The phrase "acetic ester" is correct and usable in written English.
It can be used in contexts related to chemistry, specifically when discussing organic compounds or reactions involving esters derived from acetic acid.
Example: "In the laboratory, we synthesized acetic ester to study its properties and reactions with other chemicals."
Alternatives: "ethyl acetate" or "acetate ester".
Traditionally, acetic esters were used as entrainers to separate acetic acid and water by heterogeneous azeotropic distillation (HAD).
In the study, the feasibility of using p-xylene as the entrainer is evaluated to eliminate the drawbacks of the HAD column using acetic esters as entrainers.
Bulk-imprinted artificial recognition materials for DMMP yielded detection limits of 0.2 ppm in air on quartz crystal microbalance (QCM) sensor with selectivity factors of >40 towards indoor background contaminants, such as alcohols or acetic esters.
The Acetyl Intermediates segment produces and supplies acetyl products, including acetic acid, VAM, acetic anhydride and acetate esters.
The majority of these compounds were composed of 4 and 5 carbon alcohols, acetic acid or acetate esters and compounds producing m/z 59 (acetone and/or propanal).
Lactones showed high correlation with linear esters in C7 (50 53), ethyl acetate, and acetic acid butyl ester, the only ester in C1.
The mixture was re-extracted with 800 μl acetic acid ester: cyclohexane (1 1 v/v).
Cross-linked esterified xylan and pectin in undigested residue were evident at peak 1714 cm−1 (C=O from xylan), 1738 cm−1 to 1747 cm−1 (unconjugated C=O stretch in xylan from acetic acid ester and pectin) [ 16, 17].
Flavone acetic acid ester (XXVI) (NSC 293015, LM985) emerged as a lead compound from a series of flavonoids from Lyonnaise Industrielle Pharmaceutique (Lipha) that were screened by the National Cancer Institute (NCI), and as a result of solid tumour activity in preclinical models LM985 was selected by the Phase I/II Committee.
They are typically produced by catalyzed reaction from acetic acid and the corresponding alcohol: H3C-COOH + HO-R → H3C-CO-O-R + H2O, (R = a general alkyl group) Most acetate esters, however, are produced from acetaldehyde using the Tishchenko reaction.
