Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

4- butyric acid characterization

The homogeneously catalyzed oxidation of butyraldehyde to butyric acid is a well-characterized gas/Hquid reaction for which kinetic data are available. It thus serves as a model reaction to evaluate mass transfer and reactor performance in general for new gas/liquid micro reactors to be tested. This reaction was particularly used to validate a reactor model for a micro reactor [9, 10]. [Pg.646]

Representatives of the subfamilies Omaliinae and Proteininae (omaliine group) possess an abdominal defensive gland reservoir that opens out between sternite 7 and 8 [ 120]. The multi-component mixtures contained in these glands are used for defence. In Omaliinae and Proteininae the secretion is characterized by mixtures of acids (e.g. 2-methylpropanoic acid, hexanoic acid, 2-octenoic acid, 2-methylbutanoic acid, 3-methylbutanoic acid, butyric acid, and tiglic acid), aldehydes (( )-2-hexenal, heptanal, octanal, nonanal), ketoaldehydes such as 4-oxo-2-hexenal 41 (Scheme 5), 6-methyl-5-hepten-2-one, alcohols (octanol, ( )-2-hexen-l-ol, 2-methylbutan-l-ol), alkanes (nonadecane), esters (2-methylbutyl tiglate 42, various propanoates, 2-hexenyl 3-methylbutanoate, 2-methylbutyl 2-methylbutanoate, octanoates,butanoates), and aromatic compounds (e.g. 2-phenethyl 3-methylbutanoate 43). Unusual compounds are 2-... [Pg.116]

Preschool children are reputed to differ from adults in their odor preferences. For instance children aged 3-4 years were as likely to like the odor of amyl acetate (banana) as synthetic sweat or feces odors. By 6 years of age, their preferences resembled adults, liking banana, and disliking sweaty and fecal odors (Stein et al., 1958). At 4-5 years of age, a shift occurs from positive or neutral to negative characterization of odors of sweat, feces, asa foetida, or butyric acid. However, it is increasingly becoming clear that responses by very young children... [Pg.239]

To further explore the environment inside such hexameric hosts, Atwood and coworkers performed structural characterization and spectrofluorometric studies of the capsule-bound fluorescent probe molecule pyrene butyric acid (PBA) 52 [71]. Single-crystal X-ray diffraction studies on 52 (50b)6 show not only that encapsulated guests interact with the host walls in the solid state, but also that the n surfaces of the guest molecules are well separated from one another within the capsule. The spectroscopic studies in solution corroborated this finding and revealed an average of 1.5 molecules of 52 per capsule. The assembly remains intact over four weeks in the solution phase, suggesting that the carboxylic acid groups and the polyaromatic nature of 52 do not destabilize the overall supramolecular assembly. [Pg.104]

The 2-D TLC was successfully applied to the separation of amino acids as early as the beginning of thin-layer chromatography. Separation efficiency is, by far, best with chloroform-methanol-17% ammonium hydroxide (40 40 20, v/v), n-butanol-glacial acetic acid-water (80 20 20, v/v) in combination with phenol-water (75 25, g/g). A novel 2-D TLC method has been elaborated and found suitable for the chromatographic identification of 52 amino acids. This method is based on three 2-D TLC developments on cellulose (CMN 300 50 p) using the same solvent system 1 for the first dimension and three different systems (11-IV) of suitable properties for the second dimension. System 1 n-butanol-acetone -diethylamine-water (10 10 2 5, v/v) system 11 2-propanol-formic acid-water (40 2 10, v/v) system 111 iec-butanol-methyl ethyl ketone-dicyclohexylamine-water (10 10 2 5, v/v) and system IV phenol-water (75 25, g/g) (h- 7.5 mg Na-cyanide) with 3% ammonia. With this technique, all amino acids can be differentiated and characterized by their fixed positions and also by some color reactions. Moreover, the relative merits of cellulose and silica gel are discussed in relation to separation efficiency, reproducibility, and detection sensitivity. Two-dimensional TLC separation of a performic acid oxidized mixture of 20 protein amino acids plus p-alanine and y-amino-n-butyric acid was performed in the first direction with chloroform-methanol-ammonia (17%) (40 40 20, v/v) and in the second direction with phenol-water (75 25, g/g). Detection was performed via ninhydrin reagent spray. [Pg.1667]

