1. Aldehydes, such as acetic aldehyde: minimum 3, maximum 60

2. And, in the end, it turns out that nearly every third aroma material is an Aldehyde, but some of the main Aldehydes are not Aldehydes at all.

3. Aldehyde - Aldehyde - Properties of Aldehydes: The only structural difference between hydrocarbons and Aldehydes is the presence in the latter of the carbonyl group, and it is this group that is responsible for the differences in properties, both physical and chemical

4. For the common name of Aldehydes start with the common parent chain name and add the suffix -Aldehyde

5. Aldehydes synonyms, Aldehydes pronunciation, Aldehydes translation, English dictionary definition of Aldehydes

6. Aldol definition is - a colorless beta-hydroxy aldehyde C4H8O2 used especially in organic synthesis; broadly : any of various similar aldehydes.

7. The Aldol addition of 86 occurs to a variety of aldehydes with greater than 95 : 5 facial selectivity on the aldehyde

8. Aldehyde - The Aldehydes are a very important class of organic compounds; they are characterized by the presence of the formal functional group -CHO

9. The raw alkylphenol composition is reacted directly, without pre-purification, with one or more aldehydes to form an in-situ alkylphenol-aldehyde resin.

10. Aldehydase aldehyde aldehyde base aldehyde dehydrogenase aldehyde fuchsin aldehyde-lyase aldehyde mutase aldehyde oxidoreductase aldehyde reductase aldehyde test Alden Alder Alder body alder buckthorn alder dogwood Alder flycatcher alder grove Alder's anomaly alder tree Aldercy alderfly alderman Alderney sea-lavender Alderson-Broaddus College

11. Soon it was followed by similar substances: so-called “Aldehyde C-16” (“strawberry Aldehyde”), “Aldehyde C-18” (“coconut Aldehyde”), “Aldehyde C-20” (“raspberry Aldehyde”) and others

12. This avoids the dangers of having to work with free $g(a),$g(b)-unsaturated aldehydes, the aldehydes are not liberated from their storage forms before they are required for the polymerization and a greater proportion of aldehyde groups are incorporated in the copolymers than when free aldehydes are used.

13. This invention is related to modified alkylphenol aldehyde resins and process for preparing them from the reactions of alkylphenols, aldehydes, amines, rosins and fatty acids.

14. || Aliphatic aldehydes Aromatic aldehydes Alicyclic aldehydes Aliphatic acetals Aromatic acetals Alicyclic acetals

15. Crotonic aldehyde

16. Alicyclic aldehydes

17. Ammonium aldehyde

18. Acetaldehyd (German) Acetaldehyde (ACGIH:OSHA) Acetic aldehyde Acetylaldehyde Aldehyde acetique (French)

19. However, Aldehyde abundance in the environment does not always spell doom because many familiar foods contain a variety of non-toxic Aldehydes that in addition to providing flavor to foods (e.g., aniseAldehyde, benzAldehyde, cinnamAldehyde, citral Aldehyde) and beverages (e.g., aniseAldehyde) are almost certain to stimulate beneficial actions

20. Aldehydes calculated as acetaldehyde

21. Aldehydes, whether or not with other oxygen function; cyclic polymers of aldehydes; paraformaldehyde:

22. ARTIFICIAL ALMOND OIL, Benzaldehyde, BENZENECARBONAL, BENZENECARBOXALDEHYDE, BENZOIC ALDEHYDE, PHENYLFORMALDEHYDE, and PHENYLMETHANOL ALDEHYDE

23. Aldehydes for pharmaceutical purposes

24. Formic aldehyde for pharmaceutical purposes

25. Benzaldehyde is an aromatic aldehyde

26. Benzaldehyde is an aromatic aldehyde

27. 1¿ has the same meaning as in formula (I), with the corresponding low aldehydes and the subsequent reduction of the unsaturated aldehyde thus obtained, if: i) the aldol condensation is performed in an inert organic solvent, and ii) the unsaturated aldehyde is reduced in the presence of a possibly calcined copper-zinc contact.

