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Merck
CN

136964

N-Isopropylbenzylamine

97%

Synonym(s):

N-Benzylisopropylamine

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About This Item

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

Key Documents

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InChI key

LYBKPDDZTNUNNM-UHFFFAOYSA-N

InChI

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

SMILES string

CC(C)NCc1ccccc1

assay

97%

form

liquid

drug control

Új pszichoaktív anyag / New psychoactive substance (Hungary), 78/2022. (XII. 28.) BM rendelet

Quality Level

100

bp

200 °C (lit.)

density

0.892 g/mL at 25 °C (lit.)

functional group

amine, phenyl

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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.

target_organs

Respiratory system

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

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

Storage Class

8A - Combustible corrosive hazardous materials

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Certificates of Analysis (COA)

Lot/Batch Number
WXBF4776V
BCCG6031
BCCD6714
BCCC0192
BCBW2348

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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

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