1. Starch ethers and esters

2. Polyvinyl alcohols, acetals and ethers:

3. • Ethers; Acetals; Ketals; Aldehydes; Ketones

4. Cyclic ethers are especially susceptible to ether cleavage, but acyclic ethers can be cleaved as well.

5. Ethers for pharmaceutical purposes

6. Prepare Alcohols, ethers, thiols, and sulfides

7. Method for preparing acetylated cellulose ethers having improved anti-fouling properties, and acetylated cellulose ethers prepared by same

8. Section 9 Acetylenes from Ethers

9. Polyvinyl alcohols , acetals and ethers : * *

10. Section 9 Acetylenes from Ethers

11. POLYVINYL ALCOHOLS , ACETALS AND ETHERS*21*13,5*

12. Process for preparing alkyl ethers and mixtures thereof

13. Bimolecular dehydration produces useful yields of ethers only…

14. N 1/185 . . . . Ethers; Acetals; Ketals; Aldehydes; Ketones

15. Ethers, organic peroxides, epoxides, acetals and hemiacetals and their derivatives

16. CPA #.#.#: Ethers, organic peroxides, epoxides, acetals and hemiacetals and their derivatives

17. Use of polycarboxylate ethers in combination with other additives for milling cement

18. Process for the production of alkyl ethers by the etherification of isobutene

19. Cyclic acetals and ketals were converted by this reagent into hydroxy ethers.

20. Ethers, organic peroxides, epoxides, acetals and hemiacetals; other organic compounds

21. The invention relates to a method for producing 4-amino-1-naphthol ethers which is characterized in that naphthol ethers are firstly produced from 1-naphthols, are subsequently transformed into corresponding 4-acetamino-1-naphthol ethers, whereupon the acyl group is then split off.

22. Alternatively, since the rearrangement of bis-Allylic ethers produces vinyl Allyl

23. CPA 20.14.63: Ethers, organic peroxides, epoxides, acetals and hemiacetals and their derivatives

24. In the presence of oxygen, ethers slowly Autoxidize to form hydroperoxides and dialkyl peroxides

25. In other words, Acetals are the ethers of carbonyl hydrates, or gem-diols (Sec

26. Unsaturated Anhydrides undergo additional polymerization, usually with styrene, acrylics, and vinyl ethers

27. Among the non-volatile constituents, an alkaloid Abrotin and coumarins (iso­fraxidin, umbelli­feron), flavonoids glycosides (rutin) and free flavonol ethers (various isomeric quercetin dimethyl ethers) are reported

28. In the presence of oxygen, ethers slowly Autoxidize to form hydroperoxides and dialkyl peroxides

29. The two-component absorption solution comprises ethylene glycols, glycol ethers or normal methyl pyrrolidone and alkanolamines.

30. Engineering services related to the processing and manufacturing of tert-alkyl-ethyl-ether and heavier ethers

31. • Do not pour ignitable/flammable substances (straight alcohols, ethers, acetone, xylol, chloroform) or other solvents down the drain.

32. Over time ethers that are exposed to air will Autoxidize to peroxides which are potentially explosive

33. Amides and ethers of perfluoropolyoxyalkylene sulphonic- or perfluoropolyoxyalkylene carboxylic acids of general formula (I): R¿F?

34. oxygen-containing hydrocarbons such as alcohols, aldehydes, ketones, carboxylic acids, esters, acetates, ethers, peroxides, epoxy resins

35. Functionalized alpha-hydroxy alkyl ethers have been found to perform as non (or anti-) scaling hydrogen sulfide scavengers.

36. Oxygen-containing hydrocarbons such as alcohols, aldehydes, ketones, carboxylic acids, esters, acetates, ethers, peroxides, epoxy resins

37. oxygen-containing hydrocarbons such as alcohols, aldehydes, ketones, carboxylic acids, esters, acetates, ethers, peroxides, epoxy resins;

38. In general, the cyclic compounds (crown ethers) are more effective than acyclic polyethers of comparable molecular weights.