28. Section 4 Acetylenes from Aldehydes

29. Aldehydes calculated as acetic acid

30. Catalytic antibodies, including 38C2 and 33F12, are capable of efficiently catalyzing a wide variety of ketone-ketone, ketone-aldehyde, aldehyde-ketone, and aldehyde-aldehyde intermolecular aldol reactions, and in some cases to catalyze their subsequent dehydration to yield aldol condensation products.

31. In-situ alkylphenol-aldehyde resins

32. Acyclic aldehydes without other oxygen function: |

33. Polymer aldehyde/siloxane amine networks

34. Formic aldehyde for chemical purposes

35. Section 4 Acetylenes from Aldehydes

36. Learn more about Aldehydes in …

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

38. Acyclic aldehydes without other oxygen function

39. Aldehydes Aldrich ChemFiles 2007 , 7.8 , 3

40. The Aldol condensation is a reaction that is named based on the type of product formed when two aldehydes (or ketones), in the presence of dilute base, yields a molecule having both alcohol and aldehyde functional groups

41. Aldehydes triggered a revolution in perfumery

42. Benzyl alcohols/aldehydes/acids/esters/acetals

43. Acyclic aldehydes without other oxygen function:

44. In an Aldehyde, a carbonyl group is …

45. Spinel structured catalyst for aldehyde production

46. – Acyclic aldehydes without other oxygen function:

47. – Acyclic aldehydes without other oxygen function: |

48. Some Aldehydes are made inside the body

49. Removal of aldehyde impurity by reactive polystyrene resin

50. The carbonyl stretch C=O of saturated aliphatic Aldehydes appears from 1740-1720 cm-1.As in ketones, if the carbons adjacent to the Aldehyde group are unsaturated, this vibration is shifted to lower wavenumbers, 1710-1685 cm-1.See also:

51. An Aldol addition is a reaction that occurs between the enolate of an aldehyde or ketone and the alpha-carbon of another aldehyde or ketone to form a beta-hydroxy aldehyde or ketone

52. Formaldehyde-free resins based on hydroxyl aldehydes

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

54. This makes the Aldehydes very easy to oxidise

55. Thep-nitrophenylhydrazones of aldehydes are acid-base indicators.

56. •Aldehydes are reduced to primary alcohols R R

57. Acyclic aldehydes without other oxygen function (excluding methanal, ethanal)

58. Primary Alcohols Oxidize to yield __ (functional group) Aldehyde

59. Aldehydes are readily oxidized to give carboxylic acids

60. Aldehydes are considered the most important functional group

61. Aldehyde and Ketone reduction by LiAlH 4 to Alcohols

62. Modified alkylphenol-aldehyde resins stabilized by a salicylic acid

63. LiAlH 4 can reduce Aldehyde and ketone to alcohols

64. Notice, this is an aldehyde, and it's an alcohol.

65. Method for producing primary aliphatic amines from aldehydes

66. Aldehydes can react with air to give peroxo …

67. In addition, Borane rapidly reduces aldehydes, ketones, and alkenes

68. Thus the chemical formula for an Aldehyde functional group is -CH=O, and the general formula for an Aldehyde is R-CH=O.

69. The process comprises the step of reacting a base-modified alkylphenol-aldehyde resin with a salicylic acid to stabilize the base-modified alkylphenol aldehyde resin.

70. Method for producing aldehydes from alkanes and synthesis gas

71. Aldehydes constitute a group of relatively reactive organic compounds

72. They are therefor used as sources for aldehydes and amines.

73. Carboxylic acid with alcohol, phenol, aldehyde or ketone functions

74. Aldehydes reduce the diamminesilver(I) ion to metallic silver

75. Mar 21, 2021 (The Expresswire) -- Global Aldehydes Market size …

76. Aldehydes can be prepared via a number of pathways

77. Blanche by Byredo is a Floral Aldehyde fragrance for women

78. An Aldehyde is most commonly known for their pungent smell

79. Many people have a severe problem with Aldehyde toxicity

80. It Condenses readily with aldehydes, yielding with formaldehyde, on …