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A76400

3-Amino-1-propanol

Name: 3-Amino-1-propanol
Brand: ALDRICH

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:

24891263

NACRES:

NA.22

vapor density

2.59 (vs air)

Quality Level

200

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

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Related Categories

Organic Building Blocks

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.

Pictograms

GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302,H314

Precautionary Statements

P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363

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’.

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5 `-Tethered stilbene derivatives as fidelity-and affinity-enhancing modulators of DNA duplex stability.

Dogan Z, et al.

Journal of the American Chemical Society, 126(15), 4762-4763 (2004)

Stereocontrolled total synthesis of (?)-ephedradine A (orantine).

Kurosawa W Kan T and Fukuyama T

Journal of the American Chemical Society, 125(27), 8112-8113 (2003)

A paradigmatic change: linking fullerenes to electron acceptors.

Feng L, et al.

Journal of the American Chemical Society, 134(29), 12190-12197 (2012)

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)

N-heterocyclic carbene-catalyzed amidation of unactivated esters with amino alcohols.

Movassaghi M and Schmidt M A

Organic Letters, 7(12), 2453-2456 (2005)

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