Knowledge

Tripropylene

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Johan A. Martens, Wim H. Verrelst, Georges M. Mathys, Stephen H. Brown, Pierre A. Jacobs "Tailored Catalytic Propene Trimerization over Acidic Zeolites with Tubular Pores" Angewandte Chemie International Edition Angewandte Chemie International Edition 2005, Volume 44, Issue 35, pages 5687–5690.
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In this process, two double bonds are lost and one is retained as illustrated by the isomer shown in the figure. The reaction is catalyzed by acids, such as
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G. R. Lappin, L. H. Nemec, J. D. Sauer, J. D. Wagner "Olefins, Higher" in Kirk-Othmer Encyclopedia of Chemical Technology, 2010.
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https://www.exxonmobilchemical.com/dfsmedia/f743208d804841f6ab89a60202cc3f56/3035-source?extension=pdf/options/download
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CH), which attacks another propylene unit, generating a new carbocation, etc. This kind of process affords mixtures (C
149: 500: 358: 420:. A variety of catalysts have been explored. The reaction proceeds via the formation of a carbocation ((CH 80: 166: 417: 37: 517: 378: 101: 552: 530: 513: 448: 301: 233: 47: 386: 55: 170: 329: 546: 290: 280: 194:
4,6-Dimethyl-1-heptene:: InChI=1S/C9H18/c1-5-6-9(4)7-8(2)3/h5,8-9H,1,6-7H2,2-4H3
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Except where otherwise noted, data are given for materials in their
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ExxonMobil Chemical Product Safety Summary], exxonmobilchemical.com
79: 68: 154: 346: 459:are produced by alkylation of aromatic substrates. 126: 54: 46: 285:−93.5 °C (−136.3 °F; 179.7 K) 8: 518:10.1002/0471238961.1512050612011616.a01.pub2 218:4,6-Dimethyl-1-heptene:: CC(C)CC(C)CC=C 169: 100: 15: 481: 215: 190: 165: 295:156 °C (313 °F; 429 K) 197:Key: FSWNZCWHTXTQBY-UHFFFAOYSA-N 7: 322:23 °C (73 °F; 296 K) 116: 377:, is usually sold as a mixture of 14: 447:, propylene trimer is used as an 336: 22: 385:. This mixture is obtained by 332:(at 25 °C , 100 kPa). 125:4,6-Dimethyl-1-heptene:: 99:4,6-Dimethyl-1-heptene:: 78:4,6-Dimethyl-1-heptene:: 53:4,6-Dimethyl-1-heptene:: 1: 574: 257:126.24 g/mol 326: 311: 226: 206: 181: 30: 21: 535:10.1002/anie.200463045 471:- the linear analogue 558:Trimers (chemistry) 418:polyphosphoric acid 302:Solubility in water 18: 379:structural isomers 359:Infobox references 265:colourless liquid 16: 501:Tripropylene MSDS 367:Chemical compound 365: 364: 150:CompTox Dashboard 81:Interactive image 565: 537: 526: 520: 510: 504: 498: 492: 486: 449:alkylating agent 375:propylene trimer 373:, also known as 349: 343: 340: 339: 234:Chemical formula 174: 173: 158: 156: 130: 118: 104: 83: 58: 50: 26: 19: 573: 572: 568: 567: 566: 564: 563: 562: 543: 542: 541: 540: 527: 523: 511: 507: 503:, chemexper.net 499: 495: 487: 483: 478: 465: 451:. A number of 439: 435: 431: 427: 423: 412: 408: 404: 400: 387:oligomerization 368: 361: 356: 355: 354:  ?) 345: 341: 337: 333: 304: 246: 242: 236: 222: 219: 214: 213: 202: 199: 198: 195: 189: 188: 177: 159: 152: 133: 119: 107: 86: 72: 61: 40: 12: 11: 5: 571: 569: 561: 560: 555: 545: 544: 539: 538: 521: 505: 493: 480: 479: 477: 474: 473: 472: 464: 461: 437: 433: 429: 425: 421: 414: 413: 410: 406: 402: 398: 366: 363: 362: 357: 335: 334: 330:standard state 327: 324: 323: 320: 314: 313: 309: 308: 305: 300: 297: 296: 293: 287: 286: 283: 277: 276: 273: 267: 266: 263: 259: 258: 255: 249: 248: 244: 240: 237: 232: 229: 228: 224: 223: 221: 220: 217: 209: 208: 207: 204: 203: 201: 200: 196: 193: 192: 184: 183: 182: 179: 178: 176: 175: 167:DTXSID50540820 162: 160: 148: 145: 144: 141: 135: 134: 132: 131: 122: 120: 112: 109: 108: 106: 105: 96: 94: 88: 87: 85: 84: 75: 73: 66: 63: 62: 60: 59: 51: 43: 41: 36: 33: 32: 28: 27: 13: 10: 9: 6: 4: 3: 2: 570: 559: 556: 554: 551: 550: 548: 536: 532: 525: 522: 519: 515: 509: 506: 502: 497: 494: 490: 485: 482: 475: 470: 467: 466: 462: 460: 458: 454: 450: 446: 441: 419: 396: 395: 394: 392: 388: 384: 380: 376: 372: 360: 353: 348: 331: 325: 321: 319: 316: 315: 310: 306: 303: 299: 298: 294: 292: 291:Boiling point 289: 288: 284: 282: 281:Melting point 279: 278: 274: 272: 269: 268: 264: 261: 260: 256: 254: 251: 250: 238: 235: 231: 230: 225: 216: 212: 205: 191: 187: 180: 172: 168: 164: 163: 161: 151: 147: 146: 142: 140: 137: 136: 129: 124: 123: 121: 115: 111: 110: 103: 98: 97: 95: 93: 90: 89: 82: 77: 76: 74: 70: 65: 64: 57: 52: 49: 45: 44: 42: 39: 35: 34: 29: 25: 20: 17:Tripropylene 524: 508: 496: 484: 442: 415: 374: 371:Tripropylene 370: 369: 31:Identifiers 453:surfactants 443:Like other 318:Flash point 275:1.022 g/mL 262:Appearance 227:Properties 547:Categories 476:References 457:lubricants 253:Molar mass 92:ChemSpider 67:3D model ( 48:13987-01-4 38:CAS Number 307:very low 139:UN number 56:7379-69-3 469:1-Nonene 463:See also 312:Hazards 128:13437467 102:10618997 553:Alkenes 445:alkenes 391:propene 352:what is 350: ( 271:Density 247: 114:PubChem 383:nonene 347:verify 344:  211:SMILES 405:→ C 186:InChI 143:2057 69:JSmol 455:and 531:doi 514:doi 397:3 C 389:of 381:of 155:EPA 117:CID 549:: 440:. 411:18 393:: 245:18 533:: 516:: 438:n 436:) 434:6 432:H 430:3 426:2 424:) 422:3 409:H 407:9 403:6 401:H 399:3 342:Y 243:H 241:9 239:C 157:) 153:( 71:)

Index


CAS Number
13987-01-4
7379-69-3
JSmol
Interactive image
ChemSpider
10618997
PubChem
13437467
UN number
CompTox Dashboard
DTXSID50540820
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InChI
SMILES
Chemical formula
Molar mass
Density
Melting point
Boiling point
Solubility in water
Flash point
standard state
verify
what is
Infobox references
structural isomers
nonene
oligomerization

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