1. 4-nitrobenzoic Acid, Silver Salt
2. 4-nitrobenzoic Acid, Sodium Salt
3. P-nitrobenzoic Acid
4. Para-nitrobenzoic Acid
1. P-nitrobenzoic Acid
2. 62-23-7
3. Benzoic Acid, 4-nitro-
4. Nitrodracylic Acid
5. 4-nitrodracylic Acid
6. 1-carboxy-4-nitrobenzene
7. P-nitrobenzenecarboxylic Acid
8. Benzoic Acid, P-nitro-
9. 4-nitro-benzoic Acid
10. Kyselina P-nitrobenzoova
11. P-nitrodracylic Acid
12. Para-nitrobenzoic Acid
13. Nsc 7707
14. Mfcd00007352
15. P-nitro Benzoic Acid
16. G83nwr61ow
17. Chembl101263
18. Chebi:262350
19. Nsc-7707
20. Dsstox_cid_966
21. Dsstox_rid_75894
22. Dsstox_gsid_20966
23. Cas-62-23-7
24. 4-nitrobenzoicacid
25. Ccris 1185
26. Hsdb 2140
27. Kyselina P-nitrobenzoova [czech]
28. Einecs 200-526-2
29. Unii-g83nwr61ow
30. Ai3-00149
31. P-nitro-benzoicacid
32. 4nb
33. P-carboxynitrobenzene
34. P-nitro-benzoic Acid
35. 4- Nitrobenzoic Acid
36. 4-nitro Benzoic Acid
37. Wln: Wnr Dvq
38. Ec 200-526-2
39. 4-nitrobenzoic Acid, 98%
40. Schembl43476
41. 4-nitrobenzenecarboxylic Acid
42. Para Nitrobenzoic Acid
43. Mls002454442
44. Dtxsid3020966
45. Schembl15630318
46. Amy8937
47. Nsc7707
48. Hms3041d05
49. Str01385
50. Zinc1688307
51. Tox21_201258
52. Tox21_300131
53. Bdbm50405310
54. Stl168880
55. 4-nitrobenzoic Acid, Puriss., 99%
56. 4-nitrobenzoic Acid [usp-rs]
57. Akos000118872
58. Akos015831344
59. Akos024268501
60. Cs-w020075
61. Pb43175
62. Ncgc00091607-01
63. Ncgc00091607-02
64. Ncgc00091607-03
65. Ncgc00091607-04
66. Ncgc00253917-01
67. Ncgc00258810-01
68. Ac-10993
69. Bp-30196
70. Smr001252222
71. Sy002161
72. A8599
73. Ft-0619175
74. N0156
75. C18625
76. D70606
77. 4-nitrobenzoic Acid, Purum, >=98.0% (hplc)
78. Ae-562/40227261
79. 4-nitrobenzoic Acid, Vetec(tm) Reagent Grade, 98%
80. Q2823227
81. W-105029
82. 4-aminobenzoic Acid Impurity A [ep Impurity]
83. Z57127484
84. F2191-0089
85. 4-nitrobenzoic Acid, United States Pharmacopeia (usp) Reference Standard
| Molecular Weight | 167.12 g/mol |
|---|---|
| Molecular Formula | C7H5NO4 |
| XLogP3 | 1.9 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 1 |
| Exact Mass | 167.02185764 g/mol |
| Monoisotopic Mass | 167.02185764 g/mol |
| Topological Polar Surface Area | 83.1 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 190 |
| 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 |
POSSIBLE ABSORPTION FROM SKIN OF GUINEA PIG. /FROM TABLE/
Patty, F. (ed.). Industrial Hygiene and Toxicology: Volume II: Toxicology. 2nd ed. New York: Interscience Publishers, 1963., p. 1838
EXCRETED PRINCIPALLY UNCHANGED, ABOUT 10-20% REDUCED TO P-AMINOBENZOIC ACID AND ACETYLATED. /FROM TABLE/
Patty, F. (ed.). Industrial Hygiene and Toxicology: Volume II: Toxicology. 2nd ed. New York: Interscience Publishers, 1963., p. 1838
THE NITRO GROUP OF P-NITROBENZOIC ACID IS REDUCED BY LIVER MICROSOMAL ENZYMES TO P-AMINOBENZOIC ACID. /FROM TABLE/
Hayes, W. J., Jr. Toxicology of Pesticides Baltimore: Williams & Wilkins, 1975., p. 112
Eleven strains of Pseudomonas were isolated by selective enrichment on 4-nitrotoluene. They an utilized 4-nitrotoluene, 4-nitrobenzyl alcohol or 4-nitrobenzoate as sole sources of carbon and nitrogen. One strain, TW3, was used for more detailed studies. 4-Nitrotoluene-grown cells of TW3 take up O2 when incubated in the presence of 4-nitrobenzyl alcohol, 4-nitrobenzaldehyde and 4-nitrobenzoate. PHLC analysis of culture supernatants showed that 4-nitrobenzaldehyde and 4-nitrobenzoate were formed when 4-nitrotoluene-grown cells were incubated with 4-nitrobenzyl alcohol, whereas only 4-nitrobenzoate was found when they were incubated with 4-nitrobenzaldehyde. ... It is proposed that the pathway for 4-nitrotoluene catabolism proceeds via 4-nitrobenzyl alcohol, 4-nitrobenzaldehyde and 4-nitrobenzoate and ultimately to protocatechuate with release of the nitro group as ammonium.
PMID:8245826 Rhys-Williams W et al; J Gen Microbiol 139 (9): 1967-72 (1993)
The metabolism of the nitrotoluenes was compared in hepatocytes isolated from male Fischer 344 rats. ... Metabolites were separated by reverse phase HPLC and identified by coelution with standards on HPLC, specific enzyme hydrolysis and GC-MS analysis. 4-Nitrotoluene was metabolized to s-(4-nitrobenzyl) glutathione (68%), 4-nitrobenzyl alcohol (12%), sulfate and glucuronide conjugates of 4-nitrobenzyl alcohol (6%) and 4-nitrobenzoic acid (2%) (expressed as percentage of total metabolism).
PMID:6141911 Debethizy JD, Rickert DE; Drug Metab Dispos 12 (1): 45-50 (1984)
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