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Organic acid

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Upon passive diffusion of organic acids into the bacteria, where the pH is near or above neutrality, the acids will dissociate and raise the bacteria internal pH, leading to situations that will not impair nor stop the growth of bacteria. On the other hand, the anionic part of the organic acids that
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in Petri dish. However, when they treated wood with organic acids, the acids leached out from wood and did not prevent degradation. Additionally, the organic acids' acidity may have caused chemical degradation on wood. Additionally, in a more recent study, the ecotoxicity of several natural wood
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From the use of organic acids in poultry and pigs, one can expect an improvement in performance similar to or better than that of antibiotic growth promoters, without the public health concern, a preventive effect on the intestinal problems like necrotic enteritis in chickens and
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because of their effects on bacteria. The key basic principle on the mode of action of organic acids on bacteria is that non-dissociated (non-ionized) organic acids can penetrate the bacteria cell wall and disrupt the normal physiology of certain types of bacteria that we call
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Barbero-LĂłpez and colleagues tested at the University of Eastern Finland the potential use of three organic acids, acetic, formic and propionic acids, in wood preservation. They showed a high antifungal potential against the decaying fungi tested (brown rotting fungi
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Organic acids added to feeds should be protected to avoid their dissociation in the crop and in the intestine (high pH segments) and reach far into the gastrointestinal tract, where the bulk of the bacteria population is located.
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Organic acids have been used successfully in pig production for more than 25 years. Although less research has been done in poultry, organic acids have also been found to be effective in poultry production.
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It has been well demonstrated that the state of the organic acids (undissociated or dissociated) is not important to define their capacity to inhibit the growth of bacteria, compared to undissociated acids.
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can escape the bacteria in its dissociated form will accumulate within the bacteria and disrupt few metabolic functions, leading to osmotic pressure increase, incompatible with the survival of the bacteria.
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Citric and oxalic acids are used as rust removal. As acids, they can dissolve the iron oxides, but without damaging the base metal as do stronger mineral acids. In the dissociated form, they may be able to
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acids are used for oil and gas well stimulation treatments. These organic acids are much less reactive with metals than are strong mineral acids like
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Exceptions to these solubility characteristics exist in the presence of other substituents that affect the polarity of the compound.
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is a comparatively strong acid used in organic chemistry often because it is able to dissolve in the organic reaction solvent.
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group. In biological systems, organic compounds containing these groups are generally referred to as organic acids.
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Brul, S.; Coote, P. (1999). "Preservative agents in foods, mode of action and microbial resistance mechnismes".
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Barbero-López, Aitor; Akkanen, Jarkko; Lappalainen, Reijo; Peräniemi, Sirpa; Haapala, Antti (January 2021).
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In addition to the end uses previously seen, organic acids have been tested for the following applications:
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In general, organic acids are weak acids and do not dissociate completely in water, whereas the strong
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of the acid determines its acidity. Other groups can also confer acidity, usually weakly: the
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preservatives was compared, and the results indicated a very low toxicity of propionic acid.
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Patanen, K. H.; Mroz, Z. (1999). "Organic acids for preservation". In Block, S. S. (ed.).
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infection in young pigs. Also one can expect a reduction of the carrier state for
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in food products, in particular, dairy and poultry such as ham and sausages.
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On the other hand, most organic acids are very soluble in organic solvents.
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The general structure of a few weak organic acids. From left to right:
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Barbero-LĂłpez, Aitor; Hossain, Mokbul; Haapala, Antti (2020-10-28).
