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D23602

1,3-Diaminopropane

Name: 1,3-Diaminopropane
Brand: ALDRICH

≥99%

Sinónimos:

1,3-Propanediamine, DAP, TMEDA, Trimethylenediamine

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Fórmula lineal:

NH₂(CH₂)₃NH₂

Número CAS:

109-76-2

Peso molecular:

74.12

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24893678

EC Number:

203-702-7

Beilstein/REAXYS Number:

605277

MDL number:

MFCD00008228

Assay:

≥99%

Form:

liquid

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Propiedades

vapor pressure

<8 mmHg ( 20 °C)

Quality Level

200

assay

≥99%

form

liquid

autoignition temp.

662 °F

expl. lim.

15.2 %

refractive index

n20/D 1.458 (lit.)

bp

140 °C (lit.)

mp

−12 °C (lit.)

density

0.888 g/mL at 25 °C (lit.)

SMILES string

NCCCN

InChI

1S/C3H10N2/c4-2-1-3-5/h1-5H2

InChI key

XFNJVJPLKCPIBV-UHFFFAOYSA-N

Gene Information

rat ... Grin2a(24409)

Descripción

General description

1,3-Diaminopropane is used as a monomer for the synthesis of polyamides and aliphatic polyimides. It is also utilized for the modification of carbon nanotubes and serves as a cross-linking agent in the preparation of hydrogels.

Application

Synthesis and Characterization of Bulky 1,3-Diamidopropane Complexes of Group 2 Metals (Be ‒ Sr).: Demonstrates the utility of 1,3-diaminopropane in the synthesis of metal complexes, enhancing the diversity and functionality of inorganic compounds, crucial for high purity chemical reagent applications (Jones et al., 2024).
Rational engineering of homospermidine synthase for enhanced catalytic efficiency toward spermidine synthesis.: Explores the use of 1,3-diaminopropane as a precursor in enzymatic synthesis, optimizing biotechnological processes for polyamine production, pertinent to drug delivery system research (Liu et al., 2024).
Hydroxyl-terminated dendrimers with sulfonimide linkers as binders for metals of industrial significance.: Investigates 1,3-diaminopropane′s efficacy in the synthesis of dendrimers, crucial for industrial applications in binding metals, thereby impacting industrial chemical manufacturing R&D (Abu Sbeih et al., 2024).