactions between A -(l-chloroalkyl)pyridinium chlorides 33 and amino acids in organic solvents have a low synthetic value because of the low solubility of the amine partner. A special protocol has been designed and tested in order to circumvent this drawback. Soon after the preparation of the salt, an aqueous solution of the amino acid was introduced in the reaction medium and the two-phase system obtained was heated under reflux for several hours. However, this was not too successful because sulfur dioxide, evolved during the preparation of the salt, was converted into sulfite that acted as an 5-nucleophile. As a result, A -(l-sulfonatoalkyl)pyridinium betaines such as 53 were obtained (Section IV,B,3) (97BSB383). To avoid the formation of such betaines, the salts 33 were isolated and reacted with an aqueous solution of L-cysteine (80) to afford thiazolidine-4-carboxylic acids hydrochlorides 81 (60-80% yields). 

Chloro-oxazolo[4,5-/i]quinoline-2-carboxylic acid methyl ester was the most active compound in tests for inhibitors of antigen-induced release of histamine in vitro from rat peritoneal mast cells (IC50 of 0.3 p,M) and as inhibitors of IgE-mediated passive cutaneous anaphylaxis in the rat (ED50 (intraperitoneal) of 0.1 mg/kg in dose 0.5 mg/kg as an inhibitor of the test)—10 times and 60 times more potent, respectively, than the disodium salt of cromoglycic acid (85JMC1255). 

Hydrazides of vicinal acetylene-substituted derivatives of benzoic and azole carboxylic acids are important intermediate compounds because they can be used for cyclization via both a- and /3-carbon atoms of a multiple bond involving both amine and amide nitrogen atoms (Scheme 131). Besides, the hydrazides of aromatic and heteroaromatic acids are convenient substrates for testing the proposed easy formation of a five-membered ring condensed with a benzene nucleus and the six-membered one condensed with five-membered azoles. 

An aqueous solution containing 0.10 mole/liter of chloroacetic acid, ClH2CCOOH, is tested with indicators and the concentration of H (aq) is found to be 1.2 X 10 2 M. Calculate the value of Ka (if necessary, refer back to Section 11-3.2). Compare this value with KA for acetic acid—the change is caused by the substitution of a halogen atom near a carboxylic acid group. 

Peroxides, test for, 41, 92 Peroxy acids from carboxylic acids and 70% hydrogen peroxide, 43, 96 Peroxybenzoic acid, 43,93 iodometric analysis of, 43, 94 Peroxystearic acid, 43,96 Phenacylamine hydrochloride, 41, 82... 

In 1973 it was published that in contrast to lauryl ether sulfate the lauryl ether carboxylic acid sodium salt with 3 mol EO did not disturb the skin s water loss and did not decrease the skin s resistance [74], Formulation tests for the use as emulsifier in creams were described in 1976 [75]. 

FIG. 7 Skin irritation according to the human patch test of alkyl ether carboxylic acids compared to other mild cosurfactants. CFTA-names 1, cocamidopropylbetaine 2, sodium PEG-6 cocamide carboxylate 3, sodium laureth-11 carboxylate 4, cocoamphocarboxypropionate 5, protein hydrolyzate 6, disodium laureth-3 sulfo-succinate SLES, sodium laureth sulfate. (From Ref. 68.)... 

J 3 Identify alcohols and carboxylic acids from their formulas (Self-Test D.5). 

Sf.i f-Test 10.8B List the following carboxylic acids in order of increasing strength CHCl2COOH, CH.COOH, and CH2C)COOH. 

Biological activity tests on organotin(lV) complexes with a potent antihypertensive agent, captopril[(2S)-l-[(2S)-2-methyl-3-sulfanyl propanoyl]pyrroli-dine-2-carboxylic acid cap], were carried toward the embryos of C. intestinalis. The main results obtained were as follows ... 

A preliminary test for the biodegradability of the 3-phenyl- and 3-carbamoyl-2(lH)pyridones was conducted in a barnyard humus suspension. The analysis by HPLC showed some loss, and the fluorescent compounds seemed to be adsorbed onto the solid. The 3-carbamoyl-2(lH)pyridone (II) also hydrolyzed to 3-carboxylic acid-2(lH)pyridone both in the slurry test and in water solutions that had been left standing 1-2 weeks. In preliminary tests both the 3-phenyl- and the 3-carbamoyl-2(lH)pyridones apparently adsorbed to some extent on silica sand columns. In addition, the solubility of both 1-H compounds was somewhat low, 1.3 x 10 M for II, and 1.0 x 10 M for IV. 

Phosphinous amides, based on proline and tetrahydroisoquinoline carboxylic acid, bearing a second donor center (50, Ar=Ph R =H, CH3,Tr, Ph R =H, CH3,Tr, Ph and 51, R =H,Tr R =H,Tr) (Scheme 40) have been developed for use in allylic alkylation and amination of substituted propenyl acetates, yielding the corresponding products in 87-98% (5-94% ee) and 29-97% (14-93% ee) respectively [55, 167]. With bidentate ligands of type 38 where R=(S)-PhMeCH, and with the bis(aminophosphanes) 52 (R=Ph) similar allylic alkylations have been also tested [168,169]. 

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