Skip to Content
Merck
CN
All Photos(1)

Documents

01887

Supelco

3-Amino-1-propanol

analytical standard

Sign Into View Organizational & Contract Pricing
All Photos(1)
Synonym(s):
3-Aminopropyl alcohol
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:
41116107
PubChem Substance ID:
329747368
NACRES:
NA.24

grade

analytical standard

Quality Level

100

vapor density

2.59 (vs air)

vapor pressure

2.1 mmHg ( 20 °C)

Assay

≥99.5% (GC)

autoignition temp.

770 °F

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.4598 (lit.)
n20/D 1.461

bp

184-187 °C (lit.)

mp

10-12 °C (lit.)

density

0.982 g/mL at 20 °C (lit.)

application(s)

environmental

format

neat

SMILES string

NCCCO

InChI

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

InChI key

WUGQZFFCHPXWKQ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

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

Recommended products

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302,H314

Hazard Classifications

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

WGK

WGK 1

Flash Point(F)

212.0 °F

Flash Point(C)

100 °C

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

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
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
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
Adel A A Emara et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 68(3), 592-604 (2007-02-27)
The bifunctional carbonyl compound; 4,6-diacetylresorcinol (DAR) serves as precursor for the formation of different Schiff base ligands, which are either di- or tetra-basic with two symmetrical sets of either O2N or N2O tridentate chelating sites. The condensation of 4,6-diacetylresorcinol with
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