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Details

Stereochemistry ACHIRAL
Molecular Formula C3H10N2O
Molecular Weight 90.1243
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,3-Diamino-2-propanol

SMILES

NCC(O)CN

InChI

InChIKey=UYBWIEGTWASWSR-UHFFFAOYSA-N
InChI=1S/C3H10N2O/c4-1-3(6)2-5/h3,6H,1-2,4-5H2

HIDE SMILES / InChI

Molecular Formula C3H10N2O
Molecular Weight 90.1243
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Syntheses, structures, and magnetic properties of two kinds of unique heterometallic chains with mixed-bridging ligands of tricyanometalate and alkoxide.
2010-10-18
Efficient gene transfection using novel cationic polymers poly(hydroxyalkylene imines).
2010-09-15
In vitro and in vivo degradation of poly(1,3-diamino-2-hydroxypropane-co-polyol sebacate) elastomers.
2009-12-15
Recent advances in synthetic bioelastomers.
2009-11-20
Di-, tetra- and hexanuclear iron(III), manganese(II/III) and copper(II) complexes of Schiff-base ligands derived from 6-substituted-2-formylphenols.
2009-03-14
Quantum dots for live cell and in vivo imaging.
2009-02
Synthesis and anticancer activity of [2-hydroxy-1,3-diaminopropane-kappa 2N,N'] platinum(II) complexes.
2008-10
Glass-state amorphous salt solids formed by freeze-drying of amines and hydroxy carboxylic acids: effect of hydrogen-bonding and electrostatic interactions.
2008-06
Acyclic Schiff base salts derived from 1,3-diaminopropane and 1,3-diamino-2-hydroxypropane.
2007-10
1,3-diaminopropan-2-ol sulfonamides as potent and selective inhibitors of the glycine transporter type 1.
2007-03-15
A tetradecanuclear copper dimeric macrocyclic complex with a body-centred heptanuclear core-structure and magnetism.
2007-02-28
A new 2D network built from potassium sandwiches {K[Cu(II)3(bdap)3]2} and {(micro(1,3)-SCN)3Cu(I)(NCS)} anions: structure and magnetic behaviour.
2006-08-07
Complementarity and countercomplementarity in polynuclear copper(II) complexes with R2NCH2CH(OH)CH2NR2 (R = H, CH3): crystal structures and magnetic study.
2006-06-28
Synthesis of bis-(methyl 3,4,6-tri-O-acetyl-D-glucopyranosid-2-yl)-oxamides.
2005-07-04
Copper(II) mediated anion dependent formation of Schiff base complexes.
2005-05-30
Synthesis of segmented poly(ether urethane)s and poly(ether urethane urea)s incorporating various side-chain or backbone functionalities.
2005
Molecular design of an acid-base cooperative catalyst for RNA cleavage based on a dizinc complex.
2004-10
An unprecedented trinuclear structure involving two high-spin and one spin-crossover iron(II) centers.
2004-07-26
Covalent linkage of the type-2 and type-3 structural mimics to model the active site structure of multicopper oxidases: synthesis and magneto- structural properties of two angular trinuclear copper(II) complexes.
2003-09-08
Improved synthesis and evaluation of 17-substituted aminoalkylgeldanamycin derivatives applicable to drug delivery systems.
2001-08-20
Enhanced second harmonic generation on passing from a mono- to a dicopper(II) bis(salicylaldiminato) schiff base complex.
2001-07-16
Bis-2-oxo amide triacylglycerol analogues: a novel class of potent human gastric lipase inhibitors.
2001-02-09
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:04:22 GMT 2025
Edited
by admin
on Mon Mar 31 19:04:22 GMT 2025
Record UNII
L59259H635
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,3-Diamino-2-propanol
Systematic Name English
NSC-6070
Preferred Name English
1,2-DIAMINOPROPAN-2-OL
Systematic Name English
(3-AMINO-2-HYDROXYPROPYL)AMINE
Systematic Name English
2-HYDROXYPROPYLENEDIAMINE
Systematic Name English
2-HYDROXY-1,3-PROPANEDIAMINE
Systematic Name English
2-HYDROXY-1,3-DIAMINOPROPANE
Systematic Name English
2-PROPANOL, 1,3-DIAMINO-
Systematic Name English
1,3-DIAMINO-2-HYDROXYPROPANE
Systematic Name English
DIAMINOISOPROPANOL
Systematic Name English
Code System Code Type Description
CAS
616-29-5
Created by admin on Mon Mar 31 19:04:22 GMT 2025 , Edited by admin on Mon Mar 31 19:04:22 GMT 2025
PRIMARY
PUBCHEM
61157
Created by admin on Mon Mar 31 19:04:22 GMT 2025 , Edited by admin on Mon Mar 31 19:04:22 GMT 2025
PRIMARY
EPA CompTox
DTXSID3060663
Created by admin on Mon Mar 31 19:04:22 GMT 2025 , Edited by admin on Mon Mar 31 19:04:22 GMT 2025
PRIMARY
NSC
6070
Created by admin on Mon Mar 31 19:04:22 GMT 2025 , Edited by admin on Mon Mar 31 19:04:22 GMT 2025
PRIMARY
FDA UNII
L59259H635
Created by admin on Mon Mar 31 19:04:22 GMT 2025 , Edited by admin on Mon Mar 31 19:04:22 GMT 2025
PRIMARY
ECHA (EC/EINECS)
210-474-2
Created by admin on Mon Mar 31 19:04:22 GMT 2025 , Edited by admin on Mon Mar 31 19:04:22 GMT 2025
PRIMARY