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Sigma-Aldrich

3-Amino-1-propanol

≥99%

Synonym(e):

3-Amino-propylalkohol

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About This Item

Lineare Formel:
HO(CH2)3NH2
CAS-Nummer:
156-87-6
Molekulargewicht:
75.11
Beilstein:
741855
EG-Nummer:
205-864-4
MDL-Nummer:
MFCD00008223
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24854393
NACRES:
NA.22

Dampfdichte

2.59 (vs air)

Dampfdruck

2.1 mmHg ( 20 °C)

Assay

≥99%

Form

liquid

Selbstzündungstemp.

770 °F

Brechungsindex

n20/D 1.4598 (lit.)

bp

184-187 °C (lit.)

mp (Schmelzpunkt)

10-12 °C (lit.)

Löslichkeit

water: soluble

Dichte

0.982 g/mL at 20 °C (lit.)

SMILES String

NCCCO

InChI

1S/C3H9NO/c4-2-1-3-5/h5H,1-4H2

InChIKey

WUGQZFFCHPXWKQ-UHFFFAOYSA-N

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Allgemeine Beschreibung

3-Amino-1-propanol is a linear primary alkanolamine.

Anwendung

3-Amino-1-propanol was used in the synthesis of di-tert-butyl aminopropanol derivative.

Piktogramme

CorrosionExclamation mark
GHS05,GHS07

Signalwort

Danger

H-Sätze

H302,H314

Gefahreneinstufungen

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

Lagerklassenschlüssel

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Flammpunkt (°F)

212.0 °F - Pensky-Martens closed cup

Flammpunkt (°C)

100 °C - Pensky-Martens closed cup

Persönliche Schutzausrüstung

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Rahul S Kalhapure et al.
International journal of pharmaceutics, 425(1-2), 9-18 (2012-01-24)
There is increasing demand for lipids owing to their use in formulating lipid based drug delivery systems of poorly soluble drugs. The present work discusses the synthesis, characterization of oleic acid based heterolipid and its use as oil in the
P Kovács et al.
Comparative biochemistry and physiology. Part C, Pharmacology, toxicology & endocrinology, 118(1), 83-87 (1997-11-20)
3-Amino-1-propanol (AP), a substance replacing ethanolamine in phosphatidylethanolamine (PE) significantly reduced 32P incorporation to phosphatidylinositol (PI) and glycosyl-phosphatidylinositol (GPI) in the unicellular organism Tetrahymena pyriformis. At 10 mM, AP completely inhibited the incorporation of 32P into PI. 3H-arachidonate incorporation into
Thatavarathy Rama Krishna et al.
The Journal of organic chemistry, 68(25), 9694-9704 (2003-12-06)
In this paper, we report the synthesis of several poly(propyl ether imine) dendrons and dendrimers. These dendrons and dendrimers were constructed by involving an ether as the linker component and an imine as the branching component. The divergent syntheses of
C Cacela et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 56(6), 1051-1064 (2000-06-14)
Results obtained for the isolated and liquid 3-amino-1-propanol by a concerted molecular orbital and vibrational spectroscopic approach are reported. The relative energies and both structural and vibrational data of the different conformers of the studied compound were calculated using the
Manuela L Kim et al.
Talanta, 77(3), 1068-1074 (2008-12-10)
An hybrid mesoporous material synthesised in our laboratories for solid phase extraction (SPE) in flow through systems has been used for analytical purposes. The solid was obtained from mesoporous silica MCM-41 functionalized with 3-aminopropyltriethoxy silane by Sol-Gel methodology. In order
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