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I Propylene glycol

K. Boyer-Hassen, L.V. Johson, M.I. Propylene glycol-induced proximal renal tubular cell injury. Am. J. Kidney Dis. 1997, 30 (1), 134-139. [Pg.818]

Poly(ethylene glycol-i-propylene glycol-6-ethylene glycol) dimethylsulfoxide density, F 410-411... [Pg.501]

I PEG-16 PEG-20 PEG-32 i PEG-100 PEG-150 PEG-200 i Propylene glycol laurate plasticizer, food packaging Acetyl tributyl citrate Acetyl triethyl citrate p-t-Butylphenyl salicylate n-Butyl phthalyl-n-butyl glycolate Dibutyl sebacate Diethyl phthalate Diisooctyl phthalate Distearyl citrate Epoxidized octyl stearate Glycerin... [Pg.5540]

Siloxanes and silicones, dimethyl, ether wKh ethylene glycol I propylene glycol copolymer mono dihydrogen phosphate, triethanolamine. See TEA-dime-thicone copolyol phosphate... [Pg.2422]

Propylene glycol, dipropylene glycol, and tripropylene glycol all have several isomeric forms. Propylene glycol has one asymmetric carbon and thus there are two enantiomers (R)-I,2-propanediol and (3)-1,2-propanediol. 1,3-Propanediol is a stmctural isomer. Dipropylene glycol exists in three stmctural forms and since each stmctural isomer has two asymmetric carbons there are four possible stereochemical isomers per stmcture or a total of twelve isomers. These twelve consist of four enantiomer pairs and two meso- compounds. Tripropylene glycol has four stmctural isomers and each stmctural isomer has... [Pg.366]

Propylene oxide is also produced in Hquid-phase homogeneous oxidation reactions using various molybdenum-containing catalysts (209,210), cuprous oxide (211), rhenium compounds (212), or an organomonovalent gold(I) complex (213). Whereas gas-phase oxidation of propylene on silver catalysts results primarily in propylene oxide, water, and carbon dioxide as products, the Hquid-phase oxidation of propylene results in an array of oxidation products, such as propylene oxide, acrolein, propylene glycol, acetone, acetaldehyde, and others. [Pg.141]

Elsewhere, in a series of Japanese patents, mixtures of resorcinol + sodium nitrate, glycerine + sodium nitrate, lithium hydroxide + tungstate, etc., have been claimed to be effective. An example of the use of inhibited cooling mixtures of low toxicity is provided by a patent which describes a mixture of silicate-I- polyphosphate -I- a saccharide, e.g. sucrose or fructose, as the inhibitor formulation in a propylene glycol -I- potassium-hydrogen-carbonate mixture used in aluminium cooler boxes for ice-cream. [Pg.800]

Ag+I —>AgI+e, propylene glycol, Nal, Na cetate, acetic acid -0.3468 70Kun2... [Pg.41]

Propylene glycol, i.e., 1,2-propanediol (1,2-PDO), is an important commodity chemical. It is used as biodegradable functional fluids and as precursors for the syntheses of unsaturated polyester resins and pharmaceuticals (9-10). Propylene glycol is currently produced from petroleum-derived propylene via oxidation to propylene oxide and subsequent hydrolysis (9, 11). However, the rising cost of propylene provides an incentive to find a substitute to propylene for this... [Pg.313]

Must evaluate volume of medication administered to determine total propylene glycol exposure. High-dose lorazepam (i.e., >8-10 mg/h), phenytoin loading doses, and phenobarbital are the most likely offenders. [Pg.86]

Acute Toxicity. The LD50 following oral administration of parathion, either in propylene glycol solutions or in aqueous suspensions of the 15% wettable powder, has been determined for rats, mice, and guinea pigs. The lethal dose was approximated for rabbits and dogs. The results of these experiments are summarized in Table I. Statistical evaluation was by the method of Wilcoxon and Litchfield (11). [Pg.31]

