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2D Structure
Also known as: 591-27-5, M-aminophenol, 3-hydroxyaniline, M-hydroxyaniline, Phenol, 3-amino-, 3-amino-1-hydroxybenzene
Molecular Formula
C6H7NO
Molecular Weight
109.13  g/mol
InChI Key
CWLKGDAVCFYWJK-UHFFFAOYSA-N
FDA UNII
L3WTS6QT82

1 2D Structure

2D Structure

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
3-aminophenol
2.1.2 InChI
InChI=1S/C6H7NO/c7-5-2-1-3-6(8)4-5/h1-4,8H,7H2
2.1.3 InChI Key
CWLKGDAVCFYWJK-UHFFFAOYSA-N
2.1.4 Canonical SMILES
C1=CC(=CC(=C1)O)N
2.2 Other Identifiers
2.2.1 UNII
L3WTS6QT82
2.3 Synonyms
2.3.1 MeSH Synonyms

1. 3-aminophenol Acetate

2. 3-aminophenol Hydrochloride

3. 3-aminophenol Monopotassium Salt

4. 3-aminophenol Monosodium Salt

5. 3-aminophenol Sulfate

6. M-aminophenol

7. Meta-aminophenol

2.3.2 Depositor-Supplied Synonyms

1. 591-27-5

2. M-aminophenol

3. 3-hydroxyaniline

4. M-hydroxyaniline

5. Phenol, 3-amino-

6. 3-amino-1-hydroxybenzene

7. M-hydroxyaminobenzene

8. Fouramine Eg

9. Futramine Eg

10. 1-amino-3-hydroxybenzene

11. Fourrine Eg

12. 3-amino-phenol

13. Pelagol Eg

14. Tertral Eg

15. Furro Eg

16. Renal Eg

17. Ursol Eg

18. Fourrine 65

19. Nako Teg

20. Phenol, M-amino-

21. Zoba Eg

22. M-hydroxyphenylamine

23. Basf Ursol Eg

24. M-aminofenol

25. C.i. Oxidation Base 7

26. C.i. 76545

27. Nsc 1546

28. Mfcd00007786

29. 3-azaniumylphenolate

30. 3-hydroxybenzenamine

31. Ci 76545

32. L3wts6qt82

33. Phenol, 3-amino-, Homopolymer

34. Chebi:28924

35. Nsc-1546

36. Ci Oxidation Base 7

37. M-aminofenol [czech]

38. Meta-aminophenol

39. 52984-90-4

40. Ccris 4145

41. Hsdb 2586

42. Meta Amino Phenol

43. Einecs 209-711-2

44. Unii-l3wts6qt82

45. Ai3-14871

46. M-amino-phenol

47. 3-amino Phenol

48. 3-hydroxy-aniline

49. Covastyle Map

50. Colorex Map

51. Jarocol Map

52. Amino-3-hydroxybenzene

53. Rodol Eg

54. Oristar Aph3

55. 3-aminophenol, 98%

56. Phenol,3-amino

57. Dsstox_cid_4497

58. Wln: Zr Cq

59. Ec 209-711-2

60. M-aminophenol [mi]

61. Dsstox_rid_77427

62. Dsstox_gsid_24497

63. Schembl35586

64. M-aminophenol [inci]

65. Mls002415740

66. Un 2512 (salt/mix)

67. 3-aminophenol [hsdb]

68. Bidd:er0564

69. Bidd:gt0645

70. Chembl269755

71. M-aminophenol [usp-rs]

72. 3-aminophenol, Puriss., 99%

73. Dtxsid3024497

74. Nsc1546

75. Hms3039l12

76. Zinc157527

77. Act07279

78. Str01006

79. Tox21_200706

80. Bdbm50428384

81. Stk258727

82. Akos000118984

83. M-aminophenol [un2512] [poison]

84. Am10639

85. Ps-9279

86. Ncgc00091247-01

87. Ncgc00091247-02

88. Ncgc00258260-01

89. 3-aminophenol 100 Microg/ml In Methanol

90. 3-aminophenol, Purum, >=98.0% (t)

91. Bp-13467

92. Cas-591-27-5

93. Smr001370906

94. 3-aminophenol 1000 Microg/ml In Methanol

95. Db-024153

96. Mesalazine Impurity B [ep Impurity]

97. A0383

98. Ft-0615052

99. Vu0606052-1

100. A-6901

101. C05058

102. 3-aminophenol, Pestanal(r), Analytical Standard

103. Q779427

104. J-511713

105. F3228-0191

106. Z319217206

107. M-aminophenol, United States Pharmacopeia (usp) Reference Standard

108. 3-aminophenol, Pharmaceutical Secondary Standard; Certified Reference Material

109. K5v

2.4 Create Date
2004-09-16
3 Chemical and Physical Properties
Molecular Weight 109.13 g/mol
Molecular Formula C6H7NO
XLogP30.2
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Exact Mass109.052763847 g/mol
Monoisotopic Mass109.052763847 g/mol
Topological Polar Surface Area46.2 Ų
Heavy Atom Count8
Formal Charge0
Complexity74.9
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count1
4 Pharmacology and Biochemistry
4.1 Metabolism/Metabolites

Yields m-acetamidophenol in Cordyceps. Yields 4-aminocatechol in rabbit. /From table/

Goodwin, B.L. Handbook of Intermediary Metabolism of Aromatic Compounds. New York: Wiley, 1976., p. A-48


Yields m-aminophenyl-beta-d-glucoside in housefly & in locust. Yields m-aminophenyl-beta-d-glucuronide in rabbit. /From table/

Goodwin, B.L. Handbook of Intermediary Metabolism of Aromatic Compounds. New York: Wiley, 1976., p. A-48


Yields m-aminophenyl sulfate in rat, in hen, in tick, in housefly. /From table/

Goodwin, B.L. Handbook of Intermediary Metabolism of Aromatic Compounds. New York: Wiley, 1976., p. A-48