The normal pattern of the urine is characterized by the presence of five amino acids which give prominent spots. These are glycine, serine, alanine, glutamine, and histidine. Moderate amounts to traces of lysine, threonine, glutamic acid, taurine, methylhistidine, and j8-aminoiso-butyric acid occur in some normal samples (Fig. 4). Soupart (S42) and Peters et al. (P17) have published data on the urinary excretion of the free amino acids by normal human subjects which provide a useful compilation of the current knowledge in this field (Table 4). [Pg.179]

The circulins—As early as 1949, Peterson and Reineke characterized circulin as its sulphate. Total hydrolysis yielded D-leucine, L-threonine and L-K,y-diaminobutyric acid together with an optically active isomer of pelargonic acid. The existence of two components, found by Peterson and Reineke was later confirmed by the chromatographic separation of crude circulin into two major components, named circulin A and circulin B. In addition there was evidence for at least three other ninhydrin-positive, biologically active entities. In the hydrolysate of circulin A, L-isoleucine was found besides the amino acids previously reported . Quantitative amino acid analysis showed circulin A and B to be composed of L-a,y-diamino-butyric acid, L-threonine, D-leucine, L-isoleucine and ( + )-6-methyloctanoic acid in the molar ratio 6 2 1 1 1. After partial acid hydrolysis, fractionation and structure determination of the resulting peptides, circulin A and circulin B were formulated as cyclodecapeptides . Very recently, however, Japanese workers have revised the structure of circulin A. According to them, circulin A differs from colistin A only by a replacement of L-leucine in the latter by L-isoleucine Figure 1.7). [Pg.28]

Milk fat is characterized by the presence of relatively high concentrations (about 10 wt.%) of short-chain FA (C4 0 to C10 0). Butyric acid (C4 0) is specific for milk fat of ruminants. Higher saturated FA (>C10 0) occur in amounts of approximately 57%, and palmitic, stearic, and myristic acids dominate. The 15 0 and 17 0 acids, characteristic of ruminant fat, also occur in milk fat as branched FA. [Pg.272]

When the aldehyde in the acetalization reaction is butyraldehyde, i.e., R=CH3CH2CH2-, the product is poly(vinyl butyral). Sulfuric acid is the catalyst in this reaction. Poly(vinyl butyral) is characterized by high adhesion to glass, toughness, light stability, clarity, and moisture insensitivity. It is therefore extensively used as an adhesive interlayer between glass plates in the manufacture of laminate safety glass and bullet-proof composition. [Pg.433]

S. Kim, C.M. Son, Y.S. Jeon, J.H. Kim, Characterizations of novel poly (aspartic acid). Derivahves conjugated with y-amino butyric acid (GABA) as the bioachve molecule. Bull. Korean Chem. Soc. 30 (2009) 3025-3030. [Pg.66]

Cellulose acetate (CA), cellulose acetobutyrate (CAB) cellulose propionate (CP), Thermoplastics manufactured from cellulose by esterification with acetic acid (CA), acetic acid and butyric acid (CAB), or propionic acid (CP). Their products are characterized by high impact strength, transparency (without filler), and oil resistance. Examples of applications consumer goods, toys, combs, keys for music instruments and business machines, spectacle frames, photographic films. CA fibres are used for underwear, neckties, etc. Trade names Cellidor (FRG), Setilithe (B), Tenite (USA). [Pg.14]


See other pages where 4- butyric acid characterization is mentioned: [Pg.273]    [Pg.85]    [Pg.104]    [Pg.217]    [Pg.352]    [Pg.145]    [Pg.196]    [Pg.235]    [Pg.665]    [Pg.42]    [Pg.27]    [Pg.269]    [Pg.271]    [Pg.73]    [Pg.1250]    [Pg.61]    [Pg.459]    [Pg.371]    [Pg.89]    [Pg.65]    [Pg.195]    [Pg.255]    [Pg.666]    [Pg.50]    [Pg.532]    [Pg.135]    [Pg.159]    [Pg.56]    [Pg.128]    [Pg.971]    [Pg.180]    [Pg.560]    [Pg.187]    [Pg.161]   
See also in sourсe #XX -- [ Pg.115 , Pg.117 ]




SEARCH



ACIDIC CHARACTERIZATION

Butyrate/butyric acid

Butyric acid

© 2024 chempedia.info