39. (ii) Oxygen-containing hydrocarbons such as alcohols, aldehydes, ketones, carboxylic acids, esters, acetates, ethers, peroxides, epoxy resins;

40. (ii) oxygen-containing hydrocarbons such as alcohols, aldehydes, ketones, carboxylic acids, esters, acetates, ethers, peroxides, epoxy resins;

41. Cellulose and chemical derivatives thereof, n.e.s., in primary forms (excl. cellulose acetates, cellulose nitrates and cellulose ethers)

42. There are five main classes of BFRs, listed here with their common uses: PolyBrominated diphenyl ethers (PBDEs) – plastics, textiles

43. The values of aliphatic ethers have been calculated from n.m.r. chemical shift data to be approximately −6.4.

44. The following causes of death had been chosen: electric current, Strophanthin, ethers, pneumothorax, cerebral anoxia, E 605.

45. It was found that the cleavage of glycol ethers yields chiefly ethylene and only little ethyl iodide.

46. GLYCOSIDES AND VEGETABLE ALKALOIDS, NATURAL OR REPRODUCED BY SYNTHESIS, AND THEIR SALTS, ETHERS, ESTERS AND OTHER DERIVATIVES

47. (b) oxygen-containing hydrocarbons such as alcohols, aldehydes, ketones, carboxylic acids, esters, acetates, ethers, peroxides, epoxy resins;

48. (b) oxygen-containing hydrocarbons such as alcohols, aldehydes, ketones, carboxylic acids, esters, acetates, ethers, peroxides, epoxy resins

49. (ii) Oxygen-containing hydrocarbons such as alcohols, aldehydes, ketones, carboxylic acids, esters, acetates, ethers, peroxides, epoxy resins

50. Besides increased miscarriage risk, the UC-Davis study also found a reduced ability to get pregnant linked to glycol ethers.

51. Many ethers Autoxidize so readily that peroxidic compounds form, sometimes to dangerous levels, on storage in nonairtight containers

52. Laboratory studies show that thermal maturation of methanogenic archaea generates pristane and phytane from diphytanyl glyceryl ethers (Archaeols).

53. For example, Alchemists can create consumables such as potions, ethers, elixirs, stat buffs, status cures and status inducers

54. PolyBrominated diphenyl ethers (PBDEs), a common class of Brominated flame retardants (BFRs), are a ubiquitous part of our built environment

55. Boron tribromide also mediates the dealkylation of aryl alkyl ethers, for example demethylation of 3,4-dimethoxystyrene into 3,4-dihydroxystyrene.

56. The resulting Aurated oxonium ions IIIa and IIIb can then eliminate a proton to form the Aurated vinyl ethers IV

57. They undergo a variety of secondary thermal reactions, probably acid catalyzed, to give enol ethers, enol acetates, acetophenones, and ketonylacetophenones.

58. The alcoholysis of these intermediates yields O-alkyliminium ethers which can then be easily hydrolyzed under mild acidic conditions to the corresponding esters.

59. We proposed a new route to activate aryl methyl ether bonds and synthesize aryl Acetates by carbonylation of aryl methyl ethers

60. Melamine and urea-formaldehyde resins (as solvent or Butylating agent), auxiliary agents for agriculture (butylamines), flotation agents, and ethers of ethylene and propylene glycols

61. Stick-shaped cosmetic compositions contain (a) linear fatty alcohols and (b1) 12-hydroxystearic acid, (b2) fatty ketones and/or (b) fatty ethers.

62. INTRODUCTION IN CONTINUATION of the intensive biochemical investigation of the genus Artemisial-11 we report the isolation of seven flavonoid methyl ethers from seven Artemisia taxa

63. Then we will be ready to learn about some reactions that involve Alcohols, ethers, epoxides, thiols, and sulfides as both reactants and products.

64. Cryptands are more expensive and difficult to prepare, but offer much better selectivity and strength of binding than other complexants for alkali metals, such as crown ethers.