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http://www.purac.com/purac_com/67cbf5490d83dc478dafbd96cab841b1.php
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The general structure of a few organic acids. From left to right:
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Biological systems create many more complex organic acids such as
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in water, but higher molecular mass organic acids, such as
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(2002). 671:, or even stronger double salts. 942:Science of the Total Environment 140: 34: 962:10.1016/j.scitotenv.2020.142013 459:A few common examples include: 432:, containing the group â€“SO 45:needs additional citations for 1: 1066:10.1016/s0168-1605(99)00072-0 884:Applications for lactic acid. 788:In nutrition and animal feeds 572:(HCl) or mixtures of HCl and 644:-lactic acids, derived from 1107: 719:Organic acids are used in 560:Simple organic acids like 583:of organic acids such as 856:List of carboxylic acids 232:Self-ionization of water 217:Hammett acidity function 903:Wood and Fiber Science 749:Listeria monocytogenes 711: 695: 1014:10.1093/japr/11.4.453 915:10.22382/wfs-2020-039 841:White rotting fungus 839:Gloeophyllum trabeum; 701: 677: 547:-Toluenesulfonic acid 247:Frustrated Lewis pair 207:Equilibrium chemistry 197:Dissociation constant 167:Acid–base homeostasis 861:Acid-base extraction 843:Trametes versicolor) 448:group â€“SH, the 242:Lewis acid catalysis 54:improve this article 1001:J. Appl. Poult. Res 954:2021ScTEn.75342013B 780:are widely used as 831:Coniophora puteana 712: 696: 162:Acid–base reaction 835:Rhodonia placenta 778:potassium lactate 721:food preservation 652: 643: 638:neurotransmitters 622:-glucuronic acids 621: 610: 574:hydrofluoric acid 570:hydrochloric acid 406: 405: 252:Chiral Lewis acid 130: 129: 122: 104: 16:(Redirected from 1098: 1077: 1048: 1029: 1027: 1026: 1017:. Archived from 1016: 982: 981: 933: 927: 926: 894: 888: 882: 821:Ongoing research 804:Escherichia coli 731:Escherichia coli 650: 641: 619: 608: 593:buffer solutions 422:carboxylic acids 414:organic compound 398: 391: 384: 365:Non-nucleophilic 192:Buffer solutions 177:Acidity function 144: 132: 125: 118: 114: 111: 105: 103: 62: 38: 30: 21: 1106: 1105: 1101: 1100: 1099: 1097: 1096: 1095: 1081: 1080: 1051: 1045: 1032: 1024: 1022: 994: 991: 989:Further reading 986: 985: 935: 934: 930: 896: 895: 891: 883: 879: 874: 852: 823: 790: 717: 704:carboxylic acid 666: 662: 630:carboxyl groups 581:conjugate bases 558: 517: 515:Characteristics 452:group, and the 435: 402: 227:Proton affinity 152:Acceptor number 135:Acids and bases 126: 115: 109: 106: 63: 61: 51: 39: 28: 23: 22: 15: 12: 11: 5: 1104: 1102: 1094: 1093: 1083: 1082: 1079: 1078: 1049: 1043: 1030: 1007:(4): 453–463. 990: 987: 984: 983: 928: 909:(4): 410–418. 889: 876: 875: 873: 870: 869: 868: 863: 858: 851: 848: 822: 819: 789: 786: 782:antimicrobials 774:sodium lactate 772:and its salts 743:C. perfringens 716: 713: 664: 660: 557: 554: 516: 513: 512: 511: 506: 501: 496: 491: 486: 481: 476: 471: 466: 442:conjugate base 433: 430:Sulfonic acids 426:carboxyl group 404: 403: 401: 400: 393: 386: 378: 375: 374: 373: 372: 367: 362: 357: 352: 347: 342: 337: 335:Brønsted–Lowry 329: 328: 321: 320: 319: 318: 313: 308: 303: 298: 293: 288: 283: 278: 276:Brønsted–Lowry 270: 269: 262: 261: 260: 259: 254: 249: 244: 239: 234: 229: 224: 219: 214: 209: 204: 199: 194: 189: 184: 179: 174: 169: 164: 159: 154: 146: 145: 137: 136: 128: 127: 69:"Organic acid" 42: 40: 33: 26: 24: 14: 13: 10: 9: 6: 4: 3: 2: 1103: 1092: 1091:Organic acids 1089: 1088: 1086: 1075: 1071: 1067: 1063: 1060:(1–2): 1–17. 