Resinous odor

Resinous adducts, 10 394 Resinous odor, 3 229t Resins. See also Epoxy resins Lacquer resins Novolac resins Phenolic resins Resole resins Thermoplastic resins acidic cation-exchange, 12 191 advanced materials, 1 693 antilipemic agents, 5 141 aromatic glycidyl amine, 10 372—373 chromatographic, 14 383-384 for coatings, 7 95-107 derived from furfuryl alcohol, 12 271— 272... 

Selected reactive diluents are employed to reduce the viscosity of Uvimer M formulations and to Impart a greater flexibility to the cured product. The choice of a monomer or reactive diluent for a Uvimer ig based on a number of factors, including compatibility with the base resin, odor, volatility, toxicity, and its effect on specific properties such as adhesion. Changing the diluent monomer does not drastically alter the basic properties of the resin so that it is possible to supply a given UvimerTM with a choice of diluents in order to comply with particular user requirements. 

Formula CsH5CH=CHCOOCH2CH=CHC6H5 Properties Cryst. sweet resinous odor sol. in alcohol, benzene m.w. 264.31 dens. 1.1565 (4 C) trans-trans needles pract. insol. In water sol. 

Properties Yel. brittle amorphous lumps or powd. turpentine-like fresh resinous odor sol. in alcohol, acetone insol. in benzene, aryl and aliphatic hydrocarbons, water sp.gr. 1.05-1.09 m.p. 135-150 C soften, pt. 100-130 C iodine no. 112-141 sapon. no. 145-157 ref. index 1.545 Uses Binder in lacquers and paper/picture varnishes emulsion stabilizer in cosmetics natural flavoring agent in alcoholic beverages in food-pkg. adhesives in food-contact coatings... 

Photosensitized irradiation of myrcene. Which possesses a sweet balsamic-resinous odor of poor tenacity, gives a bicyclic isomer as shown in Scheme 9 (Liu and Hammond, 1967 White and Grpta, 1969). The biradical mechanism could be used to elucidate this reaction. 

C7H4O, (CH3CH2CH2)2C0. a colourless odorous liquid b.p. 144 C. Used as a solvent for resins, particularly the glyplal and vinyloid resins, and lacquers. 

Physical Properties. Furfuryl alcohol (2-furanmethanol) [98-00-0] is aHquid, colorless, primary alcohol with a mild odor. On exposure to air, it gradually darkens in color. Furfuryl alcohol is completely miscible with water, alcohol, ether, acetone, and ethyl acetate, and most other organic solvents with the exception of paraffinic hydrocarbons. It is an exceUent, highly polar solvent, and dissolves many resins. 

If acetal resins are processed at temperatures substantially above those recommended for the particular grade, minor amounts of formaldehyde may be Hberated. Formaldehyde (qv) is a colorless, lacrimatory gas with a pungent odor and is intensely irritating to mucous membranes. The human nose is sensitive to concentrations in the range of 0.1 to 0.5 ppm. The current threshold limit value for formaldehyde is 1 ppm. 

G-9 Aromatic Petroleum Resins. Feedstocks typically used for aromatic petroleum resin synthesis boil in the approximate range of 100—300°C at atmospheric pressure, with most boiling in the 130—200°C range. The C-9 designation actually includes styrene (C-8) through C-10 hydrocarbons (eg, methylindene). Many of the polymerizable monomers identified in Table 1 for coumarone—indene type cmdes from coal tar are also present in aromatic fractions from cracked petroleum distillates. Therefore, the technology developed for the polymerization of coal-tar cmdes is also appHcable to petroleum-derived aromatic feedstocks. In addition to availabiHty, aromatic petroleum resins offer several advantages over coumarone—indene resins. These include improved color and odor, as weU as uv and thermal stabiHty (46). 

Terpene resins, because of their low odor and acceptable FDA clearance, are used as tackifiers for the natural and synthetic gum bases used in chewing gum. Selected petroleum resins are also used as gum bases. 

Uses. Diacetone alcohol is a widely used solvent in the coatings industry where it finds appHcation in hot lacquers which require high boiling components, and in bmshing lacquers where its mild odor, blush resistance, and flow-out properties are desired. Diacetone alcohol is also a solvent for nitrocellulose, cellulose acetate, and epoxy resins. 

Other. 2-Nitro-1-butanol is an excellent solvent for many polyamide resins, cellulose acetate butyrate, and ethylceUulose. It can be utilized in paint removers for epoxy-based coatings. 2-Hydroxymethyl-2-nitro-l,3-propanediol is usebil for control of odors in chemical toilets. Its slow release of formaldehyde ensures prolonged action to control odor, and there is no reodorant problem which sometimes is associated with the use of free formaldehyde. 2-Hydroxymethyl-2-nitro-l,3-propanediol solutions are effective preservative and embalming fluids. The slow Uberation of formaldehyde permits thorough penetration of the tissues before hardening. 

The function of the essential oil in the plant is not fully understood. Microscopic examination of plant parts that contain the oil sacs readily shows their presence. The odors of flowers are said to act as attractants for insects involved in pollination and thus may aid in preservation and natural selection. Essential oils are almost always bacteriostats and often bacteriocides. Many components of essential oils are chemically active and thus could participate readily in metaboHc reactions. They are sources of plant metaboHc energy, although some chemists have referred to them as waste products of plant metaboHsm. Exudates, which contain essential oils, eg, balsams and resins, act as protective seals against disease or parasites, prevent loss of sap, and are formed readily when the tree tmnks are damaged. 

Modem furniture pohshes are designed for a wide variety of surfaces, eg, plastics, metals, and synthetic and natural resin coatings. Furniture pohshes impart shine and provide protection from abrasion, marring, and spills. The formulations clean weU in many cases. In common with most other pohshes, furniture pohshes are characterized by ease and speed of apphcation and of buffing, and by either the absence of objectionable odors or the addition of pleasing ones. 

Pyrrole is a colorless, slightly hygroscopic Hquid which, if fresh, emits an odor like that of chloroform. However, it darkens on exposure to air and eventually produces a dark brown resin. It can be preserved by excluding air from the storage container, preferably by displacement with ammonia to prevent acid-catalyzed polymerization. A review of the physical and theoretical aspects of pyrrole is found in Reference 4. Some physical properties of pyrrole are Hsted in Table 1. 

Many attempts have been made to reduce the ammoniacal and sulfurous odor of the standard thioglycolate formulations. As the cosmetics market is very sensitive to the presence of impurities, odor, and color, various treatments of purification have been claimed to improve the olfactory properties of thioglycolic acid and its salts, such as distillation (33), stabilization against the formation of H2S using active ingredients (34), extraction with solvents (35), active carbon (36), and chelate resin treatments (37). 

Glycidyl and Vinyl Esters. Glycidyl neodecanoate [26761-45-5] sold commercially as GLYDEXXN-10 (Exxon) or as CarduraElO (Shell), is prepared by the reaction of neodecanoic acid and epichl orohydrin under alkaline conditions, followed by purification. Physical properties of the commercially available material are given in Table 3. The material is a mobile Hquid monomer with a mild odor and is used primarily in coatings. Eor example, it is used as an intermediate for the production of a range of alkyd resins (qv) and acryHcs, and as a reactive diluent for epoxy resins (qv). 

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