• Bulletin of the Korean Chemical Society
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• 제16권1호
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• pp.12-16
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• 1995

The diastereoselectivity of addition reaction of crotylmetal reagents to cobalt-complexed acetylenic aldehydes and metal-free aldehydes was examined. The anti-diastereomer was the predominant product when the crotyl metallics were Cr, Sn, and Zr. In THF, the uncomplexed aldehydes normally gave higher anti-diastereoselectivity. However, the cobalt-complex of silicon-substituted propynals with three bulky substituents produced increased proportions of syn-diastereomer. In DMF, the selectivity shifted towards syn-isomer except in the case of dimethylphenylsilyl substituent. When tributylstannane was used in the presence of BF3 etherate, moderate syn- selectivity was observed with uncomplexed aldehydes, but only decomposed products from complexed aldehydes.

• 한국환경보건학회지
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• 제44권2호
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• pp.169-177
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• 2018

Objectives: The emission characteristics of aldehydes were investigated in five industries for the efficient management of aldehydes. Methods: Aldehydes and THC were measured from the stack and boundary of facilities. The relative concentrations and odor contribution of aldehydes were evaluated. Results: The concentrations of aldehydes in the asphalt manufacturing and printing industries were relatively high. Formaldehyde met emission limits for all facilities. According to the odor contribution analysis of aldehydes, i-valeraldehyde and butyraldehyde, which have a relatively low odor threshold value, were found to be the major odor-causing substances in the painting and textile processing industries. Conclusions: Among the aldehydes, the major emission compounds were formaldehyde in asphalt manufacturing, acetaldehyde in the paper manufacturing and textile processing industries, and butyraldehyde in the printing and painting industries. Therefore, to increase the effectiveness of aldehyde reduction, proper control devices need to be installed and operated according to the emission characteristics of aldehydes.

• 한국환경보건학회지
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• 제32권1호
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• pp.19-26
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• 2006

This study was undertaken to determine the concentrations of 15 aldehydes in air samples collected from 21 households including 9 atopy patient's homes and to assess the extent of exposure and risk for an individual due to inhalation. Of all the aldehydes identified in both indoor and outdoor environment, formaldehyde and acetaldehyde were the most abundant aldehydes, which were occupied $60\%\;and\;17\%$ of total amount, respectively. The geometric mean concentration of formaldehyde and acetaldehyde in indoor air were $170.5\pm1.9\;{\mu}g/m^3\;and\;47.3\pm1.5\;{\mu}g/m^3$, respectively. There existed a strong correlation between formaldehyde, acetaldehyde and other aldehydes. And the ratio of indoor and outdoor concentrations (I/O) exceeded 1.0 for almost every measured aldehydes except m-tolualdehyde... No associations were found between the level of aldehydes and either housing characteristics or living habits in most of the samples with only a few exception. And the concentrations of all aldehydes indoor air between atopy patient's homes and control homes were not significant(p>0.05). Formaldehyde and acetaldehyde exposures and risks were estimated by using the inhalation unit risk, mean concentrations and the 95th percentiles, and which were $2.6\times10^{-3}\;and\;1.1\times10^{-4}$, respectively. The mean and the 95th percentile risk estimates were 25 times higher for formaldehyde than for acetaldehyde in homes.

• Environmental Analysis Health and Toxicology
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• 제22권1호
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• pp.37-47
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• 2007

Aldehydes are irritants of the upper respiratory tract with symptoms such as eye, nose, and throat. Formaldehyde classified in Group 2A by the International Agency for Research on Cancer and a probable human carcinogen by the Unite States Environmental Protection Agency due to its carcinogenicity. Aldehydes may be emitted from many other consumer products, such as permanent press fabrics, cosmetics, fiberglass insulation, paints, and coatings. The purpose of this study was to examine the does-response relationship between aldehydes levels and symptoms (eyes, nose, throat, and respiratory) for 36 dwellings and 280 households in Korea. As a result, environmental factors affecting aldehydes level were indoor smoking, ventilation, using of carpet, bed, and new furniture, painting for renovation, and indoor humidity. There wat weakly positive correlation between symptom score and aldehydes level.

• Bulletin of the Korean Chemical Society
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• 제26권2호
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• pp.265-267
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• 2005

An efficient method of addition of trimethylsilyl cyanide to aldehydes by employing a zirconium complex as the catalyst has been described. A variety of aromatic, aliphatic, cyclic and heterocyclic aldehydes has been converted into corresponding trimethylsilyl ethers in excellent yield within short reaction time.

