Big Chemical Encyclopedia

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

Articles Figures Tables About

Dimethyl-phthalate

Ketone Peroxides. These materials are mixtures of compounds with hydroperoxy groups and are composed primarily of the two stmctures shown in Table 2. Ketone peroxides are marketed as solutions in inert solvents such as dimethyl phthalate. They are primarily employed in room-temperature-initiated curing of unsaturated polyester resin compositions (usually containing styrene monomer) using transition-metal promoters such as cobalt naphthenate. Ketone peroxides contain the hydroperoxy (—OOH) group and thus are susceptible to the same ha2ards as hydroperoxides. [Pg.228]

Methyl Ethyl Ketone Peroxide in Dimethyl Phthalate (4TT3)), National Toxicology Program, Toxicity Report Series Number 18, NIH Pubhcation 93-3341, United States Department of Health and Human Services, Washington D.C., Eeb. 1993. [Pg.139]

Many other compounds are presendy in use a 1993 database search showed 27 active ingredients in 212 products registered by the U.S. EPA for human use as repellents or feeding depressants, including octyl bicycloheptene dicarboxamide (A/-2-ethylhexylbicyclo[2.2.1]-5-hepten-2,3-dicarboxamide), dipropyl isocinchomeronate (2,5-pyridine dicarboxyhc acid, dipropyl ester), dimethyl phthalate, oil of citroneUa, cedarwood oil, pyrethrins, and pine tar oil (2). Repellent—toxicant or biting depressant systems are available which are reasonably comfortable for the user and can protect completely against a number of pests for an extended period of time (2). [Pg.112]

In tests done in the 1940s, dimethyl phthalate and pyrethmm cream were found to be partially protective on skin against Phkbotomuspapatasi for 6 h... [Pg.116]

The phthalate esters are one of the most widely used classes of organic esters, and fortunately they exhibit low toxicity (82). Because of the ubiquitous nature of phthalates, many iavestigations have been conducted to determine their toxicides to marine life as well as ia mammals (83—85). Generally, phthalates are not absorbed through the skin and are not very potent when inhaled. The phthalates become less toxic as the alcohol group increases in molecular weight. For example, dimethyl phthalate has an oral LD q (mouse) of 7.2 g/kg, whereas di(2-ethylhexyl) phthalate shows an oral LD q (rat) of greater than 26 g/kg. [Pg.393]

In an attempt to generate (214), a derivative of the elusive monocyclic azete system cf. Section 5.09.5.3.1), the fused 1-azetine (213) was pyrolyzed, but gave only intractable tars in addition to low yields of dimethyl phthalate (71JOC435). [Pg.270]

Diesters Dimethyl phthalate Dibutyl phthalate Diethyl maleate... [Pg.374]

From Table 5.7 it will be seen that plasticisers for PVC such as the octyl phthalates, tritolyl phosphate and dioctyl sebacate have solubility parameters within 1 cgs unit of that of the polymer. Dimethyl phthalate and the paraffinic oils which are not PVC plasticisers fall outside the range. It will be noted that tritolyl phosphate which gels the most rapidly with PVC has the closest solubility parameter to the polymer. The sebacates which gel more slowly but give products which are flexible at lower temperatures than corresponding formulations from tritolyl phosphate have a lower solubility parameter. It is, however, likely that any difference in the effects of phthalate, phosphate and sebacate plasticisers in... [Pg.87]

Comparison of Table 5.4 and 5.7 allows the prediction that aromatic oils will be plasticisers for natural rubber, that dibutyl phthalate will plasticise poly(methyl methacrylate), that tritolyl phosphate will plasticise nitrile rubbers, that dibenzyl ether will plasticise poly(vinylidene chloride) and that dimethyl phthalate will plasticise cellulose diacetate. These predictions are found to be correct. What is not predictable is that camphor should be an effective plasticiser for cellulose nitrate. It would seem that this crystalline material, which has to be dispersed into the polymer with the aid of liquids such as ethyl alcohol, is only compatible with the polymer because of some specific interaction between the carbonyl group present in the camphor with some group in the cellulose nitrate. [Pg.88]

Although many plasticisers have been suggested for cellulose acetate very few have been used in practice. The most important of these are dimethyl phthalate (8 = 21.4), triacetin (8 = 20.3) and triphenyl phosphate (8 = 20.0), each of which have a solubility parameter within one unit of that of cellulose diacetate (-22.0). (All in units ofMPa. )... [Pg.624]

Of these dimethyl phthalate (DMP) is used in most compositions. It is cheap, has a high compatibility with secondary cellulose acetate and is efficient in increasing flexibility, toughness and the ease of flow at a given temperature. Its principal disadvantages are its high volatility and the fact that it increases the flammability of the compound. Similar in compatibility but rather less volatile is diethyl phthalate. This material has less of an influence on flexibility and flow properties than the methyl ester. [Pg.624]

Triphenyl phosphate is a crystalline solid which has less compatibility with the polymer. This may be expected from solubility parameter data. It is often used in conjunction with dimethyl phthalate and has the added virtues of imparting flame resistance and improved water resistance. It is more permanent than DMP. Triacetin is less important now than at one time since, although it is compatible, it is also highly volatile and lowers the water resistance of the compound. Today it is essential to prepare low-cost compounds to allow cellulose acetate to compete with the synthetic polymers, and plasticisers such as ethyl phthalyl ethyl glycollate, which are superior in some respects, are now rarely used. [Pg.624]

