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239844

Sigma-Aldrich

3-Amino-1-propanol

≥99%

Synonym(s):

3-Aminopropyl alcohol

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About This Item

Linear Formula:
HO(CH2)3NH2
CAS Number:
156-87-6
Molecular Weight:
75.11
Beilstein:
741855
EC Number:
205-864-4
MDL number:
MFCD00008223
UNSPSC Code:
12352100
PubChem Substance ID:
24854393
NACRES:
NA.22

vapor density

2.59 (vs air)

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.)

solubility

water: soluble

density

0.982 g/mL at 20 °C (lit.)

functional group

amine
hydroxyl

SMILES string

NCCCO

InChI

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

InChI key

WUGQZFFCHPXWKQ-UHFFFAOYSA-N

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General description

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

Application

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

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302,H314

Hazard Classifications

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

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK8753
BCCF2450
BCBV7647
BCBQ5720V
MKBL6406V

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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
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
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
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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