ライフサイエンスコーパス: dodecane

1 cluster compound (Au:SR, R = butane, hexane, dodecane).

2 r (RAFT) polymerization at 70 degrees C in n-dodecane.

3 c)(H), the acceptorless dehydrogenation of n-dodecane.

4 w that they do not cause mobilization of the dodecane.

5 multilamellar onions dispersed in deuterated dodecane.

6 icline, alpha-conotoxin MII, and bPiDDB (N,N-dodecane-1,12-diyl-bis-3-picolinium dibromide) blocked e

7 series of less volatile C12-C16 n-alkanes (n-dodecane, 349 ppb; n-tridecane, 340 ppb; n-tetradecane,

8 (23) and 7-methyl-1,5,9-triazabicyclo[5.5.0]dodecane (39) do not enhance the stabilities of their mo

9 ms, while rearrangement to the bicyclo[7,3,0]dodecane (9-5) system leads to a mixture of olefin isome

10 beaded activated carbon (BAC) loaded with n-dodecane, a high molecular weight volatile organic compo

11 s, respectively) 2-6-fold in the presence of dodecane, a lipid-solubilizing agent, with 50% maximal a

12 This conclusion was supported by dodecane adsorption/desorption, which was independent of

13 icationic 1,12-di(3-hexadecylbenzimidazolium)dodecane bis[(trifluoromethyl)sulfonyl]imide bromotrichl

14 ure helicene 3, either without solvent or in dodecane (but not in chloroform) aggregates into columna

15 r the first time for the photooxidation of n-dodecane (C12H26) in the presence of NOx in the CESAM ch

16 emperature (1)H NMR studies conducted in d26-dodecane confirm partial solvation of the PBzMA block at

17 (8)] 2[Br]) and 1,12-di (3-vinylimidazolium) dodecane dibromide ([(VIM)(2)C(12)] 2[Br]), were copolym

18 hain alkyl motifs were developed: a cysteine dodecane disulfide (Cdd) building block and a tyrosine-

19 nsitive diazatetracyclo[4.4.0.1(3,10).1(5,8)]dodecanes (DTDs) with rare alicyclic scaffolding in high

20 iers for the stabilization of emulsions of n-dodecane emulsion droplets in water.

21 Ceramide in a dodecane/ethanol delivery system inhibited the opening o

22 The relatively low volatility of n-dodecane facilitates variable-temperature rheological st

23 mass organogelator (LMOG), in n-octane and n-dodecane have been investigated as their sols were trans

24 4-trimethylpentyl)dithiophosphinic acid in n-dodecane have been studied by visible absorption spectro

25 bic effect is examined from simulations of n-dodecane in different solvents.

26 sub-CMC concentrations on solubilization of dodecane in porous media under dynamic flow conditions.

27 ctane, n-nonane, n-decane, n-undecane, and n-dodecane) in blood using headspace solid-phase microextr

28 e as a third comonomer) also formed stable n-dodecane-in-water Pickering emulsions, as judged by opti

29 bb12 = bis[4(4'-methyl-2,2'-bipyridyl)]-1,12-dodecane), incorporated into a negatively charged model

30 s containing the 12-oxatricyclo[6.3.1.0(2,7)]dodecane moiety having either the trans (8a-e) or cis (9

31 In this work a simulated collapse of an n-dodecane molecule in H2O, CCl4, and a water-like Lennard

32 size in six molecular solvents: n-hexane, n-dodecane, n-undecyl alcohol, chloroform, carbon tetrachl

33 a and log P in water versus both octanol and dodecane of 3 and a set of related agents.

34 d and 2-propanol, and one nonpolar molecule, dodecane, on LiNbO3(0001) was compared.

35 ophobic solvent components such as hexane or dodecane or by introducing hydrophobic electrolyte ions

36 altered after 1-h exposure to pure alkanes (dodecane or tetradecane) and alkane mixtures (mineral oi

37 arbamate (CNC) in an n-alkane (n-octane or n-dodecane) or 3beta-cholesteryl N-(2-naphthyl) carbamate

38 When bound to water droplets in dodecane, or to the plasma membranes of living cells, th

39 By comparison, dodecane shows a preconcentration gain of approximately

40 Two approaches to the aza-tricyclo dodecane skeleton of (-)-FR901483 are reported.

41 ts and kinetic gas-particle modeling for the dodecane SOA system, here we show that the presence of p

42 The results demonstrated the enhancement of dodecane solubility by monorhamnolipid surfactant at con

43 nel, about 15,000 plates were obtained for a dodecane test analyte.

44 e-human serum albumin clearing agent and 90Y-dodecane tetraacetic acid (DOTA)-biotin as the final ste

45 2,2,4-trimethylpentane (isooctane), decane, dodecane, tetradecane, hexadecane, and 2,6,10,14-tetrame

46 In the case of n-decane and n-dodecane, the resulting alkylarenes are exclusively unbr

47 d to be in the range of <1.0% per year for n-dodecane to n-hexadecane.

48 mputer simulations of water, n-hexane, and n-dodecane under benchtop conditions shows that the sizes

49 oil drop tensiometer at air/water (A/W) and dodecane/water (DD/W) interfaces.

50 re by 5%, the same as the surface tension of dodecane/water, in agreement again with the polymer brus

51 phobic interfaces [triolein/water (TO/W) and dodecane/water], were elastic, and were not pushed off t

52 thylamino)propane and 1,8-diazabicyclo[6.3.1]dodecane, where ten and seven low-energy conformers, res