Table 22.4 Influence of amount of plasticiser (dimethyl phthalate) on some physical properties of cellulose acetate compositions... Table 22.4 Influence of amount of plasticiser (dimethyl phthalate) on some physical properties of cellulose acetate compositions...
Benzoyl peroxide is most commonly used for elevated temperature curing. The peroxide is generally supplied as a paste (-50%) in a liquid such as dimethyl phthalate to reduce explosion hazards and to facilitate mixing. The curing cycle in pressure moulding processes is normally less than five minutes. [Pg.702]

Commercial methyl ethyl ketone peroxide (MEKP) is a mixture of compounds and is a liquid usually supplied blended into dimethyl phthalate, the mixture... [Pg.702]

Cobalt naphthenate is generally supplied in solution in styrene, the solution commonly having a cobalt concentration of 0.5-1.0%. The cobalt solution is normally used in quantities of 0.5-4.0% based on the polyester. The accelerator solution is rather unstable as the styrene will tend to polymerise and thus although the accelerator may be metered from burettes, the latter will block up unless frequently cleaned. Cobalt naphthenate solutions in white spirit and dimethyl phthalate have proved unsatisfactory. In the first case dispersion is difficult and laminates remain highly coloured whilst with the latter inferior end-products are obtained and the solution is unstable. Stable solutions of cobalt octoate in dimethyl phthalate are possible and these are often preferred because they impart less colour to the laminate. [Pg.703]

Chemical Designations — Synonyms Diacetyl Peroxide Solution Chemical Formula CH3CO(Oi)OCCH3 in dimethyl phthalate. [Pg.6]


See other pages where Dimethyl-phthalate is mentioned: [Pg.141]    [Pg.544]    [Pg.75]    [Pg.287]    [Pg.510]    [Pg.1201]    [Pg.326]    [Pg.375]    [Pg.149]    [Pg.303]    [Pg.304]    [Pg.132]    [Pg.480]    [Pg.485]    [Pg.113]    [Pg.114]    [Pg.114]    [Pg.115]    [Pg.222]    [Pg.227]    [Pg.266]    [Pg.269]    [Pg.387]    [Pg.392]    [Pg.393]    [Pg.395]    [Pg.111]    [Pg.2211]    [Pg.88]    [Pg.206]    [Pg.60]    [Pg.65]    [Pg.217]   
See also in sourсe #XX -- [ Pg.87 , Pg.88 , Pg.624 ]

See also in sourсe #XX -- [ Pg.282 ]

See also in sourсe #XX -- [ Pg.443 ]

See also in sourсe #XX -- [ Pg.126 ]

See also in sourсe #XX -- [ Pg.218 , Pg.254 , Pg.272 , Pg.273 , Pg.479 ]

See also in sourсe #XX -- [ Pg.57 ]

See also in sourсe #XX -- [ Pg.242 ]

See also in sourсe #XX -- [ Pg.103 , Pg.107 ]

See also in sourсe #XX -- [ Pg.63 ]

See also in sourсe #XX -- [ Pg.961 ]

See also in sourсe #XX -- [ Pg.307 ]

See also in sourсe #XX -- [ Pg.598 ]

See also in sourсe #XX -- [ Pg.234 , Pg.241 , Pg.248 ]

See also in sourсe #XX -- [ Pg.206 ]

See also in sourсe #XX -- [ Pg.87 , Pg.88 , Pg.624 ]

See also in sourсe #XX -- [ Pg.112 ]

See also in sourсe #XX -- [ Pg.386 , Pg.541 ]

See also in sourсe #XX -- [ Pg.67 ]

See also in sourсe #XX -- [ Pg.117 ]

See also in sourсe #XX -- [ Pg.230 ]

See also in sourсe #XX -- [ Pg.213 , Pg.592 ]

See also in sourсe #XX -- [ Pg.170 , Pg.477 ]

See also in sourсe #XX -- [ Pg.57 ]

See also in sourсe #XX -- [ Pg.74 , Pg.238 , Pg.256 , Pg.278 , Pg.279 , Pg.283 , Pg.310 , Pg.311 , Pg.499 , Pg.578 , Pg.592 , Pg.593 , Pg.602 , Pg.603 , Pg.606 , Pg.618 ]

See also in sourсe #XX -- [ Pg.343 ]

See also in sourсe #XX -- [ Pg.401 ]

See also in sourсe #XX -- [ Pg.323 ]

See also in sourсe #XX -- [ Pg.1127 ]

See also in sourсe #XX -- [ Pg.87 , Pg.88 , Pg.624 ]

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

See also in sourсe #XX -- [ Pg.302 ]

See also in sourсe #XX -- [ Pg.388 ]

See also in sourсe #XX -- [ Pg.95 , Pg.324 ]

See also in sourсe #XX -- [ Pg.732 ]

See also in sourсe #XX -- [ Pg.215 ]

See also in sourсe #XX -- [ Pg.250 , Pg.408 ]

See also in sourсe #XX -- [ Pg.108 ]




SEARCH



DIMETHYL PHTHALATE.168(Vol

Dimethyl 4-hydroxy-o-phthalate

Dimethyl cellosolve phthalate

Dimethyl o-phthalate

Dimethyl phthalate hydrogenation

Dimethyl phthalate physical properties

Dimethyl phthalate, hydrolysis

Esters dimethyl phthalate

Insect repellents dimethyl phthalate

Phthalates

Phthalation

Plasticizers dimethyl phthalate

Solvents dimethyl phthalate

© 2024 chempedia.info