Bromate, potassium: Carcinogenic Potency Database

Bromate, potassium (CAS 7758-01-2)
SMILES, InChI and Structure are below.
Rats and Mice: Cancer Test Summary

Rat Target Sites		Mouse Target Sites		TD₅₀ (mg/kg/day)
Male	Female	Male	Female	Rat	Mouse
kid per thy	kid	kid	no positive	9.82^m	53.8

Hamsters: Cancer Test Summary

Hamster Target Sites		TD₅₀ (mg/kg/day)
Male	Female	TD₅₀ (mg/kg/day)
kid	no test	533ⁿ

Key to the Table Above

Positivity: For each chemical with a positive (carcinogenic) experiment in the Carcinogenic Potency Database (CPDB), results are included on carcinogenic potency (TD₅₀) in each species and target sites in males and females. Positivity is determined by an author’s opinion in a published paper. If all experimental results in the CDPB are negative in a sex-species group, “no positive” appears. If the CPDB has no experiments in the sex-species group, “no test” appears. The summary presents the strongest evidence of carcinogenicity in each group. If there are both positive and negative experiments in a sex-species, the negative results are ignored in this Summary Table.

Target Site Codes: kid = kidney. per = peritoneal cavity. thy = thyroid gland. Target sites are listed if any author of published experimental results concluded that tumors were induced in that organ by the test agent. If there is more than one positive experiment in a sex-species, target sites listed may be from more than one experiment, e.g. if liver and lung are both listed, then liver may have been a target in one experiment and lung in another.

TD₅₀: Our standardized measure of carcinogenic potency, TD₅₀, is the daily dose rate in mg/kg body weight/day to induce tumors in half of test animals that would have remained tumor-free at zero dose. Whenever there is more than one positive experiment in a species, the reported TD₅₀ value is a Harmonic Mean calculated using the TD₅₀ value from the most potent target site in each positive experiment.

Superscripts: m = There is more than one positive experiment in the species, and TD₅₀ values from each positive experiment are used in the calculation of the reported Harmonic mean of TD₅₀. n = No positive results in this species in the CPDB are statistically significant (p<.1).

The Carcinogenic Potency Database (CPDB) is a unique and widely used international resource of the results of 6540 chronic, long-term animal cancer tests on 1547 chemicals. The CPDB provides easy access to the bioassay literature, with qualitative and quantitative analyses of both positive and negative experiments that have been published over the past 50 years in the general literature through 2001 and by the National Cancer Institute/National Toxicology Program through 2004. The CPDB standardizes the diverse literature of cancer bioassays that vary widely in protocol, histopathological examination and nomenclature, and in the published author’s choices of what information to provide in their papers. Results are reported in the CPDB for tests in rats, mice, hamsters, dogs, and nonhuman primates.

For each experiment, information is included on species, strain, and sex of test animal; features of experimental protocol such as route of administration, duration of dosing, dose level(s) in mg/kg body weight/day, and duration of experiment; experimental results are provided on target organ, tumor type, and tumor incidence; carcinogenic potency (TD₅₀) and its statistical significance; shape of the dose-response, author’s opinion as to carcinogenicity, and literature citation.

Only tests with dosing for at least ¼ the standard lifespan of the species and experiment length at least ½ the lifespan are included in the CPDB. Only routes of administration with whole body exposure are included. Doses are standardized, average dose rates in mg/kg/day. A description of methods used in the CPDB to standardize the diverse literature of animal cancer tests is presented for: 1) Criteria for inclusion of experiments 2) Standardization of average daily dose levels and 3) TD₅₀ estimation for a standard lifespan. See Methods for other details.

TD₅₀ provides a standardized quantitative measure that can be used for comparisons and analyses of many issues in carcinogenesis. The range of TD₅₀ values across chemicals that are rodent carcinogens is more than 100 million-fold. More than half the chemicals tested are positive in at least one experiment.

A plot of all results on each experiment in the CPDB for this chemical is presented below. These results are the source information for the Cancer Test Summary table above.

Bromate, potassium: All Experiments and Citations in CPDB

The definition of each code in the plot below will appear in a pop-up window when the field name in the header line is clicked, e.g., Strain, Site, Path. Each numbered line starts a new experiment and reports protocol information in black. Average daily dose-rates per kg body weight per day are in green. Remaining lines report experimental results in blue.