Propylene oxide (PO) is an important intermediate in the manufacture of a wide range of valuable products propylene glycol, ethers, isopropanolamines, and various propoxylated products for polyurethanes (1). The current processes for the large scale synthesis of PO include (i) the chlorohydrin process and (ii) the peroxide process (1, 2). [Pg.403]

The bis(jS-diketonato) Ti(IV) complex [Ti(bzac)2(OEt)2] 35 (budoti-tane, shown as the predominant cis,cis,cis isomer) entered phase I clinical trials in Germany in 1986 for the treatment of colon cancer (186). The complex is very susceptible to aquation, and to minimize this, the coprecipitate (Cremophor EL, 1,2-propylene glycol in ethanol and 35) is dissolved in water prior to administration. As for titano-cene dichloride, liver damage is the dose-limiting side-effect (187). The activity of this class of complexes shows little dependence on the nature of the leaving group (e.g., OEt, Cl), but aromatic substituents... [Pg.214]

The compound (I) was a highly crystalline, stable substance, and at that time was named dianilinofluorophosphine oxide. This compound is now called diphenylphosphorodiamidic fluoride. A solution in propylene glycol was injected into mice, and the l.d. 50 found to be about 90 mg./kg. [Pg.100]

From a study of the fluoroacetates so far mentioned, it appears that any compound which can give rise to fluoroacetic acid (or the fluoroacetate ion), either by hydrolysis or by oxidation (or both), is toxic. The toxic grouping is thus F-CH2-CO, and any substitution in this radical destroys the toxicity as far as relatively simple compounds are concerned. We had reached this conclusion by May 1943.1 We subsequently showed that esters of / -fluoropropionic acid were non-toxic, whereas esters of y-fluorobutyric acid were shown by American workers to be toxic. In 19442 we reported the synthesis of ethyl 5-fluoro-pentanecarboxylate, F,[CH2]g C02Et (I). This is a stable, colourless liquid and we showed that it possessed very potent toxic properties of the fluoroacetate type. By subcutaneous injection of the propylene glycol solution into mice the l.d. 50 was 4 mg./kg. Methyl fluoroacetate (II) may be taken as a convenient standard (p. 115) and has a l.d. 50 of about 6 mg./kg. for saline solutions, and 15 mg./kg. for propylene glycol solution.3 Therefore ethyl 5-fluoropentanecarboxylate was about 7 times as toxic as methyl fluoroacetate (molecule for molecule).4... [Pg.163]

Several polymer-related uses of brassylic acid (BA) have been investigated. For example, a BA/l,3-butanediol/lauric acid oligomer is an effective plasticizer for poljrvinyl chloride,[6] BA/ethylene glycol and BA/propylene glycol polymers function as polyester based polyurethane elastomers,[7] and BA has been patented as a cross-linker for glycidyl methacrylate copolymer powder coatings.[8] However, the most detailed studies have involved polyamides selected data from these studies are summarized in Table I. [Pg.222]


See other pages where I Propylene glycol is mentioned: [Pg.3346]    [Pg.14]    [Pg.420]    [Pg.421]    [Pg.476]    [Pg.24]    [Pg.209]    [Pg.250]    [Pg.211]    [Pg.3346]    [Pg.14]    [Pg.420]    [Pg.421]    [Pg.476]    [Pg.24]    [Pg.209]    [Pg.250]    [Pg.211]    [Pg.320]    [Pg.366]    [Pg.315]    [Pg.272]    [Pg.272]    [Pg.275]    [Pg.215]    [Pg.306]    [Pg.318]    [Pg.223]    [Pg.47]    [Pg.454]    [Pg.37]    [Pg.457]    [Pg.15]    [Pg.24]    [Pg.58]    [Pg.164]    [Pg.156]    [Pg.38]    [Pg.428]    [Pg.415]    [Pg.74]   
See also in sourсe #XX -- [ Pg.10 , Pg.84 ]




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Propylene glycol

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