butanoic acid

(redirected from Butanoate)
Also found in: Dictionary, Thesaurus, Encyclopedia.
Related to Butanoate: Ethyl butanoate

bu·ta·no·ic ac·id

(byū'tă-nō'ik as'id),
Systematic name for normal n-butyric acid.
Farlex Partner Medical Dictionary © Farlex 2012

butanoic acid

The American Heritage® Medical Dictionary Copyright © 2007, 2004 by Houghton Mifflin Company. Published by Houghton Mifflin Company. All rights reserved.

butyric acid

An oily carboxylic acid which smells like rancid butter, has an acrid taste and a sweetish aftertaste, like ether. It is present in rancid butter, parmesan cheese and vomit, and is produced in anaerobic fermentation by bacteria in the colon and axilla (resulting in body odour). It is used as a flavourant, perfume additive and cattle-feed supplement.

Fringe oncology
It is believed to have anticarcinogenic activity, especially the derivative, sodium butyrate.
Segen's Medical Dictionary. © 2012 Farlex, Inc. All rights reserved.
References in periodicals archive ?
Exceptions were methyl geranate, octyl butanoate, and bornylene, in BGM004 genotype, with concentrations about 105%, 110%, and 71% higher, respectively, in DVB/ CAR/PDMS fiber compared to CAR/PDMS.
Indeed, BGM004 presented higher concentration of all major volatile compounds, except for methyl butanoate, whose concentration was statistically similar in both genotypes.
This study showed that the S-HS optimized extraction technique was effective to recovery high concentrations of characteristics major volatile compounds in the passion fruit, such as ethyl butanoate and ethyl hexanoate, which can be advantageous due to the simplicity of the method.[beta]-Pinene, p-cymene, limonene, (Z)-[beta]-ocimene, (E)[beta]-ocimene, [gamma]-terpinene, [alpha]-terpinolene and (E) -4,8-dimethyl-1, 3,7--nonatriene terpenes were identified with the same similarity of recovery in both techniques.
In this case, according to PCA, seven are the compounds that differ in the treatments: 3-methyl-1-butanol, 3methylbutyl propanoate, 3,7-dimethyl-2,6-octadien-1-ol, 3-methylbutyl butanoate, 3-methylbutyl-3-methylbutanoate, 3-phenyl-2-propenal, and dodecanoic acid.
The principal compounds in this analysis are 3-methyl-1-butanol, 3-methylbutyl acetate, 3-methylbutyl butanoate, dodecanoic acid, and phenylmethyl butanoate.
In addition, we found greater transcript levels in liver for all enzymes of butanoate metabolism (such as butyryl Coenzyme A synthetase 1, enoyl Coenzyme A hydratase, hydroxyacyl-Coenzyme A dehydrogenase, and aldehyde dehydrogenase 1) as well as all five alcohol dehydrogenase (ADH) isoforms for metabolizing ethanol and retinol.
Among these esters, ethyl butanoate, ethyl octanoate, and ethyl decanoate were the esters found in greatest concentration.
The investigators found ethyl butanoate, ethyl hexanoate, linalool, 2-heptanone, ionone, 2-heptanol, hexanal, cis-3-hexenol, trans-2-hexenol and furaneol to be the major aroma compounds in Black Diamond.
Chemical composition and retention indices of the constituents of the essential oil of Lavandula hybrida Reverchon "Grosso" (a) Compounds KI (b) % [alpha]-Pinene 941 0.1 Camphene 955 0.1 [beta]-Pinene 974 0.2 [beta]-Myrcene 990 1.3 Hexyl acetate 1010 0.1 1,8-Cineole 1034 5.8 cis-Ocimene 1037 0.2 trans-Ocimene 1049 0.5 Linalool 1099 33.4 Octen-3-ol Acetate 1122 0.3 Camphor 1048 7.6 Hexyl isobutanoate 1153 0.2 4-Terpineol 1176 2.1 [alpha]-Terpineol 1191 1.0 Hexyl butanoate 1194 0.4 Linalyl acetate 1260 36.2 Lavandulyl acetate 1291 3.0 Neryl acetate 1363 0.7 Geranyl acetate 1384 1.4 [beta]-Caryophyllene 1421 0.6 Farnesene 1455 0.6 Caryophyllene Oxide 1585 0.6 [alpha]-Bisabolol 1690 0.2 Total identified 96.6 (a) Compounds listed in order of elution from an SE52 column.
Methyl-2,3-diacetoxy-4-oxo-4-(4`-methylphenyl amino) butanoate (3) The compound methyl-2,3-diacetoxy-4-oxo4-(4`-methylphenyl amino) butanoate (3) was synthesized by using L (+)-2,3-diacetoxy-4-methoxy- 4-oxo-butanoic acid and para-toluidine by the general procedure as described above.
Methyl-2,3-diacetoxy-4-oxo-4-(2`-bromophenyl amino) butanoate (4) Yield: 76%.