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Talk:Bisphenol A/GA1

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522: 499: 479: 463: 443: 432: 414: 403: 382: 366: 350: 332: 312: 296: 280: 264: 240: 204: 192: 1265:): CRC Handbook lists some organic solvents for it, but it doesn't give numerical values of the g/ml sort (I've taken the liberty of assuming solubility in benzene = solubility in toluene. No one uses benzene anymore). This that sufficient? I could try tracking down a Technical Data Sheet from a supplier, the values would likely be accurate but the refence is unlikely to stay put. 1289: 983: 822: 42: 1156:
Thanks. Knowledge's willingness to use 'ppm' as a unit is a pet peeve of mine; probably somewhere between meaningless and uninterpretable for novice readers - in this case it also focuses attention on the smallness of the solubility, rather than the utter enormity of available solvent. I'd never
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really thought of it as a green process but you are absolutely right, edits made to that effect. I did look at oxidation but I couldn't find a solid source and gave in, I suspect it biodegrades faster than any abiotic process. I expect photoxidation to be a path. I'll look again. --
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There appears to be no properties section. melting, boiling solubility and flash are in the chembox. But two have no references. Solubility in other solvents may be significant. Also available is the crystal structure. I would guess spectrum info is also available, IR, MR.
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Yes, I agree with the gallery change, but I still have a feeling that a duplicate picture feels strange. Maybe put another picture with a caption, then add the information you added in the caption of the duplicate picture in the text, then remove the picture.
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I've started responding to these comments on the same line you've written them, my additions in italics. Not the normal way of replying to things, but it might help to keep track of each point. If it's an issue I can revert my comments and try another way.
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I think I've addressed most of the comments raised so far. Outstanding are references for the density and water solubility in the chembox and a mechanism for abiotic decomposition. I'll continue to look for these. Additionally, this paper
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C + water. And apparently very generalizable (all kinds of phenols and carbonyls), which is very cool. Its difficult to beat the price of acetone. Also, for chemists, the prep is cute because phenol and acetone are coproduced by the
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Secondary refs query list: I've addresses the points at that section. About half the questioned refs have been deleted. The others are either fine or have been reinforced. I remain unsure about the ERRÎł binding study
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Not to worry. I've also become derailed by real life, and probably wont be able to finish the next round of edits until next week. I'm still going to try and finish this process; I feel like it's close to the end.
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Would be nice to know: to what does BPA degrade? It is popular and to some, heartwarming, that pollutants are degraded by organisms, but my guess is that at neutral pH in air, BPA undergoes some sort of
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I've reworked this, the statement did not appear to be supported by the refs given. Somewhat predictably, there are a range of reported binding affinities. General range is about right though.
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As mentioned to Praseodymium-141 on their talk-page. I feel that I've completed all of the improvements requested. It would be regrettable if the review stalled this late into the process.
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However, I've realised that you've put your comments before the text on my signing, so please can you try to move your future comments after the  ? That would be great.
177: 228: 80: 712:), I can't seem to find the link to the URL you provide. Regardless ref 66 is weak and I've deleted it. The statement is still referenced by a direct link to ECHA 835:
In the "Pharmacology" section, the last image is merely a repeat of one of the chembox images, and does the one about "diethylstilbestrol" fit in this context?
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The article presents a readable description of a highly topical and sometimes controversial chemical. Some thoughts that occurred to me but are not crucial:
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solubility of 300 g/ton of water (I like those practical units!) seems about right, in fact fairly high owing to the hydrophilic OH groups.
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Abiotic degradation (from Smokefoot): I've added a review ref which has a section on this. Did you want to know what it degraded into?
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Density: I still don't have a reference for this. I suspect it might be included in the crystal data refs, but I can't access those.
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Hello there, I will be reviewing this article. Note that I won't come Knowledge very often, so I might take a while to respond.
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Maybe you could add a bit more of the suggestions from Graeme Bartlett (e.g. solubility in other solvents)? Also check
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Yes. It's the website for the relevant Australian statutory authority. I have modified the ref to try and clarify this.
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Yes. It's the website for the relevant Canadian statutory authority. I have modified the ref to try and clarify this.
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Sorry for the delay, but I might not come back on this for a while. By the way I changed my username from Bli231957.
1329: 962:-Butylphenol. I would advise you to change "Para tertiary butyl phenol" to "4-tert-Butylphenol" in the piped link. 936: 747:
In the "History" section, what does this sentence mean: "He found BPA to be 1 / 37,000 as effective as estradiol"?
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That's ok, any improvements might take a while to push through anyhow. Thanks for accepting the job! Editors at
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I've checked the source code, and I didn't find a way to do that. Please could you open a new line instead?
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In the "Production" section, how does "para selective" have to do with "Arene substitution pattern"?
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I've made a start. I don't actually have access the the crystal data beyond what CCDC shows. --
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The section "Toxicity" is too short. Maybe expand it or merge it with the main section?
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for more suggestions with the refs. The comments from Smokefoot might also be helpful.
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I don't feel like there's anything that could be added. I'll mark this as a pass.
709: 947: 92: 858:. I'll try and clarify with captions - but I'm also comfortable with deletion. 581:
I'll do this GA review quite quickly, so it'll hopefully finish before July.
