U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C3H9NO
Molecular Weight 75.1097
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-(Methylamino)ethanol

SMILES

CNCCO

InChI

InChIKey=OPKOKAMJFNKNAS-UHFFFAOYSA-N
InChI=1S/C3H9NO/c1-4-2-3-5/h4-5H,2-3H2,1H3

HIDE SMILES / InChI
Molecular Formula C3H9NO
Molecular Weight 75.1097
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
149124
PubMed

PubMed

TitleDatePubMed
Progesterone modulation of transmembrane helix-helix interactions between the alpha-subunit of Na/K-ATPase and phospholipid N-methyltransferase in the oocyte plasma membrane.
2010-05-25
New insights into the design of inhibitors of human S-adenosylmethionine decarboxylase: studies of adenine C8 substitution in structural analogues of S-adenosylmethionine.
2009-03-12
Recovery of choline oxidase activity by in vitro recombination of individual segments.
2008-11
Photostable, amino reactive and water-soluble fluorescent labels based on sulfonated rhodamine with a rigidized xanthene fragment.
2008
4-[6-(2-Aminoethyl)naphthalen-2-yl]benzonitriles are potent histamine H3 receptor antagonists with high CNS penetration.
2007-03-01
Hybrid materials covalently incorporated with isophorone-based dyes through sol-gel process for nonlinear optical applications.
2006-10-05
Enzymatic chemoselective synthesis of secondary-amide surfactant from N-methylethanol amine.
2005-12
Transient silylation of the guanosine O6 and amino groups facilitates N-acylation.
2004-07-22
N-methylethanolamine attenuates cardiac fibrosis and improves diastolic function: inhibition of phospholipase D as a possible mechanism.
2004-07
Preliminary evaluation of anticonvulsant activity of some 4-(benzyloxy)-benzamides.
2004-04-15
Novel reactions of phosphorus(III) azides and isocyanates: unusual modes of cycloaddition with dipolarophiles and an unexpected case of ring expansion.
2002-01-07
Patents

Patents

03984228
1
04065567
2
04070176
7
04103030
1
04174958
1
04218476
2
04654369
7
04865430
2
04914092
1
04957655
1
04959366
2
04997977
2
05007696
1
05041454
1
05044725
2
05079248
1
05133037
2
05137889
17
05142056
5
05260445
2
05278174
4
05474994
10
05563142
1
05667842
2
05670675
4
05709935
3
05726313
1
05859030
1
05962458
5
06127541
3
06248739
6
06288095
1
06589963
1
06605629
4
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:42:59 GMT 2025
Edited
by admin
on Mon Mar 31 18:42:59 GMT 2025
Record UNII
ZMQ4G4V497
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-(Methylamino)ethanol
MI  
Systematic Name English
Methylethanolamine
INCI  
INCI  
Preferred Name English
2-(Methylamino)ethanol [MI]
Common Name English
Methyl ethanolamine, N-
Common Name English
NSC-62776
Code English
Methylethylolamine
Common Name English
N-Methylethanolamine
Systematic Name English
Methyl(?-hydroxyethyl)amine
Systematic Name English
2-Methylaminoethanol [HSDB]
Common Name English
Ethanol, 2-(methylamino)-
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 489200
Created by admin on Mon Mar 31 18:42:59 GMT 2025 , Edited by admin on Mon Mar 31 18:42:59 GMT 2025
Code System Code Type Description
PUBCHEM
8016
Created by admin on Mon Mar 31 18:42:59 GMT 2025 , Edited by admin on Mon Mar 31 18:42:59 GMT 2025
PRIMARY
MERCK INDEX
m7359
Created by admin on Mon Mar 31 18:42:59 GMT 2025 , Edited by admin on Mon Mar 31 18:42:59 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID5025603
Created by admin on Mon Mar 31 18:42:59 GMT 2025 , Edited by admin on Mon Mar 31 18:42:59 GMT 2025
PRIMARY
CAS
109-83-1
Created by admin on Mon Mar 31 18:42:59 GMT 2025 , Edited by admin on Mon Mar 31 18:42:59 GMT 2025
PRIMARY
WIKIPEDIA
N-METHYLETHANOLAMINE
Created by admin on Mon Mar 31 18:42:59 GMT 2025 , Edited by admin on Mon Mar 31 18:42:59 GMT 2025
PRIMARY
NSC
62776
Created by admin on Mon Mar 31 18:42:59 GMT 2025 , Edited by admin on Mon Mar 31 18:42:59 GMT 2025
PRIMARY
FDA UNII
ZMQ4G4V497
Created by admin on Mon Mar 31 18:42:59 GMT 2025 , Edited by admin on Mon Mar 31 18:42:59 GMT 2025
PRIMARY
DAILYMED
ZMQ4G4V497
Created by admin on Mon Mar 31 18:42:59 GMT 2025 , Edited by admin on Mon Mar 31 18:42:59 GMT 2025
PRIMARY
HSDB
1128
Created by admin on Mon Mar 31 18:42:59 GMT 2025 , Edited by admin on Mon Mar 31 18:42:59 GMT 2025
PRIMARY
RXCUI
2359260
Created by admin on Mon Mar 31 18:42:59 GMT 2025 , Edited by admin on Mon Mar 31 18:42:59 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-710-0
Created by admin on Mon Mar 31 18:42:59 GMT 2025 , Edited by admin on Mon Mar 31 18:42:59 GMT 2025
PRIMARY
CHEBI
21763
Created by admin on Mon Mar 31 18:42:59 GMT 2025 , Edited by admin on Mon Mar 31 18:42:59 GMT 2025
PRIMARY
NIH
NCATS
PRIVACY NOTICE
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966