Skip to Content
Merck
CN

01887

3-Amino-1-propanol

analytical standard

Synonym(s):

3-Aminopropyl alcohol

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
HO(CH2)3NH2
CAS Number:
156-87-6
Molecular Weight:
75.11
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329747368
EC Number:
205-864-4
Beilstein/REAXYS Number:
741855
MDL number:
MFCD00008223

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

3-Amino-1-propanol, analytical standard

InChI key

WUGQZFFCHPXWKQ-UHFFFAOYSA-N

InChI

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

SMILES string

NCCCO

grade

analytical standard

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

Quality Level

100

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

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

Other Notes

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

signalword

Danger

hcodes

H302,H314

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCN2386
BCCM8448
BCCM3912
BCCL2721
BCCJ9095

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

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
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
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
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