• Nutritional Sciences
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• 제3권1호
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• pp.18-24
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• 2000

Peroxidative stimuli mediated by high polyunsaturated fatty acid administration in rats induced in vivo lipid peroxidation and resulted in increased urinary excretion of a number of lipophilic aldehydes and related carbonyl compounds. These secondary lipid peroxiation products, measured as 2, 4-dinitrophenylhydrazine deritives, were detected and identified by the newly developed HPLC method. The identified urinary lipophilic nonpolar aldehydes and related carbonyl compounds were butanal, butan-2-one, pentan-2-one, hexanal, hex-2-enal, hepta-2, 4-dienal, hept-2-enal, octanal, and oct-2-enal. Lipophilic polar aldehydes such as 4-hydroxyhex-2-enal and 4-hydroxyoct-2-enal were also identified. A polyunsaturated fatty acid diet containing n-3 fatty acids generally caused high levels of urinary excretion of lipophilic aldehydes and related carbonyl compounds in rats than a normal diet. Significantly increased secondary lipid peroxidation products were hexanal, hepta-2, 4-dienal, octanal, 4-hydroxyhex-2-exal, 4-hydroxyoct-2-enal, and a number of unidentified compunds.

• Bulletin of the Korean Chemical Society
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• 제13권6호
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• pp.670-676
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• 1992

A systematic study of the partial reduction of carboxylic acids and their derivatives to the corresponding aldehydes with lithium tris(dialkylamino)aluminum hydrides under practical conditions has been carried out. The diethylaminosubstituted derivative of lithium aluminum hydride, lithium tris(diethylamino)aluminum hydride (LTDEA), shows quite general applicability in the conversion of carboxylic acids, carboxylic esters, and primary carboxamides to the corresponding aldehydes. Lithium tripiperidinoaluminum hydride (LTPDA) also appears to be a reagent of choice for such partial transformation of primary carboxamides. In additioin, both LTDEA and LTPDA reduce tertiary carboxyamides to aldehydes in high yields. Finally, lithium tris(dihexylamino)aluminum hydride (LTDHA) is capable of achieving the chemoselective reduction of aromatic nitriles to aldehydes in the presence of aliphatic nitriles under practical conditions.

• 한국물환경학회지
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• 제21권6호
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• pp.676-681
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• 2005

This study was researched for disinfection by-products (DBPs) by preozonation, prechlorination and/or postchlorination. DBPs including trihalomethanes (THMs), haloacetic acids (HAAs), halonitriles, and aldehydes were analyzed by the treatment steps of prechlorination, preozonation, sedimentation, filtration, and postchlorination comparatively. THMs were detected as $52.20{\mu}g/L$ after prechlorination and decreased during sedimentation and filtration process. The HAAs and aldehydes increased more during preozonaiton than prechlorination. However, chlorinated DBPs and aldehydes increased more by postchlorination. Chlorinated DBPs formed by preozonation increased 26% more than the chlorination process. If aldehydes were included in the total DBPs, DBPs increased up to 39% by preozonation. Preozonation could increase the removal efficiency of organic carbon during the coagulation and sedimentation processes. Ozonation might produce aldehydes that are not permitted for drinking water regulations. Also, DBPs were produced by preozonation than by chlorination. These results would bring a need for alternative disinfection studies to decrease DBPs.

• Applied Biological Chemistry
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• 제31권3호
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• pp.292-297
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• 1988

토마토 과실의 향기성분을 생체흡착법, 파쇄흡착법 및 연속 수증기증류법으로 추출하고 GC와 GC-MS에 의해 동정하였다. 생체흡착법으로 추출한 향기성분은 80여 종 이상이 분리되었고 그 중 alcohols 10종, aldehydes 6종, ester 3종, ketones 4종, phenol 1종, acid 1종으로 총 25종을 동정하였다. 파쇄흡착법으로 추출한 향기성분은 100여종 이상이 분리되었고 그중 alcohols 12종, aldehydes 6종, Ketones 5종, esters 5종, phenols 2종, hydrocarbon 1종, acid 1종으로 총 32종이 동정되었다. 연속수증기증류법으로는 향기성분 300여종 이상을 분리하였고 그 중 alcohols 19종, ester 9종, hydrocarbons 13종, aldehydes 8종, Ketones 9종, phenols 2종, lactones 2종, furans 2종, acid 1종, oters 2종으로 총 67종이 동정되었다. 연속수증기 증류법에 의해 동정한 성분 중 아직까지 MS에 의해 동정되지 않은 성분들은 hydrocarbons 11종, aldehydes, Ketones 및 other 각각 2종, alcohol, ester, lacton 및 furfural 각각 1종으로 총 21종이었다.

• Bulletin of the Korean Chemical Society
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• 제23권9호
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• pp.1340-1342
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• 2002