1059: 1055: 1050: 1046: 1044:0-683-30740-1 1040: 1036: 1031: 1021:on 2011-03-06 1020: 1015: 1010: 1006: 1002: 998: 993: 992: 988: 979: 975: 971: 967: 963: 959: 955: 951: 947: 943: 939: 932: 929: 924: 920: 916: 912: 908: 904: 900: 893: 890: 887: 881: 878: 871: 867: 864: 862: 859: 857: 854: 853: 849: 847: 844: 840: 836: 832: 826: 820: 818: 816: 815: 814:Campylobacter 810: 806: 805: 798: 794: 787: 785: 783: 779: 775: 771: 767: 763: 759: 757: 756: 755:Campylobacter 751: 750: 745: 744: 739: 738: 733: 732: 727: 722: 714: 709: 708:sulfonic acid 705: 700: 693: 689: 685: 681: 676: 672: 670: 658: 654: 647: 639: 635: 631: 627: 624:that contain 623: 616: 612: 604: 602: 596: 594: 590: 586: 582: 577: 575: 571: 567: 563: 555: 553: 550: 548: 546: 540: 538: 534: 530: 526: 522: 521:mineral acids 514: 510: 507: 505: 502: 500: 499:Tartaric acid 497: 495: 492: 490: 487: 485: 482: 480: 477: 475: 472: 470: 467: 465: 462: 461: 460: 457: 455: 451: 447: 443: 439: 431: 428: â€“COOH. 427: 423: 419: 415: 411: 399: 394: 392: 387: 385: 380: 379: 377: 376: 371: 368: 366: 363: 361: 358: 356: 353: 351: 348: 346: 343: 341: 338: 336: 333: 332: 331: 330: 326: 322: 317: 314: 312: 309: 307: 304: 302: 299: 297: 294: 292: 289: 287: 284: 282: 279: 277: 274: 273: 272: 271: 267: 263: 258: 255: 253: 250: 248: 245: 243: 240: 238: 235: 233: 230: 228: 225: 223: 220: 218: 215: 213: 210: 208: 205: 203: 200: 198: 195: 193: 190: 188: 185: 183: 180: 178: 175: 173: 172:Acid strength 170: 168: 165: 163: 160: 158: 155: 153: 150: 149: 148: 147: 143: 139: 138: 133: 124: 121: 113: 102: 99: 95: 92: 88: 85: 81: 78: 74: 71: â€“  70: 66: 65:Find sources: 59: 55: 49: 48: 43:This article 41: 37: 32: 31: 19: 18:Organic acids 1057: 1053: 1034: 1023:. Retrieved 1019:the original 1004: 1000: 945: 941: 931: 906: 902: 892: 880: 866:Organic base 842: 838: 834: 830: 827: 824: 812: 811:species and 808: 802: 799: 795: 791: 768: 764: 760: 753: 747: 741: 735: 729: 726:pH-sensitive 725: 718: 605: 597: 578: 559: 556:Applications 551: 544: 541: 537:benzoic acid 529:lactic acids 518: 504:Butyric acid 458: 410:organic acid 409: 407: 290: 202:Donor number 116: 107: 97: 90: 83: 76: 64: 52:Please help 47:verification 44: 770:Lactic acid 657:epinephrine 634:amino acids 484:Oxalic acid 479:Citric acid 474:Formic acid 469:Acetic acid 464:Lactic acid 182:Amphoterism 1025:2018-10-08 948:: 142013. 872:References 809:Salmonella 737:Salmonella 646:catabolism 509:Folic acid 494:Malic acid 360:Superbases 306:Superacids 212:Extraction 110:April 2009 80:newspapers 970:0048-9697 923:0735-6161 817:species. 758:species. 489:Uric acid 257:ECW model 237:Titration 1085:Category 1074:10488839 978:32890867 850:See also 653:-leucine 626:hydroxyl 533:miscible 950:Bibcode 715:In food 688:alcohol 611:-lactic 601:chelate 589:lactate 585:citrate 345:Organic 291:Organic 286:Mineral 94:scholar 1072:  1041:  976:  968:  921:  752:, and 740:spp., 680:phenol 617:, and 615:citric 566:acetic 562:formic 525:formic 454:phenol 418:acidic 412:is an 355:Strong 301:Strong 96:  89:  82:  75:  67:  692:thiol 669:salts 446:thiol 416:with 350:Oxide 340:Lewis 327:types 316:Solid 296:Oxide 281:Lewis 268:types 101:JSTOR 87:books 1070:PMID 1039:ISBN 974:PMID 966:ISSN 919:ISSN 837:and 776:and 684:enol 655:and 587:and 579:The 531:are 527:and 450:enol 370:Weak 325:Base 311:Weak 266:Acid 187:Base 157:Acid 73:news 1062:doi 1009:doi 958:doi 946:753 911:doi 648:of 628:or 564:or 438:–OH 408:An 56:by 1087:: 1068:. 1058:50 1056:. 1005:11 1003:. 999:. 972:. 964:. 956:. 944:. 940:. 917:. 907:52 905:. 901:. 833:, 746:, 734:, 706:, 690:, 686:, 682:, 663:–C 636:, 613:, 595:. 222:pH 1076:. 1064:: 1047:. 1028:. 1011:: 980:. 960:: 952:: 925:. 913:: 665:7 661:1 651:L 642:D 620:D 609:L 545:p 434:2 397:e 390:t 383:v 123:) 117:( 112:) 108:( 98:· 91:· 84:· 77:· 50:. 20:)

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Organic acids

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Diagrammatic representation of the dissociation of acetic acid in aqueous solution to acetate and hydronium ions.
Acceptor number
Acid
Acid–base reaction
Acid–base homeostasis
Acid strength
Acidity function
Amphoterism
Base
Buffer solutions
Dissociation constant
Donor number
Equilibrium chemistry
Extraction
Hammett acidity function
pH
Proton affinity
Self-ionization of water

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