Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

3 dodecane

Membrane retention of lipophilic molecules is significantly increased in octanol, compared to 2% DOPC. Chlorpromazine and progesterone show R 90% in octanol. Phenazopyridine, verapamil, promethazine, and imipramine show R 70%. [Pg.168]

It is also quite interesting that lipid model 4.0 may be used to obtain alkane partition coefficients at high-throughput speeds, as suggested by Faller and Wohnsland [509,554], It is also interesting to note that since our Pe are corrected for membrane retention, the slope in Fig. 7.11 corresponding to the dashed line (our data) is 1.0, whereas the data not corrected for retention (solid line) show a lesser slope. This may not matter if the objective is to obtain alkane-water log Kp values at high speeds. [Pg.169]

2 Membrane Retention (under Iso-pH and in the Absence of Sink Condition) [Pg.169]

Culture-cell assays are also subject to sample retention by the monolayer. Sawada et al. [574] studied the transport of chlorpromazine across MDCK cell [Pg.169]

Retention may be a good predictor of the PK volume of distribution, of protein binding [264,592] or possibly even of conditions suitable for P-gp binding and extrusion of drugs. Apparently, these themes have not yet been adequately explored. [Pg.170]

PROPERTIES RESEARCH GRADE PURE GRADE TECHNICAL GRADE [Pg.17]

PROPERTIES PORE GRADE TECHNICAL GRADE PROPERTIES TECHNICAL GRADE [Pg.17]

Compotitinn. wtnM pwctnt — Compositioo. Midht pascant  [Pg.17]


Fig. III-9. Representative plots of surface tension versus composition, (a) Isooctane-n-dodecane at 30°C 1 linear, 2 ideal, with a = 48.6. Isooctane-benzene at 30°C 3 ideal, with a = 35.4, 4 ideal-like with empirical a of 112, 5 unsymmetrical, with ai = 136 and U2 = 45. Isooctane- Fig. III-9. Representative plots of surface tension versus composition, (a) Isooctane-n-dodecane at 30°C 1 linear, 2 ideal, with a = 48.6. Isooctane-benzene at 30°C 3 ideal, with a = 35.4, 4 ideal-like with empirical a of 112, 5 unsymmetrical, with ai = 136 and U2 = 45. Isooctane-<yclohexane at 30°C 6 ideal, with a = 38.4, 7 ideallike with empirical a of 109.3, (a values in A /molecule) (from Ref. 93). (b) Surface tension isotherms at 350°C for the systems (Na-Rb) NO3 and (Na-Cs) NO3. Dotted lines show the fit to Eq. ni-55 (from Ref. 83). (c) Water-ethanol at 25°C. (d) Aqueous sodium chloride at 20°C. (e) Interfacial tensions between oil and water in the presence of sodium dodecylchloride (SDS) in the presence of hexanol and 0.20 M sodium chloride. Increasing both the surfactant and the alcohol concentration decreases the interfacial tension (from Ref. 92).
Tonck A, Georges J M and Loubet J L 1988 Measurements of intermoiecuiar forces and the rheology of dodecane between alumina surfaces J. Coiioid interface Sc/. 126 150-5... [Pg.1746]

Union Carbide Corp. tetraethyl-ene glycol (TETRA) the solvent is free of water a dodecane re-flux is used which is later recovered by distillation 100 reciprocating-plate extractor the extract leaving the primary ex-tractor is essen-tially free of feed ahphatics, and no further purification is necessary two-stage extraction uses dodecane as a displacement sol-vent in the second stage... [Pg.78]

In dodecane, unless otherwise noted. / fZ-Butyl peroxyoctate. [Pg.224]

Diperoxyketals. Some commercially available di(/ f2 -alkylperoxy)ketals and their corresponding 10-h half-life temperatures (deterrnined in dodecane) are hsted in Table 5 (39). Diperoxyketals thermally decompose by cleavage of only one oxygen—oxygen bond initially, usually foUowed by P-scission of the resulting alkoxy radicals (40). For acychc diperoxyketals, P-scission produces an alkyl radical and a peroxyester. [Pg.225]

Diall l Peroxides. Some commercially available diaLkyl peroxides and their corresponding 10-h half-life temperatures in dodecane are Hsted in Table 6 (44). DiaLkyl peroxides initially cleave at the oxygen—oxygen bond to generate alkoxy radical pairs ... [Pg.226]

An improved solvent extraction process, PUREX, utilizes an organic mixture of tributyl phosphate solvent dissolved in a hydrocarbon diluent, typically dodecane. This was used at Savannah River, Georgia, ca 1955 and Hanford, Washington, ca 1956. Waste volumes were reduced by using recoverable nitric acid as the salting agent. A hybrid REDOX/PUREX process was developed in Idaho Falls, Idaho, ca 1956 to reprocess high bum-up, fuUy enriched (97% u) uranium fuel from naval reactors. Other separations processes have been developed. The desirable features are compared in Table 1. [Pg.202]


