Knowledge

Alkanolamine

Source 📝

122: 155: 90: 137: 108: 439: 121: 89: 154: 422: 456: 437:
Martin Ernst; Johann-Peter Melder; Franz Ingo Berger; Christian Koch (2022). "Ethanolamines and Propanolamines".
136: 17: 412: 479: 436: 345:
contain both alcohols and amino groups. Two amino acids are alkanolamines, formally speaking:
292: 285: 281: 475: 8: 495: 452: 418: 31: 107: 444: 379: 366: 239: 194: 73: 39: 448: 500: 386: 350: 489: 326: 236: 182: 164: 95: 296: 277: 113: 99: 408: 382: 357: 300: 160: 320: 308: 246: 178: 27:
Organic compounds with hydroxyl and amino groups on an alkane backbone
361: 266: 128: 370: 304: 270: 250: 43: 375: 342: 338: 258: 254: 232: 198: 142: 414:
Advanced Organic Chemistry: Reactions, Mechanisms, and Structure
346: 262: 146: 77: 311:
is yet another medicinally useful derivative of ethanolamine.
406: 51: 249:
gives the corresponding 2-aminoalcohols. Examples include
197:
that are often generated by the reaction of amines with
314: 487: 295:. Two popular drugs, often called alkanolamine 440:Ullmann's Encyclopedia of Industrial Chemistry 417:(6th ed.), New York: Wiley-Interscience, 127:2-amino-2-methyl-1-propanol is a precursor to 80:backbone. Most alkanolamines are colorless. 193:2-Aminoalcohols are an important class of 478:at the U.S. National Library of Medicine 299:, are members of this structural class: 14: 488: 430: 245:Hydrogenation or hydride reduction of 177:1-Aminoalcohols are better known as 98:, from the reaction of ammonia with 332: 24: 315:1,3-, 1,4-, and 1,5-amino alcohols 188: 172: 25: 512: 469: 231:Simple alkanolamines are used as 153: 135: 120: 106: 88: 235:, synthetic intermediates, and 145:is derived from the amino acid 400: 13: 1: 449:10.1002/14356007.a10_001.pub2 393: 7: 10: 517: 480:Medical Subject Headings 185:is the simplest member. 443:. Weinheim: Wiley-VCH. 163:is a component of some 323:, a cardiac stimulant 38:(amino alcohols) are 293:Aminomethyl propanol 282:dimethylethanolamine 407:Smith, Michael B.; 289:-methylethanolamine 42:that contain both 424:978-0-471-72091-1 385:(adrenaline) and 380:neurotransmitters 367:Tropane alkaloids 195:organic compounds 74:functional groups 40:organic compounds 32:organic chemistry 16:(Redirected from 508: 463: 462: 434: 428: 427: 404: 333:Natural products 227: 157: 139: 124: 110: 92: 71: 64: 60: 49: 21: 516: 515: 511: 510: 509: 507: 506: 505: 486: 485: 472: 467: 466: 459: 435: 431: 425: 405: 401: 396: 389:(noradrenaline) 335: 317: 225: 221: 217: 213: 209: 205: 191: 189:2-Aminoalcohols 175: 173:1-Aminoalcohols 168: 158: 149: 140: 131: 125: 116: 111: 102: 93: 70: 66: 62: 59: 55: 47: 28: 23: 22: 15: 12: 11: 5: 514: 504: 503: 498: 484: 483: 476:Amino+Alcohols 471: 470:External links 468: 465: 464: 458:978-3527306732 457: 429: 423: 398: 397: 395: 392: 391: 390: 387:norepinephrine 373: 364: 351:hydroxyproline 334: 331: 330: 329: 327:Propanolamines 324: 316: 313: 229: 228: 223: 219: 215: 211: 207: 190: 187: 174: 171: 170: 169: 159: 152: 150: 141: 134: 132: 126: 119: 117: 112: 105: 103: 94: 87: 85: 68: 57: 26: 9: 6: 4: 3: 2: 513: 502: 499: 497: 494: 493: 491: 481: 477: 474: 473: 460: 454: 450: 446: 442: 441: 433: 426: 420: 416: 415: 410: 403: 399: 388: 384: 381: 377: 374: 372: 368: 365: 363: 359: 356: 355: 354: 352: 348: 344: 340: 328: 325: 322: 319: 318: 312: 310: 306: 302: 298: 297:beta blockers 294: 290: 288: 283: 279: 276:Key members: 274: 272: 268: 264: 260: 256: 252: 248: 243: 241: 238: 234: 204: 203: 202: 200: 196: 186: 184: 183:Methanolamine 180: 166: 165:cell membrane 162: 156: 151: 148: 144: 138: 133: 130: 123: 118: 115: 109: 104: 101: 97: 96:Methanolamine 91: 86: 84:Alkanolamines 83: 82: 81: 79: 75: 53: 45: 41: 37: 36:alkanolamines 33: 19: 18:Amino alcohol 438: 432: 413: 409:March, Jerry 402: 336: 286: 278:ethanolamine 275: 244: 237:high-boiling 230: 192: 176: 114:Ethanolamine 100:formaldehyde 35: 29: 383:epinephrine 358:Veratridine 301:propranolol 247:amino acids 179:hemiaminals 161:Sphingosine 490:Categories 394:References 321:Heptaminol 309:Isoetarine 129:oxazolines 362:veratrine 267:tyrosinol 496:Alcohols 411:(2007), 376:hormones 371:atropine 369:such as 343:peptides 339:proteins 305:pindolol 271:tyrosine 251:prolinol 233:solvents 214:O + R−NH 199:epoxides 44:hydroxyl 259:valinol 255:proline 218:→ RNHC 143:valinol 501:Amines 482:(MeSH) 455:  421:  347:serine 269:(from 263:valine 261:(from 253:(from 147:valine 78:alkane 76:on an 65:, and 50:) and 337:Most 240:bases 52:amino 453:ISBN 419:ISBN 378:and 360:and 349:and 341:and 63:−NHR 445:doi 307:. 273:). 265:), 257:), 67:−NR 56:−NH 48:−OH 30:In 492:: 451:. 353:. 303:, 291:, 284:, 280:, 242:. 226:OH 201:: 181:. 72:) 61:, 34:, 461:. 447:: 287:N 224:4 222:H 220:2 216:2 212:4 210:H 208:2 206:C 167:. 69:2 58:2 54:( 46:( 20:)

Index

Amino alcohol
organic chemistry
organic compounds
hydroxyl
amino
functional groups
alkane
Methanolamine, from the reaction of ammonia with formaldehyde
Methanolamine
formaldehyde
Ethanolamine
Ethanolamine
2-amino-2-methyl-1-propanol is a precursor to oxazolines
oxazolines
valinol is derived from the amino acid valine
valinol
valine
Sphingosine is a component of some cell membrane.
Sphingosine
cell membrane
hemiaminals
Methanolamine
organic compounds
epoxides
solvents
high-boiling
bases
amino acids
prolinol
proline

Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.