Skip to Content
Merck
All Photos(1)

Documents

386464

Sigma-Aldrich

Diisopropylamine

purified by redistillation, 99.95%

Synonym(s):

DIPA

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
(CH3)2CHNHCH(CH3)2
CAS Number:
108-18-9
Molecular Weight:
101.19
Beilstein:
605284
EC Number:
203-558-5
MDL number:
MFCD00008862
UNSPSC Code:
12352100
PubChem Substance ID:
57649857
NACRES:
NA.21

vapor density

3.5 (vs air)

Quality Level

200

vapor pressure

50 mmHg ( 20 °C)

Assay

99.95%

form

liquid

autoignition temp.

599 °F

purified by

redistillation

expl. lim.

8.5 %

refractive index

n20/D 1.392 (lit.)

bp

84 °C (lit.)

mp

−61 °C (lit.)

solubility

water: soluble 110 g/L at 25 °C

density

0.722 g/mL at 25 °C (lit.)

SMILES string

CC(C)NC(C)C

InChI

1S/C6H15N/c1-5(2)7-6(3)4/h5-7H,1-4H3

InChI key

UAOMVDZJSHZZME-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Diisopropylamine (DIPA) is an aliphatic secondary amine widely used as an organic base in organic synthesis. Its standard molar enthalpy of formation and combustion has been measured.

Application

Diisopropylamine may be used in the following processes:
  • Synthesis of diisopropylamine methyl urea (DMU).
  • Synthesis of N,N-diisopropyl quinoline-2-carboxamide.
  • Synthesis of 3-N-sulfonylamidine coumarins.
  • Synthesis of N-chloroamine, an intermediate to generate amides.

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

7.8 °F - closed cup

Flash Point(C)

-13.45 °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

Sorry, we don't have COAs for this product available online at this time.

If you need assistance, please contact Customer Support.

Already Own This Product?

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

Visit the Document Library

Customers Also Viewed

Slide 1 of 4

1 of 4

Tetrahydrofuran anhydrous, ≥99.9%, inhibitor-free

Sigma-Aldrich

401757

Tetrahydrofuran

Dipropylamine 99%

Sigma-Aldrich

D214752

Dipropylamine

Lithium diisopropylamide solution 2.0 M in THF/heptane/ethylbenzene

Sigma-Aldrich

361798

Lithium diisopropylamide solution

Dicyclohexylamine 99%

Sigma-Aldrich

185841

Dicyclohexylamine

Research on Synthesis and Corrosion Inhibitory Performance of Diisopropylamine Methyl Urea.
Zhou FR and Zhang H.
Applied Mechanics and Materials, 713, 2839-2842 (2015)
Iron-Catalyzed Direct Synthesis of Amides from Methylarenes.
Kotha SS, et al.
Advanced Synthesis & Catalysis, 357(7), 1437-1445 (2015)
Microwave-Assisted Copper-Catalyzed Four Component Tandem Synthesis of 3-N-Sulfonylamidine Coumarins.
Murugavel G and Punniyamurthy T.
The Journal of Organic Chemistry, 80 (12), 6291-6299 (2015)
A simple and novel amide ligand based on quinoline derivative used for palladium-catalyzed Suzuki coupling reaction.
Liu H, et al.
Journal of Organometallic Chemistry, 794, 27-32 (2015)
Enthalpies of combustion of di-n-propylamine, diisopropylamine, diisobutylamine, and di-sec-butylamine.
Ribeiro da Silva MAV, et al.
The Journal of Chemical Thermodynamics, 29(9), 1025-1030 (1997)
View All Related Papers

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