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Merck
CN

471224

Diisopropylamine

≥99.5%, liquid

Synonym(s):

DIPA

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About This Item

Linear Formula:
(CH3)2CHNHCH(CH3)2
CAS Number:
108-18-9
Molecular Weight:
101.19
MDL number:
MFCD00008862
NACRES:
NA.21
PubChem Substance ID:
57650897
UNSPSC Code:
12352100
EC Number:
203-558-5
Beilstein/REAXYS Number:
605284
Assay:
≥99.5%
Bp:
84 °C (lit.)
Vapor pressure:
50 mmHg ( 20 °C)

Key Documents

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Product Name

Diisopropylamine, ≥99.5%

InChI key

UAOMVDZJSHZZME-UHFFFAOYSA-N

InChI

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

SMILES string

CC(C)NC(C)C

vapor density

3.5 (vs air)

vapor pressure

50 mmHg ( 20 °C)

assay

≥99.5%

form

liquid

autoignition temp.

599 °F

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.)

functional group

amine

Quality Level

200

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Application

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

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 by static-bomb calorimetry.

signalword

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

3 - Flammable liquids

wgk

WGK 2

flash_point_f

7.8 °F - closed cup

flash_point_c

-13.45 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
SHBS9314
SHBS9117
SDBB3412
SHBS6118
SHBS6113

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Iron-Catalyzed Direct Synthesis of Amides from Methylarenes.
Kotha SS, et al.
Advanced Synthesis & Catalysis, 357(7), 1437-1445 (2015)
Research on Synthesis and Corrosion Inhibitory Performance of Diisopropylamine Methyl Urea.
Zhou FR and Zhang H.
Applied Mechanics and Materials, 713, 2839-2842 (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)
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)
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