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About This Item
Linear Formula:
HO(CH2)3NH2
CAS Number:
Molecular Weight:
75.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-864-4
Beilstein/REAXYS Number:
741855
MDL number:
Assay:
99%
Form:
liquid
vapor density
2.59 (vs air)
Quality Level
vapor pressure
2.1 mmHg ( 20 °C)
assay
99%
form
liquid
autoignition temp.
770 °F
refractive index
n20/D 1.4598 (lit.)
bp
184-187 °C (lit.)
mp
10-12 °C (lit.)
density
0.982 g/mL at 20 °C (lit.)
SMILES string
NCCCO
InChI
1S/C3H9NO/c4-2-1-3-5/h5H,1-4H2
InChI key
WUGQZFFCHPXWKQ-UHFFFAOYSA-N
General description
3-Amino-1-propanol is a linear primary alkanolamine.
Application
3-Amino-1-propanol is often used as a molecular linker. Generally, it can be used:
- In the preparation of polyurethanes and poly(propyl ether imine) dendrimers.
- As a key starting material in the total synthesis of (−)-ephedradine A (orantine), (−)-and (+)-tedanalactam.
- As a precursor to synthesize a variety of medicinally important compounds by selective O- or N-arylation and amidation of 3-amino-1-propanol.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
212.0 °F - Pensky-Martens closed cup
flash_point_c
100 °C - Pensky-Martens closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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N-heterocyclic carbene-catalyzed amidation of unactivated esters with amino alcohols.
Movassaghi M and Schmidt M A
Organic Letters, 7(12), 2453-2456 (2005)
N-versus O-arylation of aminoalcohols: Orthogonal selectivity in copper-based catalysts.
Shafir A, et al.
Journal of the American Chemical Society, 129(12), 3490-3491 (2007)
A paradigmatic change: linking fullerenes to electron acceptors.
Feng L, et al.
Journal of the American Chemical Society, 134(29), 12190-12197 (2012)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| A76400-100G | 04061833385883 |
| A76400-500G | 04061833385906 |

