Skip to Content
Merck
All Photos(1)

Documents

D18609

Sigma-Aldrich

1,3-Diamino-2-propanol

95%

Synonym(s):

2-Hydroxy-1,3-propanediamine, 1,3-Diamino-2-hydroxypropane

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
NH2CH2CH(OH)CH2NH2
CAS Number:
616-29-5
Molecular Weight:
90.12
Beilstein:
741859
EC Number:
210-474-2
MDL number:
MFCD00008142
UNSPSC Code:
12352100
PubChem Substance ID:
24893556
NACRES:
NA.22

Assay

95%

form

solid

mp

40-44 °C (lit.)

SMILES string

NCC(O)CN

InChI

1S/C3H10N2O/c4-1-3(6)2-5/h3,6H,1-2,4-5H2

InChI key

UYBWIEGTWASWSR-UHFFFAOYSA-N

Gene Information

rat ... Grin2a(24409)

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

  • 1,3-Diamino-2-propanol is a versatile bidentate diamine ligand which is used in the synthesis of a variety of organometallic compounds.
  • It is a precursor to synthesize the fluorogenic dsDNA binder, N1,N3-bis(4-amidinophenyl)propane-1,3-diamine (BAPPA).
  • It can also be used as a branching unit in the synthesis of peptide dendrimers.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Synthesis and esterolytic activity of catalytic peptide dendrimers.
Lagnoux D, et al.
Chemistry?A European Journal , 10(5), 1215-1226 (2004)
Structure? activity relationships for cytotoxic ruthenium (II) arene complexes containing N, N-, N, O-, and O, O-chelating ligands.
Habtemariam A, et al.
Journal of Medicinal Chemistry, 49(23), 6858-6868 (2006)
Syntheses, structures, and electrochemical properties of inclusion compounds of cucurbit [8] uril with cobalt (III) and nickel (II) complexes.
Mitkina T V, et al.
Inorganic Chemistry, 47(15), 6748-6755 (2008)
Bis-4-aminobenzamidines: versatile, fluorogenic A/T-selective dsDNA binders.
Vazquez O, et al.
Organic Letters, 12(2), 216-219 (2009)
M Mach et al.
The Biochemical journal, 202(1), 153-162 (1982-01-15)
Inhibitors of polyamine synthesis (alpha-methylornithine and 1,3-diaminopropan-2-ol) were used to study the relationship between polyamine synthesis and specific methylations of tRNA in Dictyostelium discoideum during vegetative growth. Polyamine concentrations were found to be 10 mM for putrescine, 1.6 mM for
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service