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Sigma-Aldrich

1,2-Diaminopropane

99%

Synonym(s):

1,2-Propanediamine, Propylenediamine

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About This Item

Linear Formula:
CH3CH(NH2)CH2NH2
CAS Number:
78-90-0
Molecular Weight:
74.12
Beilstein:
605274
EC Number:
201-155-9
MDL number:
MFCD00008089
UNSPSC Code:
12352100
eCl@ss:
39030209
PubChem Substance ID:
24847332
NACRES:
NA.22

vapor density

2.6 (vs air)

vapor pressure

14 mmHg ( 20 °C)

Assay

99%

autoignition temp.

680 °F

expl. lim.

11.1 %

refractive index

n20/D 1.446 (lit.)

bp

119-120 °C (lit.)

solubility

H2O: very soluble

density

0.87 g/mL at 25 °C (lit.)

SMILES string

CC(N)CN

InChI

1S/C3H10N2/c1-3(5)2-4/h3H,2,4-5H2,1H3

InChI key

AOHJOMMDDJHIJH-UHFFFAOYSA-N

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General description

1,2-Diaminopropane undergoes condensation with salicylaldehyde and its derivatives to form Schiff base. It reacts with formaldehyde and hydrogen peroxide in aqueous acidic solution to give cage peroxide, 1,6-diaza-3,4,8,9-tetraoxa-11-methylbicyclo[4.4.2]dodecane.

Application

1,2-Diaminopropane was used as model precursor in the electron induced deposition of amorphous carbon nitride films.

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Flam. Liq. 3 - Resp. Sens. 1 - Skin Corr. 1A - Skin Sens. 1

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

93.2 °F - closed cup

Flash Point(C)

34 °C - closed cup

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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Cage peroxides having planar bridgehead nitrogen atoms.
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Canadian Journal of Chemistry, 77(5-6), 1057-1065 (1999)
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In this work, copper pyrovanadate (Cu3V2O7(OH)2(H2O)2) nanoparticles have been synthesized by a simple and rapid chemical precipitation method. Different copper-organic complexes were used to control the size and morphology of products. The morphology and structure of the as-synthesized products were
Mononuclear and dinuclear chiral vanadium (V) complexes with tridentate Schiff bases derived from< i> R</i>(-)-1, 2-diaminopropane: Synthesis, structure, characterization and catalytic properties.
Romanowski G and Wera M.
Polyhedron, 29(13), 2747-2754 (2010)
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