Abbreviations of fields in header line: # = the line number in the plot of all CPDB chemicals; Xpo = duration of dosing; Xpt = duration of experiment; Site = tissue; Path = tumor type; DR = dose-response; AuOp = author’s opinion about carcinogenicity; LoConf, UpConf = confidence limits (99%) on TD₅₀; Inc = tumor incidence for each dose group.

See Guide to reading the plot for details on each field, using an example of one experiment.

See Help to improve readability, or to fit the plot onto the screen or a printed page.



Chemical (Synonym) CAS
# Species Sex Strain Route Xpo+Xpt PaperNum        0 Dose  1 Dose 2 Dose  3 Dose          Literature Reference or NCI/NTP:Site Path
Site Path Notes   TD50  DR Pval    AuOp LoConf UpConf   Cntrl   1 Inc  2 Inc   3 Inc                                                        Brkly Code



BROMATE, POTASSIUM   7758-01-2
828  H m syg wat 89w89 2318                          0    15.0mg  30.0mg  60.0mg  240.mg                 Takamura;srtu,32,43-46;1985
 kid rct h      533.mg * P<.2    +  202.mg n.s.s.   0/20    0/20    1/20    4/20    2/20
 liv nnd        no dre   P=1.       577.mg n.s.s.   0/20    0/20    0/20    1/20    0/20
 tba mix        no dre   P=1.       196.mg n.s.s.  10/20   14/20    7/20    8/20    9/20
829  M f b6c wat 18m24 1789                          0    75.0mg  150.mg                               Kurokawa;enhp,69,221-235;1986
 liv ade e      1.18gm * P<.05      480.mg n.s.s.   0/46    3/48    3/47
 lun mix e      1.05gm * P<.2       369.mg n.s.s.   3/46    3/48    8/47
 liv mix e      1.71gm * P<.4       449.mg n.s.s.   3/46    3/48    6/47
 lun ade e      2.03gm * P<.3       549.mg n.s.s.   2/46    1/48    5/47
 tba mix e      477.mg * P<.2       163.mg n.s.s.  15/46   16/48   22/47
830  M m b6c wat 52w53 2348m                         0    13.3mg  66.7mg  133.mg            DeAngelo;txpy,26,587-594;1998/pers.comm.
 kid tum ek     no dre   P=1.       3.79mg n.s.s.   0/7     0/7     0/7     0/6
831  M m b6c wat 78w78 2348n                         0    13.3mg  66.7mg  133.mg
 kid tum ek     no dre   P=1.       8.07mg n.s.s.   0/7     0/7     0/7     0/5
832  M m b6c wat 23m23 2348o :                       0    13.3mg  66.7mg  133.mg
 kid mix        53.8mg Z P<.008  +  20.4mg 861.mg   0/40    5/38   (3/41    1/44)
 kid rcc        92.5mg Z P<.04      28.0mg n.s.s.   0/40    3/38   (1/41    0/44)
833  M f the eat 80w80 719                           0    6.50mg  9.75mg                                Ginocchio;fctx,17,41-47;1979
 liv hem e      347.mg * P<.6    -  56.4mg n.s.s.   0/53    1/54    0/52
834  M m the eat 80w80 719                           0    6.00mg  9.00mg
 liv tum e      no dre   P=1.    -  21.3mg n.s.s.   0/35    0/46    0/53
 tba mal e      no dre   P=1.    -  63.9mg n.s.s.   1/35    1/46    0/53
835  R f f34 wat 26m26 1550                          0    14.2mg  28.3mg                               Kurokawa;jnci,71,965-972;1983
 kid mix e      13.7mg * P<.0005 +  9.90mg 19.5mg   0/47   28/50   39/49
 kid adc e      16.4mg * P<.0005    11.7mg 23.7mg   0/47   21/50   39/49
 kid ade e      87.5mg * P<.0005    49.6mg 234.mg   0/47    8/50    9/49
 thy mix e      97.6mg * P<.01      48.2mg 7.87gm   3/52   10/52   12/52
 liv mix e      no dre   P=1.       220.mg n.s.s.   2/52    1/52    2/52
 tba mix e      9.05mg * P<.003     3.96mg 62.6mg  44/52   48/52   52/52
836  R m f34 wat 26m26 1550                          0    12.4mg  22.5mg
 kid mix ev     9.62mg * P<.0005 +  6.93mg 13.9mg   3/53   32/53   46/52
 kid adc ev     12.6mg * P<.0005    9.00mg 18.6mg   3/53   24/53   44/52
 per mso ev     25.3mg * P<.0005 +  16.1mg 49.8mg   6/53   17/52   28/46
 kid ade ev     46.2mg \ P<.0005    22.5mg 124.mg   0/53   10/53   (5/52)
 liv mix ev     164.mg * P<.2       62.8mg n.s.s.   2/53    7/53    6/52
 tba mix ev     noTD50   P=1.       n.s.s. n.s.s.  53/53   53/53   52/52
837  R m f34 wat 52w52 2348m                         0    1.00mg  5.00mg  10.0mg  20.0mg    DeAngelo;txpy,26,587-594;1998/pers.comm.
 kid rca ek     16.7mg * P<.04      4.09mg n.s.s.   0/6     0/6     0/6     0/6     2/6
