Skip to Content
Merck
All Photos(2)

Key Documents

D214752

Sigma-Aldrich

Dipropylamine

99%

Synonym(s):

Di-n-propylamine, Dipropanamine, Dipropylamine (8CI), N,N-Di(n-propyl)amine, N,N-Dipropylamine, N-Propyl-1-propanamine, n-Dipropylamine

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(CH3CH2CH2)2NH
CAS Number:
Molecular Weight:
101.19
Beilstein:
505974
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

form

liquid

refractive index

n20/D 1.4049 (lit.)

bp

105-110 °C (lit.)

density

0.738 g/mL at 25 °C (lit.)

SMILES string

CCCNCCC

InChI

1S/C6H15N/c1-3-5-7-6-4-2/h7H,3-6H2,1-2H3

InChI key

WEHWNAOGRSTTBQ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Dipropylamine is an aliphatic amine, commonly used as a deprotection reagent for fluorenylmethyloxycarbonyl (Fmoc) groups. Its nucleophilic properties, due to the lone pair of electrons on the nitrogen atom, allow it to effectively participate in nucleophilic substitution reactions.

Application

  • Separation of hydrocarbons: Nitrogen-containing switchable solvents, including dipropylamine, are used for the separation of hydrocarbons and their derivatives, showcasing the compound′s versatility in solvent applications (Liu et al., 2020).
  • Microextraction techniques: Dipropylamine-based dispersive micro-solid phase extraction combined with switchable hydrophilicity solvent is employed for enriching non-steroidal anti-inflammatory drugs from environmental water samples, demonstrating its utility in complex sample preparation (Di et al., 2020).
  • Homogeneous liquid-liquid microextraction: A new pH assisted homogeneous liquid-liquid microextraction method utilizing dipropylamine as a solvent with switchable hydrophilicity was developed for the GC-MS determination of methamphetamine, highlighting its effectiveness in analytical chemistry applications (Shahvandi et al., 2018).
  • Removal of contaminants: Research demonstrated the use of zeolite and powdered activated carbon in conjunction with dipropylamine for the simultaneous removal of ammonia and N-nitrosamine precursors from high ammonia water, underscoring its environmental application (Xue et al., 2018).
  • Nanosized synthesis: Dipropylamine was used in a co-templating synthesis approach for the production of high-yield nanosized (Si)AlPO-41 using ethanol polarity equalization, illustrating its role in materials science (Majano et al., 2015).

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

44.6 °F - closed cup

Flash Point(C)

7 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

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.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Fumiki Takahashi et al.
Talanta, 188, 651-657 (2018-07-22)
A simple colorimetric method using gold nanoparticles (AuNPs) was developed as an efficient strategy for specific and sensitive detection of insecticides that are analogs of nereistoxin (NRT). The AuNPs were synthesized by a surfactant-free sonochemical reaction with ultrasonication at 430 kHz.
Siamak Kiani Shahvandi et al.
Talanta, 184, 103-108 (2018-04-21)
In this study, a new method based on homogeneous liquid-phase microextraction was developed for the determination of methamphetamine (MA) in urine samples. Dipropylamine (DPA), as a solvent with switchable hydrophilicity, was used as the extraction solvent and can be miscible/immiscible
Dipropylamine for 9-fluorenylmethyloxycarbonyl (Fmoc) deprotection with reduced aspartimide formation in solid-phase peptide synthesis
Personne et al.
ACS Omega, 8, 5050-5056 (2023)
Alexa S Kuenstler et al.
Advanced materials (Deerfield Beach, Fla.), 31(24), e1901216-e1901216 (2019-04-24)
While most photomechanical materials developed to date have relied on free-space illumination to drive actuation, this strategy fails when direct line-of-site access is precluded. In this study, waveguided light is harnessed by liquid crystal elastomer (LCE) nanocomposites to drive actuation.
Palladium-catalysed selective oxidative amination of olefins with Lewis basic amines
Jin et al.
Nature Chemistry, 14, 1118-1125 (2022)

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