1. Anthracene oil, acid ext. ; Anthracene oil extract residue

2. Dibenzo[a.h] anthracene

3. Anthracene, 2,5-furandione Adduct

4. Anthracene,maleic anhydride Adduct

5. The key difference between Anthracene and phenanthrene is that Anthracene is less stable compared to phenanthrene.

6. Anthracene is an organic semiconductor

7. Other names: Anthracene-9-carboxylic acid; 9-Anthroic acid; Anthracene-10-carboxylic acid; ANCA; 9-Carboxyanthracene

8. Anthracene-maleic anhydride diels-alder Adduct

9. Contact Us; Anthracene CASRN 120-12-7 DTXSID0023878

10. Articles of Anthracene are included as well.

11. Toxicity Profiles RAGs A Format for Anthracene - CAS Number 120127

12. Crude Anthracene crystallizes from a high-boiling coal-tar fraction

13. Anthracene is one of the smaller polynuclear aromatic hydrocarbons

14. Anthracene, 99%, ACROS Organics™ Structure Search; Print SDS

15. Anthracene is included in this fact sheet when available

16. Synonyms: 9-Anthroic acid, 9-Anthracenecarboxylic acid, 9-Carboxyanthracene, ANCA, anthracene-9-carboxylic acid, 9-AC cpd, Spectrum_001457, Tocris-0963, Spectrum3_001767, Spectrum4_000875, Spectrum5_001807, 9-ACA, 9-anthracene carboxylic acid, A89405_ALDRICH, BSPBio_003233, KBioGR_001569, KBioSS_001937, 9-Anthroic acid, sodium salt, Anthracene

17. Anthracene oil is used in the production of carbon black

18. Anthracene-D10-Other names: Anthracin; Green Oil; Paranaphthalene; Tetra Olive N2G; Anthracene oil; p-Naphthalene; Anthracen; Coal tar pitch volatiles:Anthracene; Sterilite hop defoliant Permanent link for this species

19. Like most PAHs, Anthracene is used to make dyes, plastics and pesticides

20. Anthraquinones: n.pl plant chemicals formed on anthracene (a triple benzene ring) skeleton

21. This optical absorption measurement of Anthracene were made by R.-C

22. Structure, properties, spectra, suppliers and links for: Anthracene, 120-12-7.

23. It is also a source of phenanthrene, Anthracene and carbazole

24. Anthracene is mainly converted to anthroquinone, a precursor to dyes

25. Anthracene is an aromatic hydrocarbon with the formula C 14 H 10

26. Anthracene 120-12-7 X -204-371-1X X XXKE-01825 U.S

27. When benz[a] Anthracene was oxidised in a reaction mixture containing ascorbic acid, ferrous sulphate and EDTA, the non-K-region dihydrodiols, trans-1,2-dihydro-1,2-dihydroxybenz[a] Anthracene and trans-3,4-dihydro-3,4-dihydroxybenz[a] Anthracene together with small amounts of the 8,9- and 10,11-dihydrodiols were formed.

28. What is Anthracene used for? Most of the PAHs are used to conduct research

29. Anthracene is used in the production of the red dye alizarin and other dyes.

30. Anthracene definition is - a crystalline tricyclic aromatic hydrocarbon C14H10 obtained from coal-tar distillation.

31. The whole mass dissolves on heating, and the Anthracene crystallizes out on cooling

32. Anthracene (ăn´thrəsēn), C14H10, solid organic compound derived from coal tar [1]

33. Anthracene (Anthracin, green oil, and para naphthalene) is common in the natural environment

34. Anthracene, also referred to as paranaphthalene or green oil, is a polycyclic aromatic hydrocarbon (PAH)

35. Anthracene oil, also called green oil, consists of three benzene rings derived from coal tar

36. Anthracene is a colorless to pale yellow, sand-like material with a bluish fluorescence

37. Anthracene is a solid polycyclic aromatic hydrocarbon (PAH) consisting of three fused benzene rings

38. Anthracene photodimer C28H20 CID 137122 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities

39. Acridine is structurally related to anthracene with one of the central CH groups is replaced by nitrogen

40. Anthracene is used as a scintillator for detectors of high energy photons, electrons and alpha particles

41. Chemsrc provides Anthracene(CAS#:120-12-7) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc

42. Anthracene is derived from coal tar and is primarily used as an intermediate in the production of dyes.

43. The crystallized Anthracene is then removed by a centrifugal separator and the process of solution in the

44. The self-assembly behaviors and charge transport properties of Cruciforms with anthracene as one axis were studied

45. Uses: Anthracene is an aromatic hydrocarbonwith three fused rings, and is obtained by the distillationof crude oils

46. No Significant Risk Level for Benz[a]Anthracene (Oral) and 7h-Dibenzo[c,g]carbazole (Oral) May 1, 2004

47. Thus Anthracene, now approaching its centenary still provides abundant material for scientific investigation and practical application.