 tnv mso ek     36.1mg * P<.5       5.88mg n.s.s.   0/6     0/6     0/6     1/6     0/6
838  R m f34 wat 77w77 2348n                         0    1.00mg  5.00mg  10.0mg  20.0mg
 kid rca ek     15.3mg * P<.003     5.18mg 98.3mg   0/6     0/6     0/6     0/5     4/6
 tnv mso ek     15.3mg * P<.003     5.18mg 98.3mg   0/6     0/6     0/6     0/5     4/6
 thy mix ek     21.8mg * P<.01      6.53mg 1.32gm   0/6     0/6     0/6     0/5     3/6
 thy fcc ek     34.8mg * P<.04      8.51mg n.s.s.   0/6     0/6     0/6     0/5     2/6
839  R m f34 wat 23m23 2348o :                       0    1.00mg  5.00mg  10.0mg  20.0mg
 tnv mso as     11.1mg Z P<.0005 +  7.49mg 17.8mg   0/47    4/49    5/48    9/47   27/43
 kid mix as     20.8mg Z P<.0005 +  11.8mg 45.6mg   1/45    1/41    6/45    3/38   12/31
 thy mix as     22.2mg Z P<.0005 +  12.2mg 52.2mg   0/36    4/38    1/42    4/36   14/30
 kid rca as     31.1mg Z P<.0005    15.7mg 87.6mg   1/45    1/41    4/45    2/38    9/31
 thy fca as     35.2mg Z P<.0005    17.4mg 116.mg   0/36    2/38    1/42    2/36    8/30
 kid rcc as     62.2mg * P<.0005    25.6mg 239.mg   0/45    0/41    2/45    1/38    4/31
 thy fcc as     62.9mg * P<.002     25.7mg 350.mg   0/36    2/38    0/42    2/36    6/30
840  R m f3d wat  6m24 1814m                         0    6.25mg                                 Kurokawa;gann,78,358-364;1987/1986a
 kid ade e      6.67mg   P<.0005    3.08mg 18.8mg   0/19    9/19
 kid mix e      6.67mg   P<.0005 +  3.08mg 18.8mg   0/19    9/19
 per mso e      7.84mg   P<.0005    3.50mg 24.7mg   0/19    8/19
 thy fct e      11.3mg   P<.003     4.57mg 58.1mg   0/19    6/19
 kid adc e      79.2mg   P<.3       12.9mg n.s.s.   0/19    1/19
841  R m f3d wat  9m24 1814n                         0    9.38mg
 kid mix e      4.81mg   P<.0005 +  2.42mg 10.9mg   0/19   14/19
 kid ade e      5.57mg   P<.0005    2.79mg 12.9mg   0/19   13/19
 per mso e      14.0mg   P<.002     5.97mg 52.5mg   0/19    7/19
 kid adc e      16.9mg   P<.003     6.85mg 87.2mg   0/19    6/19
842  R m f3d wat 12m24 1814o                         0    12.5mg
 kid mix e      8.32mg   P<.0005 +  3.72mg 23.3mg   0/19    9/14
 kid ade e      10.1mg   P<.0005    4.41mg 30.2mg   0/19    8/14
 per mso e      19.4mg   P<.003     7.26mg 103.mg   0/19    5/14
 thy fct e      19.4mg   P<.003     7.26mg 103.mg   0/19    5/14
 kid adc e      35.5mg   P<.02      10.7mg n.s.s.   0/19    3/14
843  R m f3d wat 52w52 1814r                         0    25.0mg                                Kurokawa;gann,78,358-364;1987/19186a
 kid ade e      4.98mg   P<.002     2.66mg 14.9mg   0/8    15/26
 per mso e      25.6mg   P<.2       8.84mg n.s.s.   0/8     4/26
844  R m f3d wat 24m24 1814s                         0    25.0mg                                 Kurokawa;gann,78,358-364;1987/1986a
 per mso e      12.4mg   P<.0005    6.33mg 27.2mg   0/19   15/20
 kid mix e      28.7mg   P<.0005 +  13.3mg 81.8mg   0/19    9/20
 thy fct e      39.8mg   P<.002     17.0mg 156.mg   0/19    7/20
 kid ade e      48.0mg   P<.004     19.4mg 271.mg   0/19    6/20
 thy fca e      59.5mg   P<.008     22.5mg 895.mg   0/19    5/20
 kid adc e      105.mg   P<.04      31.8mg n.s.s.   0/19    3/20
845  R m f3d wat 24m24 1851                          0    .750mg  1.50mg  3.00mg  6.25mg  12.5mg  25.0mg   Kurokawa;jnci,77,977-982;
                                                                                                                          1986a/1987
 per mso        19.5mg * P<.0005    12.2mg 41.2mg   0/20    0/20    3/20    4/24    2/24    3/20   15/20
 kid rct        28.9mg * P<.0005 +  17.0mg 55.2mg   0/20    0/20    0/20    1/24    5/24    5/20    9/20
 kid ade        35.7mg * P<.0005 +  20.2mg 78.3mg   0/20    0/20    0/20    1/24    5/24    5/20    6/20
 thy fct e      54.7mg * P<.0005    27.4mg 136.mg   0/16    0/19    0/20    1/24    0/24    3/20    7/19
 kid adc        224.mg * P<.006     67.7mg 2.91gm   0/20    0/20    0/20    0/24    0/24    0/20    3/20
 liv nnd        53.2mg Z P<.2       15.2mg n.s.s.   2/20    0/20    4/20    7/24    0/24    6/20   (5/20)