See other pages where 3 dodecane is mentioned: [Pg.236]    [Pg.183]    [Pg.424]    [Pg.425]    [Pg.426]    [Pg.427]    [Pg.36]    [Pg.548]    [Pg.551]    [Pg.235]    [Pg.237]    [Pg.71]    [Pg.84]    [Pg.185]    [Pg.1192]    [Pg.2]    [Pg.405]    [Pg.420]    [Pg.434]    [Pg.438]    [Pg.440]    [Pg.454]    [Pg.474]    [Pg.501]    [Pg.511]    [Pg.520]    [Pg.555]    [Pg.594]    [Pg.679]    [Pg.759]    [Pg.1095]    [Pg.1095]    [Pg.300]    [Pg.341]    [Pg.341]    [Pg.341]    [Pg.472]    [Pg.224]    [Pg.225]    [Pg.226]    [Pg.499]   
See also in sourсe #XX -- [ Pg.71 ]

See also in sourсe #XX -- [ Pg.71 ]

See also in sourсe #XX -- [ Pg.387 ]

See also in sourсe #XX -- [ Pg.138 ]

See also in sourсe #XX -- [ Pg.20 ]

See also in sourсe #XX -- [ Pg.4 ]

See also in sourсe #XX -- [ Pg.64 ]

See also in sourсe #XX -- [ Pg.183 ]

See also in sourсe #XX -- [ Pg.3 , Pg.8 ]

See also in sourсe #XX -- [ Pg.71 ]

See also in sourсe #XX -- [ Pg.480 ]

See also in sourсe #XX -- [ Pg.265 ]

See also in sourсe #XX -- [ Pg.18 ]

See also in sourсe #XX -- [ Pg.480 , Pg.486 , Pg.578 ]

See also in sourсe #XX -- [ Pg.93 , Pg.95 ]

See also in sourсe #XX -- [ Pg.480 ]

See also in sourсe #XX -- [ Pg.88 ]

See also in sourсe #XX -- [ Pg.408 , Pg.424 ]

See also in sourсe #XX -- [ Pg.4 ]

See also in sourсe #XX -- [ Pg.480 , Pg.486 , Pg.578 ]

See also in sourсe #XX -- [ Pg.331 ]

See also in sourсe #XX -- [ Pg.280 ]

See also in sourсe #XX -- [ Pg.294 , Pg.295 ]

See also in sourсe #XX -- [ Pg.437 , Pg.449 ]

See also in sourсe #XX -- [ Pg.62 ]

See also in sourсe #XX -- [ Pg.153 ]

See also in sourсe #XX -- [ Pg.38 ]

See also in sourсe #XX -- [ Pg.344 , Pg.370 , Pg.371 ]

See also in sourсe #XX -- [ Pg.30 ]

See also in sourсe #XX -- [ Pg.99 ]

See also in sourсe #XX -- [ Pg.67 ]

See also in sourсe #XX -- [ Pg.826 ]

See also in sourсe #XX -- [ Pg.826 ]

See also in sourсe #XX -- [ Pg.146 ]

See also in sourсe #XX -- [ Pg.5 , Pg.6 , Pg.7 , Pg.141 ]

See also in sourсe #XX -- [ Pg.67 ]

See also in sourсe #XX -- [ Pg.4 , Pg.93 ]

See also in sourсe #XX -- [ Pg.61 , Pg.66 , Pg.96 , Pg.217 , Pg.227 , Pg.233 , Pg.236 ]

See also in sourсe #XX -- [ Pg.140 ]

See also in sourсe #XX -- [ Pg.35 , Pg.118 , Pg.121 ]

See also in sourсe #XX -- [ Pg.826 ]

See also in sourсe #XX -- [ Pg.43 ]

See also in sourсe #XX -- [ Pg.647 , Pg.657 ]

See also in sourсe #XX -- [ Pg.32 , Pg.37 , Pg.38 , Pg.39 , Pg.47 , Pg.131 , Pg.182 ]

See also in sourсe #XX -- [ Pg.172 ]




SEARCH



1.7- Dioxaspiro- -dodecane

5 dodecane sulfonated

Bicyclo dodecanes

Cyclo-dodecane

Diamino-1,12-dodecane

Dodecan

Dodecan

Dodecanal

Dodecanal

Dodecanal production

Dodecanal titanocene dichloride

Dodecanal, reduction

Dodecane 1-chloro

Dodecane black

Dodecane derivatives

Dodecane diamine

Dodecane dispersions

Dodecane gel

Dodecane nitrile

Dodecane solvent

Dodecane sulfonates

Dodecane thiol

Dodecane thiol chain transfer agent

Dodecane thiolate

Dodecane thiols

Dodecane, 1-bromo

Dodecane, 1-bromoKomblum oxidation

Dodecane, 1-bromoKomblum oxidation solvent

Dodecane, adsorption

Dodecane, from dodecanal

Dodecane, physical

Dodecane, physical properties

Dodecane, thermodynamic properties

Dodecane-, lithium

Dodecane-, sodium

Dodecane-1,12-dicarboxylic acid

Dodecane-1,12-diol

Dodecane-2,5-dione

Dodecane-water systems

Dodecane-water systems interface

Dodecanes, nitro

Fluorescence dodecane

Fluorescence with dodecane

Hexacyclo dodecan

Interface water/dodecane

L- dodecane

N-Dodecane

Pentacyclo dodecan

Pentacyclo dodecane

Potassium dodecanate

Ra-Dodecane

Sodium dodecane sulfonate

Temperature dependence of 1 values for -butyl radicals with dodecane or 3-methyl-3-pentanol as solvent

Tetracyclo dodecan

Tetracyclo dodecane

Thermodynamic Properties of Dodecane

Tricyclo 6.2.2.0]dodecanes

Tricyclo dodecane

© 2024 chempedia.info