Skip to Content
MilliporeSigma
All Photos(1)

Documents

436860

Sigma-Aldrich

N,N-Diisopropylaniline

97%

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

About This Item

Linear Formula:
C6H5N[CH(CH3)2]2
CAS Number:
4107-98-6
Molecular Weight:
177.29
MDL number:
MFCD00048277
UNSPSC Code:
12352100
PubChem Substance ID:
24867307
NACRES:
NA.22

Quality Level

100

assay

97%

form

liquid

refractive index

n20/D 1.519 (lit.)

bp

95-96 °C/11 mmHg (lit.)

density

0.91 g/mL at 25 °C (lit.)

SMILES string

CC(C)N(C(C)C)c1ccccc1

InChI

1S/C12H19N/c1-10(2)13(11(3)4)12-8-6-5-7-9-12/h5-11H,1-4H3

InChI key

OVSARSKQWCLSJT-UHFFFAOYSA-N

Related Categories

General description

N,N-Diisopropylaniline is an N,N-dialkylaniline. Its borane adducts have been prepared and reported as hydroborating agents. Thermal dissociation of the borane-N,N-diisopropylaniline adduct has been reported to afford gaseous diborane. N,N-Diisopropylaniline is a diisoproplyamino derivative that can be prepared by reacting bromobenzene with diisopropylamine.

Application

N,N-Diisopropylaniline was used for the synthesis of 4-diisopropylamino benzonitrile. It may be used for the synthesis of 6-(4-bromophenyl)-3-methoxy-5-methyl-8-oxabicyclo[3.2.1]octa-3,6-dien-2-one and N,N,N′,N′-tetraisopropylbenzidine.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

183.2 °F - closed cup

flash_point_c

84 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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 1

1 of 1

≥99.5%

Sigma-Aldrich

471224

Diisopropylamine

Yvonne D Williams et al.
The Journal of organic chemistry, 78(23), 11707-11713 (2013-11-01)
Methoxytropolones are useful scaffolds for therapeutic development because of their known biological activity and established value in the synthesis of α-hydroxytropolones. Upon treatment with triflic acid, a series of 3-methoxy-8-oxabicyclo[3.2.1]octa-3,6-dien-2-ones rearrange rapidly and cleanly to form methoxytropolones. Interestingly, bicycles that
N-alkylation of hindered secondary aromatic amines with 2-iodobutane.
Katritzky AR, et al.
ORL; Journal for Oto-Rhino-Laryngology and Its Related Specialties, 23(4), 399-402 (1991)
Synthesis of N,N,N',N'-tetraalkylbenzidines through oxidative coupling of N,N-dialkylarylamines induced by SbCl5.
Vitale P, et al.
ARKIVOC (Gainesville, FL, United States), 3, 36-48 (2013)
Dual fluorescence and fast intramolecular charge transfer with 4-(diisopropylamino) benzonitrile in alkane solvents.
Demeter A, et al.
Chemical Physics Letters, 323(3), 351-360 (2000)
Brown et al.
The Journal of organic chemistry, 65(15), 4655-4661 (2000-08-26)
Several N,N-diethyl-tert-alkylamines, such as N,N-diethyl-2-methyl-2-butylamine (1, t-PentNEt2), N,N-diethyl-2,3-dimethyl-2-butylamine (2, t-HexNEt2), N,N-diethyl-2,3,3-trimethyl-2-butylamine (3, t-HeptNEt2), and N,N-diethyl-1,1,3,3-tetramethylbutylamine (4, t-OctNEt2) with varying steric bulk around nitrogen (by changing the tert-alkyl group) have been prepared and examined as borane carriers. The complexing ability of

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