Mutagenicity in Salmonella: positive
SMILES Code for Bromate, potassium: Br(=O)(=O)[O-].[K+]
InChI Code for Bromate, potassium: InChI=1/BrHO3.K/c2-1(3)4;/h(H,2,3,4);/q;+1/p-1
Source for SMILES and InChI: USEPA Distributed Structure-Searchable Toxicity (DSSTox) Database

Chemical Structure for Bromate, potassium:

Source for structure: National Library of Medicine ChemIDPlus

See full CPDB Summary Table on 1547 chemicals. See Full CPDB for all results on 6540 experiments of 1547 chemicals.

A complete list of CPDB chemicals, which is searchable by name or by CAS number, is available here.

For a compendium of CPDB results organized by target organ, which lists all chemicals in each species that induced tumors in each of 35 organs, see Summary Table by Target Organ.

The CPDB is available in several formats that permit printing and downloading into spreadsheets and statistical databases.

A plot of the CPDB presents results of 1547 experiments on 6540 chemicals in an easily readable format that has been used in publications of the CPDB.
A Screen version plot for use on a single computer screen, with the same data.
Excel version of the same data.
Tab-separated versions of the same data, which can be easily read into databases.

A Supplementary Dataset gives details on dosing and survival for each experiment.

Relatively precise estimates of the lower confidence limit on the TD₁₀ (LTD₁₀) are readily calculated from the TD₅₀ and its lower confidence limit, which are reported in the CPDB. For researchers and regulatory agencies interested in LTD₁₀ values, we provide them in an Excel spreadsheet.

PDF versions of our publications of analyses using the CPDB are available, organized by year and by research topic.

Carcinogenic Potency Database Project (CPDB) Home Page
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Last updated: October 3, 2007