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Martin Ernst; Johann-Peter Melder; Franz Ingo Berger; Christian Koch (2022). "Ethanolamines and
Propanolamines".
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contain both alcohols and amino groups. Two amino acids are alkanolamines, formally speaking:
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Organic compounds with hydroxyl and amino groups on an alkane backbone
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Advanced
Organic Chemistry: Reactions, Mechanisms, and Structure
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is yet another medicinally useful derivative of ethanolamine.
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gives the corresponding 2-aminoalcohols. Examples include
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that are often generated by the reaction of amines with
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429:Ullmann's Encyclopedia of Industrial Chemistry
406:(6th ed.), New York: Wiley-Interscience,
116:2-amino-2-methyl-1-propanol is a precursor to
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69:backbone. Most alkanolamines are colorless.
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220:Simple alkanolamines are used as
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438:10.1002/14356007.a10_001.pub2
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469:Medical Subject Headings
174:is the simplest member.
432:. Weinheim: Wiley-VCH.
152:is a component of some
312:, a cardiac stimulant
27:(amino alcohols) are
282:Aminomethyl propanol
271:dimethylethanolamine
396:Smith, Michael B.;
278:-methylethanolamine
31:that contain both
413:978-0-471-72091-1
374:(adrenaline) and
369:neurotransmitters
356:Tropane alkaloids
184:organic compounds
63:functional groups
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103:Ethanolamine
89:formaldehyde
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372:epinephrine
347:Veratridine
290:propranolol
236:amino acids
168:hemiaminals
150:Sphingosine
479:Categories
383:References
310:Heptaminol
298:Isoetarine
118:oxazolines
351:veratrine
256:tyrosinol
485:Alcohols
400:(2007),
365:hormones
360:atropine
358:such as
332:peptides
328:proteins
294:pindolol
260:tyrosine
240:prolinol
222:solvents
203:O + R−NH
188:epoxides
33:hydroxyl
248:valinol
244:proline
207:→ RNHC
132:valinol
490:Amines
471:(MeSH)
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336:serine
258:(from
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250:(from
242:(from
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67:alkane
65:on an
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326:Most
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41:amino
442:ISBN
408:ISBN
367:and
349:and
338:and
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52:−NHR
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56:−NR
45:−NH
37:−OH
19:In
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215:OH
190::
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276:N
213:4
211:H
209:2
205:2
201:4
199:H
197:2
195:C
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58:2
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35:(
Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.
