aldehyde

(redirected from aldehydic)
Also found in: Dictionary, Medical, Encyclopedia.
Related to aldehydic: Chypre, civet
Graphic Thesaurus  🔍
Display ON
Animation ON
Legend
Synonym
Antonym
Related
</>embed</>
aldehydealdehyde
  • noun

Words related to aldehyde

Based on WordNet 3.0, Farlex clipart collection. © 2003-2012 Princeton University, Farlex Inc.
References in periodicals archive ?
Aldehydic proton exhibited HMBC correlation (Figure 3) with three aromatic carbons at I' 116.7 (C-1), 157.8 (C-2) and 129.9 (C-6).
indicated a lethal effect of those aldehydic compounds which were much
Determination of aldehydic lipid peroxidation products malonaldehyde and 4-hydroxynonenal.
Sweet Honesty Eau de Cologne is a classic, light and playful floral Aldehydic scent that is as sweet and tender.
It also leads to formation of complex mixtures of lipid hydroperoxide aldehydic end products such as MDA.
Chitinase was assayed using 3,5-dinitrosalicylic acid reagent to determine the free aldehydic groups of hexoaminase liberated on chitin digestion according to the method described by [18]
Prof Grootveld's team measured levels of "aldehydic lipid oxidation products" (LOPs), produced when oils were heated to varying temperatures.
[sup][5],[6] As a consequence of LP-mediated membrane injury, aldehydic breakdown products like 4-hydroxynonenal (4-HNE) are generated during the first hour following TBI.
(14), (15), (16), (17), (18), (19), (20) High oxygen transmission rates, as exhibited by synthetic closures, result in wines with a high level of browning and high-oxidized characters (honey, bruised apple, cooked fruits and aldehydic port-sherry like aromas).
Lolita launched this past spring, and its a musky aldehydic floral named after the Vladimir Nabo-kov novel.
This involves the oxidation of the aldehydic and/or ketonic groups present in the sugar to the carboxylic group and 3,5-dinitrosalicylic acid is reduced to 3,5-diaminosalicylic acid under alkaline conditions.
The formation of [CMS.sup.*] radical (3) initiates a photooxidation reaction which leads to the generation of new aldehydic end groups in the CMS chain.