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Hydroxylated lecithin

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182: 109: 24: 310: 410: 86: 205:
InChI=1S/C44H88NO10P/c1-6-8-10-12-14-15-16-17-18-19-20-21-22-26-31-35-44(49)55-40(39-54-56(50,51)53-37-36-45(3,4)5)38-52-43(48)34-30-27-23-25-29-33-42(47)41(46)32-28-24-13-11-9-7-2/h40-42,46-47H,6-39H2,1-5H3/t40?,41-,42-/m1/s1
400:, which has 3 hydroxylated fatty acid chains in it. Hydroxyl groups give these oils unique polar properties that make them useful in a variety of applications, including cosmetics, pharmaceuticals, and foods. 323: 221: 438: 196: 330: 160: 23: 396:
Fatty acids with hydroxyl groups on their hydrophobic tails are rare in nature. Compare hydroxylated lecithin to
116: 382: 104: 488: 36: 454: 409: 177: 52: 434: 350: 244: 377:. The epoxides react further with water, organic acid, or peroxy acid, to ultimately form 181: 108: 62: 301: 482: 148: 97: 390: 362: 358: 354: 397: 370: 278: 346: 229:
CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCC((CCCCCCCC)O)O)COP(=O)()OCC(C)(C)C
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Except where otherwise noted, data are given for materials in their
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oxy-2-octadecanoyloxy-propyl] 2-(trimethylammonio)ethyl phosphate
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F. D. Gunstone; John L. Harwood; Albert J. Dijkstra (2007).
165: 318: 361:. In the process, some of the organic acid becomes 147: 433:. Boca Raton, FL: CRC Press. pp. 319–320. 61: 381:. Because the natural fatty acid olefins have 8: 180: 107: 15: 421: 349:. It is made by treating lecithin with 226: 201: 176: 98: 208:Key: XSEOYPMPHHCUBN-FGYWBSQSSA-N 7: 389:, the resulting vicinal diols have 138: 373:side chains creating intermediate 271: 14: 408: 308: 262: 256: 22: 393:stereochemical configurations. 304:(at 25 °C , 100 kPa). 462:US Code of Federal Regulations 365:. The peroxy acid reacts with 265: 250: 1: 294:yellow-orange viscous liquid 353:and an organic acid such as 505: 298: 237: 217: 192: 45: 35: 30: 21: 345:is chemically modified 17:Hydroxylated Lecithin 343:Hydroxylated lecithin 286: g·mol 18: 431:The Lipid Handbook 331:Infobox references 16: 440:978-0-8493-9688-5 351:hydrogen peroxide 339:Chemical compound 337: 336: 161:CompTox Dashboard 87:Interactive image 496: 473: 472: 470: 468: 459: 455:"21 CFR 172.814" 451: 445: 444: 426: 412: 387:)-configurations 321: 315: 312: 311: 285: 273: 267: 264: 258: 252: 245:Chemical formula 185: 184: 169: 167: 151: 140: 119: 111: 100: 89: 65: 26: 19: 504: 503: 499: 498: 497: 495: 494: 493: 479: 478: 477: 476: 466: 464: 457: 453: 452: 448: 441: 428: 427: 423: 418: 406: 340: 333: 328: 327: 326:  ?) 317: 313: 309: 305: 283: 270: 261: 255: 247: 233: 230: 225: 224: 213: 210: 209: 206: 200: 199: 188: 170: 163: 154: 141: 129: 92: 79: 68: 55: 41: 12: 11: 5: 502: 500: 492: 491: 481: 480: 475: 474: 446: 439: 420: 419: 417: 414: 405: 402: 338: 335: 334: 329: 307: 306: 302:standard state 299: 296: 295: 292: 288: 287: 281: 275: 274: 268: 259: 253: 248: 243: 240: 239: 235: 234: 232: 231: 228: 220: 219: 218: 215: 214: 212: 211: 207: 204: 203: 195: 194: 193: 190: 189: 187: 186: 173: 171: 159: 156: 155: 153: 152: 144: 142: 134: 131: 130: 128: 127: 123: 121: 113: 112: 102: 94: 93: 91: 90: 82: 80: 73: 70: 69: 67: 66: 58: 56: 51: 48: 47: 43: 42: 39: 33: 32: 28: 27: 13: 10: 9: 6: 4: 3: 2: 501: 490: 489:Phospholipids 487: 486: 484: 463: 456: 450: 447: 442: 436: 432: 425: 422: 415: 413: 411: 403: 401: 399: 394: 392: 388: 386: 380: 379:vicinal diols 376: 372: 368: 364: 360: 356: 352: 348: 344: 332: 325: 320: 303: 297: 293: 290: 289: 282: 280: 277: 276: 249: 246: 242: 241: 236: 227: 223: 216: 202: 198: 191: 183: 179: 178:DTXSID1093751 175: 174: 172: 162: 158: 157: 150: 146: 145: 143: 137: 133: 132: 125: 124: 122: 120: 115: 114: 110: 106: 103: 101: 99:ECHA InfoCard 96: 95: 88: 84: 83: 81: 77: 72: 71: 64: 60: 59: 57: 54: 50: 49: 44: 38: 34: 29: 25: 20: 465:. Retrieved 461: 449: 430: 424: 407: 395: 384: 342: 341: 46:Identifiers 363:peroxy acid 359:lactic acid 291:Appearance 238:Properties 105:100.029.486 416:References 398:castor oil 371:fatty acid 279:Molar mass 74:3D model ( 53:CAS Number 37:IUPAC name 404:Synthesis 126:232-440-6 118:EC Number 63:8029-76-3 483:Category 467:25 March 375:epoxides 347:lecithin 149:57508518 369:in the 367:olefins 324:what is 322: ( 284:822.159 136:PubChem 437:  355:acetic 319:verify 316:  222:SMILES 31:Names 458:(PDF) 197:InChI 76:JSmol 469:2011 435:ISBN 391:anti 357:or 166:EPA 139:CID 485:: 460:. 269:10 260:88 254:44 471:. 443:. 385:Z 383:( 314:Y 272:P 266:O 263:N 257:H 251:C 168:) 164:( 78:)

Index

Hydroxylated Lecithin
IUPAC name
CAS Number
8029-76-3
JSmol
Interactive image
ECHA InfoCard
100.029.486
Edit this at Wikidata
EC Number
PubChem
57508518
CompTox Dashboard
DTXSID1093751
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
standard state
verify
what is
Infobox references
lecithin
hydrogen peroxide
acetic
lactic acid
peroxy acid
olefins
fatty acid

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