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https://www.foodstandards.gov.au/consumer/chemicals/bpa/Pages/default.aspx
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This page gets quite a lot of pageviews, so I might be quite strict.
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I would say maybe remove the last picture, but keep the other two.
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I had though that straightforward but I have tried to clarify.
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but I don't have access to it. Are there any other issues? --
958:-Butylpheol is a piped link, but the link is a redirect to 4- 678:
https://laws-lois.justice.gc.ca/eng/acts/C-1.68/index.html
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Yeah, I've also become derailed by real life. No worries!
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I've had a crack at improving it first. Any opinions? --
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I see you've straighten it all out. Thanks for that. --
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https://news.ncsu.edu/2012/09/wms-patisaul-amygdala/
700:(cite 66) a reliable source (it is a news article)? 1280:. I'm not a pharmacologist. It appears well cited. 460:and other media, where possible and appropriate: 710:https://www.ehn.org/bisphenol-a-2639174350.html 470:(images are tagged and non-free content have 8: 553:might also be able to provide some input. -- 1119:the prep of BPA is a premier example of a 30: 61: 33: 854:Looks like an attempt at showing the 724:for some sources that might not meet 7: 905:I've redone it as a single image. -- 708:Ref 66 points to a different site ( 990:I've restructured it a bit too. -- 946:are related to Bisphenol A in the 24: 1287: 1219:Template:Chembox Thermochemistry 1217:) looks to have information for 981: 856:structure–activity relationships 820: 520: 497: 477: 461: 441: 430: 412: 409:Fair representation without bias 401: 380: 364: 348: 330: 310: 294: 278: 262: 238: 202: 190: 1044:I think it's fine, no problem. 295: 263: 239: 203: 191: 176:for what the criteria are, and 199:(prose, spelling, and grammar) 1: 680:(cite 63) a reliable source? 660:(cite 60) a reliable source? 521: 498: 478: 462: 442: 431: 413: 402: 381: 365: 349: 331: 311: 279: 931:Maybe add a comment on how 1357: 1335:18:33, 2 August 2022 (UTC) 1324:12:18, 2 August 2022 (UTC) 1310:13:51, 18 July 2022 (UTC) 1198:12:36, 29 June 2022 (UTC) 1183:22:48, 28 June 2022 (UTC) 1167:20:04, 28 June 2022 (UTC) 1151:13:39, 28 June 2022 (UTC) 1096:11:25, 24 June 2022 (UTC) 1082:19:05, 23 June 2022 (UTC) 1068:19:04, 23 June 2022 (UTC) 1054:19:02, 23 June 2022 (UTC) 1039:21:20, 22 June 2022 (UTC) 1014:16:05, 28 June 2022 (UTC) 1000:15:14, 28 June 2022 (UTC) 972:10:25, 28 June 2022 (UTC) 915:14:37, 29 June 2022 (UTC) 901:15:43, 24 June 2022 (UTC) 886:11:23, 24 June 2022 (UTC) 872:19:11, 23 June 2022 (UTC) 845:20:09, 21 June 2022 (UTC) 811:20:09, 21 June 2022 (UTC) 784:20:09, 21 June 2022 (UTC) 757:20:09, 21 June 2022 (UTC) 738:20:17, 21 June 2022 (UTC) 634:10:43, 15 July 2022 (UTC) 620:20:39, 13 July 2022 (UTC) 605:20:15, 13 July 2022 (UTC) 591:15:45, 24 June 2022 (UTC) 577:19:33, 21 June 2022 (UTC) 563:09:38, 21 June 2022 (UTC) 544:19:28, 20 June 2022 (UTC) 161:19:20, 20 June 2022 (UTC) 1250:19:00, 4 July 2022 (UTC) 1231:13:07, 1 July 2022 (UTC) 1123:process: A + 2B --: --> 472:non-free use rationales 187:reasonably well written 180:for what they are not) 454:It is illustrated by 396:neutral point of view 345:broad in its coverage 933:Dinitrobisphenol A 652:Reliable sources: 438:No edit wars, etc. 253:factually accurate 1278:10.1093/jb/mvm158 1257:Solubility (from 1215:10.1021/jp503567c 1004:Looks great now. 492:suitable captions 273:reference section 89: 88: 1348: 1295: 1291: 1290: 1264: 989: 985: 984: 828: 824: 823: 626:Praseodymium-141 597:Praseodymium-141 524: 523: 501: 500: 481: 480: 465: 464: 445: 444: 434: 433: 416: 415: 405: 404: 384: 383: 368: 367: 352: 351: 334: 333: 314: 313: 298: 297: 289:reliable sources 282: 281: 266: 265: 242: 241: 206: 205: 194: 193: 139: 130: 111: 43:Copyvio detector 31: 18:Talk:Bisphenol A 1356: 1355: 1351: 1350: 1349: 1347: 1346: 1345: 1288: 1286: 1261:Graeme Bartlett 1258: 1206: 1175:Graeme Bartlett 1121:green chemistry 1110: 1026: 982: 980: 950:section. 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Index

Talk:Bisphenol A
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Bli231957
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19:20, 20 June 2022 (UTC)
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here
MoS
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