65. Chapter 3 Alcohols, Phenols, and Ethers 2 3 Alcohols 4 The Hydroxy (—OH) Functional Group •The hydroxyl group (—OH) is found in the alcohol and phenol functional groups

66. Saturated and aromatic hydrocarbons, ethers, esters, aldehydes, alcohols, acetophenone, nitrobenzene and aniline energe rapidly from a chromatographic column of Silochrom C80 at temperatures 100–200°C with symmetrical peaks.

67. Acetals, ketals, hemiAcetals, and hemiketals react similarly to ethers, although members of this group would be less likely to form explosively unstable peroxides when exposed to oxygen

68. The reaction could proceed over RhCl3 in the presence of LiI and LiBF4, and moderate to high yields of aryl Acetates could be obtained from transformation of various aryl methyl ethers with different substituents.

69. The differing experiences which expert Anesthetizers have had in the use of ethyl ethers supplied by various manufacturers in numerous surgical cases have prompted the present investigation of the chemistry of inhalation anesthetics

70. This work was undertaken for the evaluation and revision of group-additivity values necessary for predicting standard enthalpies of formation and enthalpies of vaporization of ethers, Acetals, ketals, and ortho esters by means of Benson's group-additivity methodology

71. Azeotropic compositions include a perfluorinated alkane or alkene and an organic solvent, selected from the group consisting of hydrofluorocarbons, hydrochlorofluorocarbons, siloxanes, ethers, 2, 3-dimethyl butane, 2, 3-dimethyl pentane and 2, 2, 4-trimethylpentane.

72. The phasing out of lead Antiknock compounds in gasoline and their replacement by ‘oxygenates’ – mainly alcohols and ethers such as methyl tertiary butyl ether (MTBE) – created a need for an oxygen-selective detector, easy to use with capillary columns

73. The reactions of the trimethylsilyl enol ethers of both 4-thiochromanone and 4-thiochromanone 1,1-dioxide with various carbonyl compounds complexed with titanium tetrachloride give moderate yields of the previously unknown 3-alkylidene condensation products under mild conditions.

74. Benzyl ethers offer a versatile means of protection for the hydroxyl group, being installed under basic (Benzyl bromide, sodium hydride, DMF; Benzyl bromide, sodium hydride, tetrabutylammonium iodide, THF 76,77), acidic (Benzyl trichloroacetimidate, triflic acid; 78,79 phenyldiazomethane, tetrafluoroboric acid 80) or neutral (Benzyl bromide

75. The risk assessment has, based on the available information, determined that in the European Community the substance is mainly used as an intermediate in the production of bisphenol A, phenol resins, alkylphenols, caprolactam, salicylic acid, nitrophenols, diphenyl ethers, halogen phenols and other chemicals.

76. Ascendents grows straccio pepeljara обвалиться legal department urgirati оправдано потребно за да се спречи бегство ethers, cyclic flirter (v.) hoped for and fulfilled income bond bifurcation Gadhafi beholder Armbanduhr staviti sa strane green tuff puolipukeinen, puolittain puettu energisch (u.E

77. The DSC results showed that the compound, a colorless wax at room temperature, was amorphous with a glass transition temperature which was 80° higher than those of aliphatic crown ethers, which are crystalline compounds with melting points >40°C.

78. The risk assessment has, based on the available information, determined that in the European Community the substance is mainly used as an intermediate in the production of bisphenol A, phenol resins, alkylphenols, caprolactam, salicylic acid, nitrophenols, diphenyl ethers, halogen phenols and other chemicals

79. These agents contain at least 10 % by wt. of sodium bicarbonate with a mean particle size of 20-500 $g(m)m as a water-soluble abrasive and a surfactant mixture containing amphoteric surfactants, alkyl polyglycol ethers with a limited distribution within the homologous series and soap.

80. Amphiphilic molecules is a general term that describes any compound that contains two distinct covalently bonded components with different affinity for the solvent in the same molecule, in which one part possesses a high affinity for polar solvents (such as water), and another part has a strong affinity for nonpolar solvents, such as hydrocarbons, ethers, and esters.