Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

136964

Sigma-Aldrich

N-Isopropylbenzylamine

97%

Synonym(s):

N-Benzylisopropylamine

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

About This Item

Linear Formula:
C6H5CH2NHCH(CH3)2
CAS Number:
102-97-6
Molecular Weight:
149.23
Beilstein:
2638437
EC Number:
203-067-6
MDL number:
MFCD00008863
UNSPSC Code:
12352100
PubChem Substance ID:
24848304
NACRES:
NA.22

Assay

97%

form

liquid

refractive index

n20/D 1.502 (lit.)

bp

200 °C (lit.)

density

0.892 g/mL at 25 °C (lit.)

SMILES string

CC(C)NCc1ccccc1

InChI

1S/C10H15N/c1-9(2)11-8-10-6-4-3-5-7-10/h3-7,9,11H,8H2,1-2H3

InChI key

LYBKPDDZTNUNNM-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

N-Isopropylbenzylamine forms amine adducts with magnesocene at ambient temperature in toluene.

Application

N-Isopropylbenzylamine was used as ligand in the preparation and characterization of bis(cyclopentadienyl)magnesium. It was also used in the synthesis of N-benzylideneisopropylamine-N-oxide.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

161.6 °F - closed cup

Flash Point(C)

72 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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

Aibing Xia et al.
Journal of the American Chemical Society, 124(38), 11264-11265 (2002-09-19)
Magnesocene adducts of alkylamines were prepared and characterized. Treatment of 3-amino-2,4-dimethylpentane, isopropylamine, tert-butylamine, benzylamine, or N-isopropylbenzylamine with magnesocene at ambient temperature in toluene afforded the amine adducts Cp2Mg(NH2CH(CH(CH3)2)2) (91%), Cp2Mg(NH2iPr) (80%), Cp2Mg(NH2tBu) (67%), Cp2Mg(NH2CH2Ph) (80%), and Cp2Mg(NH(CH(CH3)2)(CH2C6H5)) (91%). These adducts
One-flask transformation of secondary amines to nitrones by oxidation with hydrogen peroxide mediated by triscetylpyridinium tetrakis oxodiperoxotungsto-phosphate (PCWP). Some mechanistic considerations.
Ballistreri FP, et al.
Tetrahedron, 48(40), 8677-8684 (1992)
O Brüggemann
Biomolecular engineering, 18(1), 1-7 (2001-06-29)
Molecular imprinting is a way of creating polymers bearing artificial receptors. It allows the fabrication of highly selective plastics by polymerizing monomers in the presence of a template. This technique primarily had been developed for the generation of biomimetic materials

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