Bisphenol A

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Bisphenol A otherwise known as BPA is a manmade polymer that could have been found in most plastics until it was tested that BPA mimics estrogen. Bisphenol A was a key ingredient in the development of many polycarbonates such as DVDs, capacitors, some modern bumpers for cars, toys and water bottles. Bisphenol A has one main property that made it stand out from other competitors, it was a clear plastic. [1] This is really important because when adding the “building blocks” to a system, the system will build off of the properties of the blocks. One example would be carbon black, carbon black is great at absorbing thermal energy, however it will turn the substance black. In addition to its clear coating that Bisphenol A has, Bisphenol A is produced …show more content…

In some ways Bisphenol A is weaker than other manufactured chemicals such as estradiol, because it takes about one hundred thousand times more Bisphenol A (ppb) to stimulate breast cancer. On the other hand, it can take .23 ppt to stimulate the development of tumors. The same amount of estradiol is required to stimulate the development of tumors. Bisphenol A is dangerous because there are endocrine-signaling pathways that act as amplifiers. Bisphenol A has a strong affinity to these pathways which connect to estrogen-binding proteins. So it will have a higher rate of absorbance and will break down faster in the blood stream. In 2000 Timms was running test experiments and found that the fetuses of pregnant mice which have been fed Bisphenol A already had Bishphenol A within their system even though the fetus has a relatively low affinity as the fetus is still under …show more content…

Beer had no trace evidence of Bisphenol A, on the other hand both food cans had Bisphenol A from 5 ppb up to 121 ppb. However, after a second test on the food groups, there were readings from 5 to 77 ppb. The amount of Bisphenol A that is absorbed by food will vary to other variables, but the average human will consume about 2.2 ppb of Bisphenol A. The numbers derived in the experimentation were taken at extreme temperature of 250°F, breaking the ester bonds allowing Bisphenol A to attach itself to the

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