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
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
| Molecular Weight | 109.13 g/mol |
|---|---|
| Molecular Formula | C6H7NO |
| XLogP3 | 0.2 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 109.052763847 g/mol |
| Monoisotopic Mass | 109.052763847 g/mol |
| Topological Polar Surface Area | 46.2 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 74.9 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
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
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