48. Anthracene, 99%, ACROS Organics™ Click to view available options Quantity: 5g 100g 500g 2.5kg 10kg

49. Anthracene with Maleic Anhydride The Diels-Alder reaction is a member of a class of reactions called cycloadditions

50. Anthraquinone definition is - a yellow crystalline ketone C14H8O2 often derived from anthracene and used especially in the manufacture of dyes.

51. The Carcinogens in tobacco include nicotine, tar, carbon monoxide, ammonia, formaldehyde, phenols, creosote, anthracene, pyrene, hydrocyanic acid,arsenic, and lead

52. Uses Anthracene is an aromatic hydrocarbonwith three fused rings, and is obtained by the distillationof crude oils

53. Anthracene, a polycyclic aromatic hydrocarbon, is an important moiety in supramolecular chemistry due to its size and shape and photophysical properties

54. Other names: Anthracin; Green Oil; Paranaphthalene; Tetra Olive N2G; Anthracene oil; p-Naphthalene; Anthracen; Coal tar pitch volatiles:anthracene; Sterilite hop defoliant

55. Anthracene is a solid poly-cyclic aromatic hydrocarbon (PAH) of formula C14H10, consisting of three fused benzene rings

56. Benz[a]Anthracene produced positive results in an assay for mutations in Drosophila melongaster (Fahmy and Fahmy, 1973)

57. ‘In animal studies, application of Anthracene to the backs of hairless mice, followed by ultraviolet radiation exposure, resulted in enhanced dermal inflammation, compared with ultraviolet radiation alone.’ ‘A positive trend was also found between the level of Anthracene in the soil and the prevalence of reported rashes.’

58. It is prepared commercially by oxidation of Anthracene or condensation of benzene and phthalic anhydride, followed by dehydration of the condensation product

59. Anthracene has been shown to be soluble in a variety of binary and ternary mixtures of cyclohexanone, ethyl acetate, and methanol 1,2

60. Anthracene and phenanthrene are structural isomers.They have the same chemical formula, but the structure of the molecule differs from each other

61. Anthracene can be synthesized by the Elbs reaction, in which o-tolyl phenyl ketone is dehydrated at 400–450 ºC

62. Anthracene has been shown to be soluble in a variety of binary and ternary mixtures of cyclohexanone, ethyl acetate, and methanol

63. Catalogue Number: A678400: Chemical Name: Anthracene: Synonyms: Anthracin; Green Oil; NSC 7958; Paranaphthalene; Tetra Olive N2G; CAS Number: 120-12-7: Molecular Formula

64. Anthraquinone, the most important quinone derivative of Anthracene and the parent substance of a large class of dyes and pigments

65. Angelicins Aniline ortho-Anisidine paræ-Anisidine Anthanthrene Anthophyllte (see Asbestos) Anthracene Anthranilic acid ANTU (see l-Naphthylthiourea) Apholate Aramitel

66. Anthraquinone, the most important quinone derivative of anthracene and the parent substance of a large class of dyes and pigments

67. Alizarin is a dihydroxyanthraquinone that is anthracene-9,10-dione in which the two hydroxy groups are located at positions 1 and 2

68. Acridine is a polycyclic heteroarene that is anthracene in which one of the central CH groups is replaced by a nitrogen atom

69. Anthraquinone definition, a yellow, water-insoluble, crystalline powder, C14H8O2, usually derived from anthracene or phthalic anhydride: used chiefly in the manufacture of Anthraquinone dyes

70. The crude Anthracene cake is purified by treatment with the higher pyridine bases, the operation being carried out in large steam-jacketed boilers

71. Anthracene is insoluble in water but is quite soluble in carbon disulfide and somewhat soluble in ethanol, methanol, benzene, chloroform, and other organic solvents

72. This IRIS assessment for Anthracene consists of hazard identification and dose-response assessment data and provides support for EPA risk management decisions

73. Anthracene has been shown to be soluble in a variety of binary and ternary mixtures of cyclohexanone, ethyl acetate, and methanol 1,2

74. The patent of Liebermann and Carl Gräbe for the synthesis of alizarin from anthracene was filed one day before the patent of William Henry Perkin.

75. Plastics such as polyvinyltolulene can be doped with Anthracene to produce a plastic scintillator that is approximately water equivalent for use in radiation therapy dosimetry.

76. The experiment involves the photochemical dimerization of Anthracene, characterization of the product by UV, IR and NMR spectroscopy, and thermolysis of the dimer.

77. REASON FOR CITATION * Anthracene is on the Hazardous Substance List because it is regulated by OSHA and cited by ACGIH, DOT, NIOSH, DEP, HHAG, NFPA and EPA

78. What does Anthracene mean? A crystalline aromatic hydrocarbon, C14 H10 , extracted from coal tar and used in the manufacture of dyes and organic ch

79. Anthracene, a tricyclic aromatic hydrocarbon found in coal tar and used as a starting material for the manufacture of dyestuffs and in scintillation counters

80. Anthracene, also called paranaphthalene or green oil, a solid polycyclic aromatic hydrocarbon (PAH) consisting of three benzene rings derived from coal-tar, is the simplest tricyclic aromatic hydrocarbon