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Key Documents

117498

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:
Molecular Weight:
74.12
Beilstein:
605274
EC Number:
MDL number:
UNSPSC Code:
12352100
eCl@ss:
39030209
PubChem Substance ID:
NACRES:
NA.22

vapor density

2.6 (vs air)

Quality Level

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.)

functional group

amine

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

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Growth and Microstructure of Nanoscale Amorphous Carbon Nitride Films Deposited by Electron Beam Irradiation of 1, 2-Diaminopropane.
Wnuk JD, et al.
The Journal of Physical Chemistry C, 113(28), 12345-12354 (2009)
Chi Chen et al.
Molecules (Basel, Switzerland), 25(18) (2020-09-16)
Utilizing liquid rubber to toughen epoxy resin is one of the most mature and promising methods. However, the dielectric relaxation characteristics of the epoxy/liquid rubber composites have not been studied systematically, while the relaxation behaviours are a critical factor for
Ekaterina Yu Bezsudnova et al.
Applied microbiology and biotechnology, 102(22), 9621-9633 (2018-09-05)
Substrate and reaction promiscuity is a remarkable property of some enzymes and facilitates the adaptation to new metabolic demands in the evolutionary process. Substrate promiscuity is also a basis for protein engineering for biocatalysis. However, molecular principles of enzyme promiscuity
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)
Cage peroxides having planar bridgehead nitrogen atoms.
Edward JT, et al.
Canadian Journal of Chemistry, 77(5-6), 1057-1065 (1999)

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