ライフサイエンスコーパス: isoamyl

1 ed CO(2), was optimized for the synthesis of isoamyl acetate (3-methylbutyl ethanoate) by response su

2 Isoamyl acetate (450.60 mug/L) and ethyl caprylate (313.

3 within the ONS, including diacetyl (sweet), isoamyl acetate (banana), dimethyl trisulfide (sulfur) a

4 ration and filtration), or ethyl alcohol and isoamyl acetate (final product).

5 cited by the bee's alarm pheromone component isoamyl acetate (IAA) is strongly suppressed by geosmin.

6 by covalent binding for use in synthesis of isoamyl acetate (IAAc), which has a typical banana flavo

7 aroma compounds and this was significant for isoamyl acetate (sweet, fruity) and methanethiol (sulfur

8 etate 39.48 ng mL(-1) (RSD mean value 4.2%), isoamyl acetate 3.88 ng mL(-1) (RSD mean value 3.4%), et

9 ts strong and pungent smell and taste, while isoamyl acetate adds intense 'fruity' and 'banana' odour

10 ost significant variations were observed for isoamyl acetate and 2-phenylethyl acetate (increasing be

11 s of isoamylalcohol and isopentyl alcohol to isoamyl acetate and isopentyl acetate using the MCH@PDA-

12 s of isoamylalcohol and isopentyl alcohol to isoamyl acetate and isopentyl acetate using the MCH@PDA-

13 f concern in e-cigarettes, only 3 (glycerol, isoamyl acetate and propylene glycol) were quantified.

14 Isoamyl acetate and whisky lactone also moderately reduc

15 tic interaction between beta-cyclocitral and isoamyl acetate but only in the case of males.

16 reen and environmentally-benign synthesis of isoamyl acetate from acetic acid and isoamyl alcohol und

17 Lilial similarly antagonized the response to isoamyl acetate in other ORNs, indicating the effect gen

18 Isoamyl acetate showed odor activity values (OAV) rangin

19 n, the onset and recovery kinetics following isoamyl acetate stimulation are prolonged in the null mi

20 Butanal and isoamyl acetate underwent metabolic reactions, which dec

21 ales (but not males) to beta-cyclocitral and isoamyl acetate when tested singly, (2) the presence of

22 labelled compounds (butanal, 2-phenyethanol, isoamyl acetate) was studied from a liquid medium into t

23 odorants were ethyl acetate, ethyl butyrate, isoamyl acetate, and isoamyl butyrate.

24 Three sweet-associated aroma compounds, isoamyl acetate, benzaldehyde and whisky lactone, were t

25 acid on sensory perception and volatility of isoamyl acetate, ethyl isobutyrate, ethyl butyrate and e

26 Six compounds (isoamyl acetate, ethyl octanoate, ethyl decanoate, 3-met

27 l butanoate, ethyl octanoate, ethyl acetate, isoamyl acetate, isobutanol, 2-methyl-1-butanol, 2-pheny

28 respectively for butanal, 2-phenyethanol and isoamyl acetate.

29 of straight-chain fatty acids, ethyl, hexyl, isoamyl acetates and superior alcohols than the control

30 e AWC-sensed odorants benzaldehyde (Bnz) and isoamyl alcohol (IsoA) and can reciprocally cross-adapt.

31 the analogous alkane of the potent inhibitor isoamyl alcohol (isopentanol), did not.

32 We found that several alcohols, notably isoamyl alcohol and 1-butanol, stimulate filamentous gro

33 lcohol, (Z)-3-hexen-1-ol, coniferyl alcohol, isoamyl alcohol and linolenic acid.

34 that C. elegans seeks bacteria that release isoamyl alcohol and support faster growth.

35 The aqueous phase contains some 0.15 M isoamyl alcohol and the unreacted hydrogen peroxide, but

36 nitrite are processed for removal of IPA and isoamyl alcohol by solvent extraction.

37 thidium bromide can be readily removed using isoamyl alcohol extractions combined with intercalator-s

38 itrite remains in the aqueous phase, whereas isoamyl alcohol forms a new organic phase along with the

39 Removal of isoamyl alcohol or traces of isoamyl nitrite is accompli

40 esis of isoamyl acetate from acetic acid and isoamyl alcohol under solvent-free conditions.

