Knowledge (XXG)

Glucic acid

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Holker, J. R. (1955). "Oxidation of Some Enediols with Selenium Dioxide".
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Except where otherwise noted, data are given for materials in their
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produced by the action of acids on cane-sugar or of
307:149 °C (300 °F; 422 K) (decomposes) 158: 89: 496: 8: 503: 489: 133: 15: 178: 424: 233: 198: 317:274 °C (525 °F; 547 K) 205:Key: NVXLIZQNSVLKPO-UHFFFAOYSA-N 7: 457: 455: 202:InChI=1S/C3H4O3/c4-1-3(6)2-5/h1-3,6H 215:Key: NVXLIZQNSVLKPO-UHFFFAOYAQ 212:InChI=1/C3H4O3/c4-1-3(6)2-5/h1-3,6H 149: 475:. You can help Knowledge (XXG) by 14: 459: 354: 263: 22: 412:Tautomeric forms of glucic acid 350:(at 25 °C , 100 kPa). 269: 257: 1: 558: 454: 344: 321: 244: 224: 189: 73: 47: 35: 30: 21: 60:2-Hydroxymalondialdehyde 467:This article about an 413: 58:2-Hydroxymalonaldehyde 411: 442:10.1039/JR9550000574 52:2-Hydroxypropanedial 50:Hydroxymalonaldehyde 37:Preferred IUPAC name 287: g·mol 18: 537:3-Hydroxypropenals 532:Secondary alcohols 414: 377:Infobox references 322:Related compounds 66:Tartronic aldehyde 41:Hydroxypropanedial 16: 484: 483: 385:Chemical compound 383: 382: 115:Interactive image 62:Glucose-reductone 549: 505: 498: 491: 463: 456: 446: 445: 429: 367: 361: 358: 357: 333:4-Hydroxynonenal 328:Related alkenals 286: 271: 265: 259: 252:Chemical formula 182: 162: 151: 137: 117: 93: 68:Triose reductone 26: 19: 557: 556: 552: 551: 550: 548: 547: 546: 512: 511: 510: 509: 452: 450: 449: 431: 430: 426: 421: 386: 379: 374: 373: 372:  ?) 363: 359: 355: 351: 338:Malondialdehyde 335: 329: 284: 274: 268: 262: 254: 240: 237: 232: 231: 220: 217: 216: 213: 207: 206: 203: 197: 196: 185: 165: 152: 140: 120: 107: 96: 83: 69: 67: 65: 63: 61: 59: 57: 56:Tartronaldehyde 55: 53: 51: 43: 42: 12: 11: 5: 555: 553: 545: 544: 539: 534: 529: 524: 514: 513: 508: 507: 500: 493: 485: 482: 481: 464: 448: 447: 423: 422: 420: 417: 416: 415: 384: 381: 380: 375: 353: 352: 348:standard state 345: 342: 341: 330: 327: 324: 323: 319: 318: 315: 309: 308: 305: 299: 298: 295: 289: 288: 282: 276: 275: 272: 266: 260: 255: 250: 247: 246: 242: 241: 239: 238: 235: 227: 226: 225: 222: 221: 219: 218: 214: 211: 210: 208: 204: 201: 200: 192: 191: 190: 187: 186: 184: 183: 175: 173: 167: 166: 164: 163: 155: 153: 145: 142: 141: 139: 138: 130: 128: 122: 121: 119: 118: 110: 108: 101: 98: 97: 95: 94: 86: 84: 79: 76: 75: 71: 70: 49: 45: 44: 40: 39: 33: 32: 28: 27: 13: 10: 9: 6: 4: 3: 2: 554: 543: 542:Alcohol stubs 540: 538: 535: 533: 530: 528: 525: 523: 522:Organic acids 520: 519: 517: 506: 501: 499: 494: 492: 487: 486: 480: 478: 474: 470: 465: 462: 458: 453: 443: 439: 435: 434:J. Chem. Soc. 428: 425: 418: 410: 406: 405: 404: 402: 398: 394: 390: 378: 371: 366: 349: 343: 340: 339: 334: 331: 326: 325: 320: 316: 314: 313:Boiling point 311: 310: 306: 304: 303:Melting point 301: 300: 296: 294: 291: 290: 283: 281: 278: 277: 256: 253: 249: 248: 243: 234: 230: 223: 209: 199: 195: 188: 181: 177: 176: 174: 172: 169: 168: 161: 157: 156: 154: 148: 144: 143: 136: 132: 131: 129: 127: 124: 123: 116: 112: 111: 109: 105: 100: 99: 92: 88: 87: 85: 82: 78: 77: 72: 46: 38: 34: 29: 25: 20: 477:expanding it 466: 451: 433: 427: 388: 387: 336: 74:Identifiers 48:Other names 17:Glucic acid 436:: 579–580. 389:Glucic acid 245:Properties 516:Categories 419:References 297:1.38 g/mL 280:Molar mass 236:O=CC(O)C=O 180:5R0YG3SBR7 126:ChemSpider 102:3D model ( 81:CAS Number 527:Aldehydes 64:Tartronal 54:Reductone 91:497-15-4 469:alcohol 401:glucose 397:alkalis 370:what is 368: ( 293:Density 160:3034155 147:PubChem 135:3650542 391:is an 365:verify 362:  285:88.062 229:SMILES 31:Names 471:is a 194:InChI 104:JSmol 473:stub 393:acid 171:UNII 438:doi 399:on 150:CID 518:: 403:. 504:e 497:t 490:v 479:. 444:. 440:: 360:N 273:3 270:O 267:4 264:H 261:3 258:C 106:)

Index


Preferred IUPAC name
CAS Number
497-15-4
JSmol
Interactive image
ChemSpider
3650542
PubChem
3034155
UNII
5R0YG3SBR7
InChI
SMILES
Chemical formula
Molar mass
Density
Melting point
Boiling point
4-Hydroxynonenal
Malondialdehyde
standard state
verify
what is
Infobox references
acid
alkalis
glucose

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