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Details

Stereochemistry ACHIRAL
Molecular Formula C4H11NO2
Molecular Weight 105.1356
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AMINOMETHYL PROPANEDIOL

SMILES

CC(N)(CO)CO

InChI

InChIKey=UXFQFBNBSPQBJW-UHFFFAOYSA-N
InChI=1S/C4H11NO2/c1-4(5,2-6)3-7/h6-7H,2-3,5H2,1H3

HIDE SMILES / InChI
Molecular Formula C4H11NO2
Molecular Weight 105.1356
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

2007
239
PubMed

PubMed

TitleDatePubMed
Comparative physical, mechanical and crystallographic properties of a series of gemfibrozil salts.
2010-11
SLUG: a new target of lymphoid enhancer factor-1 in human osteoblasts.
2010-02-03
Potential impact of stress activated retrotransposons on genome evolution in a marine diatom.
2009-12-22
Final amended report on safety assessment on aminomethyl propanol and aminomethyl propanediol.
2009-12-08
Mixed-valent Mn supertetrahedra and planar discs as enhanced magnetic coolers.
2008-08-20
Influence of additives including amine and hydroxyl groups on aqueous ammonia absorbent for CO2 capture.
2008-04-10
A new family of octanuclear Cu4Ln4 (Ln = Gd, Tb and Dy) spin clusters.
2008-01-07
Dirhodium(II)-catalyzed C-H amination reaction of (S)-3-(tert-butyldimethylsilyloxy)-2-methylpropyl carbamate: a facile preparation of optically active monoprotected 2-amino-2-methyl-1,3-propanediol.
2007-09
Mixed-valent cobalt spin clusters: a hexanuclear complex and a one-dimensional coordination polymer comprised of alternating hepta- and mononuclear fragments.
2006-10-30
ATR-FTIR characterization of transport properties of benzoic acid ion-pairs in silicone membranes.
2004-09-28
In vitro effect of a buffered chelating agent and neomycin or oxytetracycline on bacteria associated with diseases of fish.
2004-06-11
Electrospray mass spectrometry studies of macromolecules containing 1,3-oxazolidine moieties.
2004
Ultrathin-layer sodium dodecyl sulfate disc electrophoresis of proteins in the range from 10 to 220 kDa in homogeneous, low-concentrated polyacrylamide gels.
2003-07
Effect of steric hindrance on carbon dioxide absorption into new amine solutions: thermodynamic and spectroscopic verification through solubility and NMR analysis.
2003-04-15
Function of mutant (G1144A) tissue-nonspecific ALP gene from hypophosphatasia.
2002-11
Effect of a basic organic excipient on the dissolution of diclofenac salts.
2002-10
Preparation and characterisation of a range of diclofenac salts.
2001-09-11
Patents

Patents

04082892
1
04632922
1
04882358
2
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:28:03 GMT 2025
Edited
by admin
on Mon Mar 31 19:28:03 GMT 2025
Record UNII
CZ7BU4QZJZ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AMINOMETHYL PROPANEDIOL
INCI  
INCI  
Official Name English
2-AMINO-2-METHYL-1,3-PROPANEDIOL
MI  
Preferred Name English
2-AMINO-2-METHYL-1,3-PROPANEDIOL [MI]
Common Name English
1,3-PROPANEDIOL, 2-AMINO-2-METHYL-
Systematic Name English
1,1-DI(HYDROXYMETHYL)ETHYLAMINE
Systematic Name English
AMINOGLYCOL
Common Name English
AMEDIOL
Common Name English
AMMEDIOL
Common Name English
1,3-DIHYDROXY-2-AMINO-2-METHYLPROPANE
Systematic Name English
2-METHYL-2-AMINO-1,3-PROPANEDIOL
Systematic Name English
NSC-6364
Code English
1,3-DIHYDROXY-2-METHYL-2-PROPYLAMINE
Systematic Name English
AMPD
Common Name English
2-AMINO-2-METHYLPROPAN-1,3-DIOL
Systematic Name English
Code System Code Type Description
CAS
115-69-5
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
DAILYMED
CZ7BU4QZJZ
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
FDA UNII
CZ7BU4QZJZ
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
NSC
6364
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
MESH
C019250
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
MERCK INDEX
m1715
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY Merck Index
ECHA (EC/EINECS)
204-100-7
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
EPA CompTox
DTXSID7059430
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
CHEBI
991
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
PUBCHEM
1531
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY
RXCUI
1307680
Created by admin on Mon Mar 31 19:28:03 GMT 2025 , Edited by admin on Mon Mar 31 19:28:03 GMT 2025
PRIMARY RxNorm
NIH
NCATS
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