41 lta(13)C(VPDB ethyl acetate)-delta(13)C(VPDB isoamyl alcohol), delta(13)C(VPDB ethyl acetate)-delta(1

42 lta(13)C(VPDB ethyl acetate)-delta(13)C(VPDB isoamyl alcohol)-delta(13)C(VPDB n-propanol) and delta(1

43 benzyl alcohol; in Corvina, benzyl alcohol, isoamyl alcohol, 1-hexanol, p-cymen-8-ol, 2,3 pinanediol

44 o identify that these three bacteria release isoamyl alcohol, a previously described C. elegans chemo

45 ated the chemotaxis ability toward diacetyl, isoamyl alcohol, and benzaldehyde when aged.

46 ain of these alcohols, including butanol and isoamyl alcohol, bring about a rapid inhibition of trans

47 t relevant wine higher alcohols (isobutanol, isoamyl alcohol, methionol and beta-phenylethanol) on re

48 he sensory importance of the pair isobutanol-isoamyl alcohol.

49 e "burning" effects linked to high levels of isoamyl alcohol.

50 ntribution of the different players, notably isoamyl-alcohol, (Z)-1,5-octadien-3-one, benzaldehyde an

51 ldehydes, saturated-aldehydes, benzaldehyde, isoamyl-alcohol, methoxypyrazines and (Z)-1,5-octadien-3

52 l hexanoate, ethyl octanoate, butyrolactone, isoamyl alcohols, acetaldehyde, ethyl acetate, 2,3-butan

53 Within the free volatile compounds, isoamyl alcohols, benzaldehyde and guaiacol registered t

54 ile within the bound volatile compounds were isoamyl alcohols, ethyl vanillate and benzoic acid.

55 cetate, ethyl butyrate, isoamyl acetate, and isoamyl butyrate.

56 c efficiency in the solventless synthesis of isoamyl esters of natural carboxylic acids, also in mult

57 e glomerular layer responded specifically to isoamyl esters, and other regions preferred ethyl esters

58 isobutyl ketone (DIBK, yield 66%) and methyl isoamyl ketone (MIAK, yield 81%).

59 iol-disulfide interchange approach using sec-isoamyl mercaptan (SIT) as an alkyl sulfenyl-protecting

60 nd 1,4-oxathiane: tert-butyl methyl sulfide, isoamyl methyl sulfide, ethyl isoamyl sulfide, tert-buty

61 /TFAA (with [emim][CF3COO], [emim][NO3]) and isoamyl nitrate/BF3.Et2O, isoamyl nitrate/TfOH (with [em

62 ty of nitrating systems, namely NH4NO3/TFAA, isoamyl nitrate/BF3.Et2O, isoamyl nitrate/TfOH, Cu(NO3)/

63 , [emim][NO3]) and isoamyl nitrate/BF3.Et2O, isoamyl nitrate/TfOH (with [emim][OTf]) provided the bes

64 amely NH4NO3/TFAA, isoamyl nitrate/BF3.Et2O, isoamyl nitrate/TfOH, Cu(NO3)/TFAA, and AgNO3/Tf2O.

65 ydroperoxide anion (in the aqueous phase) on isoamyl nitrite (in the organic phase).

66 aryl-diazonium chemistry in the presence of isoamyl nitrite followed by condensation reaction of the

67 Removal of isoamyl alcohol or traces of isoamyl nitrite is accomplished by washing the aqueous p

68 and the unreacted hydrogen peroxide, but no isoamyl nitrite.

69 a new organic phase along with the unreacted isoamyl nitrite.

70 lves nitrosation of H2O2 at pH> or = 12.5 by isoamyl or butyl nitrite in mixed solvents of isopropyl

71 Isoamyl- or cyclopropylmethylene-substituted dipyrrole d

72 ned four filters in a 5 mL Phenol-Chloroform-Isoamyl (PCI) procedure to allow for larger volumes of w

73 content of octanoic acid, isobutanol, ethyl isoamyl succinate and catechin and a smaller amount of q

74 l sulfide, ethyl isoamyl sulfide, tert-butyl isoamyl sulfide, diisoamyl sulfide, tetrahydrothiophene,

75 ethyl sulfide, isoamyl methyl sulfide, ethyl isoamyl sulfide, tert-butyl isoamyl sulfide, diisoamyl s