Knowledge (XXG)

EDTMP

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Klinger, J.; Lang, M.; Sacher, F.; Brauch, H.-J.; Maier, D.; Worch, E. (1998). "Formation of Glyphosate and AMPA During Ozonation of Waters Containing Ethylenediaminetetra(methylenephosphonic acid)".
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Svara, J.; Weferling, N.; Hofmann, T. "Phosphorus Compounds, Organic," In 'Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2008.
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InChI=1S/C6H20N2O12P4/c9-21(10,11)3-7(4-22(12,13)14)1-2-8(5-23(15,16)17)6-24(18,19)20/h1-6H2,(H2,9,10,11)(H2,12,13,14)(H2,15,16,17)(H2,18,19,20)
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InChI=1/C6H20N2O12P4/c9-21(10,11)3-7(4-22(12,13)14)1-2-8(5-23(15,16)17)6-24(18,19)20/h1-6H2,(H2,9,10,11)(H2,12,13,14)(H2,15,16,17)(H2,18,19,20)
228: 437:. It shows excellent scale inhibition ability under temperature 200 °C. It functions by chelating with many metal ions. 537: 378: 547: 171: 441: 192: 434: 522: 517: 542: 527: 532: 134: 36: 209: 62: 417:
EDTMP is normally delivered as its sodium salt, which exhibits good solubility in water. Used in
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agent, the corrosion inhibition of EDTMP is 3–5 times better than that of inorganic
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Except where otherwise noted, data are given for materials in their
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and anti corrosion properties. EDTMP is the phosphonate analog of
95: 85: 409:. It is classified as a nitrogenous organic polyphosphonic acid. 406: 23: 197: 366: 50:
Ethylenediamine tetra(methylene phosphonic acid), EDTMP
395:ethylenediamine tetra(methylene phosphonic acid) 271:O=P(O)(O)CN(CP(=O)(O)O)CCN(CP(=O)(O)O)CP(=O)(O)O 159: 71: 41:{Ethane-1,2-diylbis}tetrakis(phosphonic acid) 8: 212: 137: 115: 15: 179: 452: 268: 233: 208: 128: 240:Key: NFDRPXJGHKJRLJ-UHFFFAOYSA-N 7: 250:Key: NFDRPXJGHKJRLJ-UHFFFAOYAV 150: 14: 479:Ozone: Science & Engineering 356: 22: 352:(at 25 °C , 100 kPa). 1: 465:10.1002/14356007.a19_545.pub2 444:is also derived from EDTMP. 413:Properties and applications 564: 435:Aminomethylphosphonic acid 491:10.1080/01919519808547279 346: 279: 259: 224: 55: 47: 35: 30: 21: 442:Samarium (Sm) lexidronam 440:The anti-cancer drug 433:. It can degrade to 538:Corrosion inhibitors 322:436.13 37:Preferred IUPAC name 548:Hexadentate ligands 337:Solubility in water 18: 379:Infobox references 16: 387:Chemical compound 385: 384: 193:CompTox Dashboard 97:Interactive image 555: 523:Chelating agents 518:Phosphonic acids 503: 502: 474: 468: 457: 369: 363: 360: 359: 287:Chemical formula 217: 216: 201: 199: 183: 163: 152: 141: 130: 119: 99: 75: 26: 19: 563: 562: 558: 557: 556: 554: 553: 552: 543:Water treatment 528:Tertiary amines 508: 507: 506: 476: 475: 471: 458: 454: 450: 419:Water treatment 415: 399:phosphonic acid 388: 381: 376: 375: 374:  ?) 365: 361: 357: 353: 339: 311: 307: 303: 299: 295: 289: 275: 272: 267: 266: 255: 252: 251: 248: 242: 241: 238: 232: 231: 220: 202: 195: 186: 166: 153: 122: 102: 89: 78: 65: 51: 43: 42: 12: 11: 5: 561: 559: 551: 550: 545: 540: 535: 533:Ethyleneamines 530: 525: 520: 510: 509: 505: 504: 469: 451: 449: 446: 427:anti corrosion 414: 411: 386: 383: 382: 377: 355: 354: 350:standard state 347: 344: 343: 340: 335: 332: 331: 328: 324: 323: 320: 314: 313: 309: 305: 301: 297: 293: 290: 285: 282: 281: 277: 276: 274: 273: 270: 262: 261: 260: 257: 256: 254: 253: 249: 246: 245: 243: 239: 236: 235: 227: 226: 225: 222: 221: 219: 218: 205: 203: 191: 188: 187: 185: 184: 176: 174: 168: 167: 165: 164: 156: 154: 146: 143: 142: 132: 124: 123: 121: 120: 112: 110: 104: 103: 101: 100: 92: 90: 83: 80: 79: 77: 76: 68: 66: 61: 58: 57: 53: 52: 49: 45: 44: 40: 39: 33: 32: 28: 27: 13: 10: 9: 6: 4: 3: 2: 560: 549: 546: 544: 541: 539: 536: 534: 531: 529: 526: 524: 521: 519: 516: 515: 513: 500: 496: 492: 488: 485:(2): 99–110. 484: 480: 473: 470: 466: 462: 456: 453: 447: 445: 443: 438: 436: 432: 431:polyphosphate 428: 424: 420: 412: 410: 408: 404: 400: 396: 392: 380: 373: 368: 351: 345: 341: 338: 334: 333: 329: 326: 325: 321: 319: 316: 315: 291: 288: 284: 283: 278: 269: 265: 258: 244: 234: 230: 223: 215: 211: 210:DTXSID3061689 207: 206: 204: 194: 190: 189: 182: 178: 177: 175: 173: 170: 169: 162: 158: 157: 155: 149: 145: 144: 140: 136: 133: 131: 129:ECHA InfoCard 126: 125: 118: 114: 113: 111: 109: 106: 105: 98: 94: 93: 91: 87: 82: 81: 74: 70: 69: 67: 64: 60: 59: 54: 46: 38: 34: 29: 25: 20: 482: 478: 472: 455: 439: 416: 394: 390: 389: 56:Identifiers 48:Other names 327:Appearance 280:Properties 135:100.014.410 512:Categories 448:References 421:as an anti 318:Molar mass 181:V4CP8RSX7V 108:ChemSpider 84:3D model ( 63:CAS Number 499:0191-9512 403:chelating 401:. It has 73:1429-50-1 342:limited 423:scaling 372:what is 370: ( 312: 148:PubChem 497:  367:verify 364:  330:solid 264:SMILES 31:Names 17:EDTMP 397:is a 391:EDTMP 229:InChI 161:15025 117:14301 86:JSmol 495:ISSN 425:and 407:EDTA 172:UNII 487:doi 461:doi 393:or 198:EPA 151:CID 514:: 493:. 483:20 481:. 306:12 298:20 501:. 489:: 467:. 463:: 362:Y 310:4 308:P 304:O 302:2 300:N 296:H 294:6 292:C 200:) 196:( 88:)

Index


Preferred IUPAC name
CAS Number
1429-50-1
JSmol
Interactive image
ChemSpider
14301
ECHA InfoCard
100.014.410
Edit this at Wikidata
PubChem
15025
UNII
V4CP8RSX7V
CompTox Dashboard
DTXSID3061689
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
Solubility in water
standard state
verify
what is
Infobox references
phosphonic acid